West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.

West Nile virus (WNV) has caused repeated large-scale human epidemics in North America since it was first detected in 1999 and is now the dominant vector-borne disease in this continent. Understanding the factors that determine the intensity of the spillover of this zoonotic pathogen from birds to h...

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Main Authors: A Marm Kilpatrick, Laura D Kramer, Matthew J Jones, Peter P Marra, Peter Daszak
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2006-04-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC1382011?pdf=render
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spelling doaj-884c97b23e2d4d1db00f77269624a5d72021-07-02T05:26:19ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852006-04-0144e8210.1371/journal.pbio.0040082West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.A Marm KilpatrickLaura D KramerMatthew J JonesPeter P MarraPeter DaszakWest Nile virus (WNV) has caused repeated large-scale human epidemics in North America since it was first detected in 1999 and is now the dominant vector-borne disease in this continent. Understanding the factors that determine the intensity of the spillover of this zoonotic pathogen from birds to humans (via mosquitoes) is a prerequisite for predicting and preventing human epidemics. We integrated mosquito feeding behavior with data on the population dynamics and WNV epidemiology of mosquitoes, birds, and humans. We show that Culex pipiens, the dominant enzootic (bird-to-bird) and bridge (bird-to-human) vector of WNV in urbanized areas in the northeast and north-central United States, shifted its feeding preferences from birds to humans by 7-fold during late summer and early fall, coinciding with the dispersal of its preferred host (American robins, Turdus migratorius) and the rise in human WNV infections. We also show that feeding shifts in Cx. tarsalis amplify human WNV epidemics in Colorado and California and occur during periods of robin dispersal and migration. Our results provide a direct explanation for the timing and intensity of human WNV epidemics. Shifts in feeding from competent avian hosts early in an epidemic to incompetent humans after mosquito infection prevalences are high result in synergistic effects that greatly amplify the number of human infections of this and other pathogens. Our results underscore the dramatic effects of vector behavior in driving the transmission of zoonotic pathogens to humans.http://europepmc.org/articles/PMC1382011?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author A Marm Kilpatrick
Laura D Kramer
Matthew J Jones
Peter P Marra
Peter Daszak
spellingShingle A Marm Kilpatrick
Laura D Kramer
Matthew J Jones
Peter P Marra
Peter Daszak
West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.
PLoS Biology
author_facet A Marm Kilpatrick
Laura D Kramer
Matthew J Jones
Peter P Marra
Peter Daszak
author_sort A Marm Kilpatrick
title West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.
title_short West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.
title_full West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.
title_fullStr West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.
title_full_unstemmed West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior.
title_sort west nile virus epidemics in north america are driven by shifts in mosquito feeding behavior.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2006-04-01
description West Nile virus (WNV) has caused repeated large-scale human epidemics in North America since it was first detected in 1999 and is now the dominant vector-borne disease in this continent. Understanding the factors that determine the intensity of the spillover of this zoonotic pathogen from birds to humans (via mosquitoes) is a prerequisite for predicting and preventing human epidemics. We integrated mosquito feeding behavior with data on the population dynamics and WNV epidemiology of mosquitoes, birds, and humans. We show that Culex pipiens, the dominant enzootic (bird-to-bird) and bridge (bird-to-human) vector of WNV in urbanized areas in the northeast and north-central United States, shifted its feeding preferences from birds to humans by 7-fold during late summer and early fall, coinciding with the dispersal of its preferred host (American robins, Turdus migratorius) and the rise in human WNV infections. We also show that feeding shifts in Cx. tarsalis amplify human WNV epidemics in Colorado and California and occur during periods of robin dispersal and migration. Our results provide a direct explanation for the timing and intensity of human WNV epidemics. Shifts in feeding from competent avian hosts early in an epidemic to incompetent humans after mosquito infection prevalences are high result in synergistic effects that greatly amplify the number of human infections of this and other pathogens. Our results underscore the dramatic effects of vector behavior in driving the transmission of zoonotic pathogens to humans.
url http://europepmc.org/articles/PMC1382011?pdf=render
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