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Female reproduction and viral infection in a long‐lived mammal

1. For energetically limited organisms, life‐history theory predicts trade‐offs between reproductive effort and somatic maintenance. This is especially true of female mammals, for whom reproduction presents multifarious energetic and physiological demands. 2. Here, we examine longitudinal changes in...

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Autores principales: Negrey, Jacob D., Emery Thompson, Melissa, Dunn, Christopher D., Otali, Emily, Wrangham, Richard W., Mitani, John C., Machanda, Zarin P., Muller, Martin N., Langergraber, Kevin E., Goldberg, Tony L.
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/PMC9532343/
https://www.ncbi.nlm.nih.gov/pubmed/35988037
http://dx.doi.org/10.1111/1365-2656.13799
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author Negrey, Jacob D.
Emery Thompson, Melissa
Dunn, Christopher D.
Otali, Emily
Wrangham, Richard W.
Mitani, John C.
Machanda, Zarin P.
Muller, Martin N.
Langergraber, Kevin E.
Goldberg, Tony L.
author_facet Negrey, Jacob D.
Emery Thompson, Melissa
Dunn, Christopher D.
Otali, Emily
Wrangham, Richard W.
Mitani, John C.
Machanda, Zarin P.
Muller, Martin N.
Langergraber, Kevin E.
Goldberg, Tony L.
author_sort Negrey, Jacob D.
collection PubMed
description 1. For energetically limited organisms, life‐history theory predicts trade‐offs between reproductive effort and somatic maintenance. This is especially true of female mammals, for whom reproduction presents multifarious energetic and physiological demands. 2. Here, we examine longitudinal changes in the gut virome (viral community) with respect to reproductive status in wild mature female chimpanzees Pan troglodytes schweinfurthii from two communities, Kanyawara and Ngogo, in Kibale National Park, Uganda. 3. We used metagenomic methods to characterize viromes of individual chimpanzees while they were cycling, pregnant and lactating. 4. Females from Kanyawara, whose territory abuts the park's boundary, had higher viral richness and loads (relative quantity of viral sequences) than females from Ngogo, whose territory is more energetically rich and located farther from large human settlements. Viral richness (total number of distinct viruses per sample) was higher when females were lactating than when cycling or pregnant. In pregnant females, viral richness increased with estimated day of gestation. Richness did not vary with age, in contrast to prior research showing increased viral abundance in older males from these same communities. 5. Our results provide evidence of short‐term physiological trade‐offs between reproduction and infection, which are often hypothesized to constrain health in long‐lived species.
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spelling pubmed-95323432022-10-05 Female reproduction and viral infection in a long‐lived mammal Negrey, Jacob D. Emery Thompson, Melissa Dunn, Christopher D. Otali, Emily Wrangham, Richard W. Mitani, John C. Machanda, Zarin P. Muller, Martin N. Langergraber, Kevin E. Goldberg, Tony L. J Anim Ecol Research Articles 1. For energetically limited organisms, life‐history theory predicts trade‐offs between reproductive effort and somatic maintenance. This is especially true of female mammals, for whom reproduction presents multifarious energetic and physiological demands. 2. Here, we examine longitudinal changes in the gut virome (viral community) with respect to reproductive status in wild mature female chimpanzees Pan troglodytes schweinfurthii from two communities, Kanyawara and Ngogo, in Kibale National Park, Uganda. 3. We used metagenomic methods to characterize viromes of individual chimpanzees while they were cycling, pregnant and lactating. 4. Females from Kanyawara, whose territory abuts the park's boundary, had higher viral richness and loads (relative quantity of viral sequences) than females from Ngogo, whose territory is more energetically rich and located farther from large human settlements. Viral richness (total number of distinct viruses per sample) was higher when females were lactating than when cycling or pregnant. In pregnant females, viral richness increased with estimated day of gestation. Richness did not vary with age, in contrast to prior research showing increased viral abundance in older males from these same communities. 5. Our results provide evidence of short‐term physiological trade‐offs between reproduction and infection, which are often hypothesized to constrain health in long‐lived species. John Wiley and Sons Inc. 2022-08-21 2022-10 /pmc/articles/PMC9532343/ /pubmed/35988037 http://dx.doi.org/10.1111/1365-2656.13799 Text en © 2022 The Authors. Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. 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 Research Articles
Negrey, Jacob D.
Emery Thompson, Melissa
Dunn, Christopher D.
Otali, Emily
Wrangham, Richard W.
Mitani, John C.
Machanda, Zarin P.
Muller, Martin N.
Langergraber, Kevin E.
Goldberg, Tony L.
Female reproduction and viral infection in a long‐lived mammal
title Female reproduction and viral infection in a long‐lived mammal
title_full Female reproduction and viral infection in a long‐lived mammal
title_fullStr Female reproduction and viral infection in a long‐lived mammal
title_full_unstemmed Female reproduction and viral infection in a long‐lived mammal
title_short Female reproduction and viral infection in a long‐lived mammal
title_sort female reproduction and viral infection in a long‐lived mammal
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532343/
https://www.ncbi.nlm.nih.gov/pubmed/35988037
http://dx.doi.org/10.1111/1365-2656.13799
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