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Social status and parasitism in male and female vertebrates: a meta-analysis

Social status is an important predictor of parasite risk in vertebrates. To date, general frameworks to explain status-related variation in parasitism have remained elusive. In this meta-analysis, we evaluated five hypotheses proposed to explain status-related variation in parasitism in male and fem...

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Autores principales: Habig, Bobby, Doellman, Meredith M., Woods, Kourtney, Olansen, Jonathan, Archie, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827031/
https://www.ncbi.nlm.nih.gov/pubmed/29483573
http://dx.doi.org/10.1038/s41598-018-21994-7
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author Habig, Bobby
Doellman, Meredith M.
Woods, Kourtney
Olansen, Jonathan
Archie, Elizabeth A.
author_facet Habig, Bobby
Doellman, Meredith M.
Woods, Kourtney
Olansen, Jonathan
Archie, Elizabeth A.
author_sort Habig, Bobby
collection PubMed
description Social status is an important predictor of parasite risk in vertebrates. To date, general frameworks to explain status-related variation in parasitism have remained elusive. In this meta-analysis, we evaluated five hypotheses proposed to explain status-related variation in parasitism in male and female vertebrates by leveraging variation in hierarchy type, mating system, parasite transmission mode, and allostatic load to test associated predictions. Our meta-analyses span 66 analyses (26 studies) of male vertebrates (two orders and five classes), and 62 analyses (13 studies) of female vertebrates (four vertebrate orders). Contrary to the prevailing paradigm that low status is linked to poor health, we found that dominant animals typically faced higher parasite risk than subordinates. This pattern was especially well-supported in analyses of males versus females, in linear versus egalitarian hierarchies, in mating systems where dominance rank predicts mating effort, and for contact- and environmentally-transmitted parasites rather than vector-borne parasites. These findings supported the priority-of-access and tradeoffs hypotheses suggesting that variation in parasitism is driven by rank-associated differences in exposure to parasites and mating effort. Together, these results suggest that high parasite risk might sometimes be an unappreciated cost of high rank, and conversely, reduced parasite risk might be a benefit of social subordination.
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spelling pubmed-58270312018-03-01 Social status and parasitism in male and female vertebrates: a meta-analysis Habig, Bobby Doellman, Meredith M. Woods, Kourtney Olansen, Jonathan Archie, Elizabeth A. Sci Rep Article Social status is an important predictor of parasite risk in vertebrates. To date, general frameworks to explain status-related variation in parasitism have remained elusive. In this meta-analysis, we evaluated five hypotheses proposed to explain status-related variation in parasitism in male and female vertebrates by leveraging variation in hierarchy type, mating system, parasite transmission mode, and allostatic load to test associated predictions. Our meta-analyses span 66 analyses (26 studies) of male vertebrates (two orders and five classes), and 62 analyses (13 studies) of female vertebrates (four vertebrate orders). Contrary to the prevailing paradigm that low status is linked to poor health, we found that dominant animals typically faced higher parasite risk than subordinates. This pattern was especially well-supported in analyses of males versus females, in linear versus egalitarian hierarchies, in mating systems where dominance rank predicts mating effort, and for contact- and environmentally-transmitted parasites rather than vector-borne parasites. These findings supported the priority-of-access and tradeoffs hypotheses suggesting that variation in parasitism is driven by rank-associated differences in exposure to parasites and mating effort. Together, these results suggest that high parasite risk might sometimes be an unappreciated cost of high rank, and conversely, reduced parasite risk might be a benefit of social subordination. Nature Publishing Group UK 2018-02-26 /pmc/articles/PMC5827031/ /pubmed/29483573 http://dx.doi.org/10.1038/s41598-018-21994-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Habig, Bobby
Doellman, Meredith M.
Woods, Kourtney
Olansen, Jonathan
Archie, Elizabeth A.
Social status and parasitism in male and female vertebrates: a meta-analysis
title Social status and parasitism in male and female vertebrates: a meta-analysis
title_full Social status and parasitism in male and female vertebrates: a meta-analysis
title_fullStr Social status and parasitism in male and female vertebrates: a meta-analysis
title_full_unstemmed Social status and parasitism in male and female vertebrates: a meta-analysis
title_short Social status and parasitism in male and female vertebrates: a meta-analysis
title_sort social status and parasitism in male and female vertebrates: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827031/
https://www.ncbi.nlm.nih.gov/pubmed/29483573
http://dx.doi.org/10.1038/s41598-018-21994-7
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