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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...

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Autores principales: Bubrig, Louis T., Janisch, Anne N., Tillet, Emily M., Gibson, Amanda Kyle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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