Cargando…
Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences
Generalist bacterial predators are likely to strongly shape many important ecological and evolutionary features of microbial communities, for example by altering the character and pace of molecular evolution, but investigations of such effects are scarce. Here we report how predator-prey interaction...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754418/ https://www.ncbi.nlm.nih.gov/pubmed/31541093 http://dx.doi.org/10.1038/s41467-019-12140-6 |
_version_ | 1783453072213671936 |
---|---|
author | Nair, Ramith R. Vasse, Marie Wielgoss, Sébastien Sun, Lei Yu, Yuen-Tsu N. Velicer, Gregory J. |
author_facet | Nair, Ramith R. Vasse, Marie Wielgoss, Sébastien Sun, Lei Yu, Yuen-Tsu N. Velicer, Gregory J. |
author_sort | Nair, Ramith R. |
collection | PubMed |
description | Generalist bacterial predators are likely to strongly shape many important ecological and evolutionary features of microbial communities, for example by altering the character and pace of molecular evolution, but investigations of such effects are scarce. Here we report how predator-prey interactions alter the evolution of fitness, genomes and phenotypic diversity in coevolving bacterial communities composed of Myxococcus xanthus as predator and Escherichia coli as prey, relative to single-species controls. We show evidence of reciprocal adaptation and demonstrate accelerated genomic evolution specific to coevolving communities, including the rapid appearance of mutator genotypes. Strong parallel evolution unique to the predator-prey communities occurs in both parties, with predators driving adaptation at two prey traits associated with virulence in bacterial pathogens—mucoidy and the outer-membrane protease OmpT. Our results suggest that generalist predatory bacteria are important determinants of how complex microbial communities and their interaction networks evolve in natural habitats. |
format | Online Article Text |
id | pubmed-6754418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67544182019-09-23 Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences Nair, Ramith R. Vasse, Marie Wielgoss, Sébastien Sun, Lei Yu, Yuen-Tsu N. Velicer, Gregory J. Nat Commun Article Generalist bacterial predators are likely to strongly shape many important ecological and evolutionary features of microbial communities, for example by altering the character and pace of molecular evolution, but investigations of such effects are scarce. Here we report how predator-prey interactions alter the evolution of fitness, genomes and phenotypic diversity in coevolving bacterial communities composed of Myxococcus xanthus as predator and Escherichia coli as prey, relative to single-species controls. We show evidence of reciprocal adaptation and demonstrate accelerated genomic evolution specific to coevolving communities, including the rapid appearance of mutator genotypes. Strong parallel evolution unique to the predator-prey communities occurs in both parties, with predators driving adaptation at two prey traits associated with virulence in bacterial pathogens—mucoidy and the outer-membrane protease OmpT. Our results suggest that generalist predatory bacteria are important determinants of how complex microbial communities and their interaction networks evolve in natural habitats. Nature Publishing Group UK 2019-09-20 /pmc/articles/PMC6754418/ /pubmed/31541093 http://dx.doi.org/10.1038/s41467-019-12140-6 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Nair, Ramith R. Vasse, Marie Wielgoss, Sébastien Sun, Lei Yu, Yuen-Tsu N. Velicer, Gregory J. Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
title | Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
title_full | Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
title_fullStr | Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
title_full_unstemmed | Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
title_short | Bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
title_sort | bacterial predator-prey coevolution accelerates genome evolution and selects on virulence-associated prey defences |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754418/ https://www.ncbi.nlm.nih.gov/pubmed/31541093 http://dx.doi.org/10.1038/s41467-019-12140-6 |
work_keys_str_mv | AT nairramithr bacterialpredatorpreycoevolutionacceleratesgenomeevolutionandselectsonvirulenceassociatedpreydefences AT vassemarie bacterialpredatorpreycoevolutionacceleratesgenomeevolutionandselectsonvirulenceassociatedpreydefences AT wielgosssebastien bacterialpredatorpreycoevolutionacceleratesgenomeevolutionandselectsonvirulenceassociatedpreydefences AT sunlei bacterialpredatorpreycoevolutionacceleratesgenomeevolutionandselectsonvirulenceassociatedpreydefences AT yuyuentsun bacterialpredatorpreycoevolutionacceleratesgenomeevolutionandselectsonvirulenceassociatedpreydefences AT velicergregoryj bacterialpredatorpreycoevolutionacceleratesgenomeevolutionandselectsonvirulenceassociatedpreydefences |