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Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction
Bacteria engage in a complex network of ecological interactions, which includes mobile genetic elements (MGEs) such as phages and plasmids. These elements play a key role in microbial communities as vectors of horizontal gene transfer but can also be important sources of selection for their bacteria...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655702/ https://www.ncbi.nlm.nih.gov/pubmed/28247474 http://dx.doi.org/10.1111/mec.14080 |
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author | Harrison, Ellie Hall, James P. J. Paterson, Steve Spiers, Andrew J. Brockhurst, Michael A. |
author_facet | Harrison, Ellie Hall, James P. J. Paterson, Steve Spiers, Andrew J. Brockhurst, Michael A. |
author_sort | Harrison, Ellie |
collection | PubMed |
description | Bacteria engage in a complex network of ecological interactions, which includes mobile genetic elements (MGEs) such as phages and plasmids. These elements play a key role in microbial communities as vectors of horizontal gene transfer but can also be important sources of selection for their bacterial hosts. In natural communities, bacteria are likely to encounter multiple MGEs simultaneously and conflicting selection among MGEs could alter the bacterial evolutionary response to each MGE. Here, we test the effect of interactions with multiple MGEs on bacterial molecular evolution in the tripartite interaction between the bacterium, Pseudomonas fluorescens, the lytic bacteriophage, SBW25φ2, and conjugative plasmid, pQBR103, using genome sequencing of experimentally evolved bacteria. We show that individually, both plasmids and phages impose selection leading to bacterial evolutionary responses that are distinct from bacterial populations evolving without MGEs, but that together, plasmids and phages impose conflicting selection on bacteria, constraining the evolutionary responses observed in pairwise interactions. Our findings highlight the likely difficulties of predicting evolutionary responses to multiple selective pressures from the observed evolutionary responses to each selective pressure alone. Understanding evolution in complex microbial communities comprising many species and MGEs will require that we go beyond studies of pairwise interactions. |
format | Online Article Text |
id | pubmed-5655702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56557022017-11-01 Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction Harrison, Ellie Hall, James P. J. Paterson, Steve Spiers, Andrew J. Brockhurst, Michael A. Mol Ecol ORIGINAL ARTICLES Bacteria engage in a complex network of ecological interactions, which includes mobile genetic elements (MGEs) such as phages and plasmids. These elements play a key role in microbial communities as vectors of horizontal gene transfer but can also be important sources of selection for their bacterial hosts. In natural communities, bacteria are likely to encounter multiple MGEs simultaneously and conflicting selection among MGEs could alter the bacterial evolutionary response to each MGE. Here, we test the effect of interactions with multiple MGEs on bacterial molecular evolution in the tripartite interaction between the bacterium, Pseudomonas fluorescens, the lytic bacteriophage, SBW25φ2, and conjugative plasmid, pQBR103, using genome sequencing of experimentally evolved bacteria. We show that individually, both plasmids and phages impose selection leading to bacterial evolutionary responses that are distinct from bacterial populations evolving without MGEs, but that together, plasmids and phages impose conflicting selection on bacteria, constraining the evolutionary responses observed in pairwise interactions. Our findings highlight the likely difficulties of predicting evolutionary responses to multiple selective pressures from the observed evolutionary responses to each selective pressure alone. Understanding evolution in complex microbial communities comprising many species and MGEs will require that we go beyond studies of pairwise interactions. John Wiley and Sons Inc. 2017-04-03 2017-05 /pmc/articles/PMC5655702/ /pubmed/28247474 http://dx.doi.org/10.1111/mec.14080 Text en © 2017 The Authors. Molecular Ecology Published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | ORIGINAL ARTICLES Harrison, Ellie Hall, James P. J. Paterson, Steve Spiers, Andrew J. Brockhurst, Michael A. Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
title | Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
title_full | Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
title_fullStr | Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
title_full_unstemmed | Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
title_short | Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
title_sort | conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria–plasmid–phage interaction |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655702/ https://www.ncbi.nlm.nih.gov/pubmed/28247474 http://dx.doi.org/10.1111/mec.14080 |
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