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Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method

BACKGROUND: Coxsackievirus A16 (CV-A16), a major etiopathologic cause of pediatric hand, foot, and mouth disease (HFMD) worldwide, has been reported to have caused several fatalities. Revealing the evolutionary and epidemiologic dynamics of CV-A16 across time and space is central to understanding it...

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Autores principales: Zhao, Guolian, Zhang, Xun, Wang, Changmin, Wang, Guoqing, Li, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963925/
https://www.ncbi.nlm.nih.gov/pubmed/27464503
http://dx.doi.org/10.1186/s12985-016-0578-3
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author Zhao, Guolian
Zhang, Xun
Wang, Changmin
Wang, Guoqing
Li, Fan
author_facet Zhao, Guolian
Zhang, Xun
Wang, Changmin
Wang, Guoqing
Li, Fan
author_sort Zhao, Guolian
collection PubMed
description BACKGROUND: Coxsackievirus A16 (CV-A16), a major etiopathologic cause of pediatric hand, foot, and mouth disease (HFMD) worldwide, has been reported to have caused several fatalities. Revealing the evolutionary and epidemiologic dynamics of CV-A16 across time and space is central to understanding its outbreak potential. METHODS: In this study, we isolated six CV-A16 strains in China’s Jilin province and construct a maximum clade credibility (MCC) tree for CV-A16 VP1 gene by the Bayesian Markov Chain Monte Carlo method using 708 strains from GenBank with epidemiological information. The evolution characteristics of CV-A16 VP1 gene was also analysed dynamicly through Bayesian skyline plot. RESULTS: All CV-A16 strains identified could be classified into five major genogroups, denoted by GI–GV. GIV and GV have co-circulated in China since 2007, and the CV-A16 epidemic strain isolated in the Jilin province, China, can be classified as GIV-3. The CV-A16 genogroups circulating recently in China have the same ancestor since 2007. The genetic diversity of the CV-A16 VP1 gene shows a continuous increase since the mid-1990s, with sharp increases in genetic diversity in 1997 and 2007 and reached peak in 2007. Very low genetic diversity existed after 2010. The CV-A16 VP1 gene evolutionary rate was 6.656E-3 substitutions per site per year. CONCLUSIONS: We predicted the dynamic phylogenetic trends, which indicate outbreak trends of CV-A16, and provide theoretical foundations for clinical prevention and treatment of HFMD which caused by a CV-A16. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-016-0578-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-49639252016-07-29 Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method Zhao, Guolian Zhang, Xun Wang, Changmin Wang, Guoqing Li, Fan Virol J Research BACKGROUND: Coxsackievirus A16 (CV-A16), a major etiopathologic cause of pediatric hand, foot, and mouth disease (HFMD) worldwide, has been reported to have caused several fatalities. Revealing the evolutionary and epidemiologic dynamics of CV-A16 across time and space is central to understanding its outbreak potential. METHODS: In this study, we isolated six CV-A16 strains in China’s Jilin province and construct a maximum clade credibility (MCC) tree for CV-A16 VP1 gene by the Bayesian Markov Chain Monte Carlo method using 708 strains from GenBank with epidemiological information. The evolution characteristics of CV-A16 VP1 gene was also analysed dynamicly through Bayesian skyline plot. RESULTS: All CV-A16 strains identified could be classified into five major genogroups, denoted by GI–GV. GIV and GV have co-circulated in China since 2007, and the CV-A16 epidemic strain isolated in the Jilin province, China, can be classified as GIV-3. The CV-A16 genogroups circulating recently in China have the same ancestor since 2007. The genetic diversity of the CV-A16 VP1 gene shows a continuous increase since the mid-1990s, with sharp increases in genetic diversity in 1997 and 2007 and reached peak in 2007. Very low genetic diversity existed after 2010. The CV-A16 VP1 gene evolutionary rate was 6.656E-3 substitutions per site per year. CONCLUSIONS: We predicted the dynamic phylogenetic trends, which indicate outbreak trends of CV-A16, and provide theoretical foundations for clinical prevention and treatment of HFMD which caused by a CV-A16. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-016-0578-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-28 /pmc/articles/PMC4963925/ /pubmed/27464503 http://dx.doi.org/10.1186/s12985-016-0578-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhao, Guolian
Zhang, Xun
Wang, Changmin
Wang, Guoqing
Li, Fan
Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method
title Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method
title_full Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method
title_fullStr Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method
title_full_unstemmed Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method
title_short Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method
title_sort characterization of vp1 sequence of coxsackievirus a16 isolates by bayesian evolutionary method
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963925/
https://www.ncbi.nlm.nih.gov/pubmed/27464503
http://dx.doi.org/10.1186/s12985-016-0578-3
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