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Rapid compensatory evolution promotes the survival of conjugative plasmids

Conjugative plasmids play a vital role in bacterial adaptation through horizontal gene transfer. Explaining how plasmids persist in host populations however is difficult, given the high costs often associated with plasmid carriage. Compensatory evolution to ameliorate this cost can rescue plasmids f...

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Autores principales: Harrison, Ellie, Dytham, Calvin, Hall, James P. J., Guymer, David, Spiers, Andrew J., Paterson, Steve, Brockhurst, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964889/
https://www.ncbi.nlm.nih.gov/pubmed/27510852
http://dx.doi.org/10.1080/2159256X.2016.1179074
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author Harrison, Ellie
Dytham, Calvin
Hall, James P. J.
Guymer, David
Spiers, Andrew J.
Paterson, Steve
Brockhurst, Michael A.
author_facet Harrison, Ellie
Dytham, Calvin
Hall, James P. J.
Guymer, David
Spiers, Andrew J.
Paterson, Steve
Brockhurst, Michael A.
author_sort Harrison, Ellie
collection PubMed
description Conjugative plasmids play a vital role in bacterial adaptation through horizontal gene transfer. Explaining how plasmids persist in host populations however is difficult, given the high costs often associated with plasmid carriage. Compensatory evolution to ameliorate this cost can rescue plasmids from extinction. In a recently published study we showed that compensatory evolution repeatedly targeted the same bacterial regulatory system, GacA/GacS, in populations of plasmid-carrying bacteria evolving across a range of selective environments. Mutations in these genes arose rapidly and completely eliminated the cost of plasmid carriage. Here we extend our analysis using an individual based model to explore the dynamics of compensatory evolution in this system. We show that mutations which ameliorate the cost of plasmid carriage can prevent both the loss of plasmids from the population and the fixation of accessory traits on the bacterial chromosome. We discuss how dependent the outcome of compensatory evolution is on the strength and availability of such mutations and the rate at which beneficial accessory traits integrate on the host chromosome.
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spelling pubmed-49648892016-08-10 Rapid compensatory evolution promotes the survival of conjugative plasmids Harrison, Ellie Dytham, Calvin Hall, James P. J. Guymer, David Spiers, Andrew J. Paterson, Steve Brockhurst, Michael A. Mob Genet Elements Commentary Conjugative plasmids play a vital role in bacterial adaptation through horizontal gene transfer. Explaining how plasmids persist in host populations however is difficult, given the high costs often associated with plasmid carriage. Compensatory evolution to ameliorate this cost can rescue plasmids from extinction. In a recently published study we showed that compensatory evolution repeatedly targeted the same bacterial regulatory system, GacA/GacS, in populations of plasmid-carrying bacteria evolving across a range of selective environments. Mutations in these genes arose rapidly and completely eliminated the cost of plasmid carriage. Here we extend our analysis using an individual based model to explore the dynamics of compensatory evolution in this system. We show that mutations which ameliorate the cost of plasmid carriage can prevent both the loss of plasmids from the population and the fixation of accessory traits on the bacterial chromosome. We discuss how dependent the outcome of compensatory evolution is on the strength and availability of such mutations and the rate at which beneficial accessory traits integrate on the host chromosome. Taylor & Francis 2016-05-04 /pmc/articles/PMC4964889/ /pubmed/27510852 http://dx.doi.org/10.1080/2159256X.2016.1179074 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Commentary
Harrison, Ellie
Dytham, Calvin
Hall, James P. J.
Guymer, David
Spiers, Andrew J.
Paterson, Steve
Brockhurst, Michael A.
Rapid compensatory evolution promotes the survival of conjugative plasmids
title Rapid compensatory evolution promotes the survival of conjugative plasmids
title_full Rapid compensatory evolution promotes the survival of conjugative plasmids
title_fullStr Rapid compensatory evolution promotes the survival of conjugative plasmids
title_full_unstemmed Rapid compensatory evolution promotes the survival of conjugative plasmids
title_short Rapid compensatory evolution promotes the survival of conjugative plasmids
title_sort rapid compensatory evolution promotes the survival of conjugative plasmids
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964889/
https://www.ncbi.nlm.nih.gov/pubmed/27510852
http://dx.doi.org/10.1080/2159256X.2016.1179074
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