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When sexual selection in hosts benefits parasites

In host-parasite coevolution, the parasite is selected to increase its infectivity while host is selected to resist the parasite infection. It is widely held that parasite-mediated sexual selection can further amplify the selective pressure on the host to overcome parasite infection. In this paper w...

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Autores principales: Aavani, Pooya, Rice, Sean H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474839/
https://www.ncbi.nlm.nih.gov/pubmed/36158519
http://dx.doi.org/10.1016/j.idm.2022.08.001
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author Aavani, Pooya
Rice, Sean H.
author_facet Aavani, Pooya
Rice, Sean H.
author_sort Aavani, Pooya
collection PubMed
description In host-parasite coevolution, the parasite is selected to increase its infectivity while host is selected to resist the parasite infection. It is widely held that parasite-mediated sexual selection can further amplify the selective pressure on the host to overcome parasite infection. In this paper we focus on certain types of parasites, those that can impair the activity of the host immune function to prevent signs of sickness. We show that the effect of sexual selection can actually reduce the selective pressure on the host immune response to adapt to the parasite infection. We design a simple mathematical model for a population of sexually reproducing organism in which individuals are choosy, preferring traits that are correlated negatively with immune system activity. We introduce to this population a parasite that can suppress activation of the host's immune response. Our results show that even though the host immune system is likely to ultimately evolve and adapt to the parasite infection, when sexual selection is part of this process, it can slow down this evolution on the host and give the parasite more time to get established.
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spelling pubmed-94748392022-09-22 When sexual selection in hosts benefits parasites Aavani, Pooya Rice, Sean H. Infect Dis Model Article In host-parasite coevolution, the parasite is selected to increase its infectivity while host is selected to resist the parasite infection. It is widely held that parasite-mediated sexual selection can further amplify the selective pressure on the host to overcome parasite infection. In this paper we focus on certain types of parasites, those that can impair the activity of the host immune function to prevent signs of sickness. We show that the effect of sexual selection can actually reduce the selective pressure on the host immune response to adapt to the parasite infection. We design a simple mathematical model for a population of sexually reproducing organism in which individuals are choosy, preferring traits that are correlated negatively with immune system activity. We introduce to this population a parasite that can suppress activation of the host's immune response. Our results show that even though the host immune system is likely to ultimately evolve and adapt to the parasite infection, when sexual selection is part of this process, it can slow down this evolution on the host and give the parasite more time to get established. KeAi Publishing 2022-08-11 /pmc/articles/PMC9474839/ /pubmed/36158519 http://dx.doi.org/10.1016/j.idm.2022.08.001 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Aavani, Pooya
Rice, Sean H.
When sexual selection in hosts benefits parasites
title When sexual selection in hosts benefits parasites
title_full When sexual selection in hosts benefits parasites
title_fullStr When sexual selection in hosts benefits parasites
title_full_unstemmed When sexual selection in hosts benefits parasites
title_short When sexual selection in hosts benefits parasites
title_sort when sexual selection in hosts benefits parasites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474839/
https://www.ncbi.nlm.nih.gov/pubmed/36158519
http://dx.doi.org/10.1016/j.idm.2022.08.001
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