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Review ARTICLE

Front. Microbiol., 26 July 2011 | http://dx.doi.org/10.3389/fmicb.2011.00158

Horizontal gene exchange in environmental microbiota

  • Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, UK

Horizontal gene transfer (HGT) plays an important role in the evolution of life on the Earth. This view is supported by numerous occasions of HGT that are recorded in the genomes of all three domains of living organisms. HGT-mediated rapid evolution is especially noticeable among the Bacteria, which demonstrate formidable adaptability in the face of recent environmental changes imposed by human activities, such as the use of antibiotics, industrial contamination, and intensive agriculture. At the heart of the HGT-driven bacterial evolution and adaptation are highly sophisticated natural genetic engineering tools in the form of a variety of mobile genetic elements (MGEs). The main aim of this review is to give a brief account of the occurrence and diversity of MGEs in natural ecosystems and of the environmental factors that may affect MGE-mediated HGT.

Historical Overview

Historically, the first portrayal of horizontal gene transfer (HGT) was made by Griffith (1928), who described the transformation of rough, avirulent live pneumococci into smooth, virulent pneumococci by the addition of factors from dead, smooth, and virulent pneumococci. The term “transformation” at the time had no genetic component in the sense it is perceived today; it simply referred to the “transformation” of pneumococcal phenotype. The transforming factor, unknown until 1944, appeared to be a desoxyribonucleic acid (DNA), thus bringing a genetic context to the original description of transformation (Avery et al., 1944). The discovery of the first mobile genetic elements (MGEs) in bacteria, phages (reviewed in Duckworth, 1976), and plasmids (Lederberg, 1952), has laid the foundation for the development of contemporary molecular biology, which has contributed enormously to many fields of biology, medicine, and biotechnology. This era began in the 1930s and 1950s, when the three main mechanisms of HGT – transduction, transformation, and conjugation – were discovered. The understanding of the fundamentals of the structure-and-function of MGEs allowed us to adapt these mechanisms to serve our needs, in the form of genetic engineering technology, in a number of applications in science, biotechnology, and everyday life.

Another factor that attracted increased attention to MGEs and HGT in bacteria is the problem of antibiotic resistance in pathogenic bacteria. Although the use of antibiotics has revolutionized the treatment of infectious diseases in humans and animals, the emergence of antibiotic resistant pathogens such as Staphylococcus aureus, Streptococcus and Enterococcus, Pseudomonas aeruginosa, Clostridium difficile, Salmonella and Escherichia coli, and Acinetobacter baumannii poses a grave concern. The question, therefore, is: why and how does this happen? Why does a recently introduced and efficient antibiotic, after some years of use, become essentially useless for treatment of an infection? The problem was first encountered in Japanese communities and hospitals in the 1950s when they faced Shigella dysentery outbreaks that resisted to treatment by usual antibiotics. Intensive clinical and genetic investigations performed by Japanese scientists during that period resulted in the concept of episome-mediated transfer of drug resistance in Enterobacteriaceae (Watanabe and Fukasawa, 1961; Watanabe, 1963). This, along with the following period of antibiotic resistance research, was an enclave within the boundaries of clinical microbiology and bacterial genetics, because it was thought that the antibiotic resistance problem was due to, and could be resolved within, the antibiotic treatment practices of human infectious diseases. The little interaction with other fields of microbiology was another contributing factor to the isolation. The realization that antibiotic resistance research should take a broader than the clinical microbiology approach to identify the factors ultimately leading to the acquisition of antibiotic resistance by pathogens entered the mainstream thinking substantially later. In particular, the placement of the problem within the evolutionary and ecological contexts appeared to be especially fruitful (Aminov and Mackie, 2007; Aminov, 2009, 2010). Two main conclusions emerged from this synthesis: firstly, it is the enormous diversity of antibiotic resistance genes existing in the environmental microbiota that has accumulated during billions of years of evolution; and, secondly, the realization that there are no barriers among the ecological compartments in the microbial world, and that the microbiota of different compartments may easily exchange the gene pool through the MGE-mediated HGT.

Clinical studies focused on molecular mechanisms of antibiotic resistance, genetic elements involved and epidemiology have been developing in parallel to, but not interactively with, the environmental studies of HGT. The first attempts to estimate the frequencies of HGT in natural settings were performed in the 1970s with the use of model bacteria, E. coli and Bacillus subtilis (Weinberg and Stotzky, 1972; Graham and Istock, 1978). Since then, the approach involving microcosm-based and field studies as well as a range of MGEs has resulted in a better understanding of how the environmental factors contribute to HGT in natural ecosystems (Van Elsas et al., 2000; Timms-Wilson et al., 2001). The analysis of gene exchange processes in natural settings was facilitated by the introduction of a variety of molecular ecology tools into the microcosm and field studies. These were the markers that allowed distinguishing the donor, recipient, and transformant/transconjugant/transductant populations; DNA hybridization and sequencing; PCR typing; and others (Akkermans et al., 1995; Götz et al., 1996; Smalla et al., 2000; Timms-Wilson et al., 2001). The visualization of gene transfer in situ was made possible with the use of the gfp gene (Christensen et al., 1996; Andersen et al., 1998; Dahlberg et al., 1998a). These technological advances allowed estimating the actual rates of HGT and factors affecting it in natural ecosystems.

Further substantiation for the important role played by HGT in the evolutionary process, especially among the Bacteria, surfaced during the last decade, commonly referred to as the “omics” era. The advent of high-throughput sequencing makes it possible to determine the genomic structure of many living organisms and apply the retrospective approach to HGT studies. Comparative genomic analyses revealed that, besides the core genes encoding essential cellular functions, the substantial part of bacterial genomes consists of auxiliary genes acquired by HGT (Ochman et al., 2000). The latter group of genes may confer adaptive advantages under certain growth or environmental conditions that may contain antimicrobials, xenobiotics, heavy metals, sucrose, and other compounds. These genes also confer the important characteristics allowing the colonization of new ecological niches governed by biotic factors such as the symbiotic and pathogenic relationships (Koonin et al., 2001).

The range of MGEs involved in the evolution and adaptation of bacteria through HGT is continuously updated and re-classified according to a better understanding of HGT mechanisms. It has been proposed, for example, to unify the heterogeneous classes of MGEs, such as conjugative transposons, integrative “plasmids,” genomic islands, and numerous unclassified elements into integrative and conjugative elements (ICEs; Burrus et al., 2002). The basis for this re-classification was that these elements share similar characteristics, such as the excision by site-specific recombination, transfer by conjugation, and integration by recombination between a specific site of elements and a site in the host’s genome. Thus, ICEs combine the features of other MGEs, such as bacteriophages (integration into and excision from the host chromosome but no transmission by conjugation), insertion sequences (ISs), and simple transposons (integration into and excision from the chromosome but no horizontal transfer), and conjugative and mobilizable plasmids (transferred from cell-to-cell by conjugation but replicated autonomously; Wozniak and Waldor, 2010). Another, even more radical, proposal was to bring a number of MGEs under the umbrella of genomic islands (GEIs; Juhas et al., 2009). According to this view, GEI would encompass other categories of elements, such as ICEs, integrated plasmids, non-replicative but excisable elements (non-replicating Bacteroides unit, NBU; Shoemaker et al., 2000), and even cryptic or damaged prophages.

Another interesting class of MGEs is the so-called gene transfer agent (GTA), which was initially described in Rhodobacter capsulatus (formerly Rhodopseudomonas capsulata; Yen et al., 1979) but was later found in many other bacteria (Lang and Beatty, 2007; Stanton, 2007). Although GTAs are similar to bacteriophages, they have two important differences: they function only in genomic DNA transfers between cells, and there are no negative effects associated with the gene transfer to the recipient. The representatives of another class of MGEs, named ISCRs, are known to move by a process called “rolling-circle replication.” A function of this process is the concomitant movement of adjacent DNA upstream of their transposase genes (Toleman et al., 2006). A recently discovered novel mechanism of HGT in E. coli, which was named “cell-to-cell transformation,” involves cell-derived DNA and, similar to Gram-positive bacteria, a putative promoting pheromone (Etchuuya et al., 2011). These examples suggest that there is a continuum of MGEs, partially overlapping in their structure-and-function, rather than separate and strictly defined MGE classes.

Even the concepts within the well-established areas of MGE research such as plasmid biology may require further clarifications and adjustments in the light of novel information coming from a broader sampling of microbial diversity and associated genetic mechanisms. For example, the original classification of plasmids into compatibility groups was based on the ability of plasmids to stably coexist in the same bacterium (Datta and Hedges, 1971). Molecular mechanisms underlying the incompatibility were explained basically as a stochastic phenomenon based on the bacterial host’s inability to differentiate among similar replicons thus giving rise to homoplasmid segregants as a direct consequence of random assortment during cell division (Novick, 1987). Within the frames of this concept, it is hard to explain the stable inheritance of multiple large plasmids in the Alphaproteobacteria (Pradella et al., 2010). The implementation of a phylogenomic approach to plasmid classification suggests that the Rhodobacterales harbor a set of at least 18 compatible plasmids, which can in principle stably coexist within the same cell (Petersen et al., 2009, 2011). Another concept that is presently undergoing an extensive reassessment is the role of prophages in bacterial genomes. The conventional view of prophages as time bombs that are ready to enter the lytic cycle and destroy the host is gradually shifting toward their perception as a key component in bacterial survival strategies (Paul, 2008). Indeed, the prophages may confer many beneficial properties on the host thus helping to withstand osmotic, oxidative, and acid stresses, as well as contributing to increased growth and biofilm formation (Wang et al., 2010).

While exploring the wealth of data collected by environmental genomics/metagenomics we may get a glimpse of the HGT events of the past, we also understandably wish to know the extent of HGT in the present-day ecosystems, especially in the face of pressing needs such as the acquisition of antibiotic resistance by pathogens or the potential risks associated with genetically modified organisms (GMO). Many microcosm and field experiments aimed at the estimation of HGT rates in natural ecosystems rely on model organisms with well-developed genetics. These organisms, however, have been selected as models due to their characteristics that are important for working under laboratory conditions, such as the simplicity of cultivation, tolerance to high nutrient concentration, the ease of genetic manipulation, and other characteristics that are not necessarily significant for the survival and multiplication in natural ecosystems. Laboratory strains of B. subtilis, for example, have been selected and manipulated to become highly competent, which is important for bacterial genetics studies (Anagnostopoulos and Spizizen, 1961). Many wild type strains of B. subtilis, however, are not naturally competent, and the transformation of these “undomesticated” strains is possible only by highly unnatural means such as protoplast electroporation (Romero et al., 2006). Another problem, which may be encountered when accessing HGT in natural ecosystems, is that different MGEs may potentially interact with each other. It is thus important to know the diversity of indigenous MGEs in microcosm and field studies. And finally, due to dispersion and population sizes, microorganisms can be transferred across distant environments (Hooper et al., 2008). This geographical component may substantially contribute to HGT, especially if the transferred genetic material confers the traits important for the survival and reproduction in the “donor” ecological niche. Thus, a certain degree of caution must be exercised when estimating the frequencies of HGT in natural ecosystems.

In this review, HGT is viewed mostly from an ecological and environmental regulation prospective rather than focusing on genetics and regulation at the cellular level. It consists of two parts. In the first part, the soil, aquatic, gut, and biofilm communities are discussed in respect to HGT processes in these ecosystems. In the second part, factors potentially affecting HGT in natural ecosystems are analyzed.

HGT in Natural Ecosystems

Soil

Soil ecosystems harbor an extremely broad diversity of microbiota reflecting plant type, soil type, soil management regime, and other factors (Garbeva et al., 2004). To begin with, the physical environment of soil is quite heterogeneous in terms of gaseous, liquid or solid phases (Smiles, 1988). Additional variables include abiotic factors such as temperature, pH, concentration of nutrients and oxygen and moisture content and biotic factors such as antagonistic, commensal, mutualistic, and other relationships among the soil inhabitants. Since the regulation of genetic machinery is highly responsive to the environment, these factors may indeed affect the frequencies of HGT. For example, the rate of conjugal plasmid transfer in soil varies depending on abiotic factors, such as soil moisture and temperature (Richaume et al., 1989), pH (Rochelle et al., 1989), and soil type (Richaume et al., 1992). Water movement in soil may influence the survival and transport of genetically engineered strains (Trevors et al., 1990). As for biotic factors, the presence of earthworms, protozoa, and fungi certainly affects the conjugal plasmid transfer in soil (Daane et al., 1996, 1997; Sørensen et al., 1999; Sengeløv et al., 2000). Bulk soil, however, is generally poor in nutrients, whereas the active metabolic state of bacteria required for HGT is possible in nutritional hot spots such as the rhizosphere, the phyllosphere, decaying plant and animal tissues, and manure-applied soil (Van Elsas and Bailey, 2002).

Indeed, conjugative plasmid transfers among plant phytosphere inhabitants have been detected on multiple occasions (Van Elsas et al., 1988; Lilley et al., 1994; Björklöf et al., 1995; Pukall et al., 1996; Lilley and Bailey, 1997; Kroer et al., 1998). Root growth and exudate production appeared to be the most important factors contributing to the frequency of horizontal plasmid transfer in the rhizosphere (Mølbak et al., 2007). Transfer ratios were about 10 times lower in control soil than in the pea and barley rhizospheres. For some plasmids, an exceptionally broad range of recipients in the rhizosphere was demonstrated (Musovic et al., 2006). It was shown that there was a high frequency conjugal transfer of an IncP-1 plasmid pKJK10 not only to bacteria belonging to the alpha, beta, and gamma subclasses of the Proteobacteria, but also to Arthrobacter sp., a Gram-positive member of the Actinobacteria. Compared to filter mating, the plant model (alfalfa sprouts) provided an environment substantially enhancing the transfer of plasmid- and transposon-encoded antibiotic resistance markers between lactic acid bacteria (Toomey et al., 2009).

Application of manure to soil is another hot spot contributing to the increase in local concentrations of MGEs and the frequency of HGT in this ecosystem. This practice, as it has been shown, may enhance plasmid mobilization and survival of the introduced donor strain (Götz and Smalla, 1997). If applied together with an antibiotic, the effect is synergistic and affects the transfer frequencies and composition of MGEs introduced with manure (Heuer and Smalla, 2007). Field application of piggery manure, which harbors a substantial reservoir of broad-host-range plasmids conferring multiple antibiotic resistance genes, results in the dissemination of IncN, IncW, IncP-1, and pHHV216-like plasmids into agricultural soils (Binh et al., 2008). Clinically relevant class 1 integrons are also introduced into soil via similar practices (Binh et al., 2009).

Besides contributing to the accumulation of MGEs and to the HGT increase, the application of manure to soil has other important consequences such as the generation of novel MGE diversity and dissemination of novel phenotypes (for example, resistance to recently introduced antibiotics) among bacterial populations. An example of this kind was described recently (Heuer et al., 2009) and deserves a more detailed discussion. A novel plasmid type with 36% G + C content was captured from manure-treated soil microbiota by conjugation to E. coli recipient. The core of plasmids of this type is probably the product of recombination, comprising transfer, and maintenance genes with moderate homology to plasmid pIPO2 and a replication module (rep and oriV) of other descent, correspondingly. These plasmids encode a number of antibiotic resistance genes including tet(X) (GenBank accession number FJ012881), which may confer resistance against a recently introduced third-generation tetracycline, tigecycline (Moore et al., 2005). The species of Acinetobacter are the putative hosts for these low G + C plasmids in soil ecosystem (Heuer et al., 2009), which is of concern because the closely related multidrug-resistant A. baumannii is one of the currently emerging threats in hospitals (Dijkshoorn et al., 2007). Tigecycline is currently proposed as a new treatment choice against A. baumannii (Bosó-Ribelles et al., 2008), but this bacterium already poses a significant problem, as the resistance, albeit conferred by a mechanism other than TetX, easily emerges during tigecycline therapy (Peleg et al., 2007; Damier-Piolle et al., 2008). The similarity of structural and replication features among low G + C plasmids from soil and the corresponding plasmids of clinical A. baumannii isolates, together with the stable inheritance of these plasmids in Acinetobacter spp. (Heuer et al., 2009), suggests that, once acquired, the plasmids may be easily accommodated by A. baumannii in the clinical environment. Given these plasmids carry resistance against the drug of last resort, their possible entry into clinical A. baumannii is a highly undesirable scenario. Disappointingly, there is some evidence that at least some clinically relevant resistance genes have an environmental origin (Wright, 2010) suggesting past horizontal gene exchange events between these ecological compartments. Thus, the microbiota of soil, especially of manure-fertilized soil, harbors a wide variety of MGEs enabling extensive HGT within and among microbial ecosystems.

At the same time, nutritionally poor soil ecosystems may also be involved in the HGT process. For example, a deep terrestrial subsurface, which is highly oligotrophic and extreme in terms of physical and chemical conditions, still harbors bacterial populations that carry MGEs and the genetic signatures of past gene transfer events, some of them apparently recent (Coombs and Barkay, 2004; Coombs, 2009). It is still more likely that the HGT rates under nutritionally favorable conditions are higher due to the substantial biosynthetic and energetic requirements of conjugation, DNA uptake, and lytic cycle.

Recent assessments of several types of soil revealed that lysogeny is relatively common in soil microbiota (Williamson et al., 2007, 2008; Ghosh et al., 2008). Similar to the plasmid-mediated HGT, the diversity, and dynamics of bacteriophages is also mostly confined to the nutritionally rich hot spots such as the rhizosphere. The decline in the introduced fluorescent Pseudomonas sp. population revealed the presence of large numbers of bacteriophages in the sugarbeet rhizosphere (Stephens et al., 1987). On the other hand, the growth and interaction dynamics of streptomycetes and a bacteriophage investigated under a less nutritionally rich condition of soil microcosm did not reveal such an effect of phages (Burroughs et al., 2000). No measurable impact on the host in terms of reduced growth by the phage was found under these conditions. Interestingly, the burst size of the phage was larger in soil relative to that observed in liquid culture, suggesting that in vitro transduction experiments may underestimate the impact of this particular HGT mechanism in natural ecosystems.

In the soil ecosystem, bacteriophages display local adaptation to their bacterial hosts (Vos et al., 2009). Sympatric phages are more infective than are phages from samples some distance away, suggesting that the phage-mediated HGT is highly localized in soil compartments. In model microcosm experiments, the presence of phages greatly reduced the sympatric diversity of the host bacterium but favored the allopatric host diversification (Buckling and Rainey, 2002).

The possibility of natural genetic transformation of B. subtilis and Pseudomonas stutzeri has been demonstrated in a soil/sediment model system (Lorenz et al., 1988; Lorenz and Wackernagel, 1990). These studies found significantly higher rates of transformation if transforming DNA was associated with mineral/particulate material and was thus protected against the nuclease degradation. The protective effect of DNA absorption on minerals comprising soil and sediments against DNases has been noticed on many occasions (Aardema et al., 1983; Romanowski et al., 1991; Demanèche et al., 2001; Cai et al., 2006). While some naturally competent bacteria, as in the examples above, indeed demonstrate a certain level of transformability, the occurrence of naturally transformable bacteria amongst bulk and rhizosphere soil microbiota is very low (Richter and Smalla, 2007). Various transformation assays were performed, but only transformants with a positive control, Acinetobacter baylyi BD413, a highly transformable strain that can be transformed by DNA from virtually any source, were obtained. Thus, the authors concluded that the proportion of native rhizosphere and bulk soil bacteria, which are naturally transformable, is negligibly low.

There have been (and indeed there still are) intensive debates surrounding the issue of possible risks associated with the release of GMO into the environment and, in particular, the impact of transgenic plants. The plant DNA may persist in soil for substantially long periods. In microcosm experiments modeling in situ transport of recombinant plant DNA (rDNA) from roundup ready (RR) corn and soybean by leachate water, half-lives of rDNA in leachate water ranged from 1.2 to 26.7 h, depending on the temperature (Gulden et al., 2005). The presence of transgenic DNA in soil where RR corn and soybean were cultivated can be detected by real-time PCR for up to 1 year after seeding (Lerat et al., 2007). In soil microcosm experiments, where the entry of rDNA from decomposing RR leaf biomass into soil was investigated, the corresponding DNA was detectable in soil after 30 days (Levy-Booth et al., 2008). At the present stage of our knowledge, HGT from transgenic plants to terrestrial bacteria is considered to be a rare event (Nielsen et al., 1998). A recent study with the use of an in situ visualization technology, nevertheless, demonstrated this process could be observed in real time (Pontiroli et al., 2009). The study, however, employed a highly transformable A. baylyi strain BD413, which may lead to the overestimation of natural transformation rates. The current view is that even if HGT from transgenic plants to soil microbiota takes place, it is not expected to influence prokaryotic evolution or have negative effects on human or animal health and the environment (Brigulla and Wackernagel, 2010).

Aquatic Ecosystems

More than 70% of the earth surface is covered with water, and the World Ocean is one of the principal components forming the climate and biosphere of the Earth. As the largest habit on the Earth, the World Ocean hosts a large diversity of life and is responsible for nearly the half of oxygen production. Besides, there are many freshwater ecosystems, such as lakes, rivers, and smaller water bodies.

One of the earliest accounts on the occurrence of antibiotic resistance in marine bacteria has found that this phenotype is common within this microbiota (Sizemore and Colwell, 1977). Interestingly, the resistance phenotype was more frequently encountered in bacteria from seawater samples collected offshore than for those collected near shore. Antibiotic resistance was even present in bacteria collected about 522 km offshore and at depths of 8,200 m. In 6 out of 10 bacterial isolates the presence of plasmid DNA was confirmed by ethidium bromide–cesium chloride density gradient centrifugation. In general, however, antibiotic resistance phenotype and the presence of plasmids in marine bacteria tend to correlate with the degree of pollution, especially by toxic chemical waste (Baya et al., 1986; Young, 1993). A recently applied cultivation-free approach for characterization of coastal Synechococcus metagenome relied on flow cytometry-based sorting of cells with a subsequent 454 shotgun pyrosequencing (Palenik et al., 2009). This approach allowed identifying novel plasmids that were not found in model strain genomes of this clade. Plasmids with an enormous size range are also widespread in the Roseobacter clade, the representatives of which constitute up to 25% of the total marine bacterial community and thus play a global role in this ecosystem (Brinkhoff et al., 2008). Some representatives may carry up to 12 extrachromosomal replicons suggesting a very sophisticated partition mechanism ensuring their stable inheritance (Pradella et al., 2010). In marine Vibrio the majority of plasmids are associated with pathogenic or symbiotic relationship with the host organism (Hazen et al., 2010).

With the advent of high-throughput sequencing technologies, it becomes possible to characterize the marine phage diversity without the isolation and cultivation steps, which are extremely time- and resource-consuming while the outcome is limited to a few phages that we are able to multiply and characterize under laboratory conditions. In fact, the metagenomic approach is the only way to characterize the viral diversity because there is no single gene common to all phages to serve as a phylogenetic marker (Edwards and Rohwer, 2005). Comparative marine virome analyses involving four oceanic regions demonstrated that the global diversity is very high – presumably several hundred thousands of species (Angly et al., 2006). The oceanic regions had different assemblages of marine phages suggesting strong local selective pressures enriching for certain viral types. Metagenomic characterization of viruses within aquatic microbial samples revealed a prevalence of genes encoding microbial physiological functions among viral sequences (Williamson et al., 2008). Screening of 113 marine bacterial genomes for prophages yielded 64 prophage-like elements, 21 of which strongly resembled GTAs (Paul, 2008). Hence, the viral- and GTA-mediated HGT is a common mechanism for generating microbial diversity in the marine environment thus contributing to the survival in different parts of this extensive ecological niche. Moreover, marine phages may directly contribute to the fitness of their hosts. It has been suggested, for example, that the auxiliary genes in marine phages may confer selective advantage to the host through the viral gene cassettes encoding core photosystems, I and II (Sharon et al., 2009).

Historically, the in situ HGT rates in aquatic ecosystems have been typically studied with the use of microcosms, and it is understandable that in a number of cases these models have certain limitations in reproducing the vast range of ecological niches present, for example, in the World Ocean. In most cases, the microcosms are limited to modeling the shallow costal or estuarine ecosystems, frequently without the presence of ambient macro- and micro-biota. Laboratory experiments also lack the scale of natural ecosystems and, as a consequence, may discount the role of important variables potentially affecting HGT. Another aspect, which needs to be taken into consideration, is the use of model donors and recipients that have been “preselected” under laboratory conditions to monitor HGT. The HGT results obtained with the use of model organisms, genetic constructs, and microcosms should be interpreted with a reasonable degree of precaution when extrapolating them in an attempt to describe a broader environment.

It has been shown that the presence of marine sediments in microcosms facilitates the uptake and expression of exogenous DNA by transformable marine Vibrio sp. (Stewart and Sinigalliano, 1990). It was concluded from this study that sediments were more likely niches for natural transformation than the water column in the marine environment. However, another study of natural plasmid transformation of a Vibrio strain in marine water column and sediment microcosms, in the presence of the ambient microbial community, arrived at the opposite conclusion (Paul et al., 1991). The authors explained this discrepancy by a differential experimental setup involving the presence of ambient microbiota in their experiments, while the previous work used sterile sediments. Estimation of transformation rates in estuarine environments based upon the distribution of competency and transformation frequencies in isolates and mixed populations ranged from 5 × 10-4 to 1.5 transformants per day (Frischer et al., 1994). Another aspect of natural transformation is that the structure-and-function of transforming DNA may be affected by the in situ microbiota. For instance, a broad-host-range plasmid pQSR50 that was introduced into the indigenous marine bacteria by natural transformation was subjected to the alteration of restriction profiles (Williams et al., 1997). This involved changes in methylation patterns as well as structural rearrangements of the plasmid following gene transfer, thus contributing to the generation of plasmid diversity among the in situ bacterial populations.

Conjugative plasmid transfers under simulated marine environment conditions have been demonstrated in many experiments. Transconjugants can be detected even under oligotrophic conditions and at very low population densities of donors and recipients (Goodman et al., 1993). The heterogeneity of the marine environment affects the HGT rates; the plasmid transfer frequency is higher among cells attached to the bead surfaces in the biofilm than among cells in the aqueous phase (Angles et al., 1993). The use of the in situ technology with the gfp-tagged conjugative plasmid pBF1 from Pseudomonas putida suggests that the directly determined rates of horizontal plasmid transfer in marine bacterial communities may be high, ranging from 2.3 × 10−6 to 2.2 × 10−4 transconjugants per recipient (Dahlberg et al., 1998b).

In one of the initial studies, transduction of P. aeruginosa streptomycin resistance by a generalized transducing phage, F116, was monitored in a flow-through chamber suspended in a freshwater reservoir (Morrison et al., 1978). The frequency of F116-mediated transduction ranged from 1.4 × 10−5 to 8.3 × 10−2 transductants per recipient during the 10-day incubation period. A recent investigation of phage-mediated gene transfer in freshwater environments used a more advanced technological tool to monitor these events at the single-cell level; the so-called cycling primed in situ amplification–fluorescent in situ hybridization (CPRINS–FISH; Kenzaka et al., 2010). The P1, T4, and EC10 phages mediated gene transfer from E. coli to both plaque-forming and non-plaque-forming Enterobacteriaceae strains at frequencies of 0.3–8 × 10−3 per plaque-forming unit (PFU). The rate of transfer of EC10 ranged from undetectable to 2 × 10−3 per total direct cell count when natural bacterial communities were the recipients. This suggests that transduction may involve a wide range of bacteria, not necessarily limited by close relatives, and that the phage-mediated HGT is a frequent event in freshwater environments.

Compared to the freshwater microcosm studies, the corresponding experiments imitating the marine environment yielded lower frequencies of plasmid transduction in the mixed bacterial communities; the values were in the range from 1.58 × 10−8 to 3.7 × 10−8 transductants/PFU (Jiang and Paul, 1998). This is not to say that the overall HGT rates in marine ecosystems are low. Other MGEs residing in marine microbiota may generate an extraordinarily extensive gene flow – one of the highest ever detected. A recent study demonstrated extremely high rates of HGT in marine ecosystems that are mediated by GTAs (McDaniel et al., 2010). The frequencies detected are by many orders of magnitude higher than those of transformation or transduction, with as high as 47% of the culturable marine microbiota being confirmed as gene recipients. Given the wide presence of GTAs in phylogenetically and ecologically diverse bacteria (Stanton, 2007), GTA-mediated HGT may be more common in other natural ecosystems and may generate more extensive gene exchange than previously anticipated.

Comparative genomics and transcriptomics of marine bacteria are consistent with the high rates of HGT in these ecosystems. The co-occurring Shewanella baltica isolates from similar depths exchanged a larger fraction of their core and auxiliary genome compared with the isolates from more different depths (Caro-Quintero et al., 2011). These HGT events took place in the very recent past reflecting the rapid adaptation to environmental settings through gene acquisition. Genomic evolution for a cold marine lifestyle and in situ explosive biodegradation in Shewanella spp. also involved an extensive gene acquisition from deep-sea bacteria (Zhao et al., 2010).

Gut

The frequencies of HGT by conjugation are usually estimated using standard mating techniques, in liquid culture or on the surface of solidified media or filters. The microcosm and field experiments that are better estimates of HGT in the environment usually deal with lower population densities, lower nutrient availability, and generally lower temperatures. The in vivo conditions, however, are substantially different, especially in the intestine, where the enormously dense and diverse microbiota performs a number of functions important for the host organism. These functions include the prevention of colonization by pathogens, degradation of dietary (polysaccharides) and in situ-produced (mucin) compounds, production of nutrients (short chain fatty acids and vitamins), shaping and maintenance of normal mucosal immunity, and contribution to intestinal epithelial homeostasis. The commensal microbiota is under constant surveillance by the innate (antimicrobial peptides) and adaptive (immunoglobulins) immunity. The effect of innate immunity breaches on gut microbiota can be seen in genetically susceptible hosts, the commensal microbiota of which is formidably restructured compared to normal subjects (Khachatryan et al., 2008).

The discovery of ICEs among the representatives of Bacteroidetes, the major bacterial phylum in the mammalian gut, brought the notion that gene transfer in this ecosystem may be intense (Salyers, 1993), and gut microbiota, therefore, may represent one of the major reservoirs for antibiotic resistance genes (Salyers et al., 2004). Indeed, the taxonomically different representatives of gut microbiota may share the pool of closely related antimicrobial resistance genes (Frye et al., 2011). The role of bacteriophages in acquisition of genes by pathogenic gut microbiota and subsequent evolution toward pathogenicity also pointed to HGT as a crucial event in the development of virulence traits and antibiotic resistance (Calderwood et al., 1987; Barondess and Beckwith, 1990; Brabban et al., 2005). More recent metagenomic studies of the human gut microbiota allowed estimating the role of MGEs without the cultivation bias. The uncultured viral community from human feces contained an estimated 1,200 viral genotypes (Breitbart et al., 2003). Interestingly, unlike the similarity of gut bacterial communities among genetically related individuals, the viral communities are unique to individuals regardless of their degree of genetic relatedness (Reyes et al., 2010). Besides viromes, a recent metagenomic inventory identified a conjugative transposon family explosively amplified in human gut microbiomes (Kurokawa et al., 2007). The culture independent TRACA system was used to sample plasmid diversity in the human gut microbiota (Jones et al., 2010). This study suggested a broad global distribution of some plasmids and plasmid families that are potentially unique to the human gut microbiome. Thus these findings further supported the earlier cultivation-based views that the intestinal microbial ecosystem is extremely enriched by MGEs thus making it the arena of a potentially extensive gene exchange. Indeed, the range of genes that have been exchanged in the past is not limited to the virulence and antibiotic resistance genes but also includes the genes of the core gut microbiome such as encoding bile salt hydrolases (Elkins et al., 2001) or butyrate metabolism enzymes (Louis et al., 2007).

Humans and agricultural animals are the main consumers of antibiotics, for therapeutic, prophylactic, and growth-promoting purposes and, as discussed before, antibiotics may substantially increase the rates of HGT. But what could be other host-mediated factors contributing to the maintenance and transfer of MGEs in gut microbiota? It seems that the in vivo environment itself may enhance the transfer frequency and contribute to the stable inheritance of MGEs even in the absence of selection by antibiotics (Johnsen et al., 2002; Dahl et al., 2007). Thus in vitro models may substantially underestimate the transfer potential of MGEs. In nutritionally poor environments, such as bulk soil, the presence of earthworms greatly enhances the transfer of plasmid pJP4 from an inoculated donor bacterium, P. fluorescens, to the indigenous soil microbiota (Daane et al., 1996). Other soil microcosm experiments, modeled with E. coli as a donor of a genetically marked large conjugative plasmid RP4luc, in the presence or absence of earthworms, provided evidence that the gut passage was a precondition for a plasmid transfer to soil microbiota (Thimm et al., 2001). Interestingly, the plasmid was transferred at higher frequencies than detected in filter mating, suggesting once again that the HGT rates in nature are higher than the laboratory estimates. This observation also confirms the earlier notion that microbial ecosystems are not isolated and there is a potential for lateral gene exchange among different microbial ecosystems. If MGEs from soil have entered the earthworm gut, then they can also enter the gut of animals that are next in the food chain, for example, moles and birds.

Another curious factor that may contribute to the enhanced HGT is the presence of ciliates. Ciliates are common in many aquatic ecosystems as well as in the rumen. Their food vacuoles are formed through phagocytosis and follow a particular path through the cell resembling a primitive gastrointestinal tract. It has been shown that ciliates may enhance the rate of conjugal transfer between E. coli strains by two orders of magnitude, and the mechanism involved is the accumulation of bacteria in vesicles (Matsuo et al., 2010). The mechanism described may contribute to the dissemination of antibiotic resistance in bacterial populations (Oguri et al., 2011).

The insect gut can also be considered as a hot spot contributing to the enhanced HGT in this ecosystem. For example, the rates of conjugative plasmid transfer between S. enterica Newport and E. coli in the gut of the lesser mealworm beetle are by two orders of magnitude higher compared to filter mating (Poole and Crippen, 2009). The occurrence of conjugal plasmid transfer and transduction was also observed in the flea and house fly gut (Hinnebusch et al., 2002; Petridis et al., 2006; Akhtar et al., 2009). An assessment of natural transformability of bacteria in the insect gut, however, failed to detect any transformation event, even with the use of A. baylyi strain BD413 as a recipient (Ray et al., 2007).

Conditions in the gut can be considered as very favorable for HGT. Firstly, the host provides a continuous inflow of nutrients that allow maintaining the active metabolism of gut microbiota. Secondly, the population densities are extremely high and thus conducive to the HGT mechanisms requiring intimate cell-to-cell contact such as conjugation. Thirdly, it is constant body temperature of homeothermic animals that allows the bacterial cells to perform at optimal efficiency. And finally, the vast diversity of gut microbiota itself may have an “amplification effect” for HGT (Dionisio et al., 2002). In addition to these well-known factors, recent investigations have uncovered the mechanisms of host–microbe molecular crosstalk that may contribute to the frequencies of HGT in the gut.

One of these mechanisms is based on the ability of bacteria to sense and respond to host signals. In particular, bacterial sensing and responding to the level of host stress hormones is a well-established fact (Sperandio et al., 2003; Clarke et al., 2006; Karavolos et al., 2008; Spencer et al., 2010). Bacterial responses to the host stress may also involve a genetic component, which is expressed through the enhanced conjugative gene transfer between enteric bacteria (Peterson et al., 2011). In these in vitro experiments, the physiological concentrations of norepinephrine stimulated the transfer of a conjugative plasmid from a clinical strain of Salmonella sp. to an E. coli recipient. Interestingly, the adrenergic receptor antagonists negated the stimulatory effect of norepinephrine on conjugation. These mediators of host stress may possibly affect HGT under the in vivo environment as well.

The issues of potential risks associated with the consumption of GMOs by humans and animals have been addressed in a number of feeding trials. In general, there is a lack of evidence that DNA of transgenic plants, in particular the markers used for their construction, can be taken up by gut microbiota or enter the organs other than the gastrointestinal tract. Neither small fragments of transgenic DNA nor immunoreactive fragments of transgenic protein were detectable in loin muscle samples from pigs fed a diet containing Roundup Ready soybean meal (Jennings et al., 2003). An assessment of the survival of transgenic plant DNA in the human gastrointestinal tract concluded that gene transfer did not occur during the feeding experiment involving GM soya (Netherwood et al., 2004). No traces of the construct or endogenous soybean DNA could be detected in muscle samples of rats fed soybean meal from roundup ready or conventional soybeans (Zhu et al., 2004). Likewise, no traces of transgenic DNA were detected in the milk of cows fed corn silage from an herbicide-tolerant genetically modified variety (Phipps et al., 2005). Plasmid and genomic DNA from GM plants were used in in vitro and in vivo (mono-associated rats) transformation studies, but no detectable transfer of DNA was found (Wilcks and Jacobsen, 2010). Attempts to detect DNA transfer from transgenic plants to bacteria in the intestine of the tobacco hornworm (Deni et al., 2005) or bees were also unsuccessful (Mohr and Tebbe, 2007).

Biofilms

Biofilms are the matrix-enclosed aggregates of microbiota, attached to each other and to biological or non-biological surfaces (Hall-Stoodley et al., 2004). This ancient form of adaptation appeared very early in the prokaryotic phase of evolution to withstand the forces of hostile environmental factors. Indeed, biofilms can be perceived as a form of primitive multicellular organisms, which use the same strategy in their interaction with the environment as their eukaryotic counterparts do. This successful trait, therefore, was replicated in many bacterial and archaeal lineages; and biofilm communities are widespread in many natural ecosystems. It is now widely acknowledged that the majority of microbiota found in natural, clinical, and industrial settings persist in association with surfaces and not in the planktonic state (Costerton, 1995; Davey and O’Toole, 2000). In natural ecosystems, biofilms are usually found in many aquatic or semi-aquatic ecosystems such as rocks and pebbles of most streams and rivers, on the surface of still water bodies, in wastewater treatment systems, in water and sewage pipes, in hot springs, in the subtidal and intertidal solid surfaces of marine ecosystems, on the teeth of humans and animals, in chronic infections of human body, and in many other ecosystems. For studies of HGT in highly organized structures as biofilms, technologies such as single-cell detection of donor, recipient, and transconjugant bacteria, combined with individual-based mathematical models, have been developed to estimate the HGT rates in situ (Sørensen et al., 2005). Raman spectrometry and environmental scanning electron microscopy analyses, combined with molecular ecology tools, allow a better understanding of structure-and-function of biofilms including the chemical composition of the matrix, microbiota embedded in the matrix, and the spatial distribution of biofilms (Schwartz et al., 2009).

Most of our knowledge regarding the biology of biofilms came from clinical microbiology. This increased attention to the clinical aspects of biofilm communities was primarily dictated by their role in human disease (Parsek and Singh, 2003; Fux et al., 2005; Lindsay and von Holy, 2006; Estrela et al., 2009; Kaplan, 2010). Biofilm formation is linked to the pathology of many infectious diseases, and biofilms are notoriously difficult to eradicate because of the increased level of resistance to antibiotics (Stewart and Costerton, 2001; Anderson and O’Toole, 2008; Høiby et al., 2010a). The ability to form highly resilient biofilms has been demonstrated for many human pathogens such as P. aeruginosa (for recent reviews, see Harmsen et al., 2010; Häussler, 2010; Høiby et al., 2010b; and Hassett et al., 2010), Staphylococcus aureus (Goerke and Wolz, 2010), S. epidermidis (Fey and Olson, 2010; Rohde et al., 2010), Streptococcus pneumoniae (Moscoso et al., 2009), S. mutans (Senadheera and Cvitkovitch, 2008), Neisseria gonorrhoeae (Greiner et al., 2005; Falsetta et al., 2009; Steichen et al., 2011), Campylobacter jejuni (Haddock et al., 2010; Naito et al., 2010), Candida sp. (Morales and Hogan, 2010; Williams et al., 2011), and others. Besides, microorganisms may form mixed-species communities and, in a number of cases, this may promote the development of biofilms (Bamford et al., 2009; Silverman et al., 2010; Teh et al., 2010).

Given their structure-and-function, biofilms are the hot spots for HGT because they provide high population densities and close proximity of cells, cells in biofilms are metabolically active, and the microbiota is protected against harsh environment, predators, and immune surveillance by the extracellular matrix in which the cells are encapsulated. Indeed, HGT occurs with enhanced efficiency in biofilms, and conjugative plasmids themselves contribute to the development, stabilization, and expansion of biofilms (Hausner and Wuertz, 1999; Ghigo, 2001; Molin and Tolker-Nielsen, 2003; Reisner et al., 2006; Burmølle et al., 2008). Conjugal plasmid transfer that is implemented through the synthesis of pili and type IV secretion system contributes to the intimate cell-to-cell contact, thus facilitating the formation and growth of biofilms. Type IV secretion systems use a pilus-based system to mediate DNA or protein transfer (Hayes et al., 2010). The involvement of type IV secretion system in biofilm formation has been demonstrated for a number of bacteria (Shime-Hattori et al., 2006; Li et al., 2007; Luke et al., 2007; Barken et al., 2008; Varga et al., 2008; Bahar et al., 2009; Gibiansky et al., 2010). Protection under the umbrella of biofilms confers a selective advantage for the bacteria as well as aids further plasmid/ICE/GEI transfers. Thus, this positive feedback sustains the diversity of MGEs in biofilms and offsets the fitness cost associated with the carriage of MGEs.

The presence of prophages in the host’s genome may have a modulatory effect on biofilm formation and physiology of the host, including central metabolism (Wang et al., 2009). Some prophage-encoded proteins are actually essential for biofilm formation (Toba et al., 2011). The modulatory effect of prophages is expressed in the enhancement of biofilm formation and the resistance of biofilms against adverse environmental conditions (Carrolo et al., 2010; Wang et al., 2010). The biofilm matrix is a conglomerate of polymers usually consisting of extracellular DNA (eDNA), proteins, and polysaccharides. In this respect, a partial phage-mediated lysis of a proportion of microbiota in biofilm, due to spontaneous phage induction, may provide the eDNA supply, thus contributing to biofilm formation and maintenance by the remaining bacterial populations (Carrolo et al., 2010; Gödeke et al., 2011). At the same time, transmission electron microscopy reveals also the presence of intact bacteriophage particles that are enmeshed in the extracellular polymeric matrix of biofilms (Kay et al., 2011). Precise deletion of E. coli prophages uncovered the role of e14 and rac proteins in the increased early biofilm formation (Wang et al., 2010). Besides, other prophages contributed to the host resistance against a variety of stresses, including osmotic, oxidative, and acid. These examples reveal the role of the phage-mediated HGT in bacterial evolution and adaptation, especially regarding the acquired ability to form biofilms as well as to withstand environmental stresses.

Natural competence and transformability in bacteria usually correlates with the presence of type IV pili or type IV pilin-like proteins (Averhoff and Friedrich, 2003). While the role of conjugation machinery and pili in biofilm formation and subsequent acceleration of conjugative element transfer is firmly established, it is not clear if the same is true for natural transformation. Given the involvement of type IV pili or type IV pilin-like proteins in natural transformation and in biofilm formation, would this result in a higher rate of transformation within biofilms? Do the large quantities of eDNA in the extracellular matrix participate in natural transformation of bacteria in biofilms? There are very few works that have addressed these questions. Horizontal transfer of non-conjugative plasmids in E. coli colony biofilms suggested the possibility of natural transformation within bacterial biofilms (Maeda et al., 2006). Later, however, it became clear that the mechanism of DNA acquisition in the biofilm is more complex and was, therefore, described as a “cell-to-cell transformation,” which also involves a peptide pheromone as a regulator (Etchuuya et al., 2011). Other circumstantial evidences of DNA transfer due to close cell-to-cell contact (Van Randen and Venema, 1984; Wang et al., 2007) may be interpreted within the frames of this hypothesis, although the transfer in these cases was between the genera, and the role of pheromones was not shown. The language of intercellular communication used in regulation of various processes within the complex structure of biofilms is indeed the language of pheromones such as N-acyl-L-homoserine lactones, furanosyl borate diester, and peptide autoinducers (Dickschat, 2010). Recently, the possibility of transfer of tetracycline resistance by transformation with eDNA within model oral biofilms was described, although without specifying the frequency of such an event (Hannan et al., 2010).

Factors Affecting HGT

Stress and SOS Response

It has been long recognized that various stress conditions may contribute to increased rates of HGT. For example, UV irradiation or starvation affects the mobility of transposons and ISs (Levy et al., 1993; Ilves et al., 2001). While the lysogenic cycle in the phage development limits its inheritance to the vertical transfer within the chromosome of the host, the stress factors such as induction of the SOS response or amino acid deprivation of the host lead to the lytic cycle and further horizontal dissemination of phage and transduced DNA (Melechen and Go, 1980; Little, 2005). Control of horizontal transfer of ICEs, which are found in many bacterial genomes and which encode a variety of properties besides antibiotic resistance and virulence, may also be regulated through stress, SOS, and other environmental signals (Auchtung et al., 2005; Bose et al., 2008). In particular, the SOS response, which is induced by DNA damaging agents such as mitomycin C and antibiotics such as fluoroquinolones and dihydrofolate reductase inhibitors, leads to the expression of the SXT activators resulting in more than 300-fold increase of HGT rates (Beaber et al., 2004). Thus the consequences of using SOS response-inducing antibiotics may result in co-selection of other antibiotic resistance genes that are physically linked in a MGE (Hastings et al., 2004). Moreover, the SOS response controls integron recombination thus enhancing the potential for cassette swapping and capture in cells (Guerin et al., 2009). Besides the antibiotic- (see the previous section) and SOS response-regulated excision, transfer, and integration of ICEs, regulatory factors include the stationary phase of growth and the presence of 3-chlorobenzoate (Sentchilo et al., 2003). Interestingly, this chlorinated compound stimulates horizontal transfer of the genes encoding its own metabolism. This may explain the previous results of the authors that suggested the need of specific substrates for genetic transfer to occur in activated-sludge microcosms (Ravatn et al., 1998). The transfer of another class of MGEs, GTA, can also be induced by mitomycin C and oxidative stress (Stanton et al., 2008).

Although it has been initially assumed that the SOS response is triggered exclusively by direct DNA damage, there is evidence that certain stimuli can indirectly generate SOS-inducing signals (Aertsen and Michiels, 2006). Some antibiotics, which do not directly interfere with DNA metabolism, may, nevertheless, induce a genuine SOS response. This was demonstrated, for example, for the β-lactam antibiotics targeting bacterial cell wall (Miller et al., 2004). The resulting effect is the elevated rate of horizontal transfer of virulence genes in staphylococci (Maiques et al., 2006; Ubeda et al., 2006). Furthermore, the presence of a functional SOS response system seems not an absolute prerequisite for the stress-induced increase in HGT frequencies. In naturally competent bacterial species such as Streptococcus pneumonia the antibiotic-imposed stress induces genetic transformation in the absence of a SOS-like system (Prudhomme et al., 2006). Another naturally competent bacterium, Legionella pneumophila, also lacks a prototypic SOS response system, but UV light, which represents a major source of genotoxic stress in the environment, effectively induces competence development in this bacterium (Charpentier et al., 2011). The authors have hypothesized that competence for natural transformation and, therefore, the ability to acquire and propagate foreign genes may have evolved as a DNA damage response in SOS-deficient bacteria. Thus, Gram-positive bacteria respond to stress conditions by induction of competence for genetic transformation to generate genetic diversity (Claverys et al., 2006). The strategy is combined with SOS induction in bacteria, such as B. subtilis, while others, such as S. pneumonia, rely solely on competence.

In naturally competent Gram-negative bacteria, the stress conditions may also enhance HGT. Vibrio cholera, for example, can acquire new genetic material by natural transformation during growth on chitin, which activates regulatory cascades leading to increased cell density, nutrient limitation, and decline in growth rate and stress (Meibom et al., 2005). Stress in the form of DNA damage induces transcription and translation of competence genes in Helicobacter pylori, thus increasing transformation frequency and genetic exchange rates (Dorer et al., 2010).

To what extent is the SOS response induced in natural ecosystems? The impact of solar UV radiation on microbiota may be profound, especially in aquatic ecosystems (Hader, 2000; Sinha and Hader, 2002). One of the major targets is DNA where UV-B irradiation results in the formation of cyclobutane-pyrimidine dimers (CPDs), 6-4 photoproducts (6-4PPs), and DNA strand breaks, thus leading to the induction of a number of repair mechanisms, including the SOS response (Rastogi et al., 2010). In photosynthetic cyanobacteria, UV-B stress is accompanied by additional stresses such as oxidative stress and oxidative damage (He et al., 2002). Despite the fact that future trends for solar UV irradiation of the Earth’s surface remain unclear, the increases in UV-B irradiance over the latter part of the twentieth century have been larger than the natural variability (McKenzie et al., 2007). Thus, this factor may play an increasingly important role in accelerating HGT in microbial ecosystems.

Sub-Inhibitory Antimicrobials

During the recent years the concept of antibiotics as solely killing agents has been substantially revised in the light of new findings suggesting that low concentrations of antibiotics may play a regulatory function in natural ecosystems (Davies et al., 2006; Fajardo and Martínez, 2008; Aminov, 2009). Moreover, the killing/therapeutic and regulatory/sub-inhibitory concentrations of an antibiotic are indeed directed toward different targets in the cell (Hoffman et al., 2005). There is a substantial body of evidence suggesting that the sub-inhibitory concentrations of antibiotics may significantly increase the frequency of horizontal transfer of many types of MGEs. It was noticed a quarter of a century ago that the sub-inhibitory concentrations of β-lactams enhanced the transfer of tetracycline resistance plasmids in Staphylococcus aureus by up to 1,000-fold (Barr et al., 1986). Pre-incubation of donor cells of Bacteroides sp. in the presence of sub-inhibitory tetracycline accelerates the mobilization of a resident non-conjugative plasmid by chromosomally encoded tetracycline conjugal elements (Valentine et al., 1988). A similar type of exposure of donor Bacteroides cells appeared to be a prerequisite for the excision and conjugal transfer of the ICE CTnDOT (Stevens et al., 1993; Whittle et al., 2002). In the absence of tetracycline induction of donor cells, practically no such transfers were detected. Addition of sub-inhibitory tetracycline into the mating medium substantially enhanced the conjugal transfer of another ICE, Tn916 (Showsh and Andrews, 1992). A similar stimulatory effect of tetracycline on conjugation transfer was demonstrated for Tn925 as well (Torres et al., 1991). A recent study has revealed the induction effect of carbadox and metronidazole on the GTA-mediated HGT in Brachyspira hyodysenteriae (Stanton et al., 2008). The induced VSH-1 particles transmitted tylosin and chloramphenicol resistances between B. hyodysenteriae strains.

These experiments described above have been performed under laboratory conditions using standard mating techniques, and the question is whether these observations reflect the real in vivo situation or these are the effects of specific in vitro conditions. The former point of view is supported by a number of experiments using animal models. For instance, the inclusion of sub-inhibitory tetracycline in drinking water resulted in a 10-fold increase of transfer of an ICE, Tn1545, from Enterococcus faecalis to Listeria monocytogenes in the intestine of gnotobiotic mice (Doucet-Populaire et al., 1991). In gnotobiotic rats, the presence of tetracycline resulted in a higher number of Tn916 transconjugants compared to control (Bahl et al., 2004). An astonishing 100% transfer rate of a small plasmid pLFE1 from Lactobacillus plantarum to E. faecalis was observed in the gut of gnotobiotic mice receiving erythromycin (Feld et al., 2008). These experiments suggest that the stimulatory effect of sub-inhibitory antibiotics on transfer of MGEs is not an artifact of in vitro conditions but happens in the real gut of real animals. It needs to be noted, however, that the transfer frequencies were estimated in gnotobiotic animals, which are lacking the highly diverse and dense microbiota in the gut.

The mechanisms contributing to the enhanced movement of MGEs in the presence of antibiotics have been established on several occasions, especially for ICEs. In Tn916, transcriptional regulation of the tra genes required for the conjugal transfer of this ICE is under the control of orf7 and orf8 products (Celli and Trieu-Cuot, 1998; Roberts and Mullany, 2009). Transcripts for these two ORFs are produced from the distant promoter of the tet(M) gene as well as from the promoter directly upstream of orf7. In the absence of tetracycline, transcription from PtetM is attenuated (Su et al., 1992), and the transcripts are very short, not covering the orf7 and orf8 genes. In addition, the product of orf9 negatively regulates the promoter upstream of orf7. In the presence of tetracycline, however, transcription from PtetM extends through orf7 and orf8 thus allowing the synthesis of these two proteins that promote transcription from Porf7. The long transcripts from PtetM are also complementary to the orf9 transcripts thus efficiently reducing the concentration of Porf7 repressor. As a result, transcription from Porf7 extends downstream of orf8 through int and xis, which encode the integrase and excisionase, respectively. Once Tn917 is circularized, transcription from Porf7 also leads to the expression of the tra genes thus initiating the conjugation machinery.

Another mechanism, also involving tetracycline as a positive regulator of HGT, is implemented in the Bacteroides ICE, CTnDOT (Whittle et al., 2002; Moon et al., 2005). In this regulatory cascade, tetracycline activates the transcription of the tet(Q) gene and the downstream genes of the two-component regulatory system, rteA and rteB. The product of rteB activates the transcription of rteC system, which, in turn, leads to the elevated transcription of the gene cluster involved in CTnDOT excision. Subsequently, the proteins encoded by the excision genes upregulate the production of tra gene mRNA thus activating the conjugation machinery (Jeters et al., 2009). In this complex regulatory system, the stimulatory effect of tetracycline on transcription of its own resistance gene (and concomitantly on the excision and conjugal transfer genes of CTnDOT) is implemented through a translation attenuation mechanism involving the leader region of tet(Q) (Wang et al., 2005).

Both regulatory mechanisms of the MGE movement discussed above display a common theme in that the primary switch for this genetic process is based on an antibiotic–antibiotic resistance gene pair. That is, the presence of a sub-inhibitory antibiotic in the environment activates the transcription of a corresponding resistance gene and, concurrently, the genes involved in the mobility of MGEs. In this regard, the interaction of an antibiotic and antibiotic resistance gene resembles a positively regulated switch, with an antibiotic possessing a signaling function, ultimately leading to the activation of horizontal gene exchange in microbiota. The recent works describing concentration-dependent bacterial responses to antibiotics have led to the development of the hormesis concept (Davies et al., 2006; Fajardo and Martínez, 2008). According to this concept, low concentrations of antibiotics may regulate a specific set of genes in target bacteria, while increasingly higher concentrations elicit a stress response, and even higher concentrations are lethal. It has been suggested that antibiotics play a regulatory role in nature at low concentrations unlike the lethal concentrations used in clinical therapy (Aminov, 2009). Given the profound stimulatory effect of low-dose antibiotics on the movement of MGEs, one of the functions of antibiotics in natural ecosystems may be the regulation of HGT between the representatives of environmental microbiota.

Despite the fact that some countries have enacted legislations limiting the non-therapeutic use of antibiotics, in particularly in food animals (http://ec.europa.eu/food/food/animalnutrition/feedadditives/index_en.htm), the use of sub-therapeutic antimicrobials in agriculture and aquaculture of other countries is still widespread. Moreover, the US Food and Drug Administration has recently approved sub-inhibitory concentrations of doxycycline and minocycline for the systemic treatment of skin infections in humans (Del Rosso, 2007). Thus, there is a high probability that the gut ecosystems may continue to be hotspots of horizontal gene exchange involving the resident and transient gut microbiota. The land application of manure with residual antibiotics and antibiotic resistance genes of the gut content may further contribute to the enhanced HGT in the environment (Chee-Sanford et al., 2009).

Indirect Mechanisms of Maintenance and Dissemination of MGEs

The “cooperation” between different mechanisms of HGT can be seen in many examples of mobility among the genetic elements that are normally not mobile on their own. For example, ICEs of Bacteroides spp. and large broad-host-range conjugative IncP plasmids R751 and RP4 are able to act in trans to excise, circularize, and transfer unlinked integrated elements called NBUs (Li et al., 1993; Shoemaker et al., 1993). Bioinformatics of plasmid mobility suggests that globally about a quarter of all plasmids are potentially mobilizable and, therefore, can be transferred if a compatible conjugation machinery is present (Smillie et al., 2010). In Sinorhizobium meliloti, conjugation functions for a 1,683-kb symbiotic megaplasmid pSymB are supplied in trans by another megaplasmid, pSymB (Blanca-Ordóñez et al., 2010). The recently described ISCR elements are thought to be the key players in IncA/C plasmid evolution serving as antibiotic resistance gene capture and movement systems that are also capable of constructing extended clusters of antibiotic resistance genes (Toleman and Walsh, 2010).

Insertion sequences constitute an important component of most bacterial genomes and are simple transposable elements consisting of inverted repeat (IR) sequences, a transposase gene, and frequently a second recombination regulation enzyme gene (Mahillon and Chandler, 1998). It has been thought that the transposition of ISs is a rare event within a bacterial genome, but the discovery of a protein called IS-excision enhancer (IEE), which promotes excision events, suggested that the rates could be high (Kusumoto et al., 2011). The IEE activity, therefore, may play an important role in bacterial genome evolution by inducing IS removal and genomic deletion. Another aspect is the transposition of an IS into a conjugative plasmid, an ICE, or a genomic island. This way, the IS elements can be disseminated to many other, not necessarily closely related, bacterial taxa. Together with prophages (Asadulghani et al., 2009), IS elements are the major contributors to the genomic diversification in pathogenic E. coli (Ooka et al., 2009). Since the IS elements are ubiquitous in many bacteria, including environmental and commensal species, these mechanisms of diversification are probably not limited exclusively to pathogens.

Since the carriage of MGEs may be associated with a considerable fitness cost, certain mechanisms of stable inheritance have been selected within the MGEs. One of these mechanisms is a toxin–antitoxin (TA) system consisting of two components, a stable toxin and its labile antitoxin. Type I and II TA systems were found on plasmids in the 1980s (Ogura and Hiraga, 1983; Jaffe et al., 1985), and type III is a more recent discovery (Fineran et al., 2009). The general mechanism of action is that if an MGE with TA system is lost during cell division, the concentrations of a labile antitoxin rapidly decreases thus releasing a stable toxin, which kills an MGE-free cell (Van Melderen, 2010). Thus, TA systems contribute to the stable maintenance and dissemination of plasmids and genomic islands in bacterial populations despite the associated fitness cost.

The size of MGEs varies from small IS elements (typically 700 to 2,500 bp; Mahillon and Chandler, 1998) to large symbiotic megaplasmids of Sinorhizobium meliloti (1.35 and 1.68 Mb; Barnett et al., 2001; Capela et al., 2001). The majority of large self-transmissible genetic elements have a sufficient capacity to carry multiple genes, including those encoding antibiotic, heavy metal and biocide resistances, metabolism of various substrates and xenobiotics, symbiosis with the host, and other auxiliary functions. The fact that R plasmids mediate resistance to mercury, nickel, and cobalt was first described more than 40 years ago (Smith, 1967). Subsequent research by other groups demonstrated that the genetic linkage between antibiotic resistance and mercury resistance in enterobacteria had occurred prior to the late 1950s in Japan (reviewed in Liebert et al., 1999). At the same time, Enterobacteriaceae strains collected by E. D. G. Murray from 1917 to 1954 contained very few antibiotic and mercury resistant bacteria, despite the finding that 25% of the strains carried conjugative functions (Hughes and Datta, 1983). Thus, the frequency of MGEs even in the “pre-antibiotic era” was sufficiently high but not associated with the adaptation to anthropogenic factors such as antibiotics or heavy metals.

The exceptional natural genetic engineering capabilities of bacteria have been profoundly demonstrated during the “antibiotic era” (Aminov, 2010). To withstand the massive pressure of antimicrobials used by humans, commensal, and pathogenic bacteria were able, within a relatively short period of time on the evolutionary scale, to mobilize a huge reservoir of antibiotic resistance genes, often from the environmental bacteria (Aminov and Mackie, 2007; Cantón, 2009; Wright, 2010). The main genetic engineering tool used by bacteria to collect antibiotic resistance genes is integrons, the genetic platform that is involved in the acquisition and functional expression of exogenous gene cassettes (Mazel, 2006). The discovery of superintegrons that contain hundreds of auxiliary genes and may occupy a significant part of many bacterial genomes has changed our initial interpretation of integrons as merely a mechanism of collecting antibiotic resistance genes. The presence of toxin/antitoxin cassettes in superintegrons further facilitates the stabilization of large cassette arrays consisting of many ancillary genes (Cambray et al., 2010).

The physical linkage of numerous and functionally diverse groups of genes within the high-capacity MGEs has implications for their persistence in the environment. Selection that is imposed toward even a single component/gene of an MGE will automatically select for the whole MGE. Thus, we should see the co-selection effect in phenotypes of bacteria that carry MGEs. Indeed, bacteria in metal-contaminated areas appeared to be more tolerant to metals and antibiotics than in control sites (Stepanauskas et al., 2005; Baker-Austin et al., 2006; Wright et al., 2006). Treatment of agricultural soils with copper may lead to a significantly higher incidence of antibiotic resistance phenotypes in indigenous soil microbiota (Berg et al., 2005). In freshwater microcosms, amendment with metal concentrations representative of industry and mining-impacted environments increased the frequency of antibiotic resistance in the microbial communities (Stepanauskas et al., 2006). Genetic mechanisms responsible for the co-selection phenomena in the contaminated environments are presently poorly understood, but it is clear that the MGE-driven HGT is the main adaptive trait in bacteria inhabiting industrially contaminated aquatic (Wright et al., 2008) and soil (Top et al., 1995; Sobecky and Coombs, 2009) ecosystems.

Quorum Sensing

The quorum sensing (QS) systems are widespread among a variety of microbiota and initially they were recognized as population-density-sensing mechanisms based on the best-studied prototype, the QS network, which regulates the lux operon in Vibrio fischeri (Eberhard et al., 1981; Fuqua et al., 1996). Since then it has become clear that the QS is involved in regulation of a much broader range of functions and activities such as pathogenicity, extracellular enzyme production, antibiotic biosynthesis, and others (Bainton et al., 1992; Jones et al., 1993; Passador et al., 1993; Pirhonen et al., 1993; Pierson et al., 1994). The QS is indeed a universal language of communication not only among the bacteria but also in the inter-kingdom interaction (Shiner et al., 2005).

One of the earliest indications of the QS involvement in HGT came from the studies of conjugal transfer of the Agrobacterium tumefaciens Ti plasmids (Zhang and Kerr, 1991; Piper et al., 1993; Fuqua and Winans, 1994). The Ti plasmid encodes a regulatory system, consisting of the acyl-homoserine lactone (AHL) synthase TraI and the transcription factor TraR. TraI synthesizes AHLs, mainly N-(3-oxo-octanoyl)-L-homoserine lactone (OOHL), while TraR is an OOHL-dependent transcription activator of conjugative transfer genes. Molecular mechanisms of this activation that leads to the enhanced conjugal transfer of the Ti plasmids are well understood (Costa et al., 2009; Qin et al., 2009).

Another well-explored area is the QS regulation of transfer of large symbiotic plasmids in rhizobia (Danino et al., 2003; He et al., 2003; Tun-Garrido et al., 2003). Analysis of plasmid transfer in several rhizobia species has revealed a regulatory relay that is specifically poised to detect AHLs made by different cells and to respond to these signals by up-regulation of conjugal transfer genes. In turn, the production of AHLs, N-(3-oxo-octanoyl)-L-homoserine lactone, and N-(octanoyl)-L-homoserine lactone, is regulated by a complex interaction of plasmid- and chromosome-encoded genes in donors and recipients in response to environmental cues. Recently it has been shown that the transfer of an ICE of Mesorhizobium loti, which carries genes for a nitrogen-fixing symbiosis with Lotus species, is also regulated by a QS mechanism (Ramsay et al., 2009). The two conserved hypothetical genes, which are essential for the QS-mediated excision and transfer, can also be found on putative ICEs in several alphaproteobacteria, indicating a broader presence of this HGT regulatory mechanism.

Recent investigations have identified an important role played by QS in regulation of phage-mediated HGT. For example, acyl-homoserine lactones (AHLs), the essential signaling molecules of QS in many Gram-negative bacteria, can trigger phage production in soil and groundwater bacteria (Ghosh et al., 2009). Interestingly, in the recA mutant of E. coli the induction responses of lambda to AHL remained unaffected, suggesting that this mechanism does not involve an SOS response.

Concluding Remarks

The high rate of horizontal gene exchange in natural ecosystems is evident from both retrospective and prospective types of studies. The microbial world around us can be seen as a giant microbiome, with the continuous flow of genes between its different compartments. This flow is sustained by a variety of sophisticated natural genetic engineering tools, MGEs, which have been selected during the evolution as providing the means for re-shuffling the available genetic material and picking the best responses possible to cope with the continuously changing environmental challenges. The recent relatively short history of the “antibiotic era” (Aminov, 2010) demonstrates the ultimate success of this strategy and urges us to rethink our own when interacting with the microbial world. Continuous discoveries of novel MGEs and mechanisms of HGT, together with the findings of unexpectedly high HGT rates in natural ecosystems, indicate that we are still far from the understanding of the true extent of HGT in nature. The contribution to the better understanding may be envisaged as the combination of retrospective and prospective approaches. On the dry lab side, the history of past HGT events, which is recorded in the wealth of genomic/genomic information, can be more vigorously interrogated on the basis of our knowledge about MGEs and with the help of bioinformatics tools that are able to detect the events consistent with HGT. On the wet lab side, it is the development of in situ technologies that are more sensitive, less intrusive and applicable to the field studies. The microcosm experiments should model real environmental situations, working with native microbiota, with a lesser dependence on model organisms. These developments may help to elaborate better strategies to deal with the pressing needs such as the emergence of novel infections and opportunistic pathogens as well as antibiotic resistance genes.

Conflict of Interest Statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The author is supported by the Rural and Environmental Science and Analytical Services (RESAS) Program of the Scottish Government.

References

Aardema, B. W., Lorenz, M. G., and Krumbein, W. E. (1983). Protection of sediment-adsorbed transforming DNA against enzymatic inactivation. Appl. Environ. Microbiol. 46, 417–420.

Pubmed Abstract | Pubmed Full Text

Aertsen, A., and Michiels, C. W. (2006). Upstream of the SOS response: figure out the trigger. Trends Microbiol. 14, 421–423.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Akhtar, M., Hirt, H., and Zurek, L. (2009). Horizontal transfer of the tetracycline resistance gene tet(M) mediated by pCF10 among Enterococcus faecalis in the house fly (Musca domestica L.) alimentary canal. Microb. Ecol. 58, 509–518.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Akkermans, A. D. L., Van Elsas, J. D., and De Bruijn, F. J. (1995). Molecular Microbial Ecology Manual. Dordrecht: Kluwer Academic Publisher.

Aminov, R. I. (2009). The role of antibiotics and antibiotic resistance in nature. Environ. Microbiol. 11, 2970–2988.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Aminov, R. I. (2010). A brief history of the antibiotic era: lessons learned and challenges for the future. Front. Microbiol. 1:134. doi: 10.3389/fmicb.2010.00134

CrossRef Full Text

Aminov, R. I., and Mackie, R. I. (2007). Evolution and ecology of antibiotic resistance genes. FEMS Microbiol. Lett. 271, 147–161.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Anagnostopoulos, C., and Spizizen, J. (1961). Requirements for transformation in Bacillus subtilis. J. Bacteriol. 81, 741–746.

Pubmed Abstract | Pubmed Full Text

Andersen, J. B., Sternberg, C., Poulsen, L. K., Bjorn, S. P., Givskov, M., and Molin, S. (1998). New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Appl. Environ. Microbiol. 64, 2240–2246.

Pubmed Abstract | Pubmed Full Text

Anderson, G. G., and O’Toole, G. A. (2008). Innate and induced resistance mechanisms of bacterial biofilms. Curr. Top. Microbiol. Immunol. 322, 85–105.

Pubmed Abstract | Pubmed Full Text

Angles, M. L., Marshall, K. C., and Goodman, A. E. (1993). Plasmid transfer between marine bacteria in the aqueous phase and biofilms in reactor microcosms. Appl. Environ. Microbiol. 59, 843–850.

Pubmed Abstract | Pubmed Full Text

Angly, F. E., Felts, B., Breitbart, M., Salamon, P., Edwards, R. A., Carlson, C., Chan, A. M., Haynes, M., Kelley, S., Liu, H., Mahaffy, J. M., Mueller, J. E., Nulton, J., Olson, R., Parsons, R., Rayhawk, S., Suttle, C. A., and Rohwer, F. (2006). The marine viromes of four oceanic regions. PLoS Biol. 4, e368. doi: 10.1371/journal.pbio.0040368

CrossRef Full Text

Asadulghani, M., Ogura, Y., Ooka, T., Itoh, T., Sawaguchi, A., Iguchi, A., Nakayama, K., and Hayashi, T. (2009). The defective prophage pool of Escherichia coli O157: prophage-prophage interactions potentiate horizontal transfer of virulence determinants. PLoS Pathog. 5, e1000408. doi: 10.1371/journal.ppat.1000408

CrossRef Full Text

Auchtung, J. M., Lee, C. A., Monson, R. E., Lehman, A. P., and Grossman, A. D. (2005). Regulation of a Bacillus subtilis mobile genetic element by intercellular signaling and the global DNA damage response. Proc. Natl. Acad. Sci. U.S.A. 102, 12554–12559.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Averhoff, B., and Friedrich, A. (2003). Type IV pili-related natural transformation systems: DNA transport in mesophilic and thermophilic bacteria. Arch. Microbiol. 180, 385–393.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Avery, O. T., MacLeod, C. M., and McCarty, M. (1944). Studies on the chemical nature of the substance inducing transformation of pneumococcal types. Induction of transformation by a desoxyribonucleic acid fraction isolated from pneumococcus type III. J. Exp. Med. 89, 137–158.

CrossRef Full Text

Bahar, O., Goffer, T., and Burdman, S. (2009). Type IV pili are required for virulence, twitching motility, and biofilm formation of Acidovorax avenae subsp. citrulli. Mol. Plant Microbe Interact. 22, 909–920.

CrossRef Full Text

Bahl, M. I., Sorensen, S. J., Hansen, L. H., and Licht, T. R. (2004). Effect of tetracycline on transfer and establishment of the tetracycline-inducible conjugative transposon Tn916 in the guts of gnotobiotic rats. Appl. Environ. Microbiol. 70, 758–764.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bainton, N. J., Bycroft, B. W., Chhabra, S. R., Stead, P., Glehill, L., Hill, P. J., Rees, C. E. D., Winson, M. K., Salmond, G. P. C., Stewart, G. S. A. B., and Williams, P. (1992). A general role for the lux autoinducer in bacterial cell signaling: control of antibiotic biosynthesis in Erwinia. Gene 116, 87–91.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Baker-Austin, C., Wright, M. S., Stepanauskas, R., and McArthur, J. V. (2006). Co-selection of antibiotic and metal resistance. Trends Microbiol. 14, 176–182.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bamford, C. V., d’Mello, A., Nobbs, A. H., Dutton, L. C., Vickerman, M. M., and Jenkinson, H. F. (2009). Streptococcus gordonii modulates Candida albicans biofilm formation through intergeneric communication. Infect. Immun. 77, 3696–3704.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Barken, K. B., Pamp, S. J., Yang, L., Gjermansen, M., Bertrand, J. J., Klausen, M., Givskov, M., Whitchurch, C. B., Engel, J. N., and Tolker-Nielsen, T. (2008). Roles of type IV pili, flagellum-mediated motility and extracellular DNA in the formation of mature multicellular structures in Pseudomonas aeruginosa biofilms. Environ. Microbiol. 10, 2331–2343.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Barnett, M. J., Fisher, R. F., Jones, T., Komp, C., Abola, A. P., Barloy-Hubler, F., Bowser, L., Capela, D., Galibert, F., Gouzy, J., Gurjal, M., Hong, A., Huizar, L., Hyman, R. W., Kahn, D., Kahn, M. L., Kalman, S., Keating, D. H., Palm, C., Peck, M. C., Surzycki, R., Wells, D. H., Yeh, K. C., Davis, R. W., Federspiel, N. A., and Long, S. R. (2001). Nucleotide sequence and predicted functions of the entire Sinorhizobium meliloti pSymA megaplasmid. Proc. Natl. Acad. Sci. U.S.A. 98, 9883–9888.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Barondess, J. J., and Beckwith, J. (1990). A bacterial virulence determinant encoded by lysogenic coliphage lambda. Nature 346, 871–874.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Barr, V., Barr, K., Millar, M. R., and Lacey, R. W. (1986). Beta-lactam antibiotics increase the frequency of plasmid transfer in Staphylococcus aureus. J. Antimicrob. Chemother. 17, 409–413.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Baya, A. M., Brayton, P. R., Brown, V. L., Grimes, D. J., Russek-Cohen, E., and Colwell, R. R. (1986). Coincident plasmids and antimicrobial resistance in marine bacteria isolated from polluted and unpolluted Atlantic Ocean samples. Appl. Environ. Microbiol. 51, 1285–1292.

Pubmed Abstract | Pubmed Full Text

Beaber, J. W., Hochhut, B., and Waldor, M. K. (2004). SOS response promotes horizontal dissemination of antibiotic resistance genes. Nature, 427, 72–74.

Berg, J., Tom-Petersen, A., and Nybroe, O. (2005). Copper amendment of agricultural soil selects for bacterial antibiotic resistance in the field. Lett. Appl. Microbiol. 40, 146–151.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Binh, C. T., Heuer, H., Kaupenjohann, M., and Smalla, K. (2008). Piggery manure used for soil fertilization is a reservoir for transferable antibiotic resistance plasmids. FEMS Microbiol. Ecol. 66, 25–37.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Binh, C. T., Heuer, H., Kaupenjohann, M., and Smalla, K. (2009). Diverse aadA gene cassettes on class 1 integrons introduced into soil via spread manure. Res. Microbiol. 160, 427–433.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Björklöf, K., Suoniemi, A., Haahtela, K., and Romantschuk, M. (1995). High frequency of conjugation versus plasmid segregation of RP1 in epiphytic Pseudomonas syringae populations. Microbiology 141, 2719–2727.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Blanca-Ordóñez, H., Oliva-García, J. J., Pérez-Mendoza, D., Soto, M. J., Olivares, J., Sanjuán, J., and Nogales, J. (2010). pSymA-dependent mobilization of the Sinorhizobium meliloti pSymB megaplasmid. J. Bacteriol. 192, 6309–6312.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bose, B., Auchtung, J. M., Lee, C. A., and Grossman, A. D. (2008). A conserved anti-repressor controls horizontal gene transfer by proteolysis. Mol. Microbiol. 70, 570–582.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bosó-Ribelles, V., Romá-Sánchez, E., Carmena, J., Cáceres, C., and Bautista, D. (2008). Tigecycline: a new treatment choice against Acinetobacter baumannii. Recent Pat. Antiinfect. Drug Discov. 3, 117–122.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Brabban, A. D., Hite, E., and Callaway, T. R. (2005). Evolution of foodborne pathogens via temperate bacteriophage-mediated gene transfer. Foodborne Pathog. Dis. 2, 287–303.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Breitbart, M., Hewson, I., Felts, B., Mahaffy, J. M., Nulton, J., Salamon, P., and Rohwer, F. (2003). Metagenomic analyses of an uncultured viral community from human feces. J. Bacteriol. 185, 6220–6223.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Brigulla, M., and Wackernagel, W. (2010). Molecular aspects of gene transfer and foreign DNA acquisition in prokaryotes with regard to safety issues. Appl. Microbiol. Biotechnol. 86, 1027–1041.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Brinkhoff, T., Giebel, H. A., and Simon, M. (2008). Diversity, ecology, and genomics of the Roseobacter clade: a short overview. Arch. Microbiol. 189, 531–539.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Buckling, A., and Rainey, P. B. (2002). The role of parasites in sympatric and allopatric host diversification. Nature 420, 496–499.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burmølle, M., Bahl, M. I., Jensen, L. B., Sørensen, S. J., and Hansen, L. H. (2008). Type 3 fimbriae, encoded by the conjugative plasmid pOLA52, enhance biofilm formation and transfer frequencies in Enterobacteriaceae strains. Microbiology 154, 187–195.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burroughs, N. J., Marsh, P., and Wellington, E. M. (2000). Mathematical analysis of growth and interaction dynamics of streptomycetes and a bacteriophage in soil. Appl. Environ. Microbiol. 66, 3868–3877.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Burrus, V., Pavlovic, G., Decaris, B., and Guédon, G. (2002). Conjugative transposons: the tip of the iceberg. Mol. Microbiol. 46, 601–610.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Cai, P., Huang, Q. Y., and Zhang, X. W. (2006). Interactions of DNA with clay minerals and soil colloidal particles and protection against degradation by DNase. Environ. Sci. Technol. 40, 2971–2976.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Calderwood, S. B., Auclair, F., Donohue-Rolfe, A., Keusch, G. T., and Mekalanos, J. J. (1987). Nucleotide sequence of the Shiga-like toxin genes of Escherichia coli. Proc. Natl. Acad. Sci. U.S.A. 84, 4364–4368.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Cambray, G., Guerout, A. M., and Mazel, D. (2010). Integrons. Annu. Rev. Genet. 44, 141–166.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Cantón, R. (2009). Antibiotic resistance genes from the environment: a perspective through newly identified antibiotic resistance mechanisms in the clinical setting. Clin. Microbiol. Infect. 15(Suppl. 1), 20–25.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Capela, D., Barloy-Hubler, F., Gouzy, J., Bothe, G., Ampe, F., Batut, J., Boistard, P., Becker, A., Boutry, M., Cadieu, E., Dreano, S., Gloux, S., Godrie, T., Goffeau, A., Kahn, D., Kiss, E., Lelaure, V., Masuy, D., Pohl, T., Portetelle, D., Pühler, A., Purnelle, B., Ramsperger, U., Renard, C., Thebault, P., Vandenbol, M., Weidner, S., and Galibert, F. (2001). Analysis of the chromosome sequence of the legume symbiont Sinorhizobium meliloti strain 1021. Proc. Natl. Acad. Sci. U.S.A. 98, 9877–9882.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Caro-Quintero, A., Deng, J., Auchtung, J., Brettar, I., Höfle, M. G., Klappenbach, J., and Konstantinidis, K. T. (2011). Unprecedented levels of horizontal gene transfer among spatially co-occurring Shewanella bacteria from the Baltic Sea. ISME J. 5, 131–140.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Carrolo, M., Frias, M. J., Pinto, F. R., Melo-Cristino, J., and Ramirez, M. (2010). Prophage spontaneous activation promotes DNA release enhancing biofilm formation in Streptococcus pneumoniae. PLoS ONE 5, e15678. doi: 10.1371/journal.pone.0015678

CrossRef Full Text

Celli, J., and Trieu-Cuot, P. (1998). Circularization of Tn916 is required for expression of the transposon-encoded transfer functions: characterization of long tetracycline-inducible transcripts reading through the attachment site. Mol. Microbiol. 28, 103–117.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Charpentier, X., Kay, E., Schneider, D., and Shuman, H. A. (2011). Antibiotics and UV radiation induce competence for natural transformation in Legionella pneumophila. J. Bacteriol. 193, 1114–1121.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chee-Sanford, J. C., Mackie, R. I., Koike, S., Krapac, I. G., Lin, Y. F., Yannarell, A. C., Maxwell, S., and Aminov, R. I. (2009). Fate and transport of antibiotic residues and antibiotic resistance genes following land application of manure waste. J. Environ. Qual. 38, 1086–1108.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Christensen, B. B., Sternberg, C., and Molin, S. (1996). Bacterial plasmid conjugation on semi-solid surfaces monitored with the green fluorescent protein from Aequorea victoria as a marker. Gene 173, 59–65.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Clarke, M. B., Hughes, D. T., Zhu, C., Boedeker, E. C., and Sperandio, V. (2006). The QseC sensor kinase: a bacterial adrenergic receptor. Proc. Natl. Acad. Sci. U.S.A. 103, 10420–10425.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Claverys, J. P., Prudhomme, M., and Martin, B. (2006). Induction of competence regulons as a general response to stress in Gram-positive bacteria. Annu. Rev. Microbiol. 60, 451–475.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Coombs, J. M. (2009). Potential for horizontal gene transfer in microbial communities of the terrestrial subsurface. Methods Mol. Biol. 532, 413–433.

Pubmed Abstract | Pubmed Full Text

Coombs, J. M., and Barkay, T. (2004). Molecular evidence for the evolution of metal homeostasis genes by lateral gene transfer in bacteria from the deep terrestrial subsurface. Appl. Environ. Microbiol. 70, 1698–1707.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Costa, E. D., Cho, H., and Winans, S. C. (2009). Identification of amino acid residues of the pheromone-binding domain of the transcription factor TraR that are required for positive control. Mol. Microbiol. 73, 341–351.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Costerton, J. W. (1995). Overview of microbial biofilms. J. Ind. Microbiol. 15, 137–140.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Daane, L. L., Molina, J. A., Berry, E. C., and Sadowsky, M. J. (1996). Influence of earthworm activity on gene transfer from Pseudomonas fluorescens to indigenous soil bacteria. Appl. Environ. Microbiol. 62, 515–521.

Pubmed Abstract | Pubmed Full Text

Daane, L. L., Molina, J. A. E., and Sadowsky, M. J. (1997). Plasmid transfer between spatially separated donor and recipient bacteria in earthworm-containing soil microcosms. Appl. Environ. Microbiol. 63, 679–686.

Pubmed Abstract | Pubmed Full Text

Dahl, K. H., Mater, D. D., Flores, M. J., Johnsen, P. J., Midtvedt, T., Corthier, G., and Sundsfjord, A. (2007). Transfer of plasmid and chromosomal glycopeptide resistance determinants occurs more readily in the digestive tract of mice than in vitro and exconjugants can persist stably in vivo in the absence of glycopeptide selection. J. Antimicrob. Chemother. 59, 478–486.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Dahlberg, C., Bergström, M., Andreasen, M., Christensen, B. B., Molin, S., and Hermansson, M. (1998a). Interspecies bacterial conjugation by plasmids from marine environments visualized by gfp expression. Mol. Biol. Evol. 15, 385–390.

Dahlberg, C., Bergström, M., and Hermansson, M. (1998b). In situ detection of high levels of horizontal plasmid transfer in marine bacterial communities. Appl. Environ. Microbiol. 64, 2670–2675.

Damier-Piolle, L., Magnet, S., Brémont, S., Lambert, T., and Courvalin, P. (2008). AdeIJK, a resistance-nodulation-cell division pump effluxing multiple antibiotics in Acinetobacter baumannii. Antimicrob. Agents Chemother. (Bethesda) 52, 557–562.

CrossRef Full Text

Danino, V. E., Wilkinson, A., Edwards, A., and Downie, J. A. (2003). Recipient-induced transfer of the symbiotic plasmid pRL1JI in Rhizobium leguminosarum bv. viciae is regulated by a quorum-sensing relay. Mol. Microbiol. 50, 511–512.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Datta, N., and Hedges, R. W. (1971). Compatibility groups among fi-R factors. Nature 234, 222–223.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Davey, M. E., and O’Toole, G. A. (2000). Microbial biofilms: from ecology to molecular genetics. Microbiol. Mol. Biol. Rev. 64, 847–867.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Davies, J., Spiegelman, G. B., and Yim, G. (2006). The world of subinhibitory antibiotic concentrations. Curr. Opin. Microbiol. 9, 445–453.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Del Rosso, J. Q. (2007). Recently approved systemic therapies for acne vulgaris and rosacea. Cutis 80, 113–120.

Pubmed Abstract | Pubmed Full Text

Demanèche, S., Jocteur-Monrozier, L., Quiquampoix, H., and Simonet, P. (2001). Evaluation of biological and physical protection against nuclease degradation of clay-bound plasmid DNA. Appl. Environ. Microbiol. 67, 293–299.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Deni, J., Message, B., Chioccioli, M., and Tepfer, D. (2005). Unsuccessful search for DNA transfer from transgenic plants to bacteria in the intestine of the tobacco hornworm, Manduca sexta. Transgenic Res. 14, 207–215.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Dickschat, J. S. (2010). Quorum sensing and bacterial biofilms. Nat. Prod. Rep. 27, 343–369.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Dijkshoorn, L., Nemec, A., and Seifert, H. (2007). An increasing threat in hospitals: multidrug-resistant Acinetobacter baumannii. Nat. Rev. Microbiol. 5, 939–951.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Dionisio, F., Matic, I., Radman, M., Rodrigues, O. R., and Taddei, F. (2002). Plasmids spread very fast in heterogeneous bacterial communities. Genetics 162, 1525–1532.

Pubmed Abstract | Pubmed Full Text

Dorer, M. S., Fero, J., and Salama, N. R. (2010). DNA damage triggers genetic exchange in Helicobacter pylori. PLoS Pathog. 6, e1001026. doi: 10.1371/journal.ppat.1001026

CrossRef Full Text

Doucet-Populaire, F., Trieu-Cuot, P., Dosbaa, I., Andremont, A., and Courvalin, P. (1991). Inducible transfer of conjugative transposon Tn1545 from Enterococcus faecalis to Listeria monocytogenes in the digestive tracts of gnotobiotic mice. Antimicrob. Agents Chemother. (Bethesda) 35, 185–187.

Duckworth, D. H. (1976). Who discovered bacteriophage? Bacteriol. Rev. 40, 793–802.

Pubmed Abstract | Pubmed Full Text

Eberhard, A., Burlingame, A. L., Eberhard, C., Kenyon, G. L., Nealson, K. H., and Oppenheimer, N. J. (1981). Structural identification of autoinducer of Photobacterium fischeri luciferase. Biochemistry 20, 2444–2449.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Edwards, R. A., and Rohwer, F. (2005). Viral metagenomics. Nat. Rev. Microbiol. 3, 504–510.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Elkins, C. A., Moser, S. A., and Savage, D. C. (2001). Genes encoding bile salt hydrolases and conjugated bile salt transporters in Lactobacillus johnsonii 100-100 and other Lactobacillus species. Microbiology 147, 3403–3412.

Pubmed Abstract | Pubmed Full Text

Estrela, A. B., Heck, M. G., and Abraham, W. R. (2009). Novel approaches to control biofilm infections. Curr. Med. Chem. 16, 1512–1530.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Etchuuya, R., Ito, M., Kitano, S., Shigi, F., Sobue, R., and Maeda, S. (2011). Cell-to-cell transformation in Escherichia coli: a novel type of natural transformation involving cell-derived DNA and a putative promoting pheromone. PLoS ONE 6, e16355. doi:10.1371/journal.pone.0016355

CrossRef Full Text

Fajardo, A., and Martínez, J. L. (2008). Antibiotics as signals that trigger specific bacterial responses. Curr. Opin. Microbiol. 11, 161–167.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Falsetta, M. L., Bair, T. B., Ku, S. C., Vanden Hoven, R. N., Steichen, C. T., McEwan, A. G., Jennings, M. P., and Apicella, M. A. (2009). Transcriptional profiling identifies the metabolic phenotype of gonococcal biofilms. Infect. Immun. 77, 3522–3532.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Feld, L., Schjørring, S., Hammer, K., Licht, T. R., Danielsen, M., Krogfelt, K., and Wilcks, A. (2008). Selective pressure affects transfer and establishment of a Lactobacillus plantarum resistance plasmid in the gastrointestinal environment. J. Antimicrob. Chemother. 61, 845–852.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Fey, P. D., and Olson, M. E. (2010). Current concepts in biofilm formation of Staphylococcus epidermidis. Future Microbiol. 5, 917–913.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Fineran, P. C., Blower, T. R., Foulds, I. J., Humphreys, D. P., Lilley, K. S., and Salmond, G. P. (2009). The phage abortive infection system, ToxIN, functions as a protein-RNA toxin–antitoxin pair. Proc. Natl. Acad. Sci. U.S.A. 106, 894–899.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Frischer, M. E., Stewartb, G. J., and Paul, J. H. (1994). Plasmid transfer to indigenous marine bacterial populations by natural transformation. FEMS Microbiol. Ecol. 15, 127–135.

CrossRef Full Text

Frye, J. G., Lindsey, R. L., Meinersmann, R. J., Berrang, M. E., Jackson, C. R., Englen, M. D., Turpin, J. B., and Fedorka-Cray, P. J. (2011). Related antimicrobial resistance genes detected in different bacterial species co-isolated from swine fecal samples. Foodborne Pathog. Dis. 8, 663–679.

CrossRef Full Text

Fuqua, C., Winans, S. C., and Greenberg, E. P. (1996). Census and consensus in bacterial ecosystems: the LuxR-LuxI family of quorum-sensing transcriptional regulators. Annu. Rev. Microbiol. 50, 727–751.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Fuqua, W. C., and Winans, S. C. (1994). A LuxR-LuxI type regulatory system activates Agrobacterium Ti plasmid conjugal transfer in the presence of a plant tumor metabolite. J. Bacteriol. 176, 2796–2806.

Pubmed Abstract | Pubmed Full Text

Fux, C. A., Costerton, J. W., Stewart, P. S., and Stoodley, P. (2005). Survival strategies of infectious biofilms. Trends Microbiol. 13, 34–40.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Garbeva, P., van Veen, J. A., and van Elsas, J. D. (2004). Microbial diversity in soil: selection microbial populations by plant and soil type and implications for disease suppressiveness. Annu. Rev. Phytopathol. 42, 243–270.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ghigo, J. M. (2001). Natural conjugative plasmids induce bacterial biofilm development. Nature 412, 442–445.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ghosh, D., Roy, K., Williamson, K. E., Srinivasiah, S., Wommack, K. E., and Radosevich, M. (2009). Acyl-homoserine lactones can induce virus production in lysogenic bacteria: an alternative paradigm for prophage induction. Appl. Environ. Microbiol. 75, 7142–7152.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ghosh, D., Roy, K., Williamson, K. E., White, D. C., Wommack, K. E., Sublette, K. L., and Radosevich, M. (2008). Prevalence of lysogeny among soil bacteria and presence of 16S rRNA and trzN genes in viral-community DNA. Appl. Environ. Microbiol. 74, 495–502.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gibiansky, M. L., Conrad, J. C., Jin, F., Gordon, V. D., Motto, D. A., Mathewson, M. A., Stopka, W. G., Zelasko, D. C., Shrout, J. D., and Wong, G. C. (2010). Bacteria use type IV pili to walk upright and detach from surfaces. Science 330, 197.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gödeke, J., Paul, K., Lassak, J., and Thormann, K. M. (2011). Phage-induced lysis enhances biofilm formation in Shewanella oneidensis MR-1. ISME J. 5, 613–626.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Goerke, C., and Wolz, C. (2010). Adaptation of Staphylococcus aureus to the cystic fibrosis lung. Int. J. Med. Microbiol. 300, 520–525.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Goodman, A. E., Hild, E., Marshall, K. C., and Hermansson, M. (1993). Conjugative plasmid transfer between bacteria under simulated marine oligotrophic conditions. Appl. Environ. Microbiol. 59, 1035–1040.

Pubmed Abstract | Pubmed Full Text

Götz, A., Pukall, R., Smit, E., Tietze, E., Prager, R., Tschäpe, H., van Elsas, J. D., and Smalla, K. (1996). Detection and characterization of broad-host-range plasmids in environmental bacteria by PCR. Appl. Environ. Microbiol. 62, 2621–2628.

Pubmed Abstract | Pubmed Full Text

Götz, A., and Smalla, K. (1997). Manure enhances plasmid mobilization and survival of Pseudomonas putida introduced into field soil. Appl. Environ. Microbiol. 63, 1980–1986.

Pubmed Abstract | Pubmed Full Text

Graham, J. B., and Istock, C. A. (1978). Genetic exchange in Bacillus subtilis in soil. Mol. Gen. Genet. 116, 287–298.

Greiner, L. L., Edwards, J. L., Shao, J., Rabinak, C., Entz, D., and Apicella, M. A. (2005). Biofilm formation by Neisseria gonorrhoeae. Infect. Immun. 73, 1964–1970.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Griffith, F. (1928). The significance of pneumococcal types. J. Hyg. 27, 113–159.

CrossRef Full Text

Guerin, E., Cambray, G., Sanchez-Alberola, N., Campoy, S., Erill, I., Da Re, S., Gonzalez-Zorn, B., Barbé, J., Ploy, M. C., and Mazel, D. (2009). The SOS response controls integron recombination. Science 324, 1034.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gulden, R. H., Lerat, S., Hart, M. M., Powell, J. R., Trevors, J. T., Pauls, K. P., Klironomos, J. N., and Swanton, C. J. (2005). Quantitation of transgenic plant DNA in leachate water: real-time polymerase chain reaction analysis. J. Agric. Food Chem. 53, 5858–5865.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Haddock, G., Mullin, M., MacCallum, A., Sherry, A., Tetley, L., Watson, E., Dagleish, M., Smith, D. G., and Everest, P. (2010). Campylobacter jejuni 81-176 forms distinct microcolonies on in vitro-infected human small intestinal tissue prior to biofilm formation. Microbiology 156, 3079–3084.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hader, D. P. (2000). Effects of solar UV-B radiation on aquatic ecosystems. Adv. Space Res. 26, 2029–2040.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hall-Stoodley, L., Costerton, J. W., and Stoodley, P. (2004). Bacterial biofilms: from the natural environment to infectious diseases. Nat. Rev. Microbiol. 2, 95–108.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hannan, S., Ready, D., Jasni, A. S., Rogers, M., Pratten, J., and Roberts, A. P. (2010). Transfer of antibiotic resistance by transformation with eDNA within oral biofilms. FEMS Immunol. Med. Microbiol. 59, 345–349.

Pubmed Abstract | Pubmed Full Text

Harmsen, M., Yang, L., Pamp, S. J., and Tolker-Nielsen, T. (2010). An update on Pseudomonas aeruginosa biofilm formation, tolerance, and dispersal. FEMS Immunol. Med. Microbiol. 59, 253–268.

Pubmed Abstract | Pubmed Full Text

Hassett, D. J., Korfhagen, T. R., Irvin, R. T., Schurr, M. J., Sauer, K., Lau, G. W., Sutton, M. D., Yu, H., and Hoiby, N. (2010). Pseudomonas aeruginosa biofilm infections in cystic fibrosis: insights into pathogenic processes and treatment strategies. Expert Opin. Ther. Targets 14, 117–130.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hastings, P. J., Rosenberg, S. M., and Slack, A. (2004). Antibiotic-induced lateral transfer of antibiotic resistance. Trends Microbiol. 12, 401–404.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hausner, M., and Wuertz, S. (1999). High rates of conjugation in bacterial biofilms as determined by quantitative in situ analysis. Appl. Environ. Microbiol. 65, 3710–3713.

Pubmed Abstract | Pubmed Full Text

Häussler, S. (2010). Multicellular signalling and growth of Pseudomonas aeruginosa. Int. J. Med. Microbiol. 300, 544–548.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hayes, C. S., Aoki, S. K., and Low, D. A. (2010). Bacterial contact-dependent delivery systems. Annu. Rev. Genet. 44, 71–90.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hazen, T. H., Pan, L., Gu, J. D., and Sobecky, P. A. (2010). The contribution of mobile genetic elements to the evolution and ecology of Vibrios. FEMS Microbiol. Ecol. 74, 485–499.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

He, X., Chang, W., Pierce, D. L., Seib, L. O., Wagner, J., and Fuqua, C. (2003). Quorum sensing in Rhizobium sp. strain NGR234 regulates conjugal transfer (tra) gene expression and influences growth rate. J. Bacteriol. 185, 809–822.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

He, Y. Y., Klisch, M., and Häder, D. P. (2002). Adaptation of cyanobacteria to UV-B stress correlated with oxidative stress and oxidative damage. Photochem. Photobiol. 76, 188–196.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Heuer, H., Kopmann, C., Binh, C. T., Top, E. M., and Smalla, K. (2009). Spreading antibiotic resistance through spread manure: characteristics of a novel plasmid type with low%G+C content. Environ. Microbiol. 11, 937–949.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Heuer, H., and Smalla, K. (2007). Manure and sulfadiazine synergistically increased bacterial antibiotic resistance in soil over at least two months. Environ. Microbiol. 9, 657–666.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hinnebusch, B. J., Rosso, M. L., Schwan, T. G., and Carniel, E. (2002). High-frequency conjugative transfer of antibiotic resistance genes to Yersinia pestis in the flea midgut. Mol. Microbiol. 46, 349–354.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hoffman, L. R., D’Argenio, D. A., MacCoss, M. J., Zhang, Z., Jones, R. A., and Miller, S. I. (2005). Aminoglycoside antibiotics induce bacterial biofilm formation. Nature 436, 1171–1175.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Høiby, N., Bjarnsholt, T., Givskov, M., Molin, S., and Ciofu, O. (2010a). Antibiotic resistance of bacterial biofilms. Int. J. Antimicrob. Agents 35, 322–332.

CrossRef Full Text

Høiby, N., Ciofu, O., and Bjarnsholt, T. (2010b). Pseudomonas aeruginosa biofilms in cystic fibrosis. Future Microbiol. 5, 1663–1667.

CrossRef Full Text

Hooper, S. D., Raes, J., Foerstner, K. U., Harrington, E. D., Dalevi, D., and Bork, P. (2008). A molecular study of microbe transfer between distant environments. PLoS ONE 3, e2607. doi: 10.1371/journal.pone.0002607

CrossRef Full Text

Hughes, V. M., and Datta, N. (1983). Conjugative plasmids in bacteria of the “pre-antibiotic” era. Nature 302, 725–726.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ilves, H., Horak, R., and Kivisaar, M. (2001). Involvement of sigma(S) in starvation-induced transposition of Pseudomonas putida transposon Tn4652. J. Bacteriol. 183, 5445–5448.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Jaffe, A., Ogura, T., and Hiraga, S. (1985). Effects of the ccd function of the F plasmid on bacterial growth. J. Bacteriol. 163, 841–849.

Pubmed Abstract | Pubmed Full Text

Jennings, J. C., Kolwyck, D. C., Kays, S. B., Whetsell, A. J., Surber, J. B., Cromwell, G. L., Lirette, R. P., and Glenn, K. C. (2003). Determining whether transgenic and endogenous plant DNA and transgenic protein are detectable in muscle from swine fed Roundup Ready soybean meal. J. Anim. Sci. 81, 1447–1455.

Pubmed Abstract | Pubmed Full Text

Jeters, R. T., Wang, G. R., Moon, K., Shoemaker, N. B., and Salyers, A. A. (2009). Tetracycline-associated transcriptional regulation of transfer genes of the Bacteroides conjugative transposon CTnDOT. J. Bacteriol. 191, 6374–6382.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Jiang, S. C., and Paul, J. H. (1998). Gene transfer by transduction in the marine environment. Appl. Environ. Microbiol. 64, 2780–2787.

Pubmed Abstract | Pubmed Full Text

Johnsen, P. J., Simonsen, G. S., Olsvik, O., Midtvedt, T., and Sundsfjord, A. (2002). Stability, persistence, and evolution of plasmid-encoded VanA glycopeptide resistance in enterococci in the absence of antibiotic selection in vitro and in gnotobiotic mice. Microb. Drug Resist. 8, 161–170.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Jones, B. V., Sun, F., and Marchesi, J. R. (2010). Comparative metagenomic analysis of plasmid encoded functions in the human gut microbiome. BMC Genomics 11, 46. doi: 10.1186/1471-2164-11-46

CrossRef Full Text

Jones, S., Yu, B., Bainton, N. J., Birdsall, M., Bycroft, B. W., Chhabra, S. R., Cox, A. J. R., Golby, P., Reeves, P. J., Stephens, S., Winson, M. K., Salmond, G. P. C., Stewart, G. S. A. B., and Williams, P. (1993). The lux autoinducer regulates the production of exoenzyme virulence determinants in Erwinia carotovora and Pseudomonas aeruginosa. EMBO J. 12, 2477–2482.

Pubmed Abstract | Pubmed Full Text

Juhas, M., van der Meer, J. R., Gaillard, M., Harding, R. M., Hood, D. W., and Crook, D. W. (2009). Genomic islands: tools of bacterial horizontal gene transfer and evolution. FEMS Microbiol. Rev. 33, 376–393.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kaplan, J. B. (2010). Biofilm dispersal: mechanisms, clinical implications, and potential therapeutic uses. J. Dent. Res. 89, 205–218.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Karavolos, M. H., Spencer, H., Bulmer, D. M., Thompson, A., Winzer, K., Williams, P., Hinton, J. C., and Khan, C. M. (2008). Adrenaline modulates the global transcriptional profile of Salmonella revealing a role in the antimicrobial peptide and oxidative stress resistance responses. BMC Genomics 9, 458. doi: 10.1186/1471-2164-9-458

CrossRef Full Text

Kay, M. K., Erwin, T. C., McLean, R. J., and Aron, G. M. (2011). Bacteriophage ecology in Escherichia coli and Pseudomonas aeruginosa mixed-biofilm communities. Appl. Environ. Microbiol. 77, 821–829.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kenzaka, T., Tani, K., and Nasu, M. (2010). High-frequency phage-mediated gene transfer in freshwater environments determined at single-cell level. ISME J. 4, 648–659.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Khachatryan, Z. A., Ktsoyan, Z. A., Manukyan, G. P., Kelly, D., Ghazaryan, K. A., and Aminov, R. I. (2008). Predominant role of host genetics in controlling the composition of gut microbiota. PLoS ONE 3, e3064. doi: 10.1371/journal.pone.0003064

CrossRef Full Text

Koonin, E. V., Makarova, K. S., and Aravind, L. (2001). Horizontal gene transfer in prokaryotes: quantification and classification. Annu. Rev. Microbiol. 55, 709–742.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kroer, N., Barkay, T., Sörensen, S., and Weber, D. (1998). Effect of root exudates and bacterial metabolic activity on conjugative gene transfer in the rhizosphere of a marsh plant. FEMS Microbiol. Ecol. 25, 375–384.

CrossRef Full Text

Kurokawa, K., Itoh, T., Kuwahara, T., Oshima, K., Toh, H., Toyoda, A., Takami, H., Morita, H., Sharma, V. K., Srivastava, T. P., Taylor, T. D., Noguchi, H., Mori, H., Ogura, Y., Ehrlich, D. S., Itoh, K., Takagi, T., Sakaki, Y., Hayashi, T., and Hattori, M. (2007). Comparative metagenomics revealed commonly enriched gene sets in human gut microbiomes. DNA Res. 14, 169–181.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kusumoto, M., Ooka, T., Nishiya, Y., Ogura, Y., Saito, T., Sekine, Y., Iwata, T., Akiba, M., and Hayashi, T. (2011). Insertion sequence-excision enhancer removes transposable elements from bacterial genomes and induces various genomic deletions. Nat. Commun. 2, 152.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Lang, A. S., and Beatty, J. T. (2007). Importance of widespread gene transfer agent genes in alpha-proteobacteria. Trends Microbiol. 15, 54–62.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Lederberg, J. (1952). Cell genetics and hereditary symbiosis. Physiol. Rev. 32, 403–430.

Pubmed Abstract | Pubmed Full Text

Lerat, S., Gulden, R. H., Hart, M. M., Powell, J. R., England, L. S., Pauls, K. P., Swanton, C. J., Klironomos, J. N., and Trevors, J. T. (2007). Quantification and persistence of recombinant DNA of Roundup Ready corn and soybean in rotation. J. Agric. Food Chem. 55, 10226–10231.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Levy, M. S., Balbinder, E., and Nagel, R. (1993). Effect of mutations in SOS genes on UV-induced precise excision of Tn10 in Escherichia coli. Mutat. Res. 293, 241–247.

Pubmed Abstract | Pubmed Full Text

Levy-Booth, D. J., Campbell, R. G., Gulden, R. H., Hart, M. M., Powell, J. R., Klironomos, J. N., Pauls, K. P., Swanton, C. J., Trevors, J. T., and Dunfield, K. E. (2008). Real-time polymerase chain reaction monitoring of recombinant DNA entry into soil from decomposing roundup ready leaf biomass. J. Agric. Food Chem. 56, 6339–6347.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Li, L.-Y., Shoemaker, N. B., and Salyers, A. A. (1993). Characterization of the mobilization region of a Bacteroides insertion element (NBU1) that is excised and transferred by Bacteroides conjugative transposons. J. Bacteriol. 175, 6588–6598.

Pubmed Abstract | Pubmed Full Text

Li, Y., Hao, G., Galvani, C. D., Meng, Y., De La Fuente, L., Hoch, H. C., and Burr, T. J. (2007). Type I and type IV pili of Xylella fastidiosa affect twitching motility, biofilm formation and cell-cell aggregation. Microbiology 153, 719–726.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Liebert, C. A., Hall, R. M., and Summers, A. O. (1999). Transposon Tn21, flagship of the floating genome. Microbiol. Mol. Biol. Rev. 63, 507–522.

Pubmed Abstract | Pubmed Full Text

Lilley, A. K., and Bailey, M. J. (1997). The acquisition of indigenous plasmids by a genetically marked pseudomonad population colonizing the sugar beet phytosphere is related to local environmental conditions. Appl. Environ. Microbiol. 63, 1577–1583.

Pubmed Abstract | Pubmed Full Text

Lilley, A. K., Fry, J. C., Day, M. J., and Bailey, M. J. (1994). In situ transfer of an exogenously isolated plasmid between indigenous donor and recipient Pseudomonas spp. in sugar beet rhizosphere. Microbiology 140, 27–33.

CrossRef Full Text

Lindsay, D., and von Holy, A. (2006). Bacterial biofilms within the clinical setting: what healthcare professionals should know. J. Hosp. Infect. 64, 313–325.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Little, J. W. (2005). “Lysogeny, prophage induction, and lysogenic conversion,” In Phages, eds M. K. Waldor, D. I. Friedman, and S. Adhya (Washington, DC: ASM Press), 37–54.

Lorenz, M. G., Aardema, B. W., and Wackernagel, W. (1988). Highly efficient genetic transformation of Bacillus subtilis attached to sand grains. J. Gen. Microbiol. 134, 107–112.

Pubmed Abstract | Pubmed Full Text

Lorenz, M. G., and Wackernagel, W. (1990). Natural genetic transformation of Pseudomonas stutzeri by sand-adsorbed DNA. Arch. Microbiol. 154, 380–385.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Louis, P., McCrae, S. I., Charrier, C., and Flint, H. J. (2007). Organization of butyrate synthetic genes in human colonic bacteria: phylogenetic conservation and horizontal gene transfer. FEMS Microbiol. Lett. 269, 240–247.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Luke, N. R., Jurcisek, J. A., Bakaletz, L. O., and Campagnari, A. A. (2007). Contribution of Moraxella catarrhalis type IV pili to nasopharyngeal colonization and biofilm formation. Infect. Immun. 75, 5559–5564.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Maeda, S., Ito, M., Ando, T., Ishimoto, Y., Fujisawa, Y., Takahashi, H., Matsuda, A., Sawamura, A., and Kato, S. (2006). Horizontal transfer of nonconjugative plasmids in a colony biofilm of Escherichia coli. FEMS Microbiol. Lett. 255, 115–120.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Mahillon, J., and Chandler, M. (1998). Insertion sequences. Microbiol. Mol. Biol. Rev. 62, 725–774.

Pubmed Abstract | Pubmed Full Text

Maiques, E., Ubeda, C., Campoy, S., Salvador, N., Lasa, I., Novick, R. P., Barbé, J., and Penadés, J. R. (2006). β-lactam antibiotics induce the SOS response and horizontal transfer of virulence factors in Staphylococcus aureus. J. Bacteriol. 188, 2726–2729.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Matsuo, J., Oguri, S., Nakamura, S., Hanawa, T., Fukumoto, T., Hayashi, Y., Kawaguchi, K., Mizutani, Y., Yao, T., Akizawa, K., Suzuki, H., Simizu, C., Matsuno, K., Kamiya, S., and Yamaguchi, H. (2010). Ciliates rapidly enhance the frequency of conjugation between Escherichia coli strains through bacterial accumulation in vesicles. Res. Microbiol. 161, 711–719.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Mazel, D. (2006). Integrons: agents of bacterial evolution. Nat. Rev. Microbiol. 4, 608–620.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

McDaniel, L. D., Young, E., Delaney, J., Ruhnau, F., Ritchie, K. B., and Paul, J. H. (2010). High frequency of horizontal gene transfer in the oceans. Science 330, 50.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

McKenzie, R. L., Aucamp, P. J., Bais, A. F., Björn, L. O., and Ilyas, M. (2007). Changes in biologically-active ultraviolet radiation reaching the earth’s surface. Photochem. Photobiol. Sci. 6, 218–231.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Meibom, K. L., Blokesch, M., Dolganov, N. A., Wu, C. Y., and Schoolnik, G. K. (2005). Chitin induces natural competence in Vibrio cholerae. Science 310, 1824–1827.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Melechen, N. E., and Go, G. (1980). Induction of lambdoid prophages by amino acid deprivation: differential inducibility; role of recA. Mol. Gen. Genet. 180, 147–155.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Miller, C., Thomsen, L. E., Gaggero, C., Mosseri, R., Ingmer, H., and Cohen, S. N. (2004). SOS response induction by beta-lactams and bacterial defense against antibiotic lethality. Science 305, 1629–1631.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Mohr, K. I., and Tebbe, C. C. (2007). Field study results on the probability and risk of a horizontal gene transfer from transgenic herbicide-resistant oilseed rape pollen to gut bacteria of bees. Appl. Microbiol. Biotechnol. 75, 573–582.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Mølbak, L., Molin, S., and Kroer, N. (2007). Root growth and exudate production define the frequency of horizontal plasmid transfer in the Rhizosphere. FEMS Microbiol. Ecol. 59, 167–176.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Molin, S., and Tolker-Nielsen, T. (2003). Gene transfer occurs with enhanced efficiency in biofilms and induces enhanced stabilisation of the biofilm structure. Curr. Opin. Biotechnol. 14, 255–261.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Moon, K., Shoemaker, N. B., Gardner, J. F., and Salyers, A. A. (2005). Regulation of excision genes of the Bacteroides conjugative transposon CTnDOT. J. Bacteriol. 187, 5732–5741.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Moore, I. F., Hughes, D. W., and Wright, G. D. (2005). Tigecycline is modified by the flavin-dependent monooxygenase TetX. Biochemistry 44, 11829–11835.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Morales, D. K., and Hogan, D. A. (2010). Candida albicans interactions with bacteria in the context of human health and disease. PLoS Pathog. 6, e1000886. doi: 10.1371/journal.ppat.1000886

CrossRef Full Text

Morrison, W. D., Miller, R. V., and Sayler, G. S. (1978). Frequency of F116-mediated transduction of Pseudomonas aeruginosa in a freshwater environment. Appl. Environ. Microbiol. 36, 724–730.

Pubmed Abstract | Pubmed Full Text

Moscoso, M., García, E., and López, R. (2009). Pneumococcal biofilms. Int. Microbiol. 12, 77–85.

Pubmed Abstract | Pubmed Full Text

Musovic, S., Oregaard, G., Kroer, N., and Sørensen, S. J. (2006). Cultivation-independent examination of horizontal transfer and host range of an IncP-1 plasmid among Gram-positive and Gram-negative bacteria indigenous to the barley rhizosphere. Appl. Environ. Microbiol. 72, 6687–6692.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Naito, M., Frirdich, E., Fields, J. A., Pryjma, M., Li, J., Cameron, A., Gilbert, M., Thompson, S. A., and Gaynor, E. C. (2010). Effects of sequential Campylobacter jejuni 81-176 lipooligosaccharide core truncations on biofilm formation, stress survival, and pathogenesis. J. Bacteriol. 192, 2182–2192.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Netherwood, T., Martín-Orúe, S. M., O’Donnell, A. G., Gockling, S., Graham, J., Mathers, J. C., and Gilbert, H. J. (2004). Assessing the survival of transgenic plant DNA in the human gastrointestinal tract. Nat. Biotechnol. 22, 204–209.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Nielsen, K. M., Bones, A. M., Smalla, K., and van Elsas, J. D. (1998). Horizontal gene transfer from transgenic plants to terrestrial bacteria – a rare event? FEMS Microbiol. Rev. 22, 79–103.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Novick, R. P. (1987). Plasmid incompatibility. Microbiol. Rev. 51, 381–395.

Pubmed Abstract | Pubmed Full Text

Ochman, H., Lawrence, J. G., and Groisman, E. A. (2000). Lateral gene transfer and the nature of bacterial innovation. Nature 405, 299–304.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ogura, T., and Hiraga, S. (1983). Mini-F plasmid genes that couple host cell division to plasmid proliferation. Proc. Natl. Acad. Sci. U.S.A. 80, 4784–4788.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Oguri, S., Matsuo, J., Hayashi, Y., Nakamura, S., Hanawa, T., Fukumoto, T., Mizutani, Y., Yao, T., Akizawa, K., Suzuki, H., Shimizu, C., Matsuno, K., Kamiya, S., and Yamaguchi, H. (2011). Ciliates promote the transfer of the gene encoding the extended-spectrum beta-lactamase CTX-M-27 between Escherichia coli strains. J. Antimicrob. Chemother. 66, 527–530.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ooka, T., Ogura, Y., Asadulghani, M., Ohnishi, M., Nakayama, K., Terajima, J., Watanabe, H., and Hayashi, T. (2009). Inference of the impact of insertion sequence (IS) elements on bacterial genome diversification through analysis of small-size structural polymorphisms in Escherichia coli O157 genomes. Genome Res. 19, 1809–1816.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Palenik, B., Ren, Q., Tai, V., and Paulsen, I. T. (2009). Coastal Synechococcus metagenome reveals major roles for horizontal gene transfer and plasmids in population diversity. Environ. Microbiol. 11, 349–359.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Parsek, M. R., and Singh, P. K. (2003). Bacterial biofilms: an emerging link to disease pathogenesis. Annu. Rev. Microbiol. 57, 677–701.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Passador, L., Cook, J. M., Gambello, M. J., Rust, L., and Iglewski, B. H. (1993). Expression of Pseudomonas aeruginosa virulence genes requires cell-to-cell communication. Science 260, 1127–1130.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Paul, J. H. (2008). Prophages in marine bacteria: dangerous molecular time bombs or the key to survival in the seas? ISME J. 2, 579–589.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Paul, J. H., Frischer, M. E., and Thurmond, J. M. (1991). Gene transfer in marine water column and sediment microcosms by natural plasmid transformation. Appl. Environ. Microbiol. 57, 1509–1515.

Pubmed Abstract | Pubmed Full Text

Peleg, A. Y., Adams, J., and Paterson, D. L. (2007). Tigecycline efflux as a mechanism for nonsusceptibility in Acinetobacter baumannii. Antimicrob. Agents Chemother. (Bethesda) 51, 2065–2069.

CrossRef Full Text

Petersen, J., Brinkmann, H., Berger, M., Brinkhoff, T., Päuker, O., and Pradella, S. (2011). Origin and evolution of a novel DnaA-like plasmid replication type in Rhodobacterales. Mol. Biol. Evol. 28, 1229–1240.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Petersen, J., Brinkmann, H., and Pradella, S. (2009). Diversity and evolution of repABC type plasmids in Rhodobacterales. Environ. Microbiol. 11, 2627–2638.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Peterson, G., Kumar, A., Gart, E., and Narayanan, S. (2011). Catecholamines increase conjugative gene transfer between enteric bacteria. Microb. Pathog. 51, 1–8.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Petridis, M., Bagdasarian, M., Waldor, M. K., and Walker, E. (2006). Horizontal transfer of Shiga toxin and antibiotic resistance genes among Escherichia coli strains in house fly (Diptera: Muscidae) gut. J. Med. Entomol. 43, 288–295.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Phipps, R. H., Jones, A. K., Tingey, A. P., and Abeyasekera, S. (2005). Effect of corn silage from an herbicide-tolerant genetically modified variety on milk production and absence of transgenic DNA in milk. J. Dairy Sci. 88, 2870–2878.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pierson, L. S., Keppenne, V. D. III, and Wood, D. W. (1994). Phenazine antibiotic biosynthesis in Pseudomonas aureofaciens 30-84 is regulated by phzR in response to cell density. J. Bacteriol. 176, 3966–3974.

Pubmed Abstract | Pubmed Full Text

Piper, K. R., Beck von Bodman, S., and Farrand, S. K. (1993). Conjugation factor of Agrobacterium tumefaciens regulates Ti plasmid transfer by autoinduction. Nature 362, 448–450.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pirhonen, M., Flego, D., Heikinheimo, R., and Palva, E. T. (1993). A small diffusible signal molecule is responsible for the global control of virulence and exoenzyme production in the plant pathogen Erwinia carotovora. EMBO J. 12, 2467–2476.

Pubmed Abstract | Pubmed Full Text

Pontiroli, A., Rizzi, A., Simonet, P., Daffonchio, D., Vogel, T. M., and Monier, J. M. (2009). Visual evidence of horizontal gene transfer between plants and bacteria in the phytosphere of transplastomic tobacco. Appl. Environ. Microbiol. 75, 3314–3322.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Poole, T., and Crippen, T. (2009). Conjugative plasmid transfer between Salmonella enterica Newport and Escherichia coli within the gastrointestinal tract of the lesser mealworm beetle, Alphitobius diaperinus (Coleoptera: Tenebrionidae). Poult. Sci. 88, 1553–1558.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pradella, S., Päuker, O., and Petersen, J. (2010). Genome organization of the marine Roseobacter clade member Marinovum algicola. Arch. Microbiol. 192, 115–126.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Prudhomme, M., Attaiech, L., Sanchez, G., Martin, B., and Claverys, J. P. (2006). Antibiotic stress induces genetic transformability in the human pathogen Streptococcus pneumoniae. Science 313, 89–92.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pukall, R., Tschape, H., and Smalla, K. (1996). Monitoring the spread of broad host and narrow host range plasmids in soil microcosms. FEMS Microbiol. Ecol. 20, 53–66.

CrossRef Full Text

Qin, Y., Keenan, C., and Farrand, S. K. (2009). N- and C-terminal regions of the quorum-sensing activator TraR cooperate in interactions with the alpha and sigma-70 components of RNA polymerase. Mol. Microbiol. 74, 330–346.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ramsay, J. P., Sullivan, J. T., Jambari, N., Ortori, C. A., Heeb, S., Williams, P., Barrett, D. A., Lamont, I. L., and Ronson, C. W. (2009). A LuxRI-family regulatory system controls excision and transfer of the Mesorhizobium loti strain R7A symbiosis island by activating expression of two conserved hypothetical genes. Mol. Microbiol. 73, 1141–1155.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Rastogi, R. P., Richa, Kumar, A., Tyagi, M. B., and Sinha, R. P. (2010). Molecular mechanisms of ultraviolet radiation-induced DNA damage and repair. J. Nucleic Acids 2010, 592980.

Pubmed Abstract | Pubmed Full Text

Ravatn, R., Zehnder, A. J., and van der Meer, J. R. (1998). Low-frequency horizontal transfer of an element containing the chlorocatechol degradation genes from Pseudomonas sp. strain B13 to Pseudomonas putida F1 and to indigenous bacteria in laboratory-scale activated-sludge microcosms. Appl. Environ. Microbiol. 64, 2126–2132.

Pubmed Abstract | Pubmed Full Text

Ray, J. L., Andersen, H. K., Young, S., Nielsen, K. M., and O’Callaghan, M. (2007). An assessment of the potential of herbivorous insect gut bacteria to develop competence for natural transformation. Environ. Biosafety Res. 6, 135–147.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Reisner, A., Höller, B. M., Molin, S., and Zechner, E. L. (2006). Synergistic effects in mixed Escherichia coli biofilms: conjugative plasmid transfer drives biofilm expansion. J. Bacteriol. 188, 3582–3588.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Reyes, A., Haynes, M., Hanson, N., Angly, F. E., Heath, A. C., Rohwer, F., and Gordon, J. I. (2010). Viruses in the faecal microbiota of monozygotic twins and their mothers. Nature 466, 334–338.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Richaume, A., Angle, J. S., and Sadowsky, M. J. (1989). Influence of soil variables on in situ plasmid transfer from Escherichia coli to Rhizobium fredii. Appl. Environ. Microbiol. 55, 1730–1734.

Pubmed Abstract | Pubmed Full Text

Richaume, A., Smit, E., Faurie, G., and van Elsas, J. D. (1992). Influence of soil type on the transfer of plasmid RP4p from Pseudomonas fluorescens to introduced recipient and to indigenous bacteria. FEMS Microbiol. Ecol. 101, 281–292.

CrossRef Full Text

Richter, B., and Smalla, K. (2007). Screening of rhizosphere and soil bacteria for transformability. Environ. Biosafety Res. 6, 91–99.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Roberts, A. P., and Mullany, P. (2009). A modular master on the move: the Tn916 family of mobile genetic elements. Trends Microbiol. 17, 251–258.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Rochelle, P. A., Fry, J. C., and Day, M. J. (1989). Factors affecting conjugal transfer of plasmids encoding mercury resistance from pure cultures and mixed natural suspensions of epilithic bacteria. J. Gen. Microbiol. 135, 409–424.

Pubmed Abstract | Pubmed Full Text

Rohde, H., Frankenberger, S., Zähringer, U., and Mack, D. (2010). Structure, function and contribution of polysaccharide intercellular adhesin (PIA) to Staphylococcus epidermidis biofilm formation and pathogenesis of biomaterial-associated infections. Eur. J. Cell Biol. 89, 103–111.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Romanowski, G., Lorenz, M. G., and Wackernagel, W. (1991). Adsorption of plasmid DNA to mineral surfaces and protection against DNase I. Appl. Environ. Microbiol. 57, 1057–1061.

Pubmed Abstract | Pubmed Full Text

Romero, D., Pérez-García, A., Veening, J. W., de Vicente, A., and Kuipers, O. P. (2006). Transformation of undomesticated strains of Bacillus subtilis by protoplast electroporation. J. Microbiol. Methods 66, 556–559.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Salyers, A. A. (1993). Gene transfer in the mammalian intestinal tract. Curr. Opin. Biotechnol. 4, 294–298.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Salyers, A. A., Gupta, A., and Wang, Y. (2004). Human intestinal bacteria as reservoirs for antibiotic resistance genes. Trends Microbiol. 12, 412–416.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Schwartz, T., Jungfer, C., Heissler, S., Friedrich, F., Faubel, W., and Obst, U. (2009). Combined use of molecular biology taxonomy, Raman spectrometry, and ESEM imaging to study natural biofilms grown on filter materials at waterworks. Chemosphere 77, 249–257.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Senadheera, D., and Cvitkovitch, D. G. (2008). Quorum sensing and biofilm formation by Streptococcus mutans. Adv. Exp. Med. Biol. 631, 178–188.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sengeløv, G., Kowalchuk, G. A., and Sørensen, S. J. (2000). Influence of fungal–bacterial interactions on bacterial conjugation in the residuesphere. FEMS Microbiol. Ecol. 31, 39–45.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sentchilo, V., Ravatn, R., Werlen, C., Zehnder, A. J., and van der Meer, J. R. (2003). Unusual integrase gene expression on the clc genomic island in Pseudomonas sp. strain B13. J. Bacteriol. 185, 4530–4538.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sharon, I., Alperovitch, A., Rohwer, F., Haynes, M., Glaser, F., Atamna-Ismaeel, N., Pinter, R. Y., Partensky, F., Koonin, E. V., Wolf, Y. I., Nelson, N., and Béjà, O. (2009). Photosystem I gene cassettes are present in marine virus genomes. Nature 461, 258–262.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Shime-Hattori, A., Iida, T., Arita, M., Park, K. S., Kodama, T., and Honda, T. (2006). Two type IV pili of Vibrio parahaemolyticus play different roles in biofilm formation. FEMS Microbiol. Lett. 264, 89–97.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Shiner, E. K., Rumbaugh, K. P., and Williams, S. C. (2005). Inter-kingdom signaling: deciphering the language of acyl homoserine lactones. FEMS Microbiol. Rev. 29, 935–947.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Shoemaker, N. B., Wang, G. R., and Salyers, A. A. (2000). Multiple gene products and sequences required for excision of the mobilizable integrated Bacteroides element NBU1. J. Bacteriol. 182, 928–936.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Shoemaker, N. B., Wang, G.-R., Stevens, A. M., and Salyers, A. A. (1993). Excision, transfer, and integration of NBU1, a mobilizable site-selective insertion element. J. Bacteriol. 175, 6578–6587.

Pubmed Abstract | Pubmed Full Text

Showsh, S. A., and Andrews, R. E. Jr. (1992). Tetracycline enhances Tn916-mediated conjugal transfer. Plasmid 28, 213–224.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Silverman, R. J., Nobbs, A. H., Vickerman, M. M., Barbour, M. E., and Jenkinson, H. F. (2010). Interaction of Candida albicans cell wall Als3 protein with Streptococcus gordonii SspB adhesin promotes development of mixed-species communities. Infect. Immun. 78, 4644–4652.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sinha, R. P., and Hader, D. P. (2002). Life under solar UV radiation in aquatic organisms. Adv. Space Res. 30, 1547–1556.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sizemore, R. K., and Colwell, R. R. (1977). Plasmids carried by antibiotic-resistant marine bacteria. Antimicrob. Agents Chemother. (Bethesda) 12, 373–382.

Smalla, K., Krögerrecklenfort, E., Heuer, H., Dejonghe, W., Top, E., Osborn, M., Niewint, J., Tebbe, C., Barr, M., Bailey, M., Greated, A., Thomas, C., Turner, S., Young, P., Nikolakopoulou, D., Karagouni, A., Wolters, A., van Elsas, J. D., Drønen, K., Sandaa, R., Borin, S., Brabhu, J., Grohmann, E., and Sobecky, P. (2000). PCR-based detection of mobile genetic elements in total community DNA. Microbiology 146, 1256–1257.

Pubmed Abstract | Pubmed Full Text

Smiles, D. E. (1988). Aspects of the physical environment of soil organisms. Biol. Fertil. Soils 6, 204–215.

CrossRef Full Text

Smillie, C., Garcillán-Barcia, M. P., Francia, M. V., Rocha, E. P., and de la Cruz, F. (2010). Mobility of plasmids. Microbiol. Mol. Biol. Rev. 74, 434–452.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Smith, D. H. (1967). R factors mediate resistance to mercury, nickel and cobalt. Science 156, 1114–1116.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sobecky, P. A., and Coombs, J. M. (2009). Horizontal gene transfer in metal and radionuclide contaminated soils. Methods Mol. Biol. 532, 455–472.

Pubmed Abstract | Pubmed Full Text

Sørensen, S. J., Bailey, M., Hansen, L. H., Kroer, N., and Wuertz, S. (2005). Studying plasmid horizontal transfer in situ: a critical review. Nat. Rev. Microbiol. 3, 700–710.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sørensen, S. J., Schyberg, T., and Rønn, R. (1999). Predation by protozoa on Escherichia coli K12 in soil and transfer of resistance plasmid RP4 to indigenous bacteria in soil. Appl. Soil Ecol. 11, 79–90.

CrossRef Full Text

Spencer, H., Karavolos, M. H., Bulmer, D. M., Aldridge, P., Chhabra, S. R., Winzer, K., Williams, P., and Khan, C. M. (2010). Genome-wide transposon mutagenesis identifies a role for host neuroendocrine stress hormones in regulating the expression of virulence genes in Salmonella. J. Bacteriol. 192, 714–724.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sperandio, V., Torres, A. G., Jarvis, B., Nataro, J. P., and Kaper, J. B. (2003). Bacteria-host communication: the language of hormones. Proc. Natl. Acad. Sci. U.S.A. 100, 8951–8956.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Stanton, T. B. (2007). Prophage-like gene transfer agents-novel mechanisms of gene exchange for Methanococcus, Desulfovibrio, Brachyspira, and Rhodobacter species. Anaerobe 13, 43–49.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Stanton, T. B., Humphrey, S. B., Sharma, V. K., and Zuerner, R. L. (2008). Collateral effects of antibiotics: carbadox and metronidazole induce VSH-1 and facilitate gene transfer among Brachyspira hyodysenteriae strains. Appl. Environ. Microbiol. 74, 2950–2956.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Steichen, C. T., Cho, C., Shao, J. Q., and Apicella, M. A. (2011). The Neisseria gonorrhoeae biofilm matrix contains DNA, and an indogenous nuclease controls its incorporation. Infect. Immun. 79, 1504–1511.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Stepanauskas, R., Glenn, T. C., Jagoe, C. H., Tuckfield, R. C., Lindell, A. H., King, C. J., and McArthur, J. V. (2006). Coselection for microbial resistance to metals and antibiotics in freshwater microcosms. Environ. Microbiol. 8, 1510–1514.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Stepanauskas, R., Glenn, T. C., Jagoe, C. H., Tuckfield, R. C., Lindell, A. H., and McArthur, J. V. (2005). Elevated microbial tolerance to metals and antibiotics in metal-contaminated industrial environments. Environ. Sci. Technol. 39, 3671–3678.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Stephens, P. M., O’Sullivan, M., and O’Gara, F. (1987). Effect of bacteriophage on colonization of sugarbeet roots by fluorescent Pseudomonas spp. Appl. Environ. Microbiol. 53, 1164–1167.

Pubmed Abstract | Pubmed Full Text

Stevens, A. M., Shoemaker, N. B., Li, L. Y., and Salyers, A. A. (1993). Tetracycline regulation of genes on Bacteroides conjugative transposons. J. Bacteriol. 175, 6134–6141.

Pubmed Abstract | Pubmed Full Text

Stewart, G. J., and Sinigalliano, C. D. (1990). Detection of horizontal gene transfer by natural transformation in native and introduced species of bacteria in marine and synthetic sediments. Appl. Environ. Microbiol. 56, 1818–1824.

Pubmed Abstract | Pubmed Full Text

Stewart, P. S., and Costerton, J. W. (2001). Antibiotic resistance of bacteria in biofilms. Lancet 358, 135–138.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Su, Y. A., He, P., and Clewell, D. B. (1992). Characterization of the tet(M) determinant of Tn916: evidence for regulation by transcription attenuation. Antimicrob. Agents Chemother. (Bethesda) 36, 769–778.

Teh, K. H., Flint, S., and French, N. (2010). Biofilm formation by Campylobacter jejuni in controlled mixed-microbial populations. Int. J. Food Microbiol. 143, 118–124.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Thimm, T., Hoffmann, A., Fritz, I., and Tebbe, C. C. (2001). Contribution of the earthworm Lumbricus rubellus (Annelida, Oligochaeta) to the establishment of plasmids in soil bacterial communities. Microb. Ecol. 41, 341–351.

Pubmed Abstract | Pubmed Full Text

Timms-Wilson, T. M., Van Overbeek, L. S., Bailey, M. J., Trevors, J. T., and Van Elsas, J. D. (2001). “Quantification of gene transfer in soil and the rhizosphere,” in Manual of Environmental Microbiology, eds C. J. Hurst, R. L. Crawford, G. R. Knudsen, M. J. McInerney, and L. D. Stetzenbach (Washington, DC: ASM Press), 648–659.

Toba, F. A., Thompson, M. G., Campbell, B. R., Junker, L. M., Ruggeberg, K. G., and Hay, A. G. (2011). Role of DLP12 lysis genes in E. coli biofilm formation. Microbiology 157, 1640–1650.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Toleman, M. A., Bennett, P. M., and Walsh, T. R. (2006). ISCR elements: novel gene-capturing systems of the 21st century? Microbiol. Mol. Biol. Rev. 70, 296–316.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Toleman, M. A., and Walsh, T. R. (2010). ISCR elements are key players in IncA/C plasmid evolution. Antimicrob. Agents Chemother. (Bethesda) 54, 3534.

CrossRef Full Text

Toomey, N., Monaghan, A., Fanning, S., and Bolton, D. (2009). Transfer of antibiotic resistance marker genes between lactic acid bacteria in model rumen and plant environments. Appl. Environ. Microbiol. 75, 3146–3152.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Top, E. M., De Rore, H., Collard, J. M., Gellens, V., and Slobodkina, G. (1995). Retromobilization of heavy metal resistance genes in unpolluted and heavy metal polluted soil. FEMS Microbiol. Ecol. 18, 191–203.

CrossRef Full Text

Torres, O. R., Korman, R. Z., Zahler, S. A., and Dunny, G. M. (1991). The conjugative transposon Tn925: enhancement of conjugal transfer by tetracycline in Enterococcus faecalis and mobilization of chromosomal genes in Bacillus subtilis and E. faecalis. Mol. Gen. Genet. 225, 395–400.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Trevors, J. T., Van Elsas, J. D., Van Overbeek, L. S., and Starodub, M. E. (1990). Transport of a genetically engineered Pseudomonas fluorescens strain through a soil microcosm. Appl. Environ. Microbiol. 56, 401–408.

Pubmed Abstract | Pubmed Full Text

Tun-Garrido, C., Bustos, P., González, V., and Brom, S. (2003). Conjugative transfer of p42a from Rhizobium etli CFN42, which is required for mobilization of the symbiotic plasmid, is regulated by quorum sensing. J. Bacteriol. 185, 1681–1692.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ubeda, C., Maiques, E., Knecht, E., Lasa, I., Novick, R. P., and Penadés, J. R. (2006). Antibiotic-induced SOS response promotes horizontal dissemination of pathogenicity island-encoded virulence factors in staphylococci. Mol. Microbiol. 56, 836–844.

CrossRef Full Text

Valentine, P. J., Shoemaker, N. B., and Salyers, A. A. (1988). Mobilization of Bacteroides plasmids by Bacteroides conjugal elements. J. Bacteriol. 170, 1319–1324.

Pubmed Abstract | Pubmed Full Text

Van Elsas, J. D., and Bailey, M. J. (2002). The ecology of transfer of mobile genetic elements. FEMS Microbiol. Ecol. 42, 187–197.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Van Elsas, J. D., Fry, J. C., Hirsch, P., and Molin, S. (2000). “Ecology of plasmid transfer and spread,” in The Horizontal Gene Pool; Bacterial Plasmids and Gene Spread, ed. C. M. Thomas (Amsterdam: Harwood Scientific Publisher), 175–206.

Van Elsas, J. D., Trevors, J. T., and Starodub, M. E. (1988). Bacterial conjugation between pseudomonads in the rhizosphere of wheat. FEMS Microbiol. Ecol. 54, 299–306.

CrossRef Full Text

Van Melderen, L. (2010). Toxin-antitoxin systems: why so many, what for? Curr. Opin. Microbiol. 13, 781–785.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Van Randen, J., and Venema, G. (1984). Direct plasmid transfer from replica-plated E. coli colonies to competent B. subtilis cells. Identification of an E. coli clone carrying the hisH and tyrA genes of B. subtilis. Mol. Gen. Genet. 195, 57–61.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Varga, J. J., Therit, B., and Melville, S. B. (2008). Type IV pili and the CcpA protein are needed for maximal biofilm formation by the Gram-positive anaerobic pathogen Clostridium perfringens. Infect. Immun. 76, 4944–4951.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Vos, M., Birkett, P. J., Birch, E., Griffiths, R. I., and Buckling, A. (2009). Local adaptation of bacteriophages to their bacterial hosts in soil. Science 325, 833.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wang, X., Kim, Y., Ma, Q., Hong, S. H., Pokusaeva, K., Sturino, J. M., and Wood, T. K. (2010). Cryptic prophages help bacteria cope with adverse environments. Nat. Commun. 1, 147.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wang, X., Kim, Y., and Wood, T. K. (2009). Control and benefits of CP4-57 prophage excision in Escherichia coli biofilms. ISME J. 3, 1164–1179.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wang, X., Li, M., Yan, Q., Chen, X., Geng, J., Xie, Z., and Shen, P. (2007). Across genus plasmid transformation between Bacillus subtilis and Escherichia coli and the effect of Escherichia coli on the transforming ability of free plasmid DNA. Curr. Microbiol. 54, 450–456.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wang, Y., Rotman, E. R., Shoemaker, N. B., and Salyers, A. A. (2005). Translational control of tetracycline resistance and conjugation in the Bacteroides conjugative transposon CTnDOT. J. Bacteriol. 187, 2673–2680.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Watanabe, T. (1963). Infective heredity of multiple drug resistance in bacteria. Bacteriol. Rev. 27, 87–115.

Pubmed Abstract | Pubmed Full Text

Watanabe, T., and Fukasawa, T. (1961). Episome-mediated transfer of drug resistance in Enterobacteriaceae. I. Transfer of resistance factors by conjugation. J. Bacteriol. 81, 669–678.

Pubmed Abstract | Pubmed Full Text

Weinberg, S. R., and Stotzky, G. (1972). Conjugation and genetic recombination of Escherichia coli in soil. Soil Biol. Biochem. 4, 171–180.

CrossRef Full Text

Whittle, G., Shoemaker, N. B., and Salyers, A. A. (2002). Identification of two genes involved in the modulation of conjugal transfer of the Bacteroides conjugative transposon CTnDOT. J. Bacteriol. 184, 3839–3847.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wilcks, A., and Jacobsen, B. B. (2010). Lack of detectable DNA uptake by transformation of selected recipients in mono-associated rats. BMC Res. Notes 3, 49. doi:10.1186/1756-0500-3-49

CrossRef Full Text

Williams, D. W., Kuriyama, T., Silva, S., Malic, S., and Lewis, M. A. O. (2011). Candida biofilms and oral candidosis: treatment and prevention. Periodontol. 2000. 55, 250–265.

CrossRef Full Text

Williams, H. G., Benstead, J., Frischer, M. E., and Paul, J. H. (1997). Alteration in plasmid DNA following natural transformation to populations of marine bacteria. Mol. Marine Biol. Biotechnol. 6, 238–247.

Pubmed Abstract | Pubmed Full Text

Williamson, K. E., Radosevich, M., Smith, D. W., and Wommack, K. E. (2007). Incidence of lysogeny within temperate and extreme soil environments. Environ. Microbiol. 9, 2563–2574.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Williamson, K. E., Schnitker, J. B., Radosevich, M., Smith, D. W., and Wommack, K. E. (2008). Cultivation-based assessment of lysogeny among soil bacteria. Microb. Ecol. 56, 437–447.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wozniak, R. A., and Waldor, M. K. (2010). Integrative and conjugative elements: mosaic mobile genetic elements enabling dynamic lateral gene flow. Nat. Rev. Microbiol. 8, 552–563.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wright, G. D. (2010). Antibiotic resistance in the environment: a link to the clinic? Curr Opin Microbiol. 13, 589–594.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wright, M. S., Baker-Austin, C., Lindell, A. H., Stepanauskas, R., Stokes, H. W., and McArthur, J. V. (2008). Influence of industrial contamination on mobile genetic elements: class 1 integron abundance and gene cassette structure in aquatic bacterial communities. ISME J. 2, 417–428.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wright, M. S., Peltier, G. L., Stepanauskas, R., and McArthur, J. V. (2006). Bacterial tolerances to metals and antibiotics in metal-contaminated and reference streams. FEMS Microbiol. Ecol. 58, 293–302.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Yen, H. C., Hu, N. T., and Marrs, B. L. (1979). Characterization of the gene transfer agent made by an overproducer mutant of Rhodopseudomonas capsulata. J. Mol. Biol. 131, 157–168.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Young, H. K. (1993). Antimicrobial resistance spread in aquatic environments. J. Antimicrob. Chemother. 31, 627–635.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Zhang, L. H., and Kerr, A. (1991). A diffusible compound can enhance conjugal transfer of the Ti plasmid in Agrobacterium tumefaciens. J. Bacteriol. 173, 1867–1872.

Pubmed Abstract | Pubmed Full Text

Zhao, J. S., Deng, Y., Manno, D., and Hawari, J. (2010). Shewanella spp. genomic evolution for a cold marine lifestyle and in-situ explosive biodegradation. PLoS ONE 5, e9109. doi: 10.1371/journal.pone.0009109

CrossRef Full Text

Zhu, Y., Li, D., Wang, F., Yin, J., and Jin, H. (2004). Nutritional assessment and fate of DNA of soybean meal from roundup ready or conventional soybeans using rats. Arch. Anim. Nutr. 58, 295–310.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Keywords: horizontal gene transfer, soil, aquatic ecosystems, gut, biofilm

Citation: Aminov RI (2011) Horizontal gene exchange in environmental microbiota. Front. Microbio. 2:158. doi: 10.3389/fmicb.2011.00158

Received: 15 April 2011; Paper pending published: 23 May 2011;
Accepted: 11 July 2011; Published online: 26 July 2011.

Edited by:

Kornelia Smalla, Julius Kühn-Institut, Germany

Reviewed by:

Charles Knapp, University of Strathclyde, UK
Ed Topp, Agriculture and Agri-Food Canada, Canada

Copyright: © 2011 Aminov. This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

*Correspondence: Rustam I. Aminov, Rowett Institute of Nutrition and Health, College of Life Sciences and Medicine, University of Aberdeen, Greenburn Road, Aberdeen AB21 9SB, UK. e-mail: r.aminov@abdn.ac.uk