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Virus shedding kinetics and unconventional virulence tradeoffs

Tradeoff theory, which postulates that virulence provides both transmission costs and benefits for pathogens, has become widely adopted by the scientific community. Although theoretical literature exploring virulence-tradeoffs is vast, empirical studies validating various assumptions still remain sp...

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Autores principales: Wargo, Andrew R., Kurath, Gael, Scott, Robert J., Kerr, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8109835/
https://www.ncbi.nlm.nih.gov/pubmed/33970967
http://dx.doi.org/10.1371/journal.ppat.1009528
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author Wargo, Andrew R.
Kurath, Gael
Scott, Robert J.
Kerr, Benjamin
author_facet Wargo, Andrew R.
Kurath, Gael
Scott, Robert J.
Kerr, Benjamin
author_sort Wargo, Andrew R.
collection PubMed
description Tradeoff theory, which postulates that virulence provides both transmission costs and benefits for pathogens, has become widely adopted by the scientific community. Although theoretical literature exploring virulence-tradeoffs is vast, empirical studies validating various assumptions still remain sparse. In particular, truncation of transmission duration as a cost of virulence has been difficult to quantify with robust controlled in vivo studies. We sought to fill this knowledge gap by investigating how transmission rate and duration were associated with virulence for infectious hematopoietic necrosis virus (IHNV) in rainbow trout (Oncorhynchus mykiss). Using host mortality to quantify virulence and viral shedding to quantify transmission, we found that IHNV did not conform to classical tradeoff theory. More virulent genotypes of the virus were found to have longer transmission durations due to lower recovery rates of infected hosts, but the relationship was not saturating as assumed by tradeoff theory. Furthermore, the impact of host mortality on limiting transmission duration was minimal and greatly outweighed by recovery. Transmission rate differences between high and low virulence genotypes were also small and inconsistent. Ultimately, more virulent genotypes were found to have the overall fitness advantage, and there was no apparent constraint on the evolution of increased virulence for IHNV. However, using a mathematical model parameterized with experimental data, it was found that host culling resurrected the virulence tradeoff and provided low virulence genotypes with the advantage. Human-induced or natural culling, as well as host population fragmentation, may be some of the mechanisms by which virulence diversity is maintained in nature. This work highlights the importance of considering non-classical virulence tradeoffs.
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spelling pubmed-81098352021-05-21 Virus shedding kinetics and unconventional virulence tradeoffs Wargo, Andrew R. Kurath, Gael Scott, Robert J. Kerr, Benjamin PLoS Pathog Research Article Tradeoff theory, which postulates that virulence provides both transmission costs and benefits for pathogens, has become widely adopted by the scientific community. Although theoretical literature exploring virulence-tradeoffs is vast, empirical studies validating various assumptions still remain sparse. In particular, truncation of transmission duration as a cost of virulence has been difficult to quantify with robust controlled in vivo studies. We sought to fill this knowledge gap by investigating how transmission rate and duration were associated with virulence for infectious hematopoietic necrosis virus (IHNV) in rainbow trout (Oncorhynchus mykiss). Using host mortality to quantify virulence and viral shedding to quantify transmission, we found that IHNV did not conform to classical tradeoff theory. More virulent genotypes of the virus were found to have longer transmission durations due to lower recovery rates of infected hosts, but the relationship was not saturating as assumed by tradeoff theory. Furthermore, the impact of host mortality on limiting transmission duration was minimal and greatly outweighed by recovery. Transmission rate differences between high and low virulence genotypes were also small and inconsistent. Ultimately, more virulent genotypes were found to have the overall fitness advantage, and there was no apparent constraint on the evolution of increased virulence for IHNV. However, using a mathematical model parameterized with experimental data, it was found that host culling resurrected the virulence tradeoff and provided low virulence genotypes with the advantage. Human-induced or natural culling, as well as host population fragmentation, may be some of the mechanisms by which virulence diversity is maintained in nature. This work highlights the importance of considering non-classical virulence tradeoffs. Public Library of Science 2021-05-10 /pmc/articles/PMC8109835/ /pubmed/33970967 http://dx.doi.org/10.1371/journal.ppat.1009528 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
Wargo, Andrew R.
Kurath, Gael
Scott, Robert J.
Kerr, Benjamin
Virus shedding kinetics and unconventional virulence tradeoffs
title Virus shedding kinetics and unconventional virulence tradeoffs
title_full Virus shedding kinetics and unconventional virulence tradeoffs
title_fullStr Virus shedding kinetics and unconventional virulence tradeoffs
title_full_unstemmed Virus shedding kinetics and unconventional virulence tradeoffs
title_short Virus shedding kinetics and unconventional virulence tradeoffs
title_sort virus shedding kinetics and unconventional virulence tradeoffs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8109835/
https://www.ncbi.nlm.nih.gov/pubmed/33970967
http://dx.doi.org/10.1371/journal.ppat.1009528
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