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The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection

The human gut harbours a large and genetically diverse population of symbiotic microbes that both feed and protect the host. Evolutionary theory, however, predicts that such genetic diversity can destabilise mutualistic partnerships. How then can the mutualism of the human microbiota be explained? H...

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Detalles Bibliográficos
Autores principales: Schluter, Jonas, Foster, Kevin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502499/
https://www.ncbi.nlm.nih.gov/pubmed/23185130
http://dx.doi.org/10.1371/journal.pbio.1001424
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author Schluter, Jonas
Foster, Kevin R.
author_facet Schluter, Jonas
Foster, Kevin R.
author_sort Schluter, Jonas
collection PubMed
description The human gut harbours a large and genetically diverse population of symbiotic microbes that both feed and protect the host. Evolutionary theory, however, predicts that such genetic diversity can destabilise mutualistic partnerships. How then can the mutualism of the human microbiota be explained? Here we develop an individual-based model of host-associated microbial communities. We first demonstrate the fundamental problem faced by a host: The presence of a genetically diverse microbiota leads to the dominance of the fastest growing microbes instead of the microbes that are most beneficial to the host. We next investigate the potential for host secretions to influence the microbiota. This reveals that the epithelium–microbiota interface acts as a selectivity amplifier: Modest amounts of moderately selective epithelial secretions cause a complete shift in the strains growing at the epithelial surface. This occurs because of the physical structure of the epithelium–microbiota interface: Epithelial secretions have effects that permeate upwards through the whole microbial community, while lumen compounds preferentially affect cells that are soon to slough off. Finally, our model predicts that while antimicrobial secretion can promote host epithelial selection, epithelial nutrient secretion will often be key to host selection. Our findings are consistent with a growing number of empirical papers that indicate an influence of host factors upon microbiota, including growth-promoting glycoconjugates. We argue that host selection is likely to be a key mechanism in the stabilisation of the mutualism between a host and its microbiota.
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spelling pubmed-35024992012-11-26 The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection Schluter, Jonas Foster, Kevin R. PLoS Biol Research Article The human gut harbours a large and genetically diverse population of symbiotic microbes that both feed and protect the host. Evolutionary theory, however, predicts that such genetic diversity can destabilise mutualistic partnerships. How then can the mutualism of the human microbiota be explained? Here we develop an individual-based model of host-associated microbial communities. We first demonstrate the fundamental problem faced by a host: The presence of a genetically diverse microbiota leads to the dominance of the fastest growing microbes instead of the microbes that are most beneficial to the host. We next investigate the potential for host secretions to influence the microbiota. This reveals that the epithelium–microbiota interface acts as a selectivity amplifier: Modest amounts of moderately selective epithelial secretions cause a complete shift in the strains growing at the epithelial surface. This occurs because of the physical structure of the epithelium–microbiota interface: Epithelial secretions have effects that permeate upwards through the whole microbial community, while lumen compounds preferentially affect cells that are soon to slough off. Finally, our model predicts that while antimicrobial secretion can promote host epithelial selection, epithelial nutrient secretion will often be key to host selection. Our findings are consistent with a growing number of empirical papers that indicate an influence of host factors upon microbiota, including growth-promoting glycoconjugates. We argue that host selection is likely to be a key mechanism in the stabilisation of the mutualism between a host and its microbiota. Public Library of Science 2012-11-20 /pmc/articles/PMC3502499/ /pubmed/23185130 http://dx.doi.org/10.1371/journal.pbio.1001424 Text en © 2012 Schluter, Foster http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schluter, Jonas
Foster, Kevin R.
The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection
title The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection
title_full The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection
title_fullStr The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection
title_full_unstemmed The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection
title_short The Evolution of Mutualism in Gut Microbiota Via Host Epithelial Selection
title_sort evolution of mutualism in gut microbiota via host epithelial selection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502499/
https://www.ncbi.nlm.nih.gov/pubmed/23185130
http://dx.doi.org/10.1371/journal.pbio.1001424
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