Cargando…

Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions

In animal populations, males are commonly more susceptible to disease-induced mortality than females. However, three competing mechanisms can cause this sex bias: weak males may simultaneously be more prone to exposure to infection and mortality; being ‘male’ may be an imperfect proxy for the underl...

Descripción completa

Detalles Bibliográficos
Autores principales: McDonald, Jennifer L., Smith, Graham C., McDonald, Robbie A., Delahay, Richard J., Hodgson, Dave
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123697/
https://www.ncbi.nlm.nih.gov/pubmed/25056621
http://dx.doi.org/10.1098/rspb.2014.0526
_version_ 1782329525444542464
author McDonald, Jennifer L.
Smith, Graham C.
McDonald, Robbie A.
Delahay, Richard J.
Hodgson, Dave
author_facet McDonald, Jennifer L.
Smith, Graham C.
McDonald, Robbie A.
Delahay, Richard J.
Hodgson, Dave
author_sort McDonald, Jennifer L.
collection PubMed
description In animal populations, males are commonly more susceptible to disease-induced mortality than females. However, three competing mechanisms can cause this sex bias: weak males may simultaneously be more prone to exposure to infection and mortality; being ‘male’ may be an imperfect proxy for the underlying driver of disease-induced mortality; or males may experience increased severity of disease-induced effects compared with females. Here, we infer the drivers of sex-specific epidemiology by decomposing fixed mortality rates into mortality trajectories and comparing their parameters. We applied Bayesian survival trajectory analysis to a 22-year longitudinal study of a population of badgers (Meles meles) naturally infected with bovine tuberculosis (bTB). At the point of infection, infected male and female badgers had equal mortality risk, refuting the hypothesis that acquisition of infection occurs in males with coincidentally high mortality. Males and females exhibited similar levels of heterogeneity in mortality risk, refuting the hypothesis that maleness is only a proxy for disease susceptibility. Instead, sex differences were caused by a more rapid increase in male mortality rates following infection. Males are indeed more susceptible to bTB, probably due to immunological differences between the sexes. We recommend this mortality trajectory approach for the study of infection in animal populations.
format Online
Article
Text
id pubmed-4123697
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-41236972014-09-07 Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions McDonald, Jennifer L. Smith, Graham C. McDonald, Robbie A. Delahay, Richard J. Hodgson, Dave Proc Biol Sci Research Articles In animal populations, males are commonly more susceptible to disease-induced mortality than females. However, three competing mechanisms can cause this sex bias: weak males may simultaneously be more prone to exposure to infection and mortality; being ‘male’ may be an imperfect proxy for the underlying driver of disease-induced mortality; or males may experience increased severity of disease-induced effects compared with females. Here, we infer the drivers of sex-specific epidemiology by decomposing fixed mortality rates into mortality trajectories and comparing their parameters. We applied Bayesian survival trajectory analysis to a 22-year longitudinal study of a population of badgers (Meles meles) naturally infected with bovine tuberculosis (bTB). At the point of infection, infected male and female badgers had equal mortality risk, refuting the hypothesis that acquisition of infection occurs in males with coincidentally high mortality. Males and females exhibited similar levels of heterogeneity in mortality risk, refuting the hypothesis that maleness is only a proxy for disease susceptibility. Instead, sex differences were caused by a more rapid increase in male mortality rates following infection. Males are indeed more susceptible to bTB, probably due to immunological differences between the sexes. We recommend this mortality trajectory approach for the study of infection in animal populations. The Royal Society 2014-09-07 /pmc/articles/PMC4123697/ /pubmed/25056621 http://dx.doi.org/10.1098/rspb.2014.0526 Text en http://creativecommons.org/licenses/by/3.0/ © 2014 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
McDonald, Jennifer L.
Smith, Graham C.
McDonald, Robbie A.
Delahay, Richard J.
Hodgson, Dave
Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
title Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
title_full Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
title_fullStr Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
title_full_unstemmed Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
title_short Mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
title_sort mortality trajectory analysis reveals the drivers of sex-specific epidemiology in natural wildlife–disease interactions
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123697/
https://www.ncbi.nlm.nih.gov/pubmed/25056621
http://dx.doi.org/10.1098/rspb.2014.0526
work_keys_str_mv AT mcdonaldjenniferl mortalitytrajectoryanalysisrevealsthedriversofsexspecificepidemiologyinnaturalwildlifediseaseinteractions
AT smithgrahamc mortalitytrajectoryanalysisrevealsthedriversofsexspecificepidemiologyinnaturalwildlifediseaseinteractions
AT mcdonaldrobbiea mortalitytrajectoryanalysisrevealsthedriversofsexspecificepidemiologyinnaturalwildlifediseaseinteractions
AT delahayrichardj mortalitytrajectoryanalysisrevealsthedriversofsexspecificepidemiologyinnaturalwildlifediseaseinteractions
AT hodgsondave mortalitytrajectoryanalysisrevealsthedriversofsexspecificepidemiologyinnaturalwildlifediseaseinteractions