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The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation

When a novel disease strikes a naïve host population, there is evidence that the most immediate response can involve host evolution while the pathogen remains relatively unchanged. When hosts also live in metapopulations, there may be critical differences in the dynamics that emerge from the synergy...

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Autores principales: Jiao, Jing, Fefferman, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149858/
https://www.ncbi.nlm.nih.gov/pubmed/34035424
http://dx.doi.org/10.1038/s41598-021-90407-z
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author Jiao, Jing
Fefferman, Nina
author_facet Jiao, Jing
Fefferman, Nina
author_sort Jiao, Jing
collection PubMed
description When a novel disease strikes a naïve host population, there is evidence that the most immediate response can involve host evolution while the pathogen remains relatively unchanged. When hosts also live in metapopulations, there may be critical differences in the dynamics that emerge from the synergy among evolutionary, ecological, and epidemiological factors. Here we used a Susceptible-Infected-Recovery model to explore how spatial and temporal ecological factors may drive the epidemiological and rapid-evolutionary dynamics of host metapopulations. For simplicity, we assumed two host genotypes: wild type, which has a positive intrinsic growth rate in the absence of disease, and robust type, which is less likely to catch the infection given exposure but has a lower intrinsic growth rate in the absence of infection. We found that the robust-type host would be strongly selected for in the presence of disease when transmission differences between the two types is large. The growth rate of the wild type had dual but opposite effects on host composition: a smaller increase in wild-type growth increased wild-type competition and lead to periodical disease outbreaks over the first generations after pathogen introduction, while larger growth increased disease by providing more susceptibles, which increased robust host density but decreased periodical outbreaks. Increased migration had a similar impact as the increased differential susceptibility, both of which led to an increase in robust hosts and a decrease in periodical outbreaks. Our study provided a comprehensive understanding of the combined effects among migration, disease epidemiology, and host demography on host evolution with an unchanging pathogen. The findings have important implications for wildlife conservation and zoonotic disease control.
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spelling pubmed-81498582021-05-26 The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation Jiao, Jing Fefferman, Nina Sci Rep Article When a novel disease strikes a naïve host population, there is evidence that the most immediate response can involve host evolution while the pathogen remains relatively unchanged. When hosts also live in metapopulations, there may be critical differences in the dynamics that emerge from the synergy among evolutionary, ecological, and epidemiological factors. Here we used a Susceptible-Infected-Recovery model to explore how spatial and temporal ecological factors may drive the epidemiological and rapid-evolutionary dynamics of host metapopulations. For simplicity, we assumed two host genotypes: wild type, which has a positive intrinsic growth rate in the absence of disease, and robust type, which is less likely to catch the infection given exposure but has a lower intrinsic growth rate in the absence of infection. We found that the robust-type host would be strongly selected for in the presence of disease when transmission differences between the two types is large. The growth rate of the wild type had dual but opposite effects on host composition: a smaller increase in wild-type growth increased wild-type competition and lead to periodical disease outbreaks over the first generations after pathogen introduction, while larger growth increased disease by providing more susceptibles, which increased robust host density but decreased periodical outbreaks. Increased migration had a similar impact as the increased differential susceptibility, both of which led to an increase in robust hosts and a decrease in periodical outbreaks. Our study provided a comprehensive understanding of the combined effects among migration, disease epidemiology, and host demography on host evolution with an unchanging pathogen. The findings have important implications for wildlife conservation and zoonotic disease control. Nature Publishing Group UK 2021-05-25 /pmc/articles/PMC8149858/ /pubmed/34035424 http://dx.doi.org/10.1038/s41598-021-90407-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jiao, Jing
Fefferman, Nina
The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
title The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
title_full The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
title_fullStr The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
title_full_unstemmed The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
title_short The dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
title_sort dynamics of evolutionary rescue from a novel pathogen threat in a host metapopulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149858/
https://www.ncbi.nlm.nih.gov/pubmed/34035424
http://dx.doi.org/10.1038/s41598-021-90407-z
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