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Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns
By altering the abundance, diversity, and distribution of species—and their pathogens—globalization may inadvertently select for more virulent pathogens. In Brazil’s Atlantic Forest, a hotspot of amphibian biodiversity, the global amphibian trade has facilitated the co-occurrence of previously isola...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502024/ https://www.ncbi.nlm.nih.gov/pubmed/37709833 http://dx.doi.org/10.1038/s42003-023-05314-y |
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author | Carvalho, Tamilie Medina, Daniel P. Ribeiro, Luisa Rodriguez, David Jenkinson, Thomas S. Becker, C. Guilherme Toledo, Luís Felipe Hite, Jessica L. |
author_facet | Carvalho, Tamilie Medina, Daniel P. Ribeiro, Luisa Rodriguez, David Jenkinson, Thomas S. Becker, C. Guilherme Toledo, Luís Felipe Hite, Jessica L. |
author_sort | Carvalho, Tamilie |
collection | PubMed |
description | By altering the abundance, diversity, and distribution of species—and their pathogens—globalization may inadvertently select for more virulent pathogens. In Brazil’s Atlantic Forest, a hotspot of amphibian biodiversity, the global amphibian trade has facilitated the co-occurrence of previously isolated enzootic and panzootic lineages of the pathogenic amphibian-chytrid (Batrachochytrium dendrobatidis, ‘Bd’) and generated new virulent recombinant genotypes (‘hybrids’). Epidemiological data indicate that amphibian declines are most severe in hybrid zones, suggesting that coinfections are causing more severe infections or selecting for higher virulence. We investigated how coinfections involving these genotypes shapes virulence and transmission. Overall, coinfection favored the more virulent and competitively superior panzootic genotype, despite dampening its transmission potential and overall virulence. However, for the least virulent and least competitive genotype, coinfection increased both overall virulence and transmission. Thus, by integrating experimental and epidemiological data, our results provide mechanistic insight into how globalization can select for, and propel, the emergence of introduced hypervirulent lineages, such as the globally distributed panzootic lineage of Bd. |
format | Online Article Text |
id | pubmed-10502024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105020242023-09-16 Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns Carvalho, Tamilie Medina, Daniel P. Ribeiro, Luisa Rodriguez, David Jenkinson, Thomas S. Becker, C. Guilherme Toledo, Luís Felipe Hite, Jessica L. Commun Biol Article By altering the abundance, diversity, and distribution of species—and their pathogens—globalization may inadvertently select for more virulent pathogens. In Brazil’s Atlantic Forest, a hotspot of amphibian biodiversity, the global amphibian trade has facilitated the co-occurrence of previously isolated enzootic and panzootic lineages of the pathogenic amphibian-chytrid (Batrachochytrium dendrobatidis, ‘Bd’) and generated new virulent recombinant genotypes (‘hybrids’). Epidemiological data indicate that amphibian declines are most severe in hybrid zones, suggesting that coinfections are causing more severe infections or selecting for higher virulence. We investigated how coinfections involving these genotypes shapes virulence and transmission. Overall, coinfection favored the more virulent and competitively superior panzootic genotype, despite dampening its transmission potential and overall virulence. However, for the least virulent and least competitive genotype, coinfection increased both overall virulence and transmission. Thus, by integrating experimental and epidemiological data, our results provide mechanistic insight into how globalization can select for, and propel, the emergence of introduced hypervirulent lineages, such as the globally distributed panzootic lineage of Bd. Nature Publishing Group UK 2023-09-14 /pmc/articles/PMC10502024/ /pubmed/37709833 http://dx.doi.org/10.1038/s42003-023-05314-y Text en © The Author(s) 2023 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 Carvalho, Tamilie Medina, Daniel P. Ribeiro, Luisa Rodriguez, David Jenkinson, Thomas S. Becker, C. Guilherme Toledo, Luís Felipe Hite, Jessica L. Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
title | Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
title_full | Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
title_fullStr | Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
title_full_unstemmed | Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
title_short | Coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
title_sort | coinfection with chytrid genotypes drives divergent infection dynamics reflecting regional distribution patterns |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502024/ https://www.ncbi.nlm.nih.gov/pubmed/37709833 http://dx.doi.org/10.1038/s42003-023-05314-y |
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