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Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate

Infectious diseases play an important role in wildlife population dynamics by altering individual fitness, but detecting disease-driven natural selection in free-ranging populations is difficult due to complex disease–host relationships. Chronic wasting disease (CWD) is a fatal infectious prion dise...

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Autores principales: LaCava, Melanie E. F., Malmberg, Jennifer L., Edwards, William H., Johnson, Laura N. L., Allen, Samantha E., Ernest, Holly B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8355672/
https://www.ncbi.nlm.nih.gov/pubmed/34430048
http://dx.doi.org/10.1098/rsos.210802
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author LaCava, Melanie E. F.
Malmberg, Jennifer L.
Edwards, William H.
Johnson, Laura N. L.
Allen, Samantha E.
Ernest, Holly B.
author_facet LaCava, Melanie E. F.
Malmberg, Jennifer L.
Edwards, William H.
Johnson, Laura N. L.
Allen, Samantha E.
Ernest, Holly B.
author_sort LaCava, Melanie E. F.
collection PubMed
description Infectious diseases play an important role in wildlife population dynamics by altering individual fitness, but detecting disease-driven natural selection in free-ranging populations is difficult due to complex disease–host relationships. Chronic wasting disease (CWD) is a fatal infectious prion disease in cervids for which mutations in a single gene have been mechanistically linked to disease outcomes, providing a rare opportunity to study disease-driven selection in wildlife. In Wyoming, USA, CWD has gradually spread across mule deer (Odocoileus hemionus) populations, producing natural variation in disease history to evaluate selection pressure. We used spatial variation and a novel temporal comparison to investigate the relationship between CWD and a mutation at codon 225 of the mule deer prion protein gene that slows disease progression. We found that individuals with the ‘slow’ 225F allele were less likely to test positive for CWD, and the 225F allele was more common in herds exposed to CWD longer. We also found that in the past 2 decades, the 225F allele frequency increased more in herds with higher CWD prevalence. This study expanded on previous research by analysing spatio-temporal patterns of individual and herd-based disease data to present multiple lines of evidence for disease-driven selection in free-ranging wildlife.
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spelling pubmed-83556722021-08-23 Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate LaCava, Melanie E. F. Malmberg, Jennifer L. Edwards, William H. Johnson, Laura N. L. Allen, Samantha E. Ernest, Holly B. R Soc Open Sci Organismal and Evolutionary Biology Infectious diseases play an important role in wildlife population dynamics by altering individual fitness, but detecting disease-driven natural selection in free-ranging populations is difficult due to complex disease–host relationships. Chronic wasting disease (CWD) is a fatal infectious prion disease in cervids for which mutations in a single gene have been mechanistically linked to disease outcomes, providing a rare opportunity to study disease-driven selection in wildlife. In Wyoming, USA, CWD has gradually spread across mule deer (Odocoileus hemionus) populations, producing natural variation in disease history to evaluate selection pressure. We used spatial variation and a novel temporal comparison to investigate the relationship between CWD and a mutation at codon 225 of the mule deer prion protein gene that slows disease progression. We found that individuals with the ‘slow’ 225F allele were less likely to test positive for CWD, and the 225F allele was more common in herds exposed to CWD longer. We also found that in the past 2 decades, the 225F allele frequency increased more in herds with higher CWD prevalence. This study expanded on previous research by analysing spatio-temporal patterns of individual and herd-based disease data to present multiple lines of evidence for disease-driven selection in free-ranging wildlife. The Royal Society 2021-08-11 /pmc/articles/PMC8355672/ /pubmed/34430048 http://dx.doi.org/10.1098/rsos.210802 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Organismal and Evolutionary Biology
LaCava, Melanie E. F.
Malmberg, Jennifer L.
Edwards, William H.
Johnson, Laura N. L.
Allen, Samantha E.
Ernest, Holly B.
Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
title Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
title_full Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
title_fullStr Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
title_full_unstemmed Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
title_short Spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
title_sort spatio-temporal analyses reveal infectious disease-driven selection in a free-ranging ungulate
topic Organismal and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8355672/
https://www.ncbi.nlm.nih.gov/pubmed/34430048
http://dx.doi.org/10.1098/rsos.210802
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