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Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil

Microbial decomposition drives the transformation of plant-derived substrates into microbial products that form stable soil organic matter (SOM). Recent theories have posited that decomposition depends on an interaction between SOM chemistry with microbial diversity and resulting function (e.g., enz...

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Autores principales: Raczka, Nanette C., Piñeiro, Juan, Tfaily, Malak M., Chu, Rosalie K., Lipton, Mary S., Pasa-Tolic, Ljiljana, Morrissey, Ember, Brzostek, Edward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481224/
https://www.ncbi.nlm.nih.gov/pubmed/34588474
http://dx.doi.org/10.1038/s41598-021-97942-9
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author Raczka, Nanette C.
Piñeiro, Juan
Tfaily, Malak M.
Chu, Rosalie K.
Lipton, Mary S.
Pasa-Tolic, Ljiljana
Morrissey, Ember
Brzostek, Edward
author_facet Raczka, Nanette C.
Piñeiro, Juan
Tfaily, Malak M.
Chu, Rosalie K.
Lipton, Mary S.
Pasa-Tolic, Ljiljana
Morrissey, Ember
Brzostek, Edward
author_sort Raczka, Nanette C.
collection PubMed
description Microbial decomposition drives the transformation of plant-derived substrates into microbial products that form stable soil organic matter (SOM). Recent theories have posited that decomposition depends on an interaction between SOM chemistry with microbial diversity and resulting function (e.g., enzymatic capabilities, growth rates). Here, we explicitly test these theories by coupling quantitative stable isotope probing and metabolomics to track the fate of (13)C enriched substrates that vary in chemical composition as they are assimilated by microbes and transformed into new metabolic products in soil. We found that differences in forest nutrient economies (e.g., nutrient cycling, microbial competition) led to arbuscular mycorrhizal (AM) soils harboring greater diversity of fungi and bacteria than ectomycorrhizal (ECM) soils. When incubated with (13)C enriched substrates, substrate type drove shifts in which species were active decomposers and the abundance of metabolic products that were reduced or saturated in the highly diverse AM soils. The decomposition pathways were more static in the less diverse, ECM soil. Importantly, the majority of these shifts were driven by taxa only present in the AM soil suggesting a strong link between microbial identity and their ability to decompose and assimilate substrates. Collectively, these results highlight an important interaction between ecosystem-level processes and microbial diversity; whereby the identity and function of active decomposers impacts the composition of decomposition products that can form stable SOM.
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spelling pubmed-84812242021-09-30 Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil Raczka, Nanette C. Piñeiro, Juan Tfaily, Malak M. Chu, Rosalie K. Lipton, Mary S. Pasa-Tolic, Ljiljana Morrissey, Ember Brzostek, Edward Sci Rep Article Microbial decomposition drives the transformation of plant-derived substrates into microbial products that form stable soil organic matter (SOM). Recent theories have posited that decomposition depends on an interaction between SOM chemistry with microbial diversity and resulting function (e.g., enzymatic capabilities, growth rates). Here, we explicitly test these theories by coupling quantitative stable isotope probing and metabolomics to track the fate of (13)C enriched substrates that vary in chemical composition as they are assimilated by microbes and transformed into new metabolic products in soil. We found that differences in forest nutrient economies (e.g., nutrient cycling, microbial competition) led to arbuscular mycorrhizal (AM) soils harboring greater diversity of fungi and bacteria than ectomycorrhizal (ECM) soils. When incubated with (13)C enriched substrates, substrate type drove shifts in which species were active decomposers and the abundance of metabolic products that were reduced or saturated in the highly diverse AM soils. The decomposition pathways were more static in the less diverse, ECM soil. Importantly, the majority of these shifts were driven by taxa only present in the AM soil suggesting a strong link between microbial identity and their ability to decompose and assimilate substrates. Collectively, these results highlight an important interaction between ecosystem-level processes and microbial diversity; whereby the identity and function of active decomposers impacts the composition of decomposition products that can form stable SOM. Nature Publishing Group UK 2021-09-29 /pmc/articles/PMC8481224/ /pubmed/34588474 http://dx.doi.org/10.1038/s41598-021-97942-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Raczka, Nanette C.
Piñeiro, Juan
Tfaily, Malak M.
Chu, Rosalie K.
Lipton, Mary S.
Pasa-Tolic, Ljiljana
Morrissey, Ember
Brzostek, Edward
Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
title Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
title_full Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
title_fullStr Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
title_full_unstemmed Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
title_short Interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
title_sort interactions between microbial diversity and substrate chemistry determine the fate of carbon in soil
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481224/
https://www.ncbi.nlm.nih.gov/pubmed/34588474
http://dx.doi.org/10.1038/s41598-021-97942-9
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