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Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific
Understanding how diversity is maintained in natural populations is a major goal of evolutionary biology. In coevolving hosts and parasites, negative frequency‐dependent selection is one mechanism predicted to maintain genetic variation. While much is known about host diversity, parasite diversity r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290032/ https://www.ncbi.nlm.nih.gov/pubmed/34431523 http://dx.doi.org/10.1111/evo.14323 |
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author | Fredericksen, Maridel Ameline, Camille Krebs, Michelle Hüssy, Benjamin Fields, Peter D. Andras, Jason P. Ebert, Dieter |
author_facet | Fredericksen, Maridel Ameline, Camille Krebs, Michelle Hüssy, Benjamin Fields, Peter D. Andras, Jason P. Ebert, Dieter |
author_sort | Fredericksen, Maridel |
collection | PubMed |
description | Understanding how diversity is maintained in natural populations is a major goal of evolutionary biology. In coevolving hosts and parasites, negative frequency‐dependent selection is one mechanism predicted to maintain genetic variation. While much is known about host diversity, parasite diversity remains understudied in coevolutionary research. Here, we survey natural diversity in a bacterial parasite by characterizing infection phenotypes for over 50 isolates in relation to 12 genotypes of their host, Daphnia magna. We find striking phenotypic variation among parasite isolates, and we discover the parasite can infect its host through at least five different attachment sites. Variation in attachment success at each site is explained to varying degrees by host and parasite genotypes. A spatial correlation analysis showed that infectivity of different isolates does not correlate with geographic distance, meaning isolates from widespread populations are equally able to infect the host. Overall, our results reveal that infection phenotypes of this parasite are highly diverse. Our results are consistent with the prediction that under Red Queen coevolutionary dynamics both the host and the parasite should show high genetic diversity for traits of functional importance in their interactions. |
format | Online Article Text |
id | pubmed-9290032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92900322022-07-20 Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific Fredericksen, Maridel Ameline, Camille Krebs, Michelle Hüssy, Benjamin Fields, Peter D. Andras, Jason P. Ebert, Dieter Evolution Original Articles Understanding how diversity is maintained in natural populations is a major goal of evolutionary biology. In coevolving hosts and parasites, negative frequency‐dependent selection is one mechanism predicted to maintain genetic variation. While much is known about host diversity, parasite diversity remains understudied in coevolutionary research. Here, we survey natural diversity in a bacterial parasite by characterizing infection phenotypes for over 50 isolates in relation to 12 genotypes of their host, Daphnia magna. We find striking phenotypic variation among parasite isolates, and we discover the parasite can infect its host through at least five different attachment sites. Variation in attachment success at each site is explained to varying degrees by host and parasite genotypes. A spatial correlation analysis showed that infectivity of different isolates does not correlate with geographic distance, meaning isolates from widespread populations are equally able to infect the host. Overall, our results reveal that infection phenotypes of this parasite are highly diverse. Our results are consistent with the prediction that under Red Queen coevolutionary dynamics both the host and the parasite should show high genetic diversity for traits of functional importance in their interactions. John Wiley and Sons Inc. 2021-08-30 2021-10 /pmc/articles/PMC9290032/ /pubmed/34431523 http://dx.doi.org/10.1111/evo.14323 Text en © 2021 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Fredericksen, Maridel Ameline, Camille Krebs, Michelle Hüssy, Benjamin Fields, Peter D. Andras, Jason P. Ebert, Dieter Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
title | Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
title_full | Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
title_fullStr | Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
title_full_unstemmed | Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
title_short | Infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
title_sort | infection phenotypes of a coevolving parasite are highly diverse, structured, and specific |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290032/ https://www.ncbi.nlm.nih.gov/pubmed/34431523 http://dx.doi.org/10.1111/evo.14323 |
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