Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783345937757765632 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6083226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sheathdannyj winningthearmsracehostparasitesharedevolutionaryhistoryreducesinfectionrisksinfishfinalhosts AT dickjaimieta winningthearmsracehostparasitesharedevolutionaryhistoryreducesinfectionrisksinfishfinalhosts AT dickeyjameswe winningthearmsracehostparasitesharedevolutionaryhistoryreducesinfectionrisksinfishfinalhosts AT guozhiqiang winningthearmsracehostparasitesharedevolutionaryhistoryreducesinfectionrisksinfishfinalhosts AT andreoudemetra winningthearmsracehostparasitesharedevolutionaryhistoryreducesinfectionrisksinfishfinalhosts AT brittonjrobert winningthearmsracehostparasitesharedevolutionaryhistoryreducesinfectionrisksinfishfinalhosts |