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Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits

The climate is warming at an unprecedented rate, pushing many species toward and beyond the upper temperatures at which they can survive. Global change is also leading to dramatic shifts in the distribution of pathogens. As a result, upper thermal limits and susceptibility to infection should be key...

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Autores principales: Laidlaw, Tess, Hector, Tobias E., Sgrò, Carla M., Hall, Matthew D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713950/
https://www.ncbi.nlm.nih.gov/pubmed/33304498
http://dx.doi.org/10.1002/ece3.6828
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author Laidlaw, Tess
Hector, Tobias E.
Sgrò, Carla M.
Hall, Matthew D.
author_facet Laidlaw, Tess
Hector, Tobias E.
Sgrò, Carla M.
Hall, Matthew D.
author_sort Laidlaw, Tess
collection PubMed
description The climate is warming at an unprecedented rate, pushing many species toward and beyond the upper temperatures at which they can survive. Global change is also leading to dramatic shifts in the distribution of pathogens. As a result, upper thermal limits and susceptibility to infection should be key determinants of whether populations continue to persist, or instead go extinct. Within a population, however, individuals vary in both their resistance to both heat stress and infection, and their contributions to vital growth rates. No more so is this true than for males and females. Each sex often varies in their response to pathogen exposure, thermal tolerances, and particularly their influence on population growth, owing to the higher parental investment that females typically make in their offspring. To date, the interplay between host sex, infection, and upper thermal limits has been neglected. Here, we explore the response of male and female Daphnia to bacterial infection and static heat stress. We find that female Daphnia, when uninfected, are much more resistant to static heat stress than males, but that infection negates any advantage that females are afforded. We discuss how the capacity of a population to cope with multiple stressors may be underestimated unless both sexes are considered simultaneously.
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spelling pubmed-77139502020-12-09 Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits Laidlaw, Tess Hector, Tobias E. Sgrò, Carla M. Hall, Matthew D. Ecol Evol Original Research The climate is warming at an unprecedented rate, pushing many species toward and beyond the upper temperatures at which they can survive. Global change is also leading to dramatic shifts in the distribution of pathogens. As a result, upper thermal limits and susceptibility to infection should be key determinants of whether populations continue to persist, or instead go extinct. Within a population, however, individuals vary in both their resistance to both heat stress and infection, and their contributions to vital growth rates. No more so is this true than for males and females. Each sex often varies in their response to pathogen exposure, thermal tolerances, and particularly their influence on population growth, owing to the higher parental investment that females typically make in their offspring. To date, the interplay between host sex, infection, and upper thermal limits has been neglected. Here, we explore the response of male and female Daphnia to bacterial infection and static heat stress. We find that female Daphnia, when uninfected, are much more resistant to static heat stress than males, but that infection negates any advantage that females are afforded. We discuss how the capacity of a population to cope with multiple stressors may be underestimated unless both sexes are considered simultaneously. John Wiley and Sons Inc. 2020-11-06 /pmc/articles/PMC7713950/ /pubmed/33304498 http://dx.doi.org/10.1002/ece3.6828 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://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 Research
Laidlaw, Tess
Hector, Tobias E.
Sgrò, Carla M.
Hall, Matthew D.
Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
title Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
title_full Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
title_fullStr Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
title_full_unstemmed Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
title_short Pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
title_sort pathogen exposure reduces sexual dimorphism in a host’s upper thermal limits
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713950/
https://www.ncbi.nlm.nih.gov/pubmed/33304498
http://dx.doi.org/10.1002/ece3.6828
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