Proceedings of the National Academy of Sciences · 2015 · 2.9K citations · 30 references
Life SciencesMicrobiologyPlant BiologyMicrobial EcologyMicrobiome ResearchPlant-microbe InteractionsPlant MicrobiomeRhizosphere BiologyRhizosphere EcologyRhizosphere MicrobiologyRoot MicrobiomeRoot-microbe InteractionsHost Genotype Effects On MicrobiomesMicrobial Colonization Of RootsRhizosphere Bacterial CommunitiesRhizosphere MicrobiomesRoot-associated Bacterial CommunitiesRoot-associated Microbial CommunitiesRoot-microbiome InteractionsRoot-pathogen Interactions
Land plants continuously interact with diverse soil microbes through their roots, yet how the root microbiome is shaped and acquired remains poorly understood. The study aims to identify distinct root niches in rice that harbor separate bacterial and archaeal communities. The authors examined rice roots, identifying three distinct niches—root surface, endosphere, and rhizosphere—each supporting unique bacterial and archaeal assemblages. Microbial communities vary with geography, soil source, host genotype, and cultivation practice, and colonization dynamics suggest rapid soil-derived acquisition and a multistep assembly model where each niche selectively shapes the microbiome.
Significance Land plants continuously contact beneficial, commensal, and pathogenic microbes in soil via their roots. There is limited knowledge as to how the totality of root-associated microbes (i.e., the microbiome) is shaped by various factors or its pattern of acquisition in the root. Using rice as a model, we show that there exist three different root niches hosting different microbial communities of eubacteria and methanogenic archaea. These microbial communities are affected by geographical location, soil source, host genotype, and cultivation practice. Dynamics of the colonization pattern for the root-associated microbiome across the three root niches provide evidence for rapid acquisition of root-associated microbiomes from soil, and support a multistep model wherein each root niche plays a selective role in microbiome assembly.
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