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Experimental evolution reveals trade-offs between mating and immunity

Immune system maintenance and upregulation is costly. Sexual selection intensity, which increases male investment into reproductive traits, is expected to create trade-offs with immune function. We assayed phenoloxidase (PO) and lytic activity of individuals from populations of the Indian meal moth,...

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Detalles Bibliográficos
Autores principales: McNamara, Kathryn B., Wedell, Nina, Simmons, Leigh W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730636/
https://www.ncbi.nlm.nih.gov/pubmed/23720521
http://dx.doi.org/10.1098/rsbl.2013.0262
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author McNamara, Kathryn B.
Wedell, Nina
Simmons, Leigh W.
author_facet McNamara, Kathryn B.
Wedell, Nina
Simmons, Leigh W.
author_sort McNamara, Kathryn B.
collection PubMed
description Immune system maintenance and upregulation is costly. Sexual selection intensity, which increases male investment into reproductive traits, is expected to create trade-offs with immune function. We assayed phenoloxidase (PO) and lytic activity of individuals from populations of the Indian meal moth, Plodia interpunctella, which had been evolving under different intensities of sexual selection. We found significant divergence among populations, with males from female-biased populations having lower PO activity than males from balanced sex ratio or male-biased populations. There was no divergence in anti-bacterial lytic activity. Our data suggest that it is the increased male mating demands in female-biased populations that trades-off against immunity, and not the increased investment in sperm transfer per mating that characterizes male-biased populations.
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spelling pubmed-37306362013-08-23 Experimental evolution reveals trade-offs between mating and immunity McNamara, Kathryn B. Wedell, Nina Simmons, Leigh W. Biol Lett Evolutionary Biology Immune system maintenance and upregulation is costly. Sexual selection intensity, which increases male investment into reproductive traits, is expected to create trade-offs with immune function. We assayed phenoloxidase (PO) and lytic activity of individuals from populations of the Indian meal moth, Plodia interpunctella, which had been evolving under different intensities of sexual selection. We found significant divergence among populations, with males from female-biased populations having lower PO activity than males from balanced sex ratio or male-biased populations. There was no divergence in anti-bacterial lytic activity. Our data suggest that it is the increased male mating demands in female-biased populations that trades-off against immunity, and not the increased investment in sperm transfer per mating that characterizes male-biased populations. The Royal Society 2013-08-23 /pmc/articles/PMC3730636/ /pubmed/23720521 http://dx.doi.org/10.1098/rsbl.2013.0262 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolutionary Biology
McNamara, Kathryn B.
Wedell, Nina
Simmons, Leigh W.
Experimental evolution reveals trade-offs between mating and immunity
title Experimental evolution reveals trade-offs between mating and immunity
title_full Experimental evolution reveals trade-offs between mating and immunity
title_fullStr Experimental evolution reveals trade-offs between mating and immunity
title_full_unstemmed Experimental evolution reveals trade-offs between mating and immunity
title_short Experimental evolution reveals trade-offs between mating and immunity
title_sort experimental evolution reveals trade-offs between mating and immunity
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3730636/
https://www.ncbi.nlm.nih.gov/pubmed/23720521
http://dx.doi.org/10.1098/rsbl.2013.0262
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