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Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus

West Nile virus (WNV) has become the most epidemiologically important mosquito-borne disease in the United States, causing ~50,000 cases since its introduction in 1999. Transmitted primarily by Culex species, WNV transmission requires the complex interplay between bird reservoirs and mosquito vector...

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Autores principales: Dunphy, Brendan M., Kovach, Kristofer B., Gehrke, Ella J., Field, Eleanor N., Rowley, Wayne A., Bartholomay, Lyric C., Smith, Ryan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488619/
https://www.ncbi.nlm.nih.gov/pubmed/31036953
http://dx.doi.org/10.1038/s41598-019-43246-y
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author Dunphy, Brendan M.
Kovach, Kristofer B.
Gehrke, Ella J.
Field, Eleanor N.
Rowley, Wayne A.
Bartholomay, Lyric C.
Smith, Ryan C.
author_facet Dunphy, Brendan M.
Kovach, Kristofer B.
Gehrke, Ella J.
Field, Eleanor N.
Rowley, Wayne A.
Bartholomay, Lyric C.
Smith, Ryan C.
author_sort Dunphy, Brendan M.
collection PubMed
description West Nile virus (WNV) has become the most epidemiologically important mosquito-borne disease in the United States, causing ~50,000 cases since its introduction in 1999. Transmitted primarily by Culex species, WNV transmission requires the complex interplay between bird reservoirs and mosquito vectors, with human cases the result of epizootic spillover. To better understand the intrinsic factors that drive these interactions, we have compiled infection data from sentinel chickens, mosquito vectors, and human cases in Iowa over a 15 year period (2002–2016) to better understand the spatial and temporal components that drive WNV transmission. Supplementing these findings with mosquito abundance, distribution, and host preferences data, we provide strong support that Culex tarsalis is the most important vector of human WNV infections in the region. Together, our analysis provides new insights into WNV infection patterns in multiple hosts and highlights the importance of long-term surveillance to understand the dynamics of mosquito-borne-disease transmission.
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spelling pubmed-64886192019-05-16 Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus Dunphy, Brendan M. Kovach, Kristofer B. Gehrke, Ella J. Field, Eleanor N. Rowley, Wayne A. Bartholomay, Lyric C. Smith, Ryan C. Sci Rep Article West Nile virus (WNV) has become the most epidemiologically important mosquito-borne disease in the United States, causing ~50,000 cases since its introduction in 1999. Transmitted primarily by Culex species, WNV transmission requires the complex interplay between bird reservoirs and mosquito vectors, with human cases the result of epizootic spillover. To better understand the intrinsic factors that drive these interactions, we have compiled infection data from sentinel chickens, mosquito vectors, and human cases in Iowa over a 15 year period (2002–2016) to better understand the spatial and temporal components that drive WNV transmission. Supplementing these findings with mosquito abundance, distribution, and host preferences data, we provide strong support that Culex tarsalis is the most important vector of human WNV infections in the region. Together, our analysis provides new insights into WNV infection patterns in multiple hosts and highlights the importance of long-term surveillance to understand the dynamics of mosquito-borne-disease transmission. Nature Publishing Group UK 2019-04-29 /pmc/articles/PMC6488619/ /pubmed/31036953 http://dx.doi.org/10.1038/s41598-019-43246-y Text en © The Author(s) 2019 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
Dunphy, Brendan M.
Kovach, Kristofer B.
Gehrke, Ella J.
Field, Eleanor N.
Rowley, Wayne A.
Bartholomay, Lyric C.
Smith, Ryan C.
Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
title Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
title_full Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
title_fullStr Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
title_full_unstemmed Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
title_short Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
title_sort long-term surveillance defines spatial and temporal patterns implicating culex tarsalis as the primary vector of west nile virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488619/
https://www.ncbi.nlm.nih.gov/pubmed/31036953
http://dx.doi.org/10.1038/s41598-019-43246-y
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