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Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation

Coxsackievirus A16 (CA16) is one of the major pathogens associated with human hand, foot, and mouth disease (HFMD) in the Asia-pacific region. Although CA16 infections are generally mild, severe neurological manifestations or even death has been reported. Studies on CA16 pathogenesis and vaccine dev...

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Autores principales: Sun, Yi-Sheng, Li, Ya-jing, Xia, Yong, Xu, Fang, Wang, Wei-wei, Yang, Zhang-Nv, Lu, Hang-Jing, Chen, Zhi-Ping, Miao, Zi-Ping, Liang, Wei-Feng, Xu, Zhi-Yao, Dong, Hong-Jun, Qiu, Dan-Hong, Zhu, Zhi-Yong, van der Veen, Stijn, Qian, Jie, Zhou, Bin, Yao, Ping-Ping, Zhu, Han-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035925/
https://www.ncbi.nlm.nih.gov/pubmed/27667023
http://dx.doi.org/10.1038/srep34299
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author Sun, Yi-Sheng
Li, Ya-jing
Xia, Yong
Xu, Fang
Wang, Wei-wei
Yang, Zhang-Nv
Lu, Hang-Jing
Chen, Zhi-Ping
Miao, Zi-Ping
Liang, Wei-Feng
Xu, Zhi-Yao
Dong, Hong-Jun
Qiu, Dan-Hong
Zhu, Zhi-Yong
van der Veen, Stijn
Qian, Jie
Zhou, Bin
Yao, Ping-Ping
Zhu, Han-Ping
author_facet Sun, Yi-Sheng
Li, Ya-jing
Xia, Yong
Xu, Fang
Wang, Wei-wei
Yang, Zhang-Nv
Lu, Hang-Jing
Chen, Zhi-Ping
Miao, Zi-Ping
Liang, Wei-Feng
Xu, Zhi-Yao
Dong, Hong-Jun
Qiu, Dan-Hong
Zhu, Zhi-Yong
van der Veen, Stijn
Qian, Jie
Zhou, Bin
Yao, Ping-Ping
Zhu, Han-Ping
author_sort Sun, Yi-Sheng
collection PubMed
description Coxsackievirus A16 (CA16) is one of the major pathogens associated with human hand, foot, and mouth disease (HFMD) in the Asia-pacific region. Although CA16 infections are generally mild, severe neurological manifestations or even death has been reported. Studies on CA16 pathogenesis and vaccine development are severely hampered because the small animal models that are currently available show major limitations. In this study, gerbils (Meriones unguiculatus) were investigated for their suitability as an animal model to study CA16 pathogenesis and vaccine development. Our results showed that gerbils up to the age of 21 days were fully susceptible to CA16 and all died within five days post-infection. CA16 showed a tropism towards the skeletal muscle, spinal cord and brainstem of gerbils, and severe lesions, including necrosis, were observed. In addition, an inactivated CA16 whole-virus vaccine administrated to gerbils was able to provide full protection to the gerbils against lethal doses of CA16 strains. These results demonstrate that gerbils are a suitable animal model to study CA16 infection and vaccine development.
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spelling pubmed-50359252016-09-30 Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation Sun, Yi-Sheng Li, Ya-jing Xia, Yong Xu, Fang Wang, Wei-wei Yang, Zhang-Nv Lu, Hang-Jing Chen, Zhi-Ping Miao, Zi-Ping Liang, Wei-Feng Xu, Zhi-Yao Dong, Hong-Jun Qiu, Dan-Hong Zhu, Zhi-Yong van der Veen, Stijn Qian, Jie Zhou, Bin Yao, Ping-Ping Zhu, Han-Ping Sci Rep Article Coxsackievirus A16 (CA16) is one of the major pathogens associated with human hand, foot, and mouth disease (HFMD) in the Asia-pacific region. Although CA16 infections are generally mild, severe neurological manifestations or even death has been reported. Studies on CA16 pathogenesis and vaccine development are severely hampered because the small animal models that are currently available show major limitations. In this study, gerbils (Meriones unguiculatus) were investigated for their suitability as an animal model to study CA16 pathogenesis and vaccine development. Our results showed that gerbils up to the age of 21 days were fully susceptible to CA16 and all died within five days post-infection. CA16 showed a tropism towards the skeletal muscle, spinal cord and brainstem of gerbils, and severe lesions, including necrosis, were observed. In addition, an inactivated CA16 whole-virus vaccine administrated to gerbils was able to provide full protection to the gerbils against lethal doses of CA16 strains. These results demonstrate that gerbils are a suitable animal model to study CA16 infection and vaccine development. Nature Publishing Group 2016-09-26 /pmc/articles/PMC5035925/ /pubmed/27667023 http://dx.doi.org/10.1038/srep34299 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Sun, Yi-Sheng
Li, Ya-jing
Xia, Yong
Xu, Fang
Wang, Wei-wei
Yang, Zhang-Nv
Lu, Hang-Jing
Chen, Zhi-Ping
Miao, Zi-Ping
Liang, Wei-Feng
Xu, Zhi-Yao
Dong, Hong-Jun
Qiu, Dan-Hong
Zhu, Zhi-Yong
van der Veen, Stijn
Qian, Jie
Zhou, Bin
Yao, Ping-Ping
Zhu, Han-Ping
Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
title Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
title_full Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
title_fullStr Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
title_full_unstemmed Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
title_short Coxsackievirus A16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
title_sort coxsackievirus a16 induced neurological disorders in young gerbils which could serve as a new animal model for vaccine evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035925/
https://www.ncbi.nlm.nih.gov/pubmed/27667023
http://dx.doi.org/10.1038/srep34299
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