Cargando…

West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis

In nature, arthropod-borne viruses (arboviruses) perpetuate through alternating replication in vertebrate and invertebrate hosts. The trade-off hypothesis proposes that these viruses maintain adequate replicative fitness in two disparate hosts in exchange for superior fitness in one host. Releasing...

Descripción completa

Detalles Bibliográficos
Autores principales: Deardorff, Eleanor R., Fitzpatrick, Kelly A., Jerzak, Greta V. S., Shi, Pei-Yong, Kramer, Laura D., Ebel, Gregory D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213084/
https://www.ncbi.nlm.nih.gov/pubmed/22102808
http://dx.doi.org/10.1371/journal.ppat.1002335
_version_ 1782216075498225664
author Deardorff, Eleanor R.
Fitzpatrick, Kelly A.
Jerzak, Greta V. S.
Shi, Pei-Yong
Kramer, Laura D.
Ebel, Gregory D.
author_facet Deardorff, Eleanor R.
Fitzpatrick, Kelly A.
Jerzak, Greta V. S.
Shi, Pei-Yong
Kramer, Laura D.
Ebel, Gregory D.
author_sort Deardorff, Eleanor R.
collection PubMed
description In nature, arthropod-borne viruses (arboviruses) perpetuate through alternating replication in vertebrate and invertebrate hosts. The trade-off hypothesis proposes that these viruses maintain adequate replicative fitness in two disparate hosts in exchange for superior fitness in one host. Releasing the virus from the constraints of a two-host cycle should thus facilitate adaptation to a single host. This theory has been addressed in a variety of systems, but remains poorly understood. We sought to determine the fitness implications of alternating host replication for West Nile virus (WNV) using an in vivo model system. Previously, WNV was serially or alternately passed 20 times in vivo in chicks or mosquitoes and resulting viruses were characterized genetically. In this study, these test viruses were competed in vivo in fitness assays against an unpassed marked reference virus. Fitness was assayed in chicks and in two important WNV vectors, Culex pipiens and Culex quinquefasciatus. Chick-specialized virus displayed clear fitness gains in chicks and in Cx. pipiens but not in Cx. quinquefasciatus. Cx. pipiens-specialized virus experienced reduced fitness in chicks and little change in either mosquito species. These data suggest that when fitness is measured in birds the trade-off hypothesis is supported; but in mosquitoes it is not. Overall, these results suggest that WNV evolution is driven by alternate cycles of genetic expansion in mosquitoes, where purifying selection is weak and genetic diversity generated, and restriction in birds, where purifying selection is strong.
format Online
Article
Text
id pubmed-3213084
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32130842011-11-18 West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis Deardorff, Eleanor R. Fitzpatrick, Kelly A. Jerzak, Greta V. S. Shi, Pei-Yong Kramer, Laura D. Ebel, Gregory D. PLoS Pathog Research Article In nature, arthropod-borne viruses (arboviruses) perpetuate through alternating replication in vertebrate and invertebrate hosts. The trade-off hypothesis proposes that these viruses maintain adequate replicative fitness in two disparate hosts in exchange for superior fitness in one host. Releasing the virus from the constraints of a two-host cycle should thus facilitate adaptation to a single host. This theory has been addressed in a variety of systems, but remains poorly understood. We sought to determine the fitness implications of alternating host replication for West Nile virus (WNV) using an in vivo model system. Previously, WNV was serially or alternately passed 20 times in vivo in chicks or mosquitoes and resulting viruses were characterized genetically. In this study, these test viruses were competed in vivo in fitness assays against an unpassed marked reference virus. Fitness was assayed in chicks and in two important WNV vectors, Culex pipiens and Culex quinquefasciatus. Chick-specialized virus displayed clear fitness gains in chicks and in Cx. pipiens but not in Cx. quinquefasciatus. Cx. pipiens-specialized virus experienced reduced fitness in chicks and little change in either mosquito species. These data suggest that when fitness is measured in birds the trade-off hypothesis is supported; but in mosquitoes it is not. Overall, these results suggest that WNV evolution is driven by alternate cycles of genetic expansion in mosquitoes, where purifying selection is weak and genetic diversity generated, and restriction in birds, where purifying selection is strong. Public Library of Science 2011-11-10 /pmc/articles/PMC3213084/ /pubmed/22102808 http://dx.doi.org/10.1371/journal.ppat.1002335 Text en Deardorff et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Deardorff, Eleanor R.
Fitzpatrick, Kelly A.
Jerzak, Greta V. S.
Shi, Pei-Yong
Kramer, Laura D.
Ebel, Gregory D.
West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis
title West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis
title_full West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis
title_fullStr West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis
title_full_unstemmed West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis
title_short West Nile Virus Experimental Evolution in vivo and the Trade-off Hypothesis
title_sort west nile virus experimental evolution in vivo and the trade-off hypothesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213084/
https://www.ncbi.nlm.nih.gov/pubmed/22102808
http://dx.doi.org/10.1371/journal.ppat.1002335
work_keys_str_mv AT deardorffeleanorr westnilevirusexperimentalevolutioninvivoandthetradeoffhypothesis
AT fitzpatrickkellya westnilevirusexperimentalevolutioninvivoandthetradeoffhypothesis
AT jerzakgretavs westnilevirusexperimentalevolutioninvivoandthetradeoffhypothesis
AT shipeiyong westnilevirusexperimentalevolutioninvivoandthetradeoffhypothesis
AT kramerlaurad westnilevirusexperimentalevolutioninvivoandthetradeoffhypothesis
AT ebelgregoryd westnilevirusexperimentalevolutioninvivoandthetradeoffhypothesis