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Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes
Sexual interactions have a potent influence on health in several species, including mammals. Previous work in C. elegans identified strategies used by males to accelerate the demise of the opposite sex (hermaphrodites). But whether hermaphrodites evolved counter-strategies against males remains unkn...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697445/ https://www.ncbi.nlm.nih.gov/pubmed/31282863 http://dx.doi.org/10.7554/eLife.46418 |
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author | Booth, Lauren N Maures, Travis J Yeo, Robin W Tantilert, Cindy Brunet, Anne |
author_facet | Booth, Lauren N Maures, Travis J Yeo, Robin W Tantilert, Cindy Brunet, Anne |
author_sort | Booth, Lauren N |
collection | PubMed |
description | Sexual interactions have a potent influence on health in several species, including mammals. Previous work in C. elegans identified strategies used by males to accelerate the demise of the opposite sex (hermaphrodites). But whether hermaphrodites evolved counter-strategies against males remains unknown. Here we discover that young C. elegans hermaphrodites are remarkably resistant to brief sexual encounters with males, whereas older hermaphrodites succumb prematurely. Surprisingly, it is not their youthfulness that protects young hermaphrodites, but the fact that they have self-sperm. The beneficial effect of self-sperm is mediated by a sperm-sensing pathway acting on the soma rather than by fertilization. Activation of this pathway in females triggers protection from the negative impact of males. Interestingly, the role of self-sperm in protecting against the detrimental effects of males evolved independently in hermaphroditic nematodes. Endogenous strategies to delay the negative effect of mating may represent a key evolutionary innovation to maximize reproductive success. |
format | Online Article Text |
id | pubmed-6697445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-66974452019-08-19 Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes Booth, Lauren N Maures, Travis J Yeo, Robin W Tantilert, Cindy Brunet, Anne eLife Evolutionary Biology Sexual interactions have a potent influence on health in several species, including mammals. Previous work in C. elegans identified strategies used by males to accelerate the demise of the opposite sex (hermaphrodites). But whether hermaphrodites evolved counter-strategies against males remains unknown. Here we discover that young C. elegans hermaphrodites are remarkably resistant to brief sexual encounters with males, whereas older hermaphrodites succumb prematurely. Surprisingly, it is not their youthfulness that protects young hermaphrodites, but the fact that they have self-sperm. The beneficial effect of self-sperm is mediated by a sperm-sensing pathway acting on the soma rather than by fertilization. Activation of this pathway in females triggers protection from the negative impact of males. Interestingly, the role of self-sperm in protecting against the detrimental effects of males evolved independently in hermaphroditic nematodes. Endogenous strategies to delay the negative effect of mating may represent a key evolutionary innovation to maximize reproductive success. eLife Sciences Publications, Ltd 2019-07-08 /pmc/articles/PMC6697445/ /pubmed/31282863 http://dx.doi.org/10.7554/eLife.46418 Text en © 2019, Booth et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Booth, Lauren N Maures, Travis J Yeo, Robin W Tantilert, Cindy Brunet, Anne Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
title | Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
title_full | Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
title_fullStr | Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
title_full_unstemmed | Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
title_short | Self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
title_sort | self-sperm induce resistance to the detrimental effects of sexual encounters with males in hermaphroditic nematodes |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697445/ https://www.ncbi.nlm.nih.gov/pubmed/31282863 http://dx.doi.org/10.7554/eLife.46418 |
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