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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6488619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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