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Host population bottlenecks drive parasite extinction during antagonistic coevolution

Host–parasite interactions are often characterized by large fluctuations in host population size, and we investigated how such host bottlenecks affected coevolution between a bacterium and a virus. Previous theory suggests that host bottlenecks should provide parasites with an evolutionary advantage...

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Detalles Bibliográficos
Autores principales: Hesse, Elze, Buckling, Angus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736460/
https://www.ncbi.nlm.nih.gov/pubmed/26661325
http://dx.doi.org/10.1111/evo.12837
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author Hesse, Elze
Buckling, Angus
author_facet Hesse, Elze
Buckling, Angus
author_sort Hesse, Elze
collection PubMed
description Host–parasite interactions are often characterized by large fluctuations in host population size, and we investigated how such host bottlenecks affected coevolution between a bacterium and a virus. Previous theory suggests that host bottlenecks should provide parasites with an evolutionary advantage, but instead we found that phages were rapidly driven to extinction when coevolving with hosts exposed to large genetic bottlenecks. This was caused by the stochastic loss of sensitive bacteria, which are required for phage persistence and infectivity evolution. Our findings emphasize the importance of feedbacks between ecological and coevolutionary dynamics, and how this feedback can qualitatively alter coevolutionary dynamics.
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spelling pubmed-47364602016-02-18 Host population bottlenecks drive parasite extinction during antagonistic coevolution Hesse, Elze Buckling, Angus Evolution Brief Communications Host–parasite interactions are often characterized by large fluctuations in host population size, and we investigated how such host bottlenecks affected coevolution between a bacterium and a virus. Previous theory suggests that host bottlenecks should provide parasites with an evolutionary advantage, but instead we found that phages were rapidly driven to extinction when coevolving with hosts exposed to large genetic bottlenecks. This was caused by the stochastic loss of sensitive bacteria, which are required for phage persistence and infectivity evolution. Our findings emphasize the importance of feedbacks between ecological and coevolutionary dynamics, and how this feedback can qualitatively alter coevolutionary dynamics. John Wiley and Sons Inc. 2015-12-30 2016-01 /pmc/articles/PMC4736460/ /pubmed/26661325 http://dx.doi.org/10.1111/evo.12837 Text en © 2015 The Author(s). Evolution published by Wiley Periodicals, Inc. on behalf of The Society for the Study of Evolution. 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 Brief Communications
Hesse, Elze
Buckling, Angus
Host population bottlenecks drive parasite extinction during antagonistic coevolution
title Host population bottlenecks drive parasite extinction during antagonistic coevolution
title_full Host population bottlenecks drive parasite extinction during antagonistic coevolution
title_fullStr Host population bottlenecks drive parasite extinction during antagonistic coevolution
title_full_unstemmed Host population bottlenecks drive parasite extinction during antagonistic coevolution
title_short Host population bottlenecks drive parasite extinction during antagonistic coevolution
title_sort host population bottlenecks drive parasite extinction during antagonistic coevolution
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736460/
https://www.ncbi.nlm.nih.gov/pubmed/26661325
http://dx.doi.org/10.1111/evo.12837
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