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A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation

Males are typically the sicker sex. Data from multiple taxa indicate that they are more likely to be infected with parasites, and are less “tolerant,” or less able to mitigate the fitness costs of a given infection, than females. One cost of infection for many animals is an increased probability of...

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Autores principales: Stephenson, Jessica F., Kinsella, Cormac, Cable, Joanne, van Oosterhout, Cock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797162/
https://www.ncbi.nlm.nih.gov/pubmed/27066240
http://dx.doi.org/10.1002/ece3.2049
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author Stephenson, Jessica F.
Kinsella, Cormac
Cable, Joanne
van Oosterhout, Cock
author_facet Stephenson, Jessica F.
Kinsella, Cormac
Cable, Joanne
van Oosterhout, Cock
author_sort Stephenson, Jessica F.
collection PubMed
description Males are typically the sicker sex. Data from multiple taxa indicate that they are more likely to be infected with parasites, and are less “tolerant,” or less able to mitigate the fitness costs of a given infection, than females. One cost of infection for many animals is an increased probability of being captured by a predator. A clear, hitherto untested, prediction is therefore that this parasite‐induced vulnerability to predation is more pronounced among males than females. We tested this prediction in the sexually size dimorphic guppy, Poecilia reticulata, in which females are typically larger than males. We either sham or experimentally infected guppies with Gyrodactylus turnbulli, elicited their escape response using an established protocol and measured the distance they covered during 60 ms. To discriminate between the effects of body size and those of other inherent sex differences, we size‐matched fish across treatment groups. Infection with G. turnbulli reduced the distance covered during the escape response of small adults by 20.1%, whereas that of large fish was unaffected. This result implies that parasite‐induced vulnerability to predation is male‐biased in the wild: although there was no difference in escape response between our experimentally size‐matched groups of males and females, males are significantly smaller across natural guppy populations. These results are consistent with Bateman's principle for immunity: Natural selection for larger body sizes and longevity in females seems to have resulted in the evolution of increased infection tolerance. We discuss the potential implications of sex‐ and size‐biased parasite‐induced vulnerability to predation for the evolutionary ecology of this host–parasite interaction in natural communities.
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spelling pubmed-47971622016-04-08 A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation Stephenson, Jessica F. Kinsella, Cormac Cable, Joanne van Oosterhout, Cock Ecol Evol Original Research Males are typically the sicker sex. Data from multiple taxa indicate that they are more likely to be infected with parasites, and are less “tolerant,” or less able to mitigate the fitness costs of a given infection, than females. One cost of infection for many animals is an increased probability of being captured by a predator. A clear, hitherto untested, prediction is therefore that this parasite‐induced vulnerability to predation is more pronounced among males than females. We tested this prediction in the sexually size dimorphic guppy, Poecilia reticulata, in which females are typically larger than males. We either sham or experimentally infected guppies with Gyrodactylus turnbulli, elicited their escape response using an established protocol and measured the distance they covered during 60 ms. To discriminate between the effects of body size and those of other inherent sex differences, we size‐matched fish across treatment groups. Infection with G. turnbulli reduced the distance covered during the escape response of small adults by 20.1%, whereas that of large fish was unaffected. This result implies that parasite‐induced vulnerability to predation is male‐biased in the wild: although there was no difference in escape response between our experimentally size‐matched groups of males and females, males are significantly smaller across natural guppy populations. These results are consistent with Bateman's principle for immunity: Natural selection for larger body sizes and longevity in females seems to have resulted in the evolution of increased infection tolerance. We discuss the potential implications of sex‐ and size‐biased parasite‐induced vulnerability to predation for the evolutionary ecology of this host–parasite interaction in natural communities. John Wiley and Sons Inc. 2016-03-14 /pmc/articles/PMC4797162/ /pubmed/27066240 http://dx.doi.org/10.1002/ece3.2049 Text en © 2016 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. 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 Original Research
Stephenson, Jessica F.
Kinsella, Cormac
Cable, Joanne
van Oosterhout, Cock
A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation
title A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation
title_full A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation
title_fullStr A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation
title_full_unstemmed A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation
title_short A further cost for the sicker sex? Evidence for male‐biased parasite‐induced vulnerability to predation
title_sort further cost for the sicker sex? evidence for male‐biased parasite‐induced vulnerability to predation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797162/
https://www.ncbi.nlm.nih.gov/pubmed/27066240
http://dx.doi.org/10.1002/ece3.2049
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