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Parasite-mediated disruptive selection in a natural Daphnia population

BACKGROUND: A mismatch has emerged between models and data of host-parasite evolution. Theory readily predicts that parasites can promote host diversity through mechanisms such as disruptive selection. Yet, despite these predictions, empirical evidence for parasite-mediated increases in host diversi...

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Autores principales: Duffy, Meghan A, Brassil, Chad E, Hall, Spencer R, Tessier, Alan J, Cáceres, Carla E, Conner, Jeffrey K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276202/
https://www.ncbi.nlm.nih.gov/pubmed/18328099
http://dx.doi.org/10.1186/1471-2148-8-80
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author Duffy, Meghan A
Brassil, Chad E
Hall, Spencer R
Tessier, Alan J
Cáceres, Carla E
Conner, Jeffrey K
author_facet Duffy, Meghan A
Brassil, Chad E
Hall, Spencer R
Tessier, Alan J
Cáceres, Carla E
Conner, Jeffrey K
author_sort Duffy, Meghan A
collection PubMed
description BACKGROUND: A mismatch has emerged between models and data of host-parasite evolution. Theory readily predicts that parasites can promote host diversity through mechanisms such as disruptive selection. Yet, despite these predictions, empirical evidence for parasite-mediated increases in host diversity remains surprisingly scant. RESULTS: Here, we document parasite-mediated disruptive selection on a natural Daphnia population during a parasite epidemic. The mean susceptibility of clones collected from the population before and after the epidemic did not differ, but clonal variance and broad-sense heritability of post-epidemic clones were significantly greater, indicating disruptive selection and rapid evolution. A maximum likelihood method that we developed for detecting selection on natural populations also suggests disruptive selection during the epidemic: the distribution of susceptibilities in the population shifted from unimodal prior to the epidemic to bimodal after the epidemic. Interestingly, this same bimodal distribution was retained after a generation of sexual reproduction. CONCLUSION: These results provide rare empirical support for parasite-driven increases in host genetic diversity, and suggest that this increase can occur rapidly.
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spelling pubmed-22762022008-03-28 Parasite-mediated disruptive selection in a natural Daphnia population Duffy, Meghan A Brassil, Chad E Hall, Spencer R Tessier, Alan J Cáceres, Carla E Conner, Jeffrey K BMC Evol Biol Research Article BACKGROUND: A mismatch has emerged between models and data of host-parasite evolution. Theory readily predicts that parasites can promote host diversity through mechanisms such as disruptive selection. Yet, despite these predictions, empirical evidence for parasite-mediated increases in host diversity remains surprisingly scant. RESULTS: Here, we document parasite-mediated disruptive selection on a natural Daphnia population during a parasite epidemic. The mean susceptibility of clones collected from the population before and after the epidemic did not differ, but clonal variance and broad-sense heritability of post-epidemic clones were significantly greater, indicating disruptive selection and rapid evolution. A maximum likelihood method that we developed for detecting selection on natural populations also suggests disruptive selection during the epidemic: the distribution of susceptibilities in the population shifted from unimodal prior to the epidemic to bimodal after the epidemic. Interestingly, this same bimodal distribution was retained after a generation of sexual reproduction. CONCLUSION: These results provide rare empirical support for parasite-driven increases in host genetic diversity, and suggest that this increase can occur rapidly. BioMed Central 2008-03-07 /pmc/articles/PMC2276202/ /pubmed/18328099 http://dx.doi.org/10.1186/1471-2148-8-80 Text en Copyright ©2008 Duffy et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Duffy, Meghan A
Brassil, Chad E
Hall, Spencer R
Tessier, Alan J
Cáceres, Carla E
Conner, Jeffrey K
Parasite-mediated disruptive selection in a natural Daphnia population
title Parasite-mediated disruptive selection in a natural Daphnia population
title_full Parasite-mediated disruptive selection in a natural Daphnia population
title_fullStr Parasite-mediated disruptive selection in a natural Daphnia population
title_full_unstemmed Parasite-mediated disruptive selection in a natural Daphnia population
title_short Parasite-mediated disruptive selection in a natural Daphnia population
title_sort parasite-mediated disruptive selection in a natural daphnia population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276202/
https://www.ncbi.nlm.nih.gov/pubmed/18328099
http://dx.doi.org/10.1186/1471-2148-8-80
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