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Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird

Animal hosts can adapt to emerging infectious disease through both disease resistance, which decreases pathogen numbers, and disease tolerance, which limits damage during infection without limiting pathogen replication. Both resistance and tolerance mechanisms can drive pathogen transmission dynamic...

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Autores principales: Henschen, Amberleigh E., Vinkler, Michal, Langager, Marissa M., Rowley, Allison A., Dalloul, Rami A., Hawley, Dana M., Adelman, James S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287013/
https://www.ncbi.nlm.nih.gov/pubmed/37294834
http://dx.doi.org/10.1371/journal.ppat.1011408
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author Henschen, Amberleigh E.
Vinkler, Michal
Langager, Marissa M.
Rowley, Allison A.
Dalloul, Rami A.
Hawley, Dana M.
Adelman, James S.
author_facet Henschen, Amberleigh E.
Vinkler, Michal
Langager, Marissa M.
Rowley, Allison A.
Dalloul, Rami A.
Hawley, Dana M.
Adelman, James S.
author_sort Henschen, Amberleigh E.
collection PubMed
description Animal hosts can adapt to emerging infectious disease through both disease resistance, which decreases pathogen numbers, and disease tolerance, which limits damage during infection without limiting pathogen replication. Both resistance and tolerance mechanisms can drive pathogen transmission dynamics. However, it is not well understood how quickly host tolerance evolves in response to novel pathogens or what physiological mechanisms underlie this defense. Using natural populations of house finches (Haemorhous mexicanus) across the temporal invasion gradient of a recently emerged bacterial pathogen (Mycoplasma gallisepticum), we find rapid evolution of tolerance (<25 years). In particular, populations with a longer history of MG endemism have less pathology but similar pathogen loads compared with populations with a shorter history of MG endemism. Further, gene expression data reveal that more-targeted immune responses early in infection are associated with tolerance. These results suggest an important role for tolerance in host adaptation to emerging infectious diseases, a phenomenon with broad implications for pathogen spread and evolution.
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spelling pubmed-102870132023-06-23 Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird Henschen, Amberleigh E. Vinkler, Michal Langager, Marissa M. Rowley, Allison A. Dalloul, Rami A. Hawley, Dana M. Adelman, James S. PLoS Pathog Research Article Animal hosts can adapt to emerging infectious disease through both disease resistance, which decreases pathogen numbers, and disease tolerance, which limits damage during infection without limiting pathogen replication. Both resistance and tolerance mechanisms can drive pathogen transmission dynamics. However, it is not well understood how quickly host tolerance evolves in response to novel pathogens or what physiological mechanisms underlie this defense. Using natural populations of house finches (Haemorhous mexicanus) across the temporal invasion gradient of a recently emerged bacterial pathogen (Mycoplasma gallisepticum), we find rapid evolution of tolerance (<25 years). In particular, populations with a longer history of MG endemism have less pathology but similar pathogen loads compared with populations with a shorter history of MG endemism. Further, gene expression data reveal that more-targeted immune responses early in infection are associated with tolerance. These results suggest an important role for tolerance in host adaptation to emerging infectious diseases, a phenomenon with broad implications for pathogen spread and evolution. Public Library of Science 2023-06-09 /pmc/articles/PMC10287013/ /pubmed/37294834 http://dx.doi.org/10.1371/journal.ppat.1011408 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Henschen, Amberleigh E.
Vinkler, Michal
Langager, Marissa M.
Rowley, Allison A.
Dalloul, Rami A.
Hawley, Dana M.
Adelman, James S.
Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
title Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
title_full Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
title_fullStr Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
title_full_unstemmed Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
title_short Rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
title_sort rapid adaptation to a novel pathogen through disease tolerance in a wild songbird
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287013/
https://www.ncbi.nlm.nih.gov/pubmed/37294834
http://dx.doi.org/10.1371/journal.ppat.1011408
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