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...
Autores principales: | , , , , |
---|---|
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 |