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Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments

Parasite local adaptation, the greater performance of parasites on their local compared with foreign hosts, has important consequences for the maintenance of diversity and epidemiology. While the abiotic environment may significantly affect local adaptation, most studies to date have failed either t...

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Detalles Bibliográficos
Autores principales: Gorter, Florien A., Scanlan, Pauline D., Buckling, Angus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780547/
https://www.ncbi.nlm.nih.gov/pubmed/26888914
http://dx.doi.org/10.1098/rsbl.2015.0879
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author Gorter, Florien A.
Scanlan, Pauline D.
Buckling, Angus
author_facet Gorter, Florien A.
Scanlan, Pauline D.
Buckling, Angus
author_sort Gorter, Florien A.
collection PubMed
description Parasite local adaptation, the greater performance of parasites on their local compared with foreign hosts, has important consequences for the maintenance of diversity and epidemiology. While the abiotic environment may significantly affect local adaptation, most studies to date have failed either to incorporate the effects of the abiotic environment, or to separate them from those of the biotic environment. Here, we tease apart biotic and abiotic components of local adaptation using the bacterium Pseudomonas fluorescens and its viral parasite bacteriophage Φ2. We coevolved replicate populations of bacteria and phages at three different temperatures, and determined their performance against coevolutionary partners from the same and different temperatures. Crucially, we measured performance at different assay temperatures, which allowed us to disentangle adaptation to biotic and abiotic habitat components. Our results show that bacteria and phages are more resistant and infectious, respectively, at the temperature at which they previously coevolved, confirming that local adaptation to abiotic conditions can play a crucial role in determining parasite infectivity and host resistance. Our work underlines the need to assess host–parasite interactions across multiple relevant abiotic environments, and suggests that microbial adaption to local temperatures can create ecological barriers to dispersal across temperature gradients.
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spelling pubmed-47805472016-03-18 Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments Gorter, Florien A. Scanlan, Pauline D. Buckling, Angus Biol Lett Evolutionary Biology Parasite local adaptation, the greater performance of parasites on their local compared with foreign hosts, has important consequences for the maintenance of diversity and epidemiology. While the abiotic environment may significantly affect local adaptation, most studies to date have failed either to incorporate the effects of the abiotic environment, or to separate them from those of the biotic environment. Here, we tease apart biotic and abiotic components of local adaptation using the bacterium Pseudomonas fluorescens and its viral parasite bacteriophage Φ2. We coevolved replicate populations of bacteria and phages at three different temperatures, and determined their performance against coevolutionary partners from the same and different temperatures. Crucially, we measured performance at different assay temperatures, which allowed us to disentangle adaptation to biotic and abiotic habitat components. Our results show that bacteria and phages are more resistant and infectious, respectively, at the temperature at which they previously coevolved, confirming that local adaptation to abiotic conditions can play a crucial role in determining parasite infectivity and host resistance. Our work underlines the need to assess host–parasite interactions across multiple relevant abiotic environments, and suggests that microbial adaption to local temperatures can create ecological barriers to dispersal across temperature gradients. The Royal Society 2016-02 /pmc/articles/PMC4780547/ /pubmed/26888914 http://dx.doi.org/10.1098/rsbl.2015.0879 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolutionary Biology
Gorter, Florien A.
Scanlan, Pauline D.
Buckling, Angus
Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
title Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
title_full Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
title_fullStr Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
title_full_unstemmed Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
title_short Adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
title_sort adaptation to abiotic conditions drives local adaptation in bacteria and viruses coevolving in heterogeneous environments
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780547/
https://www.ncbi.nlm.nih.gov/pubmed/26888914
http://dx.doi.org/10.1098/rsbl.2015.0879
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