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Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution

The Red Queen hypothesis proposes that coevolving parasites select for outcrossing in the host. Outcrossing relies on males, which often show lower immune investment due to, for example, sexual selection. Here, we demonstrate that such sex differences in immunity interfere with parasite-mediated sel...

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Autores principales: Masri, Leila, Schulte, Rebecca D, Timmermeyer, Nadine, Thanisch, Stefanie, Crummenerl, Lena Luise, Jansen, Gunther, Michiels, Nico K, Schulenburg, Hinrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655609/
https://www.ncbi.nlm.nih.gov/pubmed/23301667
http://dx.doi.org/10.1111/ele.12068
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author Masri, Leila
Schulte, Rebecca D
Timmermeyer, Nadine
Thanisch, Stefanie
Crummenerl, Lena Luise
Jansen, Gunther
Michiels, Nico K
Schulenburg, Hinrich
author_facet Masri, Leila
Schulte, Rebecca D
Timmermeyer, Nadine
Thanisch, Stefanie
Crummenerl, Lena Luise
Jansen, Gunther
Michiels, Nico K
Schulenburg, Hinrich
author_sort Masri, Leila
collection PubMed
description The Red Queen hypothesis proposes that coevolving parasites select for outcrossing in the host. Outcrossing relies on males, which often show lower immune investment due to, for example, sexual selection. Here, we demonstrate that such sex differences in immunity interfere with parasite-mediated selection for outcrossing. Two independent coevolution experiments with Caenorhabditis elegans and its microparasite Bacillus thuringiensis produced decreased yet stable frequencies of outcrossing male hosts. A subsequent systematic analysis verified that male C. elegans suffered from a direct selective disadvantage under parasite pressure (i.e. lower resistance, decreased sexual activity, increased escape behaviour), which can reduce outcrossing and thus male frequencies. At the same time, males offered an indirect selective benefit, because male-mediated outcrossing increased offspring resistance, thus favouring male persistence in the evolving populations. As sex differences in immunity are widespread, such interference of opposing selective constraints is likely of central importance during host adaptation to a coevolving parasite.
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spelling pubmed-36556092013-05-17 Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution Masri, Leila Schulte, Rebecca D Timmermeyer, Nadine Thanisch, Stefanie Crummenerl, Lena Luise Jansen, Gunther Michiels, Nico K Schulenburg, Hinrich Ecol Lett Letters The Red Queen hypothesis proposes that coevolving parasites select for outcrossing in the host. Outcrossing relies on males, which often show lower immune investment due to, for example, sexual selection. Here, we demonstrate that such sex differences in immunity interfere with parasite-mediated selection for outcrossing. Two independent coevolution experiments with Caenorhabditis elegans and its microparasite Bacillus thuringiensis produced decreased yet stable frequencies of outcrossing male hosts. A subsequent systematic analysis verified that male C. elegans suffered from a direct selective disadvantage under parasite pressure (i.e. lower resistance, decreased sexual activity, increased escape behaviour), which can reduce outcrossing and thus male frequencies. At the same time, males offered an indirect selective benefit, because male-mediated outcrossing increased offspring resistance, thus favouring male persistence in the evolving populations. As sex differences in immunity are widespread, such interference of opposing selective constraints is likely of central importance during host adaptation to a coevolving parasite. Blackwell Publishing Ltd 2013-04 2013-01-10 /pmc/articles/PMC3655609/ /pubmed/23301667 http://dx.doi.org/10.1111/ele.12068 Text en Copyright © 2013 Blackwell Publishing Ltd/CNRS http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Letters
Masri, Leila
Schulte, Rebecca D
Timmermeyer, Nadine
Thanisch, Stefanie
Crummenerl, Lena Luise
Jansen, Gunther
Michiels, Nico K
Schulenburg, Hinrich
Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
title Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
title_full Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
title_fullStr Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
title_full_unstemmed Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
title_short Sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
title_sort sex differences in host defence interfere with parasite-mediated selection for outcrossing during host–parasite coevolution
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655609/
https://www.ncbi.nlm.nih.gov/pubmed/23301667
http://dx.doi.org/10.1111/ele.12068
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