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Kin selection for cooperation in natural bacterial populations
Bacteria produce a range of molecules that are secreted from the cell and can provide a benefit to the local population of cells. Laboratory experiments have suggested that these “public goods” molecules represent a form of cooperation, favored because they benefit closely related cells (kin selecti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892524/ https://www.ncbi.nlm.nih.gov/pubmed/35193981 http://dx.doi.org/10.1073/pnas.2119070119 |
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author | Belcher, Laurence J. Dewar, Anna E. Ghoul, Melanie West, Stuart A. |
author_facet | Belcher, Laurence J. Dewar, Anna E. Ghoul, Melanie West, Stuart A. |
author_sort | Belcher, Laurence J. |
collection | PubMed |
description | Bacteria produce a range of molecules that are secreted from the cell and can provide a benefit to the local population of cells. Laboratory experiments have suggested that these “public goods” molecules represent a form of cooperation, favored because they benefit closely related cells (kin selection). However, there is a relative lack of data demonstrating kin selection for cooperation in natural populations of bacteria. We used molecular population genetics to test for signatures of kin selection at the genomic level in natural populations of the opportunistic pathogen Pseudomonas aeruginosa. We found consistent evidence from multiple traits that genes controlling putatively cooperative traits have higher polymorphism and greater divergence and are more likely to harbor deleterious mutations relative to genes controlling putatively private traits, which are expressed at similar rates. These patterns suggest that cooperative traits are controlled by kin selection, and we estimate that the relatedness for social interactions in P. aeruginosa is r = 0.84. More generally, our results demonstrate how molecular population genetics can be used to study the evolution of cooperation in natural populations. |
format | Online Article Text |
id | pubmed-8892524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-88925242022-08-22 Kin selection for cooperation in natural bacterial populations Belcher, Laurence J. Dewar, Anna E. Ghoul, Melanie West, Stuart A. Proc Natl Acad Sci U S A Biological Sciences Bacteria produce a range of molecules that are secreted from the cell and can provide a benefit to the local population of cells. Laboratory experiments have suggested that these “public goods” molecules represent a form of cooperation, favored because they benefit closely related cells (kin selection). However, there is a relative lack of data demonstrating kin selection for cooperation in natural populations of bacteria. We used molecular population genetics to test for signatures of kin selection at the genomic level in natural populations of the opportunistic pathogen Pseudomonas aeruginosa. We found consistent evidence from multiple traits that genes controlling putatively cooperative traits have higher polymorphism and greater divergence and are more likely to harbor deleterious mutations relative to genes controlling putatively private traits, which are expressed at similar rates. These patterns suggest that cooperative traits are controlled by kin selection, and we estimate that the relatedness for social interactions in P. aeruginosa is r = 0.84. More generally, our results demonstrate how molecular population genetics can be used to study the evolution of cooperation in natural populations. National Academy of Sciences 2022-02-22 2022-03-01 /pmc/articles/PMC8892524/ /pubmed/35193981 http://dx.doi.org/10.1073/pnas.2119070119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Belcher, Laurence J. Dewar, Anna E. Ghoul, Melanie West, Stuart A. Kin selection for cooperation in natural bacterial populations |
title | Kin selection for cooperation in natural bacterial populations |
title_full | Kin selection for cooperation in natural bacterial populations |
title_fullStr | Kin selection for cooperation in natural bacterial populations |
title_full_unstemmed | Kin selection for cooperation in natural bacterial populations |
title_short | Kin selection for cooperation in natural bacterial populations |
title_sort | kin selection for cooperation in natural bacterial populations |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892524/ https://www.ncbi.nlm.nih.gov/pubmed/35193981 http://dx.doi.org/10.1073/pnas.2119070119 |
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