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Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context

An extensive body of theory addresses the topic of pathogen virulence evolution, yet few studies have empirically demonstrated the presence of fitness trade-offs that would select for intermediate virulence. Here we show the presence of transmission-clearance trade-offs in dengue virus using viremia...

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Autores principales: Ben-Shachar, Rotem, Koelle, Katia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003961/
https://www.ncbi.nlm.nih.gov/pubmed/29907741
http://dx.doi.org/10.1038/s41467-018-04595-w
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author Ben-Shachar, Rotem
Koelle, Katia
author_facet Ben-Shachar, Rotem
Koelle, Katia
author_sort Ben-Shachar, Rotem
collection PubMed
description An extensive body of theory addresses the topic of pathogen virulence evolution, yet few studies have empirically demonstrated the presence of fitness trade-offs that would select for intermediate virulence. Here we show the presence of transmission-clearance trade-offs in dengue virus using viremia measurements. By fitting a within-host model to these data, we further find that the interaction between dengue and the host immune response can account for the observed trade-offs. Finally, we consider dengue virulence evolution when selection acts on the virus’s production rate. By combining within-host model simulations with empirical findings on how host viral load affects human-to-mosquito transmission success, we show that the virus’s transmission potential is maximized at production rates associated with intermediate virulence and that the optimal production rate critically depends on dengue’s epidemiological context. These results indicate that long-term changes in dengue’s global distribution impact the invasion and spread of virulent dengue virus genotypes.
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spelling pubmed-60039612018-06-18 Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context Ben-Shachar, Rotem Koelle, Katia Nat Commun Article An extensive body of theory addresses the topic of pathogen virulence evolution, yet few studies have empirically demonstrated the presence of fitness trade-offs that would select for intermediate virulence. Here we show the presence of transmission-clearance trade-offs in dengue virus using viremia measurements. By fitting a within-host model to these data, we further find that the interaction between dengue and the host immune response can account for the observed trade-offs. Finally, we consider dengue virulence evolution when selection acts on the virus’s production rate. By combining within-host model simulations with empirical findings on how host viral load affects human-to-mosquito transmission success, we show that the virus’s transmission potential is maximized at production rates associated with intermediate virulence and that the optimal production rate critically depends on dengue’s epidemiological context. These results indicate that long-term changes in dengue’s global distribution impact the invasion and spread of virulent dengue virus genotypes. Nature Publishing Group UK 2018-06-15 /pmc/articles/PMC6003961/ /pubmed/29907741 http://dx.doi.org/10.1038/s41467-018-04595-w Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ben-Shachar, Rotem
Koelle, Katia
Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
title Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
title_full Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
title_fullStr Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
title_full_unstemmed Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
title_short Transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
title_sort transmission-clearance trade-offs indicate that dengue virulence evolution depends on epidemiological context
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003961/
https://www.ncbi.nlm.nih.gov/pubmed/29907741
http://dx.doi.org/10.1038/s41467-018-04595-w
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