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Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts

Parasite manipulation of intermediate hosts evolves to increase parasite trophic transmission to final hosts, yet counter selection should act on the final host to reduce infection risk and costs. However, determining who wins this arms race and to what extent is challenging. Here, for the first tim...

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Detalles Bibliográficos
Autores principales: Sheath, Danny J., Dick, Jaimie T. A., Dickey, James W. E., Guo, Zhiqiang, Andreou, Demetra, Britton, J. Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083226/
https://www.ncbi.nlm.nih.gov/pubmed/30045905
http://dx.doi.org/10.1098/rsbl.2018.0363
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author Sheath, Danny J.
Dick, Jaimie T. A.
Dickey, James W. E.
Guo, Zhiqiang
Andreou, Demetra
Britton, J. Robert
author_facet Sheath, Danny J.
Dick, Jaimie T. A.
Dickey, James W. E.
Guo, Zhiqiang
Andreou, Demetra
Britton, J. Robert
author_sort Sheath, Danny J.
collection PubMed
description Parasite manipulation of intermediate hosts evolves to increase parasite trophic transmission to final hosts, yet counter selection should act on the final host to reduce infection risk and costs. However, determining who wins this arms race and to what extent is challenging. Here, for the first time, comparative functional response analysis quantified final host consumption patterns with respect to intermediate host parasite status. Experiments used two evolutionarily experienced fish hosts and two naive hosts, and their amphipod intermediate hosts of the acanthocephalan parasite Pomphorhynchus tereticollis. The two experienced fish consumed significantly fewer infected than non-infected prey, with lower attack rates and higher handling times towards the former. Conversely, the two naive fish consumed similar numbers of infected and non-infected prey at most densities, with similar attack rates and handling times towards both. Thus, evolutionarily experienced final hosts can reduce their infection risks and costs via reduced intermediate host consumption, with this not apparent in naive hosts.
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spelling pubmed-60832262018-08-13 Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts Sheath, Danny J. Dick, Jaimie T. A. Dickey, James W. E. Guo, Zhiqiang Andreou, Demetra Britton, J. Robert Biol Lett Community Ecology Parasite manipulation of intermediate hosts evolves to increase parasite trophic transmission to final hosts, yet counter selection should act on the final host to reduce infection risk and costs. However, determining who wins this arms race and to what extent is challenging. Here, for the first time, comparative functional response analysis quantified final host consumption patterns with respect to intermediate host parasite status. Experiments used two evolutionarily experienced fish hosts and two naive hosts, and their amphipod intermediate hosts of the acanthocephalan parasite Pomphorhynchus tereticollis. The two experienced fish consumed significantly fewer infected than non-infected prey, with lower attack rates and higher handling times towards the former. Conversely, the two naive fish consumed similar numbers of infected and non-infected prey at most densities, with similar attack rates and handling times towards both. Thus, evolutionarily experienced final hosts can reduce their infection risks and costs via reduced intermediate host consumption, with this not apparent in naive hosts. The Royal Society 2018-07 2018-07-25 /pmc/articles/PMC6083226/ /pubmed/30045905 http://dx.doi.org/10.1098/rsbl.2018.0363 Text en © 2018 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 Community Ecology
Sheath, Danny J.
Dick, Jaimie T. A.
Dickey, James W. E.
Guo, Zhiqiang
Andreou, Demetra
Britton, J. Robert
Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
title Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
title_full Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
title_fullStr Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
title_full_unstemmed Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
title_short Winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
title_sort winning the arms race: host–parasite shared evolutionary history reduces infection risks in fish final hosts
topic Community Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083226/
https://www.ncbi.nlm.nih.gov/pubmed/30045905
http://dx.doi.org/10.1098/rsbl.2018.0363
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