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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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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. |
format | Online Article Text |
id | pubmed-4736460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT hesseelze hostpopulationbottlenecksdriveparasiteextinctionduringantagonisticcoevolution AT bucklingangus hostpopulationbottlenecksdriveparasiteextinctionduringantagonisticcoevolution |