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...

Full description

Bibliographic Details
Main Authors: Jonas Schluter, Kevin R Foster
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23185130/?tool=EBI
id doaj-31d1996787df41e4ab96333c1ca59e9c
record_format Article
spelling doaj-31d1996787df41e4ab96333c1ca59e9c2021-07-02T17:07:48ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852012-01-011011e100142410.1371/journal.pbio.1001424The evolution of mutualism in gut microbiota via host epithelial selection.Jonas SchluterKevin R FosterThe 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.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23185130/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Jonas Schluter
Kevin R Foster
spellingShingle Jonas Schluter
Kevin R Foster
The evolution of mutualism in gut microbiota via host epithelial selection.
PLoS Biology
author_facet Jonas Schluter
Kevin R Foster
author_sort Jonas Schluter
title 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_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_sort evolution of mutualism in gut microbiota via host epithelial selection.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2012-01-01
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.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23185130/?tool=EBI
work_keys_str_mv AT jonasschluter theevolutionofmutualismingutmicrobiotaviahostepithelialselection
AT kevinrfoster theevolutionofmutualismingutmicrobiotaviahostepithelialselection
AT jonasschluter evolutionofmutualismingutmicrobiotaviahostepithelialselection
AT kevinrfoster evolutionofmutualismingutmicrobiotaviahostepithelialselection
_version_ 1721325982727536640