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Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host
Host and parasites interact across spatial scales, but parasite‐mediated fitness effects are typically measured only at local scales. Recent work suggests that parasites can reduce host fitness during dispersal between patches, highlighting the potential for both within‐ and between‐patch effects to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329228/ https://www.ncbi.nlm.nih.gov/pubmed/35652582 http://dx.doi.org/10.1111/evo.14521 |
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author | Bubrig, Louis T. Janisch, Anne N. Tillet, Emily M. Gibson, Amanda Kyle |
author_facet | Bubrig, Louis T. Janisch, Anne N. Tillet, Emily M. Gibson, Amanda Kyle |
author_sort | Bubrig, Louis T. |
collection | PubMed |
description | Host and parasites interact across spatial scales, but parasite‐mediated fitness effects are typically measured only at local scales. Recent work suggests that parasites can reduce host fitness during dispersal between patches, highlighting the potential for both within‐ and between‐patch effects to contribute to the net fitness consequences of parasitism. Building on this work, we measured the contribution of the dispersal phase to parasite‐mediated reductions in host fitness. We used the nematode Caenorhabditis elegans and its natural microsporidian parasite Nematocida parisii to quantify the fitness consequences of parasitism at the individual, population, and metapopulation level. Nematocida parisii reduced individual fecundity and population growth but had its greatest fitness impact at the dispersal stage: parasitism reduced the fitness of dispersing larvae by 62%–100%. These results indicate that the cost of parasitism in this system is greatly underestimated if the metapopulation level is not taken into account. We also found that the effects of N. parisii vary with host genotype, and the relative advantage of the most resistant genotype increases with inclusion of the dispersal stage. Taken together, our findings demonstrate that host‐parasite interactions at the dispersal stage can magnify selection for parasite resistance. |
format | Online Article Text |
id | pubmed-9329228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93292282022-10-14 Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host Bubrig, Louis T. Janisch, Anne N. Tillet, Emily M. Gibson, Amanda Kyle Evolution Original Articles Host and parasites interact across spatial scales, but parasite‐mediated fitness effects are typically measured only at local scales. Recent work suggests that parasites can reduce host fitness during dispersal between patches, highlighting the potential for both within‐ and between‐patch effects to contribute to the net fitness consequences of parasitism. Building on this work, we measured the contribution of the dispersal phase to parasite‐mediated reductions in host fitness. We used the nematode Caenorhabditis elegans and its natural microsporidian parasite Nematocida parisii to quantify the fitness consequences of parasitism at the individual, population, and metapopulation level. Nematocida parisii reduced individual fecundity and population growth but had its greatest fitness impact at the dispersal stage: parasitism reduced the fitness of dispersing larvae by 62%–100%. These results indicate that the cost of parasitism in this system is greatly underestimated if the metapopulation level is not taken into account. We also found that the effects of N. parisii vary with host genotype, and the relative advantage of the most resistant genotype increases with inclusion of the dispersal stage. Taken together, our findings demonstrate that host‐parasite interactions at the dispersal stage can magnify selection for parasite resistance. John Wiley and Sons Inc. 2022-06-17 2022-07 /pmc/articles/PMC9329228/ /pubmed/35652582 http://dx.doi.org/10.1111/evo.14521 Text en © 2022 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Bubrig, Louis T. Janisch, Anne N. Tillet, Emily M. Gibson, Amanda Kyle Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
title | Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
title_full | Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
title_fullStr | Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
title_full_unstemmed | Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
title_short | Contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
title_sort | contrasting parasite‐mediated reductions in fitness within versus between patches of a nematode host |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329228/ https://www.ncbi.nlm.nih.gov/pubmed/35652582 http://dx.doi.org/10.1111/evo.14521 |
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