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Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field

Research suggests that microbiomes play a major role in structuring plant communities and influencing ecosystem processes, however, the relative roles and strength of change of microbial components have not been identified. We measured the response of fungal, arbuscular mycorrhizal fungal (AMF), bac...

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Autores principales: Burrill, Haley M., Wang, Guangzhou, Bever, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115818/
https://www.ncbi.nlm.nih.gov/pubmed/37076650
http://dx.doi.org/10.1038/s43705-023-00237-5
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author Burrill, Haley M.
Wang, Guangzhou
Bever, James D.
author_facet Burrill, Haley M.
Wang, Guangzhou
Bever, James D.
author_sort Burrill, Haley M.
collection PubMed
description Research suggests that microbiomes play a major role in structuring plant communities and influencing ecosystem processes, however, the relative roles and strength of change of microbial components have not been identified. We measured the response of fungal, arbuscular mycorrhizal fungal (AMF), bacteria, and oomycete composition 4 months after planting of field plots that varied in plant composition and diversity. Plots were planted using 18 prairie plant species from three plant families (Poaceae, Fabaceae, and Asteraceae) in monoculture, 2, 3, or 6 species richness mixtures and either species within multiple families or one family. Soil cores were collected and homogenized per plot and DNA were extracted from soil and roots of each plot. We found that all microbial groups responded to the planting design, indicating rapid microbiome response to plant composition. Fungal pathogen communities were strongly affected by plant diversity. We identified OTUs from genera of putatively pathogenic fungi that increased with plant family, indicating likely pathogen specificity. Bacteria were strongly differentiated by plant family in roots but not soil. Fungal pathogen diversity increased with planted species richness, while oomycete diversity, as well as bacterial diversity in roots, decreased. AMF differentiation in roots was detected with individual plant species, but not plant family or richness. Fungal saprotroph composition differentiated between plant family composition in plots, providing evidence for decomposer home-field advantage. The observed patterns are consistent with rapid microbiome differentiation with plant composition, which could generate rapid feedbacks on plant growth in the field, thereby potentially influencing plant community structure, and influence ecosystem processes. These findings highlight the importance of native microbial inoculation in restoration.
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spelling pubmed-101158182023-04-21 Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field Burrill, Haley M. Wang, Guangzhou Bever, James D. ISME Commun Article Research suggests that microbiomes play a major role in structuring plant communities and influencing ecosystem processes, however, the relative roles and strength of change of microbial components have not been identified. We measured the response of fungal, arbuscular mycorrhizal fungal (AMF), bacteria, and oomycete composition 4 months after planting of field plots that varied in plant composition and diversity. Plots were planted using 18 prairie plant species from three plant families (Poaceae, Fabaceae, and Asteraceae) in monoculture, 2, 3, or 6 species richness mixtures and either species within multiple families or one family. Soil cores were collected and homogenized per plot and DNA were extracted from soil and roots of each plot. We found that all microbial groups responded to the planting design, indicating rapid microbiome response to plant composition. Fungal pathogen communities were strongly affected by plant diversity. We identified OTUs from genera of putatively pathogenic fungi that increased with plant family, indicating likely pathogen specificity. Bacteria were strongly differentiated by plant family in roots but not soil. Fungal pathogen diversity increased with planted species richness, while oomycete diversity, as well as bacterial diversity in roots, decreased. AMF differentiation in roots was detected with individual plant species, but not plant family or richness. Fungal saprotroph composition differentiated between plant family composition in plots, providing evidence for decomposer home-field advantage. The observed patterns are consistent with rapid microbiome differentiation with plant composition, which could generate rapid feedbacks on plant growth in the field, thereby potentially influencing plant community structure, and influence ecosystem processes. These findings highlight the importance of native microbial inoculation in restoration. Nature Publishing Group UK 2023-04-19 /pmc/articles/PMC10115818/ /pubmed/37076650 http://dx.doi.org/10.1038/s43705-023-00237-5 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Burrill, Haley M.
Wang, Guangzhou
Bever, James D.
Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
title Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
title_full Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
title_fullStr Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
title_full_unstemmed Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
title_short Rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
title_sort rapid differentiation of soil and root microbiomes in response to plant composition and biodiversity in the field
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115818/
https://www.ncbi.nlm.nih.gov/pubmed/37076650
http://dx.doi.org/10.1038/s43705-023-00237-5
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