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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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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. |
format | Online Article Text |
id | pubmed-3655609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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