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Genetic slippage after sex maintains diversity for parasite resistance in a natural host population

Although parasite-mediated selection is a major driver of host evolution, its influence on genetic variation for parasite resistance is not yet well understood. We monitored resistance in a large population of the planktonic crustacean Daphnia magna over 8 years, as it underwent yearly epidemics of...

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Autores principales: Ameline, Camille, Voegtli, Felix, Andras, Jason, Dexter, Eric, Engelstädter, Jan, Ebert, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674289/
https://www.ncbi.nlm.nih.gov/pubmed/36399570
http://dx.doi.org/10.1126/sciadv.abn0051
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author Ameline, Camille
Voegtli, Felix
Andras, Jason
Dexter, Eric
Engelstädter, Jan
Ebert, Dieter
author_facet Ameline, Camille
Voegtli, Felix
Andras, Jason
Dexter, Eric
Engelstädter, Jan
Ebert, Dieter
author_sort Ameline, Camille
collection PubMed
description Although parasite-mediated selection is a major driver of host evolution, its influence on genetic variation for parasite resistance is not yet well understood. We monitored resistance in a large population of the planktonic crustacean Daphnia magna over 8 years, as it underwent yearly epidemics of the bacterial pathogen Pasteuria ramosa. We observed cyclic dynamics of resistance: Resistance increased throughout the epidemics, but susceptibility was restored each spring when hosts hatched from sexual resting stages. Host resting stages collected across the year showed that largely resistant host populations can produce susceptible sexual offspring. A genetic model of resistance developed for this host-parasite system, based on multiple loci and strong epistasis, is in partial agreement with our findings. Our results reveal that, despite strong selection for resistance in a natural host population, genetic slippage after sexual reproduction can be a strong factor for the maintenance of genetic diversity of host resistance.
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spelling pubmed-96742892022-11-29 Genetic slippage after sex maintains diversity for parasite resistance in a natural host population Ameline, Camille Voegtli, Felix Andras, Jason Dexter, Eric Engelstädter, Jan Ebert, Dieter Sci Adv Biomedicine and Life Sciences Although parasite-mediated selection is a major driver of host evolution, its influence on genetic variation for parasite resistance is not yet well understood. We monitored resistance in a large population of the planktonic crustacean Daphnia magna over 8 years, as it underwent yearly epidemics of the bacterial pathogen Pasteuria ramosa. We observed cyclic dynamics of resistance: Resistance increased throughout the epidemics, but susceptibility was restored each spring when hosts hatched from sexual resting stages. Host resting stages collected across the year showed that largely resistant host populations can produce susceptible sexual offspring. A genetic model of resistance developed for this host-parasite system, based on multiple loci and strong epistasis, is in partial agreement with our findings. Our results reveal that, despite strong selection for resistance in a natural host population, genetic slippage after sexual reproduction can be a strong factor for the maintenance of genetic diversity of host resistance. American Association for the Advancement of Science 2022-11-18 /pmc/articles/PMC9674289/ /pubmed/36399570 http://dx.doi.org/10.1126/sciadv.abn0051 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Ameline, Camille
Voegtli, Felix
Andras, Jason
Dexter, Eric
Engelstädter, Jan
Ebert, Dieter
Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
title Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
title_full Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
title_fullStr Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
title_full_unstemmed Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
title_short Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
title_sort genetic slippage after sex maintains diversity for parasite resistance in a natural host population
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674289/
https://www.ncbi.nlm.nih.gov/pubmed/36399570
http://dx.doi.org/10.1126/sciadv.abn0051
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