Cargando…
Social status, immune response and parasitism in males: a meta-analysis
In male vertebrates, two conflicting paradigms—the energetic costs of high dominance rank and the chronic stress of low rank—have been proposed to explain patterns of immune function and parasitism. To date, neither paradigm has provided a complete explanation for status-related differences in male...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410375/ https://www.ncbi.nlm.nih.gov/pubmed/25870395 http://dx.doi.org/10.1098/rstb.2014.0109 |
_version_ | 1782368315671314432 |
---|---|
author | Habig, Bobby Archie, Elizabeth A. |
author_facet | Habig, Bobby Archie, Elizabeth A. |
author_sort | Habig, Bobby |
collection | PubMed |
description | In male vertebrates, two conflicting paradigms—the energetic costs of high dominance rank and the chronic stress of low rank—have been proposed to explain patterns of immune function and parasitism. To date, neither paradigm has provided a complete explanation for status-related differences in male health. Here, we applied meta-analyses to test for correlations between male social status, immune responses and parasitism. We used an ecoimmunological framework, which proposes that males should re-allocate investment in different immune components depending on the costs of dominance or subordination. Spanning 297 analyses, from 77 studies on several vertebrate taxa, we found that most immune responses were similar between subordinate and dominant males, and neither dominant nor subordinate males consistently invested in predictable immune components. However, subordinate males displayed significantly lower delayed-type hypersensitivity and higher levels of some inflammatory cytokines than dominant males, while dominant males exhibited relatively lower immunoglobulin responses than subordinate males. Despite few differences in immunity, dominant males exhibited consistently higher parasitism than subordinate males, including protozoan blood parasites, ectoparasites and gastrointestinal helminths. We discuss our results in the context of the costs of dominance and subordination and advocate future work that measures both parasitism and immune responses in wild systems. |
format | Online Article Text |
id | pubmed-4410375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44103752015-05-26 Social status, immune response and parasitism in males: a meta-analysis Habig, Bobby Archie, Elizabeth A. Philos Trans R Soc Lond B Biol Sci Articles In male vertebrates, two conflicting paradigms—the energetic costs of high dominance rank and the chronic stress of low rank—have been proposed to explain patterns of immune function and parasitism. To date, neither paradigm has provided a complete explanation for status-related differences in male health. Here, we applied meta-analyses to test for correlations between male social status, immune responses and parasitism. We used an ecoimmunological framework, which proposes that males should re-allocate investment in different immune components depending on the costs of dominance or subordination. Spanning 297 analyses, from 77 studies on several vertebrate taxa, we found that most immune responses were similar between subordinate and dominant males, and neither dominant nor subordinate males consistently invested in predictable immune components. However, subordinate males displayed significantly lower delayed-type hypersensitivity and higher levels of some inflammatory cytokines than dominant males, while dominant males exhibited relatively lower immunoglobulin responses than subordinate males. Despite few differences in immunity, dominant males exhibited consistently higher parasitism than subordinate males, including protozoan blood parasites, ectoparasites and gastrointestinal helminths. We discuss our results in the context of the costs of dominance and subordination and advocate future work that measures both parasitism and immune responses in wild systems. The Royal Society 2015-05-26 /pmc/articles/PMC4410375/ /pubmed/25870395 http://dx.doi.org/10.1098/rstb.2014.0109 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. 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 | Articles Habig, Bobby Archie, Elizabeth A. Social status, immune response and parasitism in males: a meta-analysis |
title | Social status, immune response and parasitism in males: a meta-analysis |
title_full | Social status, immune response and parasitism in males: a meta-analysis |
title_fullStr | Social status, immune response and parasitism in males: a meta-analysis |
title_full_unstemmed | Social status, immune response and parasitism in males: a meta-analysis |
title_short | Social status, immune response and parasitism in males: a meta-analysis |
title_sort | social status, immune response and parasitism in males: a meta-analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410375/ https://www.ncbi.nlm.nih.gov/pubmed/25870395 http://dx.doi.org/10.1098/rstb.2014.0109 |
work_keys_str_mv | AT habigbobby socialstatusimmuneresponseandparasitisminmalesametaanalysis AT archieelizabetha socialstatusimmuneresponseandparasitisminmalesametaanalysis |