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Sex-specific effects of a parasite evolving in a female-biased host population

BACKGROUND: Males and females differ in many ways and might present different opportunities and challenges to their parasites. In the same way that parasites adapt to the most common host type, they may adapt to the characteristics of the host sex they encounter most often. To explore this hypothesi...

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Detalles Bibliográficos
Autores principales: Duneau, David, Luijckx, Pepijn, Ruder, Ludwig F, Ebert, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568004/
https://www.ncbi.nlm.nih.gov/pubmed/23249484
http://dx.doi.org/10.1186/1741-7007-10-104
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author Duneau, David
Luijckx, Pepijn
Ruder, Ludwig F
Ebert, Dieter
author_facet Duneau, David
Luijckx, Pepijn
Ruder, Ludwig F
Ebert, Dieter
author_sort Duneau, David
collection PubMed
description BACKGROUND: Males and females differ in many ways and might present different opportunities and challenges to their parasites. In the same way that parasites adapt to the most common host type, they may adapt to the characteristics of the host sex they encounter most often. To explore this hypothesis, we characterized host sex-specific effects of the parasite Pasteuria ramosa, a bacterium evolving in naturally, strongly, female-biased populations of its host Daphnia magna. RESULTS: We show that the parasite proliferates more successfully in female hosts than in male hosts, even though males and females are genetically identical. In addition, when exposure occurred when hosts expressed a sexual dimorphism, females were more infected. In both host sexes, the parasite causes a similar reduction in longevity and leads to some level of castration. However, only in females does parasite-induced castration result in the gigantism that increases the carrying capacity for the proliferating parasite. CONCLUSIONS: We show that mature male and female Daphnia represent different environments and reveal one parasite-induced symptom (host castration), which leads to increased carrying capacity for parasite proliferation in female but not male hosts. We propose that parasite induced host castration is a property of parasites that evolved as an adaptation to specifically exploit female hosts.
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spelling pubmed-35680042013-02-12 Sex-specific effects of a parasite evolving in a female-biased host population Duneau, David Luijckx, Pepijn Ruder, Ludwig F Ebert, Dieter BMC Biol Research Article BACKGROUND: Males and females differ in many ways and might present different opportunities and challenges to their parasites. In the same way that parasites adapt to the most common host type, they may adapt to the characteristics of the host sex they encounter most often. To explore this hypothesis, we characterized host sex-specific effects of the parasite Pasteuria ramosa, a bacterium evolving in naturally, strongly, female-biased populations of its host Daphnia magna. RESULTS: We show that the parasite proliferates more successfully in female hosts than in male hosts, even though males and females are genetically identical. In addition, when exposure occurred when hosts expressed a sexual dimorphism, females were more infected. In both host sexes, the parasite causes a similar reduction in longevity and leads to some level of castration. However, only in females does parasite-induced castration result in the gigantism that increases the carrying capacity for the proliferating parasite. CONCLUSIONS: We show that mature male and female Daphnia represent different environments and reveal one parasite-induced symptom (host castration), which leads to increased carrying capacity for parasite proliferation in female but not male hosts. We propose that parasite induced host castration is a property of parasites that evolved as an adaptation to specifically exploit female hosts. BioMed Central 2012-12-18 /pmc/articles/PMC3568004/ /pubmed/23249484 http://dx.doi.org/10.1186/1741-7007-10-104 Text en Copyright ©2012 Duneau 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
Duneau, David
Luijckx, Pepijn
Ruder, Ludwig F
Ebert, Dieter
Sex-specific effects of a parasite evolving in a female-biased host population
title Sex-specific effects of a parasite evolving in a female-biased host population
title_full Sex-specific effects of a parasite evolving in a female-biased host population
title_fullStr Sex-specific effects of a parasite evolving in a female-biased host population
title_full_unstemmed Sex-specific effects of a parasite evolving in a female-biased host population
title_short Sex-specific effects of a parasite evolving in a female-biased host population
title_sort sex-specific effects of a parasite evolving in a female-biased host population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568004/
https://www.ncbi.nlm.nih.gov/pubmed/23249484
http://dx.doi.org/10.1186/1741-7007-10-104
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