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Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes
It is unclear if coexistence theory can be applied to gut microbiomes to understand their characteristics and modulate their composition. Through experiments in gnotobiotic mice with complex microbiomes, we demonstrated that strains of Akkermansia muciniphila and Bacteroides vulgatus could only be e...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122919/ https://www.ncbi.nlm.nih.gov/pubmed/35210551 http://dx.doi.org/10.1038/s41396-022-01208-9 |
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author | Segura Munoz, Rafael R. Mantz, Sara Martínez, Ines Li, Fuyong Schmaltz, Robert J. Pudlo, Nicholas A. Urs, Karthik Martens, Eric C. Walter, Jens Ramer-Tait, Amanda E. |
author_facet | Segura Munoz, Rafael R. Mantz, Sara Martínez, Ines Li, Fuyong Schmaltz, Robert J. Pudlo, Nicholas A. Urs, Karthik Martens, Eric C. Walter, Jens Ramer-Tait, Amanda E. |
author_sort | Segura Munoz, Rafael R. |
collection | PubMed |
description | It is unclear if coexistence theory can be applied to gut microbiomes to understand their characteristics and modulate their composition. Through experiments in gnotobiotic mice with complex microbiomes, we demonstrated that strains of Akkermansia muciniphila and Bacteroides vulgatus could only be established if microbiomes were devoid of these species. Strains of A. muciniphila showed strict competitive exclusion, while B. vulgatus strains coexisted but populations were still influenced by competitive interactions. These differences in competitive behavior were reflective of genomic variation within the two species, indicating considerable niche overlap for A. muciniphila strains and a broader niche space for B. vulgatus strains. Priority effects were detected for both species as strains’ competitive fitness increased when colonizing first, which resulted in stable persistence of the A. muciniphila strain colonizing first and competitive exclusion of the strain arriving second. Based on these observations, we devised a subtractive strategy for A. muciniphila using antibiotics and showed that a strain from an assembled community can be stably replaced by another strain. By demonstrating that competitive outcomes in gut ecosystems depend on niche differences and are historically contingent, our study provides novel information to explain the ecological characteristics of gut microbiomes and a basis for their modulation. |
format | Online Article Text |
id | pubmed-9122919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91229192022-05-22 Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes Segura Munoz, Rafael R. Mantz, Sara Martínez, Ines Li, Fuyong Schmaltz, Robert J. Pudlo, Nicholas A. Urs, Karthik Martens, Eric C. Walter, Jens Ramer-Tait, Amanda E. ISME J Article It is unclear if coexistence theory can be applied to gut microbiomes to understand their characteristics and modulate their composition. Through experiments in gnotobiotic mice with complex microbiomes, we demonstrated that strains of Akkermansia muciniphila and Bacteroides vulgatus could only be established if microbiomes were devoid of these species. Strains of A. muciniphila showed strict competitive exclusion, while B. vulgatus strains coexisted but populations were still influenced by competitive interactions. These differences in competitive behavior were reflective of genomic variation within the two species, indicating considerable niche overlap for A. muciniphila strains and a broader niche space for B. vulgatus strains. Priority effects were detected for both species as strains’ competitive fitness increased when colonizing first, which resulted in stable persistence of the A. muciniphila strain colonizing first and competitive exclusion of the strain arriving second. Based on these observations, we devised a subtractive strategy for A. muciniphila using antibiotics and showed that a strain from an assembled community can be stably replaced by another strain. By demonstrating that competitive outcomes in gut ecosystems depend on niche differences and are historically contingent, our study provides novel information to explain the ecological characteristics of gut microbiomes and a basis for their modulation. Nature Publishing Group UK 2022-02-24 2022-06 /pmc/articles/PMC9122919/ /pubmed/35210551 http://dx.doi.org/10.1038/s41396-022-01208-9 Text en © The Author(s) 2022, corrected publication 2022 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 Segura Munoz, Rafael R. Mantz, Sara Martínez, Ines Li, Fuyong Schmaltz, Robert J. Pudlo, Nicholas A. Urs, Karthik Martens, Eric C. Walter, Jens Ramer-Tait, Amanda E. Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
title | Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
title_full | Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
title_fullStr | Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
title_full_unstemmed | Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
title_short | Experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
title_sort | experimental evaluation of ecological principles to understand and modulate the outcome of bacterial strain competition in gut microbiomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122919/ https://www.ncbi.nlm.nih.gov/pubmed/35210551 http://dx.doi.org/10.1038/s41396-022-01208-9 |
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