Journal
MOLECULAR PLANT
Volume 14, Issue 3, Pages 503-516Publisher
CELL PRESS
DOI: 10.1016/j.molp.2020.12.002
Keywords
arbuscular mycorrhizae; rhizobia; symbiosis; rhizosphere microbiota; quantitative microbiota profiling; rpoB
Categories
Funding
- Chinese Academy of Sciences [ZDRW-ZS-2019-2]
- National Natural Science Foundation of China [31825003, 31730103, 31970323]
- Strategic Priority Research Program Molecular Mechanism of Plant Growth and Development of the Chinese Academy of Sciences [XDB27040207]
- China National GeneBank (CNGB)
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Plants establish symbiotic relationships with mutualistic fungi and bacteria, such as arbuscular mycorrhizal (AM) fungi and rhizobia, to exchange key nutrients and promote growth. Our research demonstrates that the AM symbiosis is crucial for assembling a normal quantitative root-associated microbiota in native soil, impacting Rhizobiales hubs among plant microbiota and benefiting the plant holobiont. Furthermore, our findings suggest that the interactions between AM and rhizobial symbioses play a key role in promoting nodulation in legume plants in native soil, with implications for agricultural management strategies.
Plants establish symbioses with mutualistic fungi, such as arbuscular mycorrhizal (AM) fungi, and bacteria, such as rhizobia, to exchange key nutrients and thrive. Plants and symbionts have coevolved and represent vital components of terrestrial ecosystems. Plants employ an ancestral AM signaling pathway to establish intracellular symbioses, including the legume-rhizobia symbiosis, in their roots. Nevertheless, the relationship between the AM and rhizobial symbioses in native soil is poorly understood. Here, we examined how these distinct symbioses affect root-associated bacterial communities in Medicago truncatula by performing quantitative microbiota profiling (QMP) of 16S rRNA genes. We found that M. truncatula mutants that cannot establish AM or rhizobia symbiosis have an altered microbial load (quantitative abundance) in the rhizosphere and roots, and in particular that AM symbiosis is required to assemble a normal quantitative root-associated microbiota in native soil. Moreover, quantitative microbial co-abundance network analyses revealed that AM symbiosis affects Rhizobiales hubs among plant microbiota and benefits the plant holobiont. Through QMP of rhizobial rpoB and AM fungal SSU rRNA genes, we revealed a new layer of interaction whereby AM symbiosis promotes rhizobia accumulation in the rhizosphere of M. truncatula. We further showed that AM symbiosis-conditioned microbial communities within the M. truncatula rhizosphere could promote nodulation in different legume plants in native soil. Given that the AM and rhizobial symbioses are critical for crop growth, our findings might inform strategies to improve agricultural management. Moreover, our work sheds light on the co-evolution of these intracellular symbioses during plant adaptation to native soil conditions.
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