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Eaten alive: cannibalism is enhanced by parasites

Cannibalism is ubiquitous in nature and especially pervasive in consumers with stage-specific resource utilization in resource-limited environments. Cannibalism is thus influential in the structure and functioning of biological communities. Parasites are also pervasive in nature and, we hypothesize,...

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Detalles Bibliográficos
Autores principales: Bunke, Mandy, Alexander, Mhairi E., Dick, Jaimie T. A., Hatcher, Melanie J., Paterson, Rachel, Dunn, Alison M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4448826/
https://www.ncbi.nlm.nih.gov/pubmed/26064614
http://dx.doi.org/10.1098/rsos.140369
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author Bunke, Mandy
Alexander, Mhairi E.
Dick, Jaimie T. A.
Hatcher, Melanie J.
Paterson, Rachel
Dunn, Alison M.
author_facet Bunke, Mandy
Alexander, Mhairi E.
Dick, Jaimie T. A.
Hatcher, Melanie J.
Paterson, Rachel
Dunn, Alison M.
author_sort Bunke, Mandy
collection PubMed
description Cannibalism is ubiquitous in nature and especially pervasive in consumers with stage-specific resource utilization in resource-limited environments. Cannibalism is thus influential in the structure and functioning of biological communities. Parasites are also pervasive in nature and, we hypothesize, might affect cannibalism since infection can alter host foraging behaviour. We investigated the effects of a common parasite, the microsporidian Pleistophora mulleri, on the cannibalism rate of its host, the freshwater amphipod Gammarus duebeni celticus. Parasitic infection increased the rate of cannibalism by adults towards uninfected juvenile conspecifics, as measured by adult functional responses, that is, the rate of resource uptake as a function of resource density. This may reflect the increased metabolic requirements of the host as driven by the parasite. Furthermore, when presented with a choice, uninfected adults preferred to cannibalize uninfected rather than infected juvenile conspecifics, probably reflecting selection pressure to avoid the risk of parasite acquisition. By contrast, infected adults were indiscriminate with respect to infection status of their victims, probably owing to metabolic costs of infection and the lack of risk as the cannibals were already infected. Thus parasitism, by enhancing cannibalism rates, may have previously unrecognized effects on stage structure and population dynamics for cannibalistic species and may also act as a selective pressure leading to changes in resource use.
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spelling pubmed-44488262015-06-10 Eaten alive: cannibalism is enhanced by parasites Bunke, Mandy Alexander, Mhairi E. Dick, Jaimie T. A. Hatcher, Melanie J. Paterson, Rachel Dunn, Alison M. R Soc Open Sci Biology (Whole Organism) Cannibalism is ubiquitous in nature and especially pervasive in consumers with stage-specific resource utilization in resource-limited environments. Cannibalism is thus influential in the structure and functioning of biological communities. Parasites are also pervasive in nature and, we hypothesize, might affect cannibalism since infection can alter host foraging behaviour. We investigated the effects of a common parasite, the microsporidian Pleistophora mulleri, on the cannibalism rate of its host, the freshwater amphipod Gammarus duebeni celticus. Parasitic infection increased the rate of cannibalism by adults towards uninfected juvenile conspecifics, as measured by adult functional responses, that is, the rate of resource uptake as a function of resource density. This may reflect the increased metabolic requirements of the host as driven by the parasite. Furthermore, when presented with a choice, uninfected adults preferred to cannibalize uninfected rather than infected juvenile conspecifics, probably reflecting selection pressure to avoid the risk of parasite acquisition. By contrast, infected adults were indiscriminate with respect to infection status of their victims, probably owing to metabolic costs of infection and the lack of risk as the cannibals were already infected. Thus parasitism, by enhancing cannibalism rates, may have previously unrecognized effects on stage structure and population dynamics for cannibalistic species and may also act as a selective pressure leading to changes in resource use. The Royal Society Publishing 2015-03-18 /pmc/articles/PMC4448826/ /pubmed/26064614 http://dx.doi.org/10.1098/rsos.140369 Text en © 2015 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 Biology (Whole Organism)
Bunke, Mandy
Alexander, Mhairi E.
Dick, Jaimie T. A.
Hatcher, Melanie J.
Paterson, Rachel
Dunn, Alison M.
Eaten alive: cannibalism is enhanced by parasites
title Eaten alive: cannibalism is enhanced by parasites
title_full Eaten alive: cannibalism is enhanced by parasites
title_fullStr Eaten alive: cannibalism is enhanced by parasites
title_full_unstemmed Eaten alive: cannibalism is enhanced by parasites
title_short Eaten alive: cannibalism is enhanced by parasites
title_sort eaten alive: cannibalism is enhanced by parasites
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4448826/
https://www.ncbi.nlm.nih.gov/pubmed/26064614
http://dx.doi.org/10.1098/rsos.140369
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