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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10287013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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