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The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations
Epidemics commonly exert parasite-mediated selection and cause declines in host population genetic diversity. This can lead to evolution of resistance in the long term and smaller subsequent epidemics. Alternatively, the loss of genetic diversity can increase host vulnerability to future disease spr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031403/ https://www.ncbi.nlm.nih.gov/pubmed/36946108 http://dx.doi.org/10.1098/rspb.2022.2139 |
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author | Auld, Stuart K. J. R. Brand, June Bussière, Luc F. |
author_facet | Auld, Stuart K. J. R. Brand, June Bussière, Luc F. |
author_sort | Auld, Stuart K. J. R. |
collection | PubMed |
description | Epidemics commonly exert parasite-mediated selection and cause declines in host population genetic diversity. This can lead to evolution of resistance in the long term and smaller subsequent epidemics. Alternatively, the loss of genetic diversity can increase host vulnerability to future disease spread and larger future epidemics. Matters are made more complex by the fact that a great many host organisms produce diapausing life stages in response to environmental change (often as a result of sexual reproduction; e.g. plant seeds and invertebrate resting eggs). These diapausing stages can disrupt the relationship between past epidemics, host genetic diversity and future epidemics because they allow host dispersal through time. Specifically, temporally dispersing hosts avoid infection and thus selection from contemporary parasites, and also archive genetic variation for the future. We studied 80 epidemics in 20 semi-natural populations of the temporally dispersing crustacean Daphnia magna and its sterilizing bacterial parasite Pasteuria ramosa, and half of these populations experienced a simulated environmental disturbance treatment. We found that early initiation of diapause relative to the timing of the epidemic led to greater host genetic diversity and reduced epidemic size in the subsequent year, but this was unaffected by environmental disturbance. |
format | Online Article Text |
id | pubmed-10031403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100314032023-03-23 The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations Auld, Stuart K. J. R. Brand, June Bussière, Luc F. Proc Biol Sci Ecology Epidemics commonly exert parasite-mediated selection and cause declines in host population genetic diversity. This can lead to evolution of resistance in the long term and smaller subsequent epidemics. Alternatively, the loss of genetic diversity can increase host vulnerability to future disease spread and larger future epidemics. Matters are made more complex by the fact that a great many host organisms produce diapausing life stages in response to environmental change (often as a result of sexual reproduction; e.g. plant seeds and invertebrate resting eggs). These diapausing stages can disrupt the relationship between past epidemics, host genetic diversity and future epidemics because they allow host dispersal through time. Specifically, temporally dispersing hosts avoid infection and thus selection from contemporary parasites, and also archive genetic variation for the future. We studied 80 epidemics in 20 semi-natural populations of the temporally dispersing crustacean Daphnia magna and its sterilizing bacterial parasite Pasteuria ramosa, and half of these populations experienced a simulated environmental disturbance treatment. We found that early initiation of diapause relative to the timing of the epidemic led to greater host genetic diversity and reduced epidemic size in the subsequent year, but this was unaffected by environmental disturbance. The Royal Society 2023-03-29 2023-03-22 /pmc/articles/PMC10031403/ /pubmed/36946108 http://dx.doi.org/10.1098/rspb.2022.2139 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Ecology Auld, Stuart K. J. R. Brand, June Bussière, Luc F. The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations |
title | The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations |
title_full | The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations |
title_fullStr | The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations |
title_full_unstemmed | The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations |
title_short | The timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in Daphnia–parasite populations |
title_sort | timings of host diapause and epidemic progression mediate host genetic diversity and future epidemic size in daphnia–parasite populations |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031403/ https://www.ncbi.nlm.nih.gov/pubmed/36946108 http://dx.doi.org/10.1098/rspb.2022.2139 |
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