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The imperative to develop a human vaccine for the Hendra virus in Australia

The Hendra virus (HeV) poses a significant challenge to public health in Australia. Expanding migratory patterns observed among bats and the mutation of the virus to seek and successfully infect new hosts is a significant departure from the generalized epidemiological trend. The recent discovery of...

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Detalles Bibliográficos
Autores principales: Zahoor, Bilal A., Mudie, Lucy I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627939/
https://www.ncbi.nlm.nih.gov/pubmed/26519254
http://dx.doi.org/10.3402/iee.v5.29619
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author Zahoor, Bilal A.
Mudie, Lucy I.
author_facet Zahoor, Bilal A.
Mudie, Lucy I.
author_sort Zahoor, Bilal A.
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description The Hendra virus (HeV) poses a significant challenge to public health in Australia. Expanding migratory patterns observed among bats and the mutation of the virus to seek and successfully infect new hosts is a significant departure from the generalized epidemiological trend. The recent discovery of equine-related infections and deaths in addition to a canine infection demonstrates the inadequacy of the current equine vaccine developed in 2012. Traditional models for controlling the spread of the vector are futile given the rapid pace at which bats' habitats are eroded. Recent ongoing zoonotic epidemics, for example, Ebola and Middle East respiratory syndrome coronavirus, demonstrate that human-to-human transmission is a distinct reality rather than an obscure possibility. The development of a human HeV vaccine is essential for the biosecurity of Australia, as part of a multipronged strategy to control HeV in Australia.
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spelling pubmed-46279392015-11-24 The imperative to develop a human vaccine for the Hendra virus in Australia Zahoor, Bilal A. Mudie, Lucy I. Infect Ecol Epidemiol Commentary The Hendra virus (HeV) poses a significant challenge to public health in Australia. Expanding migratory patterns observed among bats and the mutation of the virus to seek and successfully infect new hosts is a significant departure from the generalized epidemiological trend. The recent discovery of equine-related infections and deaths in addition to a canine infection demonstrates the inadequacy of the current equine vaccine developed in 2012. Traditional models for controlling the spread of the vector are futile given the rapid pace at which bats' habitats are eroded. Recent ongoing zoonotic epidemics, for example, Ebola and Middle East respiratory syndrome coronavirus, demonstrate that human-to-human transmission is a distinct reality rather than an obscure possibility. The development of a human HeV vaccine is essential for the biosecurity of Australia, as part of a multipronged strategy to control HeV in Australia. Co-Action Publishing 2015-10-29 /pmc/articles/PMC4627939/ /pubmed/26519254 http://dx.doi.org/10.3402/iee.v5.29619 Text en © 2015 Bilal A. Zahoor and Lucy I. Mudie http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Zahoor, Bilal A.
Mudie, Lucy I.
The imperative to develop a human vaccine for the Hendra virus in Australia
title The imperative to develop a human vaccine for the Hendra virus in Australia
title_full The imperative to develop a human vaccine for the Hendra virus in Australia
title_fullStr The imperative to develop a human vaccine for the Hendra virus in Australia
title_full_unstemmed The imperative to develop a human vaccine for the Hendra virus in Australia
title_short The imperative to develop a human vaccine for the Hendra virus in Australia
title_sort imperative to develop a human vaccine for the hendra virus in australia
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627939/
https://www.ncbi.nlm.nih.gov/pubmed/26519254
http://dx.doi.org/10.3402/iee.v5.29619
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