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Kin selection explains the evolution of cooperation in the gut microbiota
Through the secretion of “public goods” molecules, microbes cooperatively exploit their habitat. This is known as a major driver of the functioning of microbial communities, including in human disease. Understanding why microbial species cooperate is therefore crucial to achieve successful microbial...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017935/ https://www.ncbi.nlm.nih.gov/pubmed/33526674 http://dx.doi.org/10.1073/pnas.2016046118 |
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author | Simonet, Camille McNally, Luke |
author_facet | Simonet, Camille McNally, Luke |
author_sort | Simonet, Camille |
collection | PubMed |
description | Through the secretion of “public goods” molecules, microbes cooperatively exploit their habitat. This is known as a major driver of the functioning of microbial communities, including in human disease. Understanding why microbial species cooperate is therefore crucial to achieve successful microbial community management, such as microbiome manipulation. A leading explanation is that of Hamilton’s inclusive-fitness framework. A cooperator can indirectly transmit its genes by helping the reproduction of an individual carrying similar genes. Therefore, all else being equal, as relatedness among individuals increases, so should cooperation. However, the predictive power of relatedness, particularly in microbes, is surrounded by controversy. Using phylogenetic comparative analyses across the full diversity of the human gut microbiota and six forms of cooperation, we find that relatedness is predictive of the cooperative gene content evolution in gut-microbe genomes. Hence, relatedness is predictive of cooperation over broad microbial taxonomic levels that encompass variation in other life-history and ecology details. This supports the generality of Hamilton’s central insights and the relevance of relatedness as a key parameter of interest to advance microbial predictive and engineering science. |
format | Online Article Text |
id | pubmed-8017935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-80179352021-04-12 Kin selection explains the evolution of cooperation in the gut microbiota Simonet, Camille McNally, Luke Proc Natl Acad Sci U S A Biological Sciences Through the secretion of “public goods” molecules, microbes cooperatively exploit their habitat. This is known as a major driver of the functioning of microbial communities, including in human disease. Understanding why microbial species cooperate is therefore crucial to achieve successful microbial community management, such as microbiome manipulation. A leading explanation is that of Hamilton’s inclusive-fitness framework. A cooperator can indirectly transmit its genes by helping the reproduction of an individual carrying similar genes. Therefore, all else being equal, as relatedness among individuals increases, so should cooperation. However, the predictive power of relatedness, particularly in microbes, is surrounded by controversy. Using phylogenetic comparative analyses across the full diversity of the human gut microbiota and six forms of cooperation, we find that relatedness is predictive of the cooperative gene content evolution in gut-microbe genomes. Hence, relatedness is predictive of cooperation over broad microbial taxonomic levels that encompass variation in other life-history and ecology details. This supports the generality of Hamilton’s central insights and the relevance of relatedness as a key parameter of interest to advance microbial predictive and engineering science. National Academy of Sciences 2021-02-09 2021-02-01 /pmc/articles/PMC8017935/ /pubmed/33526674 http://dx.doi.org/10.1073/pnas.2016046118 Text en Copyright © 2021 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Simonet, Camille McNally, Luke Kin selection explains the evolution of cooperation in the gut microbiota |
title | Kin selection explains the evolution of cooperation in the gut microbiota |
title_full | Kin selection explains the evolution of cooperation in the gut microbiota |
title_fullStr | Kin selection explains the evolution of cooperation in the gut microbiota |
title_full_unstemmed | Kin selection explains the evolution of cooperation in the gut microbiota |
title_short | Kin selection explains the evolution of cooperation in the gut microbiota |
title_sort | kin selection explains the evolution of cooperation in the gut microbiota |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017935/ https://www.ncbi.nlm.nih.gov/pubmed/33526674 http://dx.doi.org/10.1073/pnas.2016046118 |
work_keys_str_mv | AT simonetcamille kinselectionexplainstheevolutionofcooperationinthegutmicrobiota AT mcnallyluke kinselectionexplainstheevolutionofcooperationinthegutmicrobiota |