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MINI REVIEW article

Front. Plant Sci., 09 September 2015
Sec. Plant Pathogen Interactions
This article is part of the Research Topic Signaling in the phytomicrobiome View all 12 articles

Signaling in the phytomicrobiome: breadth and potential

  • 1Plant Science Department, McGill University/Macdonald Campus, Sainte-Anne-de-Bellevue, QC, Canada
  • 2Inocucor Technologies Inc., Montréal, QC, Canada

Higher plants have evolved intimate, complex, subtle, and relatively constant relationships with a suite of microbes, the phytomicrobiome. Over the last few decades we have learned that plants and microbes can use molecular signals to communicate. This is well-established for the legume-rhizobia nitrogen-fixing symbiosis, and reasonably elucidated for mycorrhizal associations. Bacteria within the phytomircobiome communicate among themselves through quorum sensing and other mechanisms. Plants also detect materials produced by potential pathogens and activate pathogen-response systems. This intercommunication dictates aspects of plant development, architecture, and productivity. Understanding this signaling via biochemical, genomics, proteomics, and metabolomic studies has added valuable knowledge regarding development of effective, low-cost, eco-friendly crop inputs that reduce fossil fuel intense inputs. This knowledge underpins phytomicrobiome engineering: manipulating the beneficial consortia that manufacture signals/products that improve the ability of the plant-phytomicrobiome community to deal with various soil and climatic conditions, leading to enhanced overall crop plant productivity.

Background

Most energy in the terrestrial biosphere enters it through photosynthesis (Imhoff et al., 2004) carried out by plant leaves (Luo et al., 2006). Non-photosynthetic organisms with reliable access to plant energy are in an advantaged situation. Under natural conditions higher plants are always associated with a complex and relatively constant microflora (Rout and Southworth, 2013; Turner et al., 2013a). Terrestrial plants release ∼20% of photosynthetically fixed carbon as root exudates, resulting in an energy rich rhizosphere (Kuzyakov and Domanski, 2000), and a rich, generally compositionally consistent phytomicrobiome (Bulgarelli et al., 2012; Hirsch and Mauchline, 2012; Lundberg et al., 2012). These exudates vary among species, specific genotypes within species, stages of plant development and growing conditions, and influence the composition of the rhizomicrobiome (Bascom-Slack et al., 2012; Marasco et al., 2012; Badri et al., 2013a,b; Turner et al., 2013a,b; Chaparro et al., 2014).

Phytomicrobiome associations are analogous to the animal microbiome (Koenig et al., 2011); microbiome diversity, stability, and resilience play a large role in human health and disease (Cho and Blaser, 2012). Plants have likely had associated microbes since they colonized the land, almost half a billion years ago; roots of the first terrestrial plants were almost certainly less sophisticated than those that followed, making these early plants more in need of microbial assistance (Knack et al., 2015). Fossil endomycorrhizal associations occur in the early Devonian period, demonstrating association of plant roots with fungal elements of the rhizomicrobiome (Taylor, 1995; Bonfante and Genre, 2008; Porras-Alfaro and Bayman, 2011). Mycorrhizal relationships are sophisticated and their presence >400 million years ago indicates that the phytomicrobiome had already been developing for some time; it seems likely that bacterial associations have been present for at least as long. As plants adapted to and spread through diverse terrestrial environments, evolving to grow under a range of conditions, it is probable that their associations with microbes also evolved. This community of microbes is the phytomicrobiome (Smith and Zhou, 2014), with its root associated (Hirsch and Mauchline, 2012; Lundberg et al., 2012; rhizomicrobiome), above ground associated (Rastogi et al., 2012, 2013; Badri et al., 2013b; Kembel et al., 2014; phyllomicrobiome) and interior (Berg et al., 2014; endosphere) components. Even “lower plants” such as Sphagnum sp. have complex phytomicrobiomes, including highly specific associations with diazotrophs (Bragina et al., 2013).

Hence, a plant growing in nature is not a single organism; it is a community: a holobiont (Hartmann et al., 2014). While a plant growing in isolation can be very useful for research purposes, it is an anomaly. Like the human microbiome, the phytomicrobiome constitutes an underappreciated biological aspect (physiology, genome, metabolome, etc.) of plants. Plants and their associated phytomicrobiome affect each other in various and subtle ways (Berendsen et al., 2012); a field-grown plant is a meta-organism (Berg et al., 2013), having a persistent and regulated relationship with its phytomicrobiome. The composition of the phytomicrobiome is regulated by numerous biotic and abiotic factors including the complex matrix of plant–microbe and microbe–microbe communications. This communication is carried out through the release of signaling compounds, the forms and functions of which are currently being elucidated. This new understanding can be exploited to: (1) develop new approaches to crop growth promotion, (2) optimize related fermentation and formulation processess, and (3) develop novel and more consistent biocontrol mechanisms for field crops (East, 2013).

The Phytomicrobiome and Plant Growth

There has been an upsurge in phytomicrobiome publications; this community of microbes is now seen as key to the growth and health of plants (Schmidt et al., 2014); there is still a great deal to be learned about the composition and nature of interactions among members of this community, and its interactions with the host plant.

Microbes associate with the phyllosphere (as both epi- and endophytes, of leaves and stems), rhizosphere and reproductive structures such as flowers, fruits and seeds. In grape, Pseudomonas and Bacillus spp. colonize the epidermis and xylem of the ovary and ovules, while Bacillus spp. colonize berries and seed cell walls (Lugtenberg and Kamilova, 2009; Compant et al., 2010a,b). Nitrogen-fixing plant growth promoting rhizobacteria (PGPR; Loiret et al., 2004; Quecine et al., 2012; e.g., Acetobacter diazotrophicus, Pantoea agglomerans 33.1) associate with plant roots (Pisa et al., 2011), and stems of sugarcane (Velázquez et al., 2008), residing in the apoplast in a low-nitrogen, high-sucrose environment (Dong et al., 1994). Other nitrogen-fixing bacteria (Azotobacter, Enterobacter, Bacillus, Klebsiella, Azospirillum, Herbaspirillum, Gluconacetobacter, Burkholderia, Azoarcus) are found in grasses such as rice and maize (Von Bulow and Dobereiner, 1975; James, 2000; Baldani et al., 2002; Boddey et al., 2003; Santi et al., 2013). Phyllomicrobiome communities influence plant development and ecosystem function, while the host controls aspects of phytomicrobiome composition and function. Environmental factors are known to alter biosynthesis of many metabolites within plants; specific members of the rhizomicrobiome also alter plant development, growth, and composition. Treatment of leaves with specific phyllomicrobiome components suppresses feeding by insect larvae (Badri et al., 2013b). The distribution and community composition of microbes in the phyllosphere is thought to be somewhat random, whereas plants create niches in the rhizosphere and endosphere to accommodate specific microbial communities (Lebeis, 2015).

The rhizomicrobiome is comprised of diverse root endophytes (Gaiero et al., 2013), some of which are PGPRs. Compositionally the rhizomicrobiome is dynamic in time and space, in response to environmental conditions, the presence of other soil organisms, soil physical conditions, plant species and genotype and interactions between a specific microbe and a specific plant type. The best characterized microbes in the rhizomicrobiome are the PGPR. These include bacteria in the soil near plant roots, on the surface of plant root systems, in spaces between root cells or inside specialized cells of root nodules; they stimulate plant growth through a wide range of mechanisms (Gray and Smith, 2005; Mabood et al., 2014), such as: (1) nutrient solubilization (particularly phosphorus – Boddey et al., 2003; Kennedy et al., 2004; Trabelsi and Mhamdi, 2013), (2) production of metal chelating siderophores, (3) nitrogen fixation (Vessey, 2003; Bhattacharyya and Jha, 2012; Drogue et al., 2012), (4) production of phytohormones, (5) production of 1-aminocyclopropane-1-carboxylate deaminase, (6) production of volatile organic compounds, (7) induction of systemic resistance [induced systemic resistance (ISR) and systemic required resistance (SAR) – Jung et al., 2008b, 2011], and (8) suppression of disease through antibiosis (Bhattacharyya and Jha, 2012; Spence et al., 2014). It has also been shown that “signal” compounds produced by bacteria in the phytomicrobiome stimulate plant growth (Prithiviraj et al., 2003; Mabood et al., 2006a; Lee et al., 2009), particularly in the presence of abiotic stress (Wang et al., 2012; Subramanian, 2014; Prudent et al., 2015). In the broadest sense PGPR include legume-nodulating rhizobia. PGPR reside outside plant cells (extracellular – ePGPR) or, like rhizobia, live inside them (intracellular – iPGPR; Gray and Smith, 2005). Application of PGPR to crops, except for rhizobia, has met with mixed results in the field, causing increased growth sometimes and not others (Nelson, 2004). Elements of the phytomicrobiome also assist plants in dealing with abiotic stress. The Arabidopsis phytomicrobiome, for instance, can sense drought stress and help the plant maintain productivity (Zolla et al., 2013). Further, mycorrhizal associations enhance crop salinity tolerance (Porcel et al., 2012; Ruiz-Lozano et al., 2012). At a time when we are looking to crop plants to provide biofuels and other bioproducts while still feeding the world’s growing population, against a background of climate change, understanding and developing technologies that can increase overall plant productivity is imperative (Ragauskas et al., 2006; Babalola, 2010; Dutta and Podile, 2010; Beneduzi et al., 2012; Orrell and Bennett, 2013).

Newer deployments of PGPR and/or arbuscular mycorrhizal fungi (AMF) consortia that promote crop productivity by mimicking, or partially reconstructing, the phytomicrobiome are being developed. Application of a PGPR consortium (Bacillus amyloliquefaciens IN937a, Bacillus pumilus T4, AMF Glomus intraradices) to greenhouse tomato resulted in full yield with 30% less fertilizer (Adesemoye et al., 2009). Co-inoculation of B. japonicum 532C, RCR3407 and B. subtilis MIB600 increased biomass for two soybean cultivars (Atieno et al., 2012). Co-inoculation of B. japonicum E109 and Bacillus amyloliquefaciens LL2012 improved soybean nodulation efficiency. Phytohormone production by B. amyloliquefaciens LL2012 improved nodulation efficiency for B. japonicum E109 (Masciarelli et al., 2014). A consortium of B. megaterium, Enterobacter sp., B. thuringiensis and Bacillus sp., plus composted sugar beet residue, on Lavandula dentata L. helped restore soils by increasing phosphorus availability, soil nitrogen fixation and foliar NPK content (Mengual et al., 2014).

Signaling in the Phytomicrobiome

The complex community formed by the plant and its phytomicrobiome is carefully orchestrated; there is signal exchange among the various microbes involved, and also between the host plant and the microbe community (Engelmoer et al., 2014). These signals regulate aspects of each other’s activities and the community overall. Microbial chemical signals can help plants initiate immune responses to harmful pathogens or allow the entry of beneficial endophytes (Hartmann et al., 2014). Microbe associated molecular patterns (MAMPs) play a key role in plant immune response and antibiotic secretion in microbes. Plant associated Bacillus strains have been shown to down-regulate MAMP-regulated immune response including antibiotic secretion in the presence of plant root exudates to better facilitate root infection (Lakshmanan et al., 2012). Bacteria can also interfere with signaling between plants and other microbial strains. LCOs are similar in structure to chitin and can be cleaved by bacterially produced chitinases, thus interfering with plant microbe symbioses (Jung et al., 2008a). Other aspects plant–microbe symbiosis follow pathways similar to pathogen infection (Barea, 2015).

Signaling compounds produced by plants include a variety of root exudates such as primary metabolites (carbohydrates, proteins, organic acids, etc.) and secondary metabolites (flavonoids, phenol, phytohormones, etc.). Plants often excrete more of these signaling compounds in response to stress. PGPR-to-plant signaling compounds include phytohormones, acyl homoserine lactones, phenols and peptides and can also act as microbe to microbe signals (Barea, 2015). Root exudates signal and recruit specific microbial communities. Secretion of malic acid in Arabidopsis thaliana in response to foliage pathogen attack stimulates the formation of beneficial biofilms in the rhizosphere (Rudrappa et al., 2008).

That plants and microbes use signal compounds to communicate during establishment of beneficial plant-microbe interactions (Desbrosses and Stougaard, 2011), is well-described for the legume-rhizobia nitrogen fixing symbiosis (Oldroyd et al., 2010; Giles et al., 2011; Oldroyd, 2013), and somewhat elucidated for mycorrhizal associations (Gough and Cullimore, 2011). In the legume-rhizobia relationship the plant releases flavonoid signals to rhizobia (Hassan and Mathesius, 2012) or, in some cases, jasmonate signals (Mabood et al., 2006a,b; Mabood et al., 2014), followed by rhizobial production of lipo-chitooligosaccharides (LCOs) as return signals (Oldroyd, 2013). The LCOs are bound by LysM receptors, which have kinase activity (Antolin-Llovera et al., 2012), changing root hormone profile (Zamioudis et al., 2013) and triggering development of root nodules. Plants also communicate with, or otherwise influence the phytomicrobiome, affecting its composition and structure (Delaux et al., 2012; Badri et al., 2013a; Bálint et al., 2013; Peiffer et al., 2013; Turner et al., 2013b; Venkateshwaran et al., 2013; Chaparro et al., 2014; Evangelisti et al., 2014). Bacteria also communicate among themselves (Cretoiu et al., 2013); quorum sensing via N-acyl homoserine lactone (Teplitski et al., 2000) is well-characterized, and there are likely other, as of yet unknown, mechanisms (Lv et al., 2013). Quorum sensing signals can trigger immune responses and changes in hormone profiles in plants, leading to growth responses (Hartmann and Schikora, 2012). Quorum sensing in the phytomicrobiome will be the subject of an upcoming Frontiers in Plant Science theme volume (Plant responses to bacterial quorum sensing signal molecules, topic editors Schikora A, Hartmann A, and Munchen HZ). This sort of signaling almost certainly occurs in the phytomicrobiome. Plants also detect materials produced by potential pathogens and respond by activating response systems (Tena et al., 2011). Phytomicrobiome intercommunication in the rhizosphere dictates aspects of above-ground plant architecture and above-ground symbiotic/pathogenic microbial communities (Segonzac and Zipfel, 2011; Tena et al., 2011). Similarly, pathogen or herbivore attacks above ground can effect microbial community composition in the rhizosphere. Above ground injury has been shown to stimulate the production of signaling compounds in plant roots (Lakshmanan et al., 2012). Greater photosynthetic rates under elevated CO2 conditions have been shown to change microbial community composition in the rhizosphere (Berlec, 2012; He et al., 2012). Understanding plant responses to microbial signals via proteomics (Elmore et al., 2012; Nguyen et al., 2012; Rose et al., 2012) and metabolomics (Watrous et al., 2012; Zhang et al., 2012) studies has added valuable knowledge toward developing effective low-cost and eco-friendly practices to reduce fossil-fuel dependent crop inputs, leading to interest in phytomicrobiomes engineered to enhanced plant growth under variable soil and climatic conditions, improving global crop productivity.

Surprisingly, LCOs are also able to stimulate plant growth directly (Souleimanov et al., 2002; Prithiviraj et al., 2003; Almaraz et al., 2007; Khan et al., 2008; Wang et al., 2012); confirmed by Oláh et al. (2005) for root growth in Medicago truncatula, Chen et al. (2007) for accelerated flowering (a typical response to stress) and increased yield in tomato, and stimulation of early somatic embryo development in Norway spruce (Dyachok et al., 2002). Enhanced germination and seedling growth, along with the mitogenic nature of LCOs, suggest accelerated meristem activity. Products based on LCOs are now used to treat seed sown into several 10s of million ha of crop land each year, largely corn and soybean. A similar jasmonate product is now available. The effects of LCOs are much greater when stress (salt, drought, cold) is present than under optimum conditions (Smith, 2009, 2010; Subramanian et al., 2009, 2010, 2011; Schwinghamer et al., 2014; Subramanian, 2014; Prudent et al., 2015). Thuricin 17, a bacteriocin produced by Bacillus thuringiensis NEB17 isolated from soybean roots, improves plant growth and resilience to stress (Schwinghamer et al., 2014; Subramanian, 2014). Inhibition of legume nodulation, and of overall plant growth, by stressful conditions can be overcome by LCOs (nodulation – Zhang and Smith, 1995, 2002; plant growth – Schwinghamer et al., 2014; Prudent et al., 2015); Estévez et al. (2009) showed that at least one rhizobial strain produce different LCOs when grown under salt stress, and that salt stress itself can induce the nod genes of this strain (Guasch-Vidal et al., 2013).

Future Directions

We now understand that the phytomicrobiome is a complex, structured and dynamic community with a relatively constant set of potential members, whose relative abundances can shift within plant species and their genotypes, and in response to both abiotic conditions and plant development, leading to dynamism in the communications among the microbial community and the host plants. Methods, such as high throughput genotyping, are allowing us to determine the taxonomic diversity of the phytomicrobiome (Hirsch and Mauchline, 2012; Peiffer et al., 2013; Turner et al., 2013b). A better understanding of plant signaling may also become a tool for investigating community composition of the phytomicrobiome. Root exudates play an important role in the formation of microbial communities in the rhizosphere and can be useful in predicting community compositions (Berg et al., 2014). Correlations between phytomicrobiome bacterial diversity and host growth, mortality, and function suggest that incorporating information on plant–microbe associations will improve our ability to understand plant functional biogeography and drivers of variation in plant and ecosystem function (Kembel et al., 2014). It has even been suggested that beneficial effects of the phytomicrobiome could be enhanced through plant breeding, developing genotypes that encourage best membership in the phytomicrobiome (Bakker et al., 2012). More effective methods to study plant MAMP receptors are being developed (Wittulsky et al., 2014) and could lead to ways to engineer plant recognition receptors.

Novel methods of manipulating signaling in the phytomicrobiome could lead to crop production practices that are less reliant on non-renewable resources and crops more resilient in the face of stresses (Marasco et al., 2012), most crucially, those associated with climate change. Plant stress response seems to play an important role in the release of signaling compounds in the rhizosphere but the specifics of this interaction are still unclear. A better understanding of the relationship between environmental plant stress and signaling could help in developing technologies that utilize plant signaling in crop stress alleviation (Barea, 2015).

Recent developments have shown that temperature (Schwinghamer et al., 2014) and water stress (Prudent et al., 2015) can influence plant microbe communication. Environmental factors likely play an important and underdescribed role in signaling in the phytomicrobiome. Variable environmental factors may account for some of the inconsistency observed in field trials of microbial products that previously yielded favorable results in laboratory conditions. A more complete understanding of how plant–microbe communication is influenced by environmental factors will likely be useful in achieving more consistent results with agricultural microbial products.

Despite being at an early stage in understanding these communities, it is clear that there is considerable potential for application of coordinated microbial consortia to crop agriculture and, thus, to enhancing global food security. While advances in methods and technologies in microbiology used to investigate non-culturable microbial strains have led to a stronger focus on a community level approach to plant–microbe interaction research (Berlec, 2012; Rastogi et al., 2013), isolated, culturable microbial strains are still required for most plant–microbe signaling research, particularly if the research is aimed at developing commercial microbial products. Culturable strains are needed both to produce a consistent product and to verify growth promotion through plant growth trials. There are clear opportunities for development of products for more sustainable agronomic production systems (Kloepper et al., 2004; De-la-Peña and Loyola-Vargas, 2014). A range of PGPR have been identified, and even developed into products utilized in crop production. Signaling compounds that directly stimulate plant growth or improve stress tolerance have great potential because they can be produced by microbes in a controlled bioreactor rather than in variable field conditions as with inoculants. The global market for biostimulants has been projected to reach $2.241 million by 2018 and to have a compounded annual growth rate of 12.5% from 2013 to 2018 (Calvo et al., 2014). Products based on multispecies consortia may address consistency in performance observed in single species inoculants. Industry is working to harness the knowledge surrounding the phytomicrobiome, to quickly bring sustainable, consortia-based products to production agriculture.

Conflict of Interest Statement

The fourth author is Executive Vice President of Technology and Innovation at Inocucor Technologies, a company that manufactures and sells microbial consortia for plants; the first author conducts research in collaboration with this company, where the research is funded through a Canadian Federal Government program (Mitacs) which levers industrial funding.

References

Adesemoye, A. O., Torbert, H. A., and Kloepper, J. W. (2009). Plant growth promoting rhizobacteria allow reduced application rates of chemical fertilizers. Microb. Ecol. 58, 921–929. doi: 10.1007/s00248-009-9531-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Almaraz, J., Zhou, X., and Smith, D. L. (2007). Gas exchange characteristics and dry matter accumulation of soybean treated with Nod factors. J. Plant. Phys. 164, 1391–1393. doi: 10.1016/j.jplph.2006.12.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Antolin-Llovera, M. A., Ried, M. K., Binder, A., and Parniske, M. (2012). Receptor kinase signaling pathways in plant-microbe interactions. Annu. Rev. Phytopathol. 50, 451–473. doi: 10.1146/annurev-phyto-081211-173002

PubMed Abstract | CrossRef Full Text | Google Scholar

Atieno, M., Herrmann, L., Okalebo, R., and Lesueur, D. (2012). Efficiency of different formulations of Bradyrhizobium japonicum and effect of co-inoculation of Bacillus subtilis with two different strains of Bradyrhizobium japonicum. World. J. Microbol. Biotechnol. 28, 2541–2550. doi: 10.1007/s11274-012-1062-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Babalola, O. O. (2010). Beneficial bacteria of agricultural importance. Biotechnol. Lett. 32, 1559–1570. doi: 10.1007/s10529-010-0347-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Badri, D. V., Chaparro, J. M., Zhang, R., Shen, Q., and Vivanco, J. M. (2013a). Application of natural blends of phytochemicals derived from the root exudates of Arabidopsis to the soil reveal that phenolic-related compounds predominantly modulate the soil microbiome. J.Biol. Chem. 288, 4502–4512. doi: 10.1074/jbc.M112.433300

PubMed Abstract | CrossRef Full Text | Google Scholar

Badri, D. V., Zolla, G., Bakker, M. G., Manter, D. K., and Vivanco, J. M. (2013b). Potential impact of soil microbiomes on the leaf metabolome and on herbivore feeding behavior. New Phytol. 198, 264–273. doi: 10.1111/nph.12124

PubMed Abstract | CrossRef Full Text | Google Scholar

Bakker, M. G., Manter, D. K., Sheflin, A. M., Weir, T. L., and Vivanco, J. M. (2012). Harnessing the rhizosphere microbiome through plant breeding and agricultural management. Plant Soil 360, 1–13. doi: 10.1007/s11104-012-1361-x

CrossRef Full Text | Google Scholar

Baldani, J. I., Reis, V. M., Baldani, V. L. D., and Dobereiner, J. (2002). A brief story of nitrogen fixation in sugarcane – reasons for success in Brazil. Funct. Plant Biol. 29, 417–423. doi: 10.1071/PP01083

CrossRef Full Text | Google Scholar

Bálint, M., Tiffin, P., Hallström, B., O’Hara, R. B., Olson, M. S., Fankhauser, J. D., et al. (2013). Host genotype shapes the foliar fungal microbiome of Balsam Poplar (Populus balsamifera). PLoS ONE 8:e53987. doi: 10.1371/journal.pone.0053987

PubMed Abstract | CrossRef Full Text | Google Scholar

Barea, J. M. (2015). Future challenges and perspectives for applying microbial biotechnology in sustainable agriculture based on a better understanding of plant-microbe interactions. J. Soil Sci. Plant Nutr. 15, 261–282. doi: 10.4067/S0718-95162015005000021

CrossRef Full Text | Google Scholar

Bascom-Slack, C. A., Arnold, A. E., and Strobel, S. A. (2012). Student-directed discovery of the plant microbiome and its products. Science 338, 485–486. doi: 10.1126/science.1215227

PubMed Abstract | CrossRef Full Text | Google Scholar

Beneduzi, A., Ambrosini, A., and Passaglia, L. M. P. (2012). Plant growth-promoting rhizobacteria (PGPR): their potential as antagonists and biocontrol agents. Genet. Mol. Biol. 35, 1044–1051. doi: 10.1590/S1415-47572012000600020

PubMed Abstract | CrossRef Full Text | Google Scholar

Berendsen, R. L., Pieterse, C. M. J., and Bakker, P. A. H. M. (2012). The rhizosphere microbiome and plant health. Trends Plant Sci. 8, 478–486. doi: 10.1016/j.tplants.2012.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Berg, G., Grube, M., Schloter, and Kronelia, S. (2014). Unraveling the plant microbe: looking back and future perspectives. Front. Microbiol. 5:148. doi: 10.3389/fmicb.2014.00148

PubMed Abstract | CrossRef Full Text | Google Scholar

Berg, G., Zachow, C., Müller, H., Philipps, J., and Tilcher, R. (2013). Next-generation bio-products sowing the seeds of success for sustainable agriculture. Agronomy 3, 648–656. doi: 10.3390/agronomy3040648

CrossRef Full Text | Google Scholar

Berlec, A. (2012). Novel techniques and findings in the study of plant microbiota: search for plant probiotics. Plant Sci. 19, 96–102. doi: 10.1016/j.plantsci.2012.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Bhattacharyya, P. N., and Jha, D. K. (2012). Plant growth-promoting rhizobacteria (PGPR): emergence in agriculture. World J. Microbiol. Biotechnol. 28, 1327–1350. doi: 10.1007/s11274-011-0979-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Boddey, R. M., Urquiaga, S., Alves, B. J. R., and Reis, V. (2003). Endophytic nitrogen fixation in sugarcane: present knowledge and future applications. Plant Soil 252, 139–149. doi: 10.1023/A:1024152126541

CrossRef Full Text | Google Scholar

Bonfante, P., and Genre, A. (2008). Plants and arbuscular mycorrhizal fungi: an evolutionary-developmental perspective. Trends Plant Sci. 9, 402–498. doi: 10.1016/j.tplants.2008.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Bragina, A., Berg, C., Müller, H., Moser, D., and Berg, G. (2013). Insights into functional bacterial diversity and its effects on Alpine bog ecosystem functioning. Sci. Rep. 3, 1955. doi: 10.1038/srep01955

PubMed Abstract | CrossRef Full Text | Google Scholar

Bulgarelli, D., Rott, M., Schlaeppi, K., van Themaat, E. V. L., Ahmadinejad, N., Assenza, F., et al. (2012). Revealing structure and assembly cues for Arabidopsis root-inhibitiing bacterial microbiota. Nature 488, 91–95. doi: 10.1038/nature11336

PubMed Abstract | CrossRef Full Text | Google Scholar

Calvo, P., Nelson, L., and Kloepper, J. W. (2014). Agricultural uses of plant biostimulants. Plant Soil 383, 3–41. doi: 10.1007/s11104-014-2131-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Chaparro, J. M., Badri, V. D., and Vivanco, M. J. (2014). Rhizosphere microbiome assemblage is affected by plant development. ISME J. 8, 790–803. doi: 10.1038/ismej.2013.196

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, C., McIver, J., Yang, Y., Bai, Y., Schultz, B., and McIver, A. (2007). Foliar application of lipo-chitooligosaccharides (Nod factors) to tomato (Lycopersicon esculentum) enhances flowering and fruit production. Can. J. Plant Sci. 87, 365–372. doi: 10.4141/P06-164

CrossRef Full Text | Google Scholar

Cho, I., and Blaser, M. J. (2012). The human microbiome: at the interface of health and disease. Nat. Rev. Genet. 13, 260–270. doi: 10.1038/nrg3182

PubMed Abstract | CrossRef Full Text | Google Scholar

Compant, S., Clement, C., and Sessitsch, A. (2010a). Plant growth-promoting bacteria in the rhizo- and endosphere of plants: their role, colonization, mechanisms involved and prospects for utilization. Soil Biol. Biochem. 42, 669–678. doi: 10.1016/j.soilbio.2009.11.024

CrossRef Full Text | Google Scholar

Compant, S., van der Heijden, M. G. A., and Sessitsch, A. (2010b). Climate change effects on beneficial plant-microorganism interactions. FEMS Microbiol. Ecol. 73, 197–214. doi: 10.1111/j.1574-6941.2010.00900.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Cretoiu, M. S., Korthals, G. W., Visser, J. H. M., and van Elsas, J. D. (2013). Chitin amendment increases soil suppressiveness toward plant pathogens and modulates the actinobacterial and oxalobacteraceal communities in an experimental agricultural field. Appl. Evniron. Microbiol. 17, 5291–5301. doi: 10.1128/AEM.01361-13

PubMed Abstract | CrossRef Full Text | Google Scholar

Delaux, P.-M., Xie, X., Timme, R. E., Puech-Pages, V., Dunand, C., Lecompte, E., et al. (2012). Origin of strigolactones in the green lineage. New Phytologist 195, 857–871. doi: 10.1111/j.1469-8137.2012.04209.x

PubMed Abstract | CrossRef Full Text | Google Scholar

De-la-Peña, C., and Loyola-Vargas, V. M. (2014). Biotic interactions in the rhizosphere: A diverse cooperative enterprise for plant productivity. Plant Physiol. 166, 701–719. doi: 10.1104/pp.114.241810

PubMed Abstract | CrossRef Full Text | Google Scholar

Desbrosses, G. J., and Stougaard, J. (2011). Root nodulation: A paradigm for how plant-microbe symbiosis influences host developmental pathways. Cell Host Microbe 10, 348–358. doi: 10.1016/j.chom.2011.09.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Dong, Z., Canny, M. J., McCully, M. E., Roboredo, M. R., Cabadilla, C. F., Ortega, E., et al. (1994). A nitrogen-fixing endophyte of sugarcane stems’. A new role for the apoplast. Plant Physiol. 105, 1139–1147.

Google Scholar

Drogue, B., Doré, H., Borland, S., Wisniewski-Dyé, F., and Prigent-Combaret, C. (2012). Which specificity in cooperation between phytostimulating rhizobacteria and plants? Res. Microbiol. 163, 500–510. doi: 10.1016/j.resmic.2012.08.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Dutta, S., and Podile, A. R. (2010). Plant growth promoting rhizobacteria (PGPR): the bugs to debug the root zone. Crit. Rev. Microbiol. 36, 232. doi: 10.3109/10408411003766806

PubMed Abstract | CrossRef Full Text | Google Scholar

Dyachok, J., Wiweger, M., Kenne, L., and von Arnold, S. (2002). Endogenous nod-factor-like signal molecules promote early somatic embryo development in Norway spruce. Plant Physiol. 128, 523–533. doi: 10.1104/pp.010547

PubMed Abstract | CrossRef Full Text | Google Scholar

East, R. (2013). Soil science comes to life: Plants may be getting a little help with their tolerance of drought and heat. Nature 501, 18–19. doi: 10.1038/501S18a

PubMed Abstract | CrossRef Full Text | Google Scholar

Elmore, J. M., Liu, J., Smith, B., Phinney, B., and Coaker, G. (2012). Quantitative proteomics reveals dynamic changes in the plasma membrane during Arabidopsis immune signaling. Mol. Cell. Proteom. 14, 1796–1813. doi: 10.1074/mcp.M111.014555

PubMed Abstract | CrossRef Full Text | Google Scholar

Engelmoer, D. J. P., Behm, J. E., and Kiers, E. T. (2014). Intense competition between arbuscular mycorrhizal mutualists in an in vitro root microbiome negatively affects total fungal abundance. Mol. Ecol. 23, 1584–1593. doi: 10.1111/mec.12451

PubMed Abstract | CrossRef Full Text | Google Scholar

Estévez, J., Soria Díaz, M. E., Fernández de Córdoba, F., Móron, B., Manyan, H., Gil, A., et al. (2009). Different andnew Nod factors produced by Rhizobium tropici CIAT899 following Na stress. FEMS Microbiol. Lett. 293, 220–231. doi: 10.1111/j.1574-6968.2009.01540.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Evangelisti, E., Rey, T., and Schornack, S. (2014). Cross-interference of plant development and plant–microbe interactions. Curr. Opin. Plant Biol. 20, 118–126. doi: 10.1016/j.pbi.2014.05.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Gaiero, J. R., Mccall, C. A., Thompson, K. A., Day, N. J., Best, A. S., and Dunfield, K. E. (2013). Inside the root microbiome: bacterial root endophytes and plant growth promotion. Am. J. Bot. 100, 1738–1750. doi: 10.3732/ajb.1200572

PubMed Abstract | CrossRef Full Text | Google Scholar

Giles, E. D., Oldroyd, J. D., Murray, P. S. P., and Downie, J. A. (2011). The rules of engagement in the legume-rhizobial symbiosis. Annu. Rev. Genet. 45, 119–144. doi: 10.1146/annurev-genet-110410-132549

PubMed Abstract | CrossRef Full Text | Google Scholar

Gough, C., and Cullimore, J. (2011). Lipo-chitooligosaccharide signaling in endosymbiotic plant-microbe interactions. Mol. Plant Microb. Interact. 8, 867–878. doi: 10.1094/MPMI-01-11-0019

PubMed Abstract | CrossRef Full Text | Google Scholar

Gray, E. J., and Smith, D. L. (2005). Intracellular and extracellular PGPR: commonalities and distinctions in the plant-bacterium signaling processes. Soil Biol. Biochem. 37, 395–412. doi: 10.1016/j.soilbio.2004.08.030

CrossRef Full Text | Google Scholar

Guasch-Vidal, B., Estévez, J., Dardanelli, M. S., Soria-Díaz, M. E., de Córdoba, F. F., Balog, C. I., et al. (2013). High NaCl concentrations induce the nod genes of Rhizobium tropici CIAT899 in the absence of flavonoid inducers. Mol. Plant Microbe Interact. 26, 451–460. doi: 10.1094/MPMI-09-12-0213-R

PubMed Abstract | CrossRef Full Text | Google Scholar

Hartmann, A., and Schikora, A. (2012). Quorum sensing of bacteria and trans-kingdom interactions of N-acyl homoserine lactones with eukaryotes. J. Chem. Ecol. 38, 704–713. doi: 10.1007/s10886-012-0141-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Hartmann, A., Rothballer, M., Hense, B. A., and Schröder, P. (2014). Bacterial quorum sensing compounds are important modulators of microbe-plant interactions. Front. Plant Sci. 5:131. doi: 10.3389/fpls.2014.00131

PubMed Abstract | CrossRef Full Text | Google Scholar

Hassan, S., and Mathesius, U. (2012). The role of flavonoids in root–rhizosphere signalling: opportunities and challenges for improving plant–microbe interactions. J. Exp. Bot. 9, 3429–3444. doi: 10.1093/jxb/err430

PubMed Abstract | CrossRef Full Text | Google Scholar

He, Z., Piceno, Y., Deng, Y., Xu, M., Lu, Z., DeSantis, T., et al. (2012). The phylogenic composition and structure of soil microbial communities shifts in response to elevated carbon dioxide. Int. Soc. Microb. Ecol. 6, 259–272. doi: 10.1038/ismej.2011.99

PubMed Abstract | CrossRef Full Text | Google Scholar

Hirsch, P. R., and Mauchline, T. H. (2012). Who’s who in the plant root microbiome? Nat. Biotechnol. 30, 961–962. doi: 10.1038/nbt.2387

PubMed Abstract | CrossRef Full Text | Google Scholar

Imhoff, M. L., Bounoua, L., Ricketts, T., Loucks, C., Harriss, R., and Lawrence, W. T. (2004). Global patterns in human consumption of net primary production. Nature 429, 870–873. doi: 10.1038/nature02619

PubMed Abstract | CrossRef Full Text | Google Scholar

James, E. K. (2000). Nitrogen fixation in endophytic and associative symbiosis. Field Crops Res. 65, 197–209. doi: 10.1016/S0378-4290(99)00087-8

CrossRef Full Text | Google Scholar

Jung, W. J., Mabood, F., Souleimanov, A., Park, R. D., and Smith, D. L. (2008a). Chitinases produced by Paenibacillus illinoisensis and Bacillus thuringensis subsp. pakistani degrade Nod factor from Bradyrhizobium japonicum. Microbiol. Res. 163, 345–349. doi: 10.1016/j.micres.2006.06.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Jung, W. J., Mabood, F., Souleimanov, A., and Smith, D. L. (2008b). Effect of chitin hexamer and Thuricin 17 on lignification related and antioxidative enzymes of soybean plants. J. Plant. Biol. 51, 145–149. doi: 10.1007/BF03030724

CrossRef Full Text | Google Scholar

Jung, W. J., Mabood, F., Souleimanov, A., and Smith, D. L. (2011). Induction of defense-related enzymes in soybean leaves by class IId bacteriocins (thuricin 17 and bacthuricin F4) purified from Bacillus strains. Microbiol. Res. 167, 14–19. doi: 10.1016/j.micres.2011.02.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Kembel, S. W., O’Connor, T. K., Arnold, H. K., Hubbell, S. P., Wright, S. J., and Green, J. L. (2014). Relationships between phyllosphere bacterial communities and plant functional traits in a neotropical forest. Proc. Natl. Acad. Sci. U.S.A. 38, 13715–13720. doi: 10.1073/pnas.1216057111

PubMed Abstract | CrossRef Full Text | Google Scholar

Kennedy, I. R., Choudhury, A. I. M. A., and Kecske, M. L. (2004). Non-symbiotic bacterial diazotrophs in crop-farming systems: can their potential for plant growth promotion be better exploited. Soil Biol. Biochem. 36, 1229–1244. doi: 10.1016/j.soilbio.2004.04.006

CrossRef Full Text | Google Scholar

Khan, W., Prithiviraj, B., and Smith, D. L. (2008). Nod factor [Nod Bj V (C18: 1, MeFuc)] and lumichrome enhance photosynthesis and growth of corn and soybean. J. Plant Physiol. 165, 1342–1351. doi: 10.1016/j.jplph.2007.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Kloepper, J. W., Ryu, C. M., and Zhang, S. (2004). Induced systemic resistance and promotion of plant growth by Bacillus spp. Phytopathology 94, 1259–1266. doi: 10.1094/PHYTO.2004.94.11.1259

PubMed Abstract | CrossRef Full Text | Google Scholar

Knack, J. J., Wilcox, L. W., Ané, J.-M., Piotrowski, M. J., Cook, M. E., Graham, J. M., et al. (2015). Microbiomes of streptophyte algae and bryophytes suggest that a functional suite of microbiota fostered plant colonization of land. Int. J. Plant Sci. 176, 405–420. doi: 10.1086/681161

CrossRef Full Text | Google Scholar

Koenig, J. E., Spor, A., Scalfone, N., Fricker, A. D., Stombaugh, J., Knight, R., et al. (2011). Succession of microbial consortia in the developing infant gut microbiome. Proc. Natl. Acad. Sci. U.S.A. 108, 4578–4585. doi: 10.1073/pnas.1000081107

PubMed Abstract | CrossRef Full Text | Google Scholar

Kuzyakov, Y., and Domanski, G. (2000). Carbon input by plants into the soil. Rev. J. Plant Nutr. Soil Sci. 163, 421–431. doi: 10.1002/1522-2624(200008)163:4<421::AID-JPLN421>3.0.CO;2-R

CrossRef Full Text | Google Scholar

Lakshmanan, V., Kitto, S. L., Caplan, J. L., Hsueh, Y.-H., Kearns, D. B., Wu, Y.-S., et al. (2012). Microbe-associated molecular patterns-triggered root responses mediate beneficial rhizobacterial recruitment in Arabidopsis. Plant Physiol. 160, 1642–1661. doi: 10.1104/pp.112.200386

PubMed Abstract | CrossRef Full Text | Google Scholar

Lebeis, S. L. (2015). Greater than the sum of their parts: characterizing plant microbiomes at the community level. Curr. Opin. Plant Biol. 24, 82–86. doi: 10.1016/j.pbi.2015.02.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, K. D., Gray, E. J., Mabood, F., Jung, W. J., Charles, T., Clark, S. R. D., et al. (2009). The class IId bacteriocin thuricin 17 increases plant growth. Planta 229, 747–755. doi: 10.1007/s00425-008-0870-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Loiret, F. G., Ortega, E., Kleiner, D., Ortega-Rode’s, P., Rode’s, R., and Dong, Z. (2004). A putative new endophytic nitrogen-fixing bacterium Pantoea sp. from sugarcane. J. Appl. Microbiol. 97, 504. doi: 10.1111/j.1365-2672.2004.02329.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lugtenberg, B., and Kamilova, F. (2009). Plant-growth-promoting rhizobacteria. Annu. Rev. Microbiol. 63, 541–556. doi: 10.1146/annurev.micro.62.081307.162918

CrossRef Full Text | Google Scholar

Lundberg, D. S., Lebeis, S. L., Paredes, S. H., Yourstone, S., Gehring, J., Malfatti, S., et al. (2012). Defining the core Arabidopsis thaliana root. Nature 488, 86–90. doi: 10.1038/nature11237

PubMed Abstract | CrossRef Full Text | Google Scholar

Luo, Y., Hui, D., and Zhang, D. (2006). Elevated CO2 stimulates net accumulations of carbon and nitrogen in land ecosystems: a meta-analysis. Ecology 87, 53–63. doi: 10.1890/04-1724

CrossRef Full Text | Google Scholar

Lv, D., Ma, A., Tang, X., Bai, Z., Qi, H., and Zhuang, G. (2013). Profile of the culturable microbiome capable of producing acyl-homoserine lactone in the tobacco phyllosphere. J. Environ. Sci. 25, 357–366. doi: 10.1016/S1001-0742(12)60027-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Mabood, F., Gray, E. J., Lee, K. D., Supanjani, S., and Smith, D. L. (2006a). Exploiting inter-organismal chemical communication for improved inoculants. Can. J. Plant Sci. 86, 951–966. doi: 10.4141/P05-102

CrossRef Full Text | Google Scholar

Mabood, F., Zhou, X., Lee, K. D., and Smith, D. L. (2006b). Methyl jasmonate, alone or in combination with genistein, and Bradyrhizobium japonicum increases soybean (Glycine max L.) plant dry matter production and grain yield under short season conditions. Field Crops Res. 95, 412–419. doi: 10.1016/j.fcr.2005.04.013

CrossRef Full Text | Google Scholar

Mabood, F., Zhou, X., and Smith, D. L. (2014). Microbial signaling and plant growth promotion. Can. J. Plant Sci. 94, 1051–1063. doi: 10.4141/cjps2013-148

CrossRef Full Text | Google Scholar

Marasco, R., Rolli, E., Ettoumi, B., Vigani, G., Mapelli, F., Borin, S., et al. (2012). A drought resistance-promoting microbiome is selected by root system under desert farming. PLoS ONE 7:e48479. doi: 10.1371/journal.pone.0048479

PubMed Abstract | CrossRef Full Text | Google Scholar

Masciarelli, O., Llanes, A., and Luna, V. (2014). A new PGPR co-inoculated with Bradyrhizobium japonicum enhances soybean nodulation. Microbiol. Res. 169, 609–615. doi: 10.1016/j.micres.2013.10.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Mengual, C., Schoebitz, M., Azcón, R., and Roldán, A. (2014). Microbial inoculants and organic amendment improves plant establishment and soil rehabilitation under semiarid conditions. J. Environ. Manag. 134, 1–7. doi: 10.1016/j.jenvman.2014.01.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Nelson, L. M. (2004). Plant growth promoting rhizobacteria (PGPR): prospects for new inoculants. Crop Manag. 3. doi: 10.1094/CM-2004-0301-05-RV

CrossRef Full Text | Google Scholar

Nguyen, T. H. N., Brechenmacher, L., Aldrich, J. T., Clauss, T. R., Gritsenko, M. A., Hixton, K. K., et al. (2012). Quantitative phosphoproeomic analysis of soybean root hairs inoculated with Bradyrhisobium japonicum. Mol. Cell. Proteom. 11, 1140–1155. doi: 10.1074/mcp.M112.018028

PubMed Abstract | CrossRef Full Text | Google Scholar

Oláh, B., Brière, C., Bécard, G., Dénarié, J., and Gough, C. (2005). Nod factors and a diffusible factor from arbuscular mycorrhizal fungi stimulate lateral root formation in Medicago truncatula via the DMI1/DMI2 signalling pathway. Plant J. 44, 195–207. doi: 10.1111/j.1365-313X.2005.02522.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Oldroyd, G. E. D. (2013). Speak, friend, and enter: signalling systems that promote beneficial symbiotic associations in plants. Nat. Rev. Microbiol. 11, 252–263. doi: 10.1038/nrmicro2990

PubMed Abstract | CrossRef Full Text | Google Scholar

Oldroyd, G. E., Murray, J. D., Poole, P. S., and Downie, J. A. (2010). The rules of engagement in the legume5 rhizobial symbiosis. Annu. Rev. Genet. 45, 119–144. doi: 10.1146/annurev-genet-110410-132549

PubMed Abstract | CrossRef Full Text | Google Scholar

Orrell, P., and Bennett, A. E. (2013). How can we exploit above-belowground interactions to assist in addressing the challenges of food security? Front. Plant Sci. 4:432. doi: 10.3389/fpls.2013.00432

PubMed Abstract | CrossRef Full Text | Google Scholar

Peiffer, J. A., Spor, A., Koren, O., Jin, Z., Tring, S. G., Dangl, J. L., et al. (2013). Diversity and heritability of the maize rhizosphere microbiome under field conditions. Proc. Natl. Acad. Sci. U.S.A. 16, 6548–6553. doi: 10.1073/pnas.1302837110

PubMed Abstract | CrossRef Full Text | Google Scholar

Pisa, G., Magnani, G. S., Weber, H., Souza, E. M., Faoro, H., Monteiro, R. A., et al. (2011). Diversity of 16S rRNA genes from bacteria of sugarcane rhizosphere soil. Braz. J. Med. Biol. Res. 44, 1215–1221. doi: 10.1590/S0100-879X2011007500148

PubMed Abstract | CrossRef Full Text | Google Scholar

Porcel, R., Aroca, R., and Ruiz-Lozano, J. M. (2012). Salinity stress alleviation using arbuscular mycorrhizal fungi. A review. Agron. Sustain. Dev. 32, 181–200. doi: 10.1007/s13593-011-0029-x

CrossRef Full Text | Google Scholar

Porras-Alfaro, A., and Bayman, P. (2011). Hidden fungi, emergent properties: endophytes and microbiomes. Annu. Rev. Phytopathol. 49, 291–315. doi: 10.1146/annurev-phyto-080508-081831

PubMed Abstract | CrossRef Full Text | Google Scholar

Prithiviraj, B., Zhou, X., Souleimanov, A., Khan, W. K., and Smith, D. L. (2003). A host specific bacteria-to-plant signal molecule (Nod factor) enhances germination and early growth of diverse crop plants. Planta 216, 437–445.

PubMed Abstract | Google Scholar

Prudent, M., Salon, C., Souleimanov, A., Emery, R. J. N., and Smith, D. L. (2015). Soybean is less impacted by water stress using Bradyrhizobium japonicum and thuricin-17 from Bacillus thuringiensis. Agron. Sustain. Dev. 35, 749–757. doi: 10.1007/s13593-014-0256-z

CrossRef Full Text | Google Scholar

Quecine, M. C., Araújo, W. L., Rossetto, P. B., Ferreira, A., Tsui, S., Lacava, P. T., et al. (2012). Sugarcane growth promotion by the endophytic bacterium Pantoea agglomerans 33.1. Appl. Environ. Microbiol. 78, 7511–7518. doi: 10.1128/AEM.00836-12

PubMed Abstract | CrossRef Full Text | Google Scholar

Ragauskas, A. J., Williams, C. K., Davison, B. H., Britovsek, G., Cairney, J., Eckert, C. A., et al. (2006). The path forward for biofuels and biomaterials. Science 311, 484–489. doi: 10.1126/science.1114736

PubMed Abstract | CrossRef Full Text | Google Scholar

Rastogi, G., Coaker, G. L., and Leveau, J. H. J. (2013). New insights into the structure and function of phyllosphere microbiota through high-throughput molecular approaches. FEMS Microbiol. Lett. 348, 1–10. doi: 10.1111/1574-6968.12225

PubMed Abstract | CrossRef Full Text | Google Scholar

Rastogi, G., Sbodio, A., Tech, J. J., Suslow, T. V., Coaker, G. L., and Leveau, J. H. J. (2012). Leaf microbiota in an agroecosystem: spatiotemporal variation in bacterial community composition on field-grown lettuce. ISME J. 6, 1812–1822. doi: 10.1038/ismej.2012.32

PubMed Abstract | CrossRef Full Text | Google Scholar

Rose, C. M., Venkateshwaren, M., Volkening, J. D., Grimsrud, P. A., Maeda, J., Bailey, D. J., et al. (2012). Rapid phosphoproteomic and transcriptomic changes in the rhizobia-legume symbiosis. Mol. Cell. Proteom. 11, 724–744. doi: 10.1074/mcp.M112.019208

PubMed Abstract | CrossRef Full Text | Google Scholar

Rout, M. E., and Southworth, D. (2013). The root microbiome influences scales from molecules to ecosystems: the unseen majority. Am. J. Bot. 100, 1689–1691. doi: 10.3732/ajb.1300291

PubMed Abstract | CrossRef Full Text | Google Scholar

Rudrappa, T., Czymmek, K. J., Paré, P. W., and Bais, H. P. (2008). Root-secreted malic acid recruits beneficial soil bacteria. Plant Physiol. 148, 1547–1556. doi: 10.1104/pp.108.127613

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruiz-Lozano, J. M., Porcel, R., Azcon, C., and Aroca, R. (2012). Regulation by arbuscular mycorrhizae of the integrated physiological response to salinity in plants: new challenges in physiological and molecular studies. J. Exp. Bot. 11, 4033–4044. doi: 10.1093/jxb/ers126

PubMed Abstract | CrossRef Full Text | Google Scholar

Santi, C., Bogusz, D., and Franche, C. (2013). Biological nitrogen fixation in non-legume plants. Ann. Bot. 111, 743–767. doi: 10.1093/aob/mct048

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmidt, R., Köberl, M., Mostafa, A., Ramadan, E. M., Monschein, M., Jensen, K. B., et al. (2014). Effects of bacterial inoculants on the indigenous microbiome and secondary metabolites of chamomile plants. Front. Microbiol. 64:111. doi: 10.3389/fmicb.2014.00064

PubMed Abstract | CrossRef Full Text | Google Scholar

Schwinghamer, T., Souleimanov, A., Dutilleul, P., and Smith, D. L. (2014). The plant growth regulator lipo-chitooligosaccharide (LCO) can enhance the germination of canola (Brassica napus [L.]). J. Plant Growth Regul. 34, 183–195. doi: 10.1007/s00344-014-9456-7

CrossRef Full Text | Google Scholar

Segonzac, C., and Zipfel, C. (2011). Activation of plant pattern-recognition receptors by bacteria. Curr. Opin. Microbiol. 14, 54–61. doi: 10.1016/j.mib.2010.12.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Smith, D. L. (2009). “Signals in the underground: microbial signals and plant productivity,” in Proceedings of the International Society for Molecular Plant Microbe Interactions Meeting, July 19–23, Quebec City.

PubMed Abstract | Google Scholar

Smith, D. L. (2010). “Signals coming in from the cold: inter-organismal communication and abiotic stress,” in Proceedings of the the 21st North American Symbiotic Nitrogen Fixation Conference (Columbia, MI: University of California Energy Week).

Google Scholar

Smith, D. L., and Zhou, X. (2014). An effective integrated research approach to study climate change in Canada. Can. J. Plant. Sci. 94, 995–1008. doi: 10.4141/cjps-2014-503

CrossRef Full Text | Google Scholar

Souleimanov, A., Prithiviraj, B., and Smith, D. L. (2002). The major Nod factor of Bradyrhizobium japonicum promotes early growth of soybean and corn. J. Exp. Bot. 53, 1929–1934. doi: 10.1093/jxb/erf034

PubMed Abstract | CrossRef Full Text | Google Scholar

Spence, C., Alff, E., Johnson, C., Ramos, C., Donofrio, N., Sundarsan, V., et al. (2014). Natural rice rhizospheric microbes suppress rice blast infections. BMC Plant Biol. 14:130. doi: 10.1186/1471-2229-14-130

PubMed Abstract | CrossRef Full Text | Google Scholar

Subramanian, S. (2014). Mass Spectrometry Based Proteome Profiling to Understand the Effects of Lipo-Chitooligosaccharide and Thuricin 17 in Arabidopsis thaliana and Glycine max under Salt Stress. Ph.D. Thesis, McGill University, Montréal, QC.

Google Scholar

Subramanian, S., Mitkus, E., Souleimanov, A., and Smith, D. L. (2011). “Thuricin 17 and lipo-chito oligosaccharide act as plant growth promoters and alleviate drought stress in Arabidopsis thaliana,” in Proceedings of the Eastern Regional Meeting of the Canadian Society of Plant Physiologists (Ottawa: Carleton University).

Google Scholar

Subramanian, S., Schwinghamer, T., Souleimanov, A., and Smith, D. L. (2009). “Evaluating thuricin 17 (TH17) and lipo-chito oligosaccharide (LCO) as plant growth promoter in Arabidopsis thaliana,” in Proceedings of the MPMI International Meeting, Quebec City.

Google Scholar

Subramanian, S., Souleimanov, A., and Smith, D. L. (2010). “Thuricin 17 and lipo-chitooligosaccharide act as plant growth promoters and alleviate low temperature stress in Arabidopsis thaliana,” in Proceedings of the North American Symbiotic Nitrogen Fixation Conference, June 14-17, 2010, Columbia, MI.

Google Scholar

Taylor, T. N. (1995). Fossil arbuscular mycorrhizae from the Early Devonian. Mycologia 87, 560–573. doi: 10.1098/rsbl.2010.1203

PubMed Abstract | CrossRef Full Text | Google Scholar

Tena, G., Boudsocq, M., and Sheen, J. (2011). Protein kinase signaling networks in plant innate immunity. Curr. Opin. Plant Biol. 14, 519–529. doi: 10.1016/j.pbi.2011.05.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Teplitski, M., Robinson, J. B., and Bauer, W. D. (2000). Plants secrete substances that mimic bacterial N-Acyl homoserine lactone signal activities and affect population density-dependent behaviors in associated bacteria. Mol. Plant Microbe Interact. 6, 637–648. doi: 10.1094/MPMI.2000.13.6.637

PubMed Abstract | CrossRef Full Text | Google Scholar

Trabelsi, D., and Mhamdi, R. (2013). Microbial inoculants and their impact on soil microbial communities: a review. Biomed. Res. Int. 1, 13. doi: 10.1155/2013/863240

PubMed Abstract | CrossRef Full Text | Google Scholar

Turner, T. R., James, E. K., and Poole, P. S. (2013a). The plant microbiome. Genome Biol. 14, 209–219. doi: 10.1186/gb-2013-14-6-209

PubMed Abstract | CrossRef Full Text | Google Scholar

Turner, T. R., Ramakrishnan, K., Walshaw, J., Heavens, D., Alston, M., Swarbreck, D., et al. (2013b). Comparative metatranscriptomics reveals kingdom level changes in the rhizosphere microbiome of plants. ISME J. 7, 2248–2258. doi: 10.1038/ismej.2013.119

PubMed Abstract | CrossRef Full Text | Google Scholar

Velázquez, E., Rojas, M., Lorite, M. J., Rivas, R., Zurdo-Piñeiro, J. L., Heydrich, M., et al. (2008). Genetic diversity of endophytic bacteria which could be find in the apoplastic sap of the medullary parenchyma of the stem of healthy sugarcane plants. J. Basic Microbiol. 48, 118–124. doi: 10.1002/jobm.200700161

PubMed Abstract | CrossRef Full Text | Google Scholar

Venkateshwaran, M., Volkening, J. D., Sussman, M. R., and Ané, J.-M. (2013). Symbiosis and the social network of higher plants. Curr. Opin. Plant Biol. 16, 118–127. doi: 10.1016/j.pbi.2012.11.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Vessey, J. K. (2003). Plant growth promoting rhizobacteria as biofertilizers. Plant Soil 255, 571–586. doi: 10.1023/A:1026037216893

CrossRef Full Text | Google Scholar

Von Bulow, J. F. W., and Dobereiner, J. (1975). Potential for nitrogen fixation in maize genotypes in Brazil. Proc. Natl. Acad. Sci. U.S.A. 72, 2389–2393. doi: 10.1073/pnas.72.6.2389

CrossRef Full Text | Google Scholar

Wang, N., Khan, W., and Smith, D. L. (2012). Soybean global gene expression after application of lipo-chitooligosaccharide from Bradyrhizobium japonicum under sub-optimal temperature. PLoS ONE 7:e31571. doi: 10.1371/journal.pone.0031571

PubMed Abstract | CrossRef Full Text | Google Scholar

Watrous, J., Roach, P., Alexandrov, T., Heath, B. S., Yang, J. Y., Kersten, R. D., et al. (2012). Mass spectral molecular networking of living microbial colonies. Proc. Natl. Acad. Sci. U.S.A. 109, E1743–E1752. doi: 10.1073/pnas.1203689109

PubMed Abstract | CrossRef Full Text | Google Scholar

Wittulsky, S., Pellegrin, C., Giannakopoulou, A., and Böni, R. (2014). A snapshot of molecular plant-microbe interaction research. New Phytol. 205, 468–471. doi: 10.1111/nph.13194

PubMed Abstract | CrossRef Full Text | Google Scholar

Zamioudis, C., Mastranesti, P., Dhonukshe, P., Blilou, I., and Pieterse, C. M. J. (2013). Unraveling root developmental programs initiated by beneficial pseudomonas spp. Bacteria. Plant Physiol. 162, 304–318. doi: 10.1104/pp.112.212597

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, F., and Smith, D. L. (1995). Preincubation of Bradyrhizobium japonicum with genistein accelerates nodule development of soybean at suboptimal root zone temperatures. Plant Phys. 108, 961–986.

PubMed Abstract | Google Scholar

Zhang, F., and Smith, D. L. (2002). Interorganismal signaling in suboptimal environments: The legume-rhizobia symbiosis. Adv. Agron. 76, 125–161. doi: 10.1016/S0065-2113(02)76004-5

CrossRef Full Text | Google Scholar

Zhang, H., Gao, Z.-Q., Wang, W.-J., Liu, G.-F., Shtykova, E. V., Xu, J.-H., et al. (2012). The crystal structure of the MPN domain from the COP9 signalosome subunit CSN6. FEBS Lett. 586, 1147–1153. doi: 10.1016/j.febslet.2012.03.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Zolla, G., Badri, D. V., Bakker, M. G., Manter, D. K., and Vivanco, J. M. (2013). Soil microbiomes vary in their ability to confer drought tolerance to Arabidopsis. Appl. Soil Ecol. 68, 1–9. doi: 10.1016/j.apsoil.2013.03.007

CrossRef Full Text | Google Scholar

Keywords: molecular signals, plant growth promoting rhizobacteria, phytomicrobiome, holobiont, crop

Citation: Smith DL, Subramanian S, Lamont JR and Bywater-Ekegärd M (2015) Signaling in the phytomicrobiome: breadth and potential. Front. Plant Sci. 6:709. doi: 10.3389/fpls.2015.00709

Received: 20 April 2015; Accepted: 24 August 2015;
Published: 09 September 2015.

Edited by:

Jean-Michel Ané, University of Wisconsin – Madison, USA

Reviewed by:

Sen Subramanian, South Dakota State University, USA
Muthu Venkateshwaran, University of Wisconsin-Platteville, USA

Copyright © 2015 Smith, Subramanian, Lamont and Bywater-Ekegärd. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Donald L. Smith, Plant Science Department, McGill University/Macdonald Campus, 21,111 Lakeshore Road, Sainte-Anne-de-Bellevue, QC H9X 3V9, Canada, Donald.Smith@McGill.Ca

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