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Evolution of Virulence in Emerging Epidemics

Theory predicts that selection for pathogen virulence and horizontal transmission is highest at the onset of an epidemic but decreases thereafter, as the epidemic depletes the pool of susceptible hosts. We tested this prediction by tracking the competition between the latent bacteriophage λ and its...

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Detalles Bibliográficos
Autores principales: Berngruber, Thomas W., Froissart, Rémy, Choisy, Marc, Gandon, Sylvain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597519/
https://www.ncbi.nlm.nih.gov/pubmed/23516359
http://dx.doi.org/10.1371/journal.ppat.1003209
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author Berngruber, Thomas W.
Froissart, Rémy
Choisy, Marc
Gandon, Sylvain
author_facet Berngruber, Thomas W.
Froissart, Rémy
Choisy, Marc
Gandon, Sylvain
author_sort Berngruber, Thomas W.
collection PubMed
description Theory predicts that selection for pathogen virulence and horizontal transmission is highest at the onset of an epidemic but decreases thereafter, as the epidemic depletes the pool of susceptible hosts. We tested this prediction by tracking the competition between the latent bacteriophage λ and its virulent mutant λcI857 throughout experimental epidemics taking place in continuous cultures of Escherichia coli. As expected, the virulent λcI857 is strongly favored in the early stage of the epidemic, but loses competition with the latent virus as prevalence increases. We show that the observed transient selection for virulence and horizontal transmission can be fully explained within the framework of evolutionary epidemiology theory. This experimental validation of our predictions is a key step towards a predictive theory for the evolution of virulence in emerging infectious diseases.
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spelling pubmed-35975192013-03-20 Evolution of Virulence in Emerging Epidemics Berngruber, Thomas W. Froissart, Rémy Choisy, Marc Gandon, Sylvain PLoS Pathog Research Article Theory predicts that selection for pathogen virulence and horizontal transmission is highest at the onset of an epidemic but decreases thereafter, as the epidemic depletes the pool of susceptible hosts. We tested this prediction by tracking the competition between the latent bacteriophage λ and its virulent mutant λcI857 throughout experimental epidemics taking place in continuous cultures of Escherichia coli. As expected, the virulent λcI857 is strongly favored in the early stage of the epidemic, but loses competition with the latent virus as prevalence increases. We show that the observed transient selection for virulence and horizontal transmission can be fully explained within the framework of evolutionary epidemiology theory. This experimental validation of our predictions is a key step towards a predictive theory for the evolution of virulence in emerging infectious diseases. Public Library of Science 2013-03-14 /pmc/articles/PMC3597519/ /pubmed/23516359 http://dx.doi.org/10.1371/journal.ppat.1003209 Text en © 2013 Berngruber et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Berngruber, Thomas W.
Froissart, Rémy
Choisy, Marc
Gandon, Sylvain
Evolution of Virulence in Emerging Epidemics
title Evolution of Virulence in Emerging Epidemics
title_full Evolution of Virulence in Emerging Epidemics
title_fullStr Evolution of Virulence in Emerging Epidemics
title_full_unstemmed Evolution of Virulence in Emerging Epidemics
title_short Evolution of Virulence in Emerging Epidemics
title_sort evolution of virulence in emerging epidemics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597519/
https://www.ncbi.nlm.nih.gov/pubmed/23516359
http://dx.doi.org/10.1371/journal.ppat.1003209
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