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Parasite intensity drives fetal development and sex allocation in a wild ungulate

An understanding of the mechanisms influencing prenatal characteristics is fundamental to comprehend the role of ecological and evolutionary processes behind survival and reproductive success in animals. Although the negative influence of parasites on host fitness is undisputable, we know very littl...

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Autores principales: Aleuy, O. Alejandro, Serrano, Emmanuel, Ruckstuhl, Kathreen E., Hoberg, Eric P., Kutz, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518422/
https://www.ncbi.nlm.nih.gov/pubmed/32973197
http://dx.doi.org/10.1038/s41598-020-72376-x
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author Aleuy, O. Alejandro
Serrano, Emmanuel
Ruckstuhl, Kathreen E.
Hoberg, Eric P.
Kutz, Susan
author_facet Aleuy, O. Alejandro
Serrano, Emmanuel
Ruckstuhl, Kathreen E.
Hoberg, Eric P.
Kutz, Susan
author_sort Aleuy, O. Alejandro
collection PubMed
description An understanding of the mechanisms influencing prenatal characteristics is fundamental to comprehend the role of ecological and evolutionary processes behind survival and reproductive success in animals. Although the negative influence of parasites on host fitness is undisputable, we know very little about how parasitic infection in reproductive females might influence prenatal factors such as fetal development and sex allocation. Using an archival collection of Dall’s sheep (Ovis dalli dalli), a capital breeder that depends on its body reserves to overcome the arctic winter, we investigated the direct and indirect impacts of the parasite community on fetal development and sex allocation. Using partial least squares modelling, we observed a negative effect of parasite community on fetal development, driven primarily by the nematode Marshallagia marshalli. Principal component analysis demonstrated that mothers with low parasite burden and in good body condition were more likely to have female versus male fetuses. This association was primarily driven by the indirect effect of M. marshalli on ewe body condition. Refining our knowledge of the direct and indirect impact that parasite communities can have on reproduction in mammals is critical for understanding the effects of infectious diseases on wildlife populations. This can be particularly relevant for species living in ecosystems sensitive to the effects of global climate change.
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spelling pubmed-75184222020-09-29 Parasite intensity drives fetal development and sex allocation in a wild ungulate Aleuy, O. Alejandro Serrano, Emmanuel Ruckstuhl, Kathreen E. Hoberg, Eric P. Kutz, Susan Sci Rep Article An understanding of the mechanisms influencing prenatal characteristics is fundamental to comprehend the role of ecological and evolutionary processes behind survival and reproductive success in animals. Although the negative influence of parasites on host fitness is undisputable, we know very little about how parasitic infection in reproductive females might influence prenatal factors such as fetal development and sex allocation. Using an archival collection of Dall’s sheep (Ovis dalli dalli), a capital breeder that depends on its body reserves to overcome the arctic winter, we investigated the direct and indirect impacts of the parasite community on fetal development and sex allocation. Using partial least squares modelling, we observed a negative effect of parasite community on fetal development, driven primarily by the nematode Marshallagia marshalli. Principal component analysis demonstrated that mothers with low parasite burden and in good body condition were more likely to have female versus male fetuses. This association was primarily driven by the indirect effect of M. marshalli on ewe body condition. Refining our knowledge of the direct and indirect impact that parasite communities can have on reproduction in mammals is critical for understanding the effects of infectious diseases on wildlife populations. This can be particularly relevant for species living in ecosystems sensitive to the effects of global climate change. Nature Publishing Group UK 2020-09-24 /pmc/articles/PMC7518422/ /pubmed/32973197 http://dx.doi.org/10.1038/s41598-020-72376-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Aleuy, O. Alejandro
Serrano, Emmanuel
Ruckstuhl, Kathreen E.
Hoberg, Eric P.
Kutz, Susan
Parasite intensity drives fetal development and sex allocation in a wild ungulate
title Parasite intensity drives fetal development and sex allocation in a wild ungulate
title_full Parasite intensity drives fetal development and sex allocation in a wild ungulate
title_fullStr Parasite intensity drives fetal development and sex allocation in a wild ungulate
title_full_unstemmed Parasite intensity drives fetal development and sex allocation in a wild ungulate
title_short Parasite intensity drives fetal development and sex allocation in a wild ungulate
title_sort parasite intensity drives fetal development and sex allocation in a wild ungulate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518422/
https://www.ncbi.nlm.nih.gov/pubmed/32973197
http://dx.doi.org/10.1038/s41598-020-72376-x
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