4.6 Article

Variation in Root Exudate Composition Influences Soil Microbiome Membership and Function

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/aem.00226-22

关键词

exometabolomics; metagenomics; rhizodeposition; root exudates; sorghum

资金

  1. National Science Foundation [1750189]
  2. Early Career Award from the U.S. Department of Energy
  3. Office of Science, Office of Biological and Environmental Research [DE-SC0019746]
  4. Office of the U.S. Department of Energy [DE-AC02-05CH11231, 2049]
  5. Cancer Center Support Grant [P30CA046934]
  6. DOE DER award [DE-SC0014395]
  7. U.S. Department of Energy (DOE) [DE-SC0019746, DE-SC0014395] Funding Source: U.S. Department of Energy (DOE)
  8. Direct For Biological Sciences
  9. Div Of Molecular and Cellular Bioscience [1750189] Funding Source: National Science Foundation

向作者/读者索取更多资源

Root exudation plays a crucial role in mediating interactions between plant roots, microorganisms, and the soil matrix. This study investigated the chemical heterogeneity of root exudates and its effects on soil microbial membership and metabolism. The findings highlight the potential of high-resolution multiomics tools to study soil microbiomes and provide valuable information for the development of effective microbiota management strategies in agriculture.
Root exudation is one of the primary processes that mediate interactions between plant roots, microorganisms, and the soil matrix, yet the mechanisms by which exudation alters microbial metabolism in soils have been challenging to unravel. Here, utilizing distinct sorghum genotypes, we characterized the chemical heterogeneity between root exudates and the effects of that variability on soil microbial membership and metabolism. Distinct exudate chemical profiles were quantified and used to formulate synthetic root exudate treatments: a high-organic-acid treatment (HOT) and a high-sugar treatment (HST). To parse the response of the soil microbiome to different exudate regimens, laboratory soil reactors were amended with these root exudate treatments as well as a nonexudate control. Amplicon sequencing of the 16S rRNA gene illustrated distinct microbial diversity patterns and membership in response to HST, HOT, or control amendments. Exometabolite changes reflected these microbial community changes, and we observed enrichment of organic and amino acids, as well as possible phytohormones in the HST relative to the HOT and control. Linking the metabolic capacity of metagenome-assembled genomes in the HST to the exometabolite patterns, we identified microorganisms that could produce these phytohormones. Our findings emphasize the tractability of high-resolution multiomics tools to investigate soil microbiomes, opening the possibility of manipulating native microbial communities to improve specific soil microbial functions and enhance crop production. IMPORTANCE Decrypting the chemical interactions between plant roots and the soil microbiome is a gateway for future manipulation and management of the rhizosphere, a soil compartment critical to promoting plant fitness and yields. Our experimental results demonstrate how soil microbial community and genomic diversity is influenced by root exudates of differing chemical compositions and how changes in this microbiome result in altered production of plant-relevant metabolites. Together, these findings demonstrate the tractability of high-resolution multiomics tools to investigate soil microbiomes and provide new information on plant-soil environments useful for the development of efficient and precise microbiota management strategies in agricultural systems. Decrypting the chemical interactions between plant roots and the soil microbiome is a gateway for future manipulation and management of the rhizosphere, a soil compartment critical to promoting plant fitness and yields. Our experimental results demonstrate how soil microbial community and genomic diversity is influenced by root exudates of differing chemical compositions and how changes in this microbiome result in altered production of plant-relevant metabolites.

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