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The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution

BACKGROUND: Virulence is often coupled with replicative fitness of viruses in vertebrate systems, yet the relationship between virulence and fitness of arthropod-borne viruses (arboviruses) in invertebrates has not been evaluated. Although the interactions between vector-borne pathogens and their in...

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Autores principales: Ciota, Alexander T, Ehrbar, Dylan J, Matacchiero, Amy C, Van Slyke, Greta A, Kramer, Laura D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626576/
https://www.ncbi.nlm.nih.gov/pubmed/23514328
http://dx.doi.org/10.1186/1471-2148-13-71
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author Ciota, Alexander T
Ehrbar, Dylan J
Matacchiero, Amy C
Van Slyke, Greta A
Kramer, Laura D
author_facet Ciota, Alexander T
Ehrbar, Dylan J
Matacchiero, Amy C
Van Slyke, Greta A
Kramer, Laura D
author_sort Ciota, Alexander T
collection PubMed
description BACKGROUND: Virulence is often coupled with replicative fitness of viruses in vertebrate systems, yet the relationship between virulence and fitness of arthropod-borne viruses (arboviruses) in invertebrates has not been evaluated. Although the interactions between vector-borne pathogens and their invertebrate hosts have been characterized as being largely benign, some costs of arbovirus exposure have been identified for mosquitoes. The extent to which these costs may be strain-specific and the subsequent consequences of these interactions on vector and virus evolution has not been adequately explored. RESULTS: Using West Nile virus (WNV) and Culex pipiens mosquitoes, we tested the hypothesis that intrahost fitness is correlated with virulence in mosquitoes by evaluating life history traits following exposure to either non-infectious bloodmeals or bloodmeals containing wildtype (WNV WT) or the high fitness, mosquito-adapted strain, WNV MP20 derived from WNV WT. Our results demonstrate strain-specific effects on mosquito survival, fecundity, and blood feeding behavior. Specifically, both resistance to and infection with WNV MP20, but not WNV WT, decreased survival of Cx. pipiens and altered fecundity and bloodfeeding such that early egg output was enhanced at a later cost. CONCLUSIONS: As predicted by the trade-off hypothesis of virulence, costs of infection with WNV MP20 in terms of survival were directly correlated to viral load, yet resistance to infection with this virulent strain was equally costly. Taken together, these results demonstrate that WNV MP20 infection decreases the transmission potential of Cx. pipiens populations despite the increased intrahost fitness of this strain, indicating that a virulence-transmission trade-off in invertebrates could contribute significantly to the adaptive and evolutionary constraint of arboviruses.
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spelling pubmed-36265762013-04-16 The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution Ciota, Alexander T Ehrbar, Dylan J Matacchiero, Amy C Van Slyke, Greta A Kramer, Laura D BMC Evol Biol Research Article BACKGROUND: Virulence is often coupled with replicative fitness of viruses in vertebrate systems, yet the relationship between virulence and fitness of arthropod-borne viruses (arboviruses) in invertebrates has not been evaluated. Although the interactions between vector-borne pathogens and their invertebrate hosts have been characterized as being largely benign, some costs of arbovirus exposure have been identified for mosquitoes. The extent to which these costs may be strain-specific and the subsequent consequences of these interactions on vector and virus evolution has not been adequately explored. RESULTS: Using West Nile virus (WNV) and Culex pipiens mosquitoes, we tested the hypothesis that intrahost fitness is correlated with virulence in mosquitoes by evaluating life history traits following exposure to either non-infectious bloodmeals or bloodmeals containing wildtype (WNV WT) or the high fitness, mosquito-adapted strain, WNV MP20 derived from WNV WT. Our results demonstrate strain-specific effects on mosquito survival, fecundity, and blood feeding behavior. Specifically, both resistance to and infection with WNV MP20, but not WNV WT, decreased survival of Cx. pipiens and altered fecundity and bloodfeeding such that early egg output was enhanced at a later cost. CONCLUSIONS: As predicted by the trade-off hypothesis of virulence, costs of infection with WNV MP20 in terms of survival were directly correlated to viral load, yet resistance to infection with this virulent strain was equally costly. Taken together, these results demonstrate that WNV MP20 infection decreases the transmission potential of Cx. pipiens populations despite the increased intrahost fitness of this strain, indicating that a virulence-transmission trade-off in invertebrates could contribute significantly to the adaptive and evolutionary constraint of arboviruses. BioMed Central 2013-03-20 /pmc/articles/PMC3626576/ /pubmed/23514328 http://dx.doi.org/10.1186/1471-2148-13-71 Text en Copyright © 2013 Ciota et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ciota, Alexander T
Ehrbar, Dylan J
Matacchiero, Amy C
Van Slyke, Greta A
Kramer, Laura D
The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
title The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
title_full The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
title_fullStr The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
title_full_unstemmed The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
title_short The evolution of virulence of West Nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
title_sort evolution of virulence of west nile virus in a mosquito vector: implications for arbovirus adaptation and evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626576/
https://www.ncbi.nlm.nih.gov/pubmed/23514328
http://dx.doi.org/10.1186/1471-2148-13-71
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