Genomic Epidemiology and Transmission Dynamics of Global Coxsackievirus B4
Author:
Xiao Jinbo1, Wang Jianxing2, Lu Huanhuan1, Song Yang1ORCID, Sun Dapeng2, Han Zhenzhi3ORCID, Li Jichen1, Yang Qian1, Yan Dongmei1, Zhu Shuangli1, Pei Yaowen2, Wang Xianjun2, Xu Wenbo14, Zhang Yong14ORCID
Affiliation:
1. WHO WPRO Regional Polio Reference Laboratory, National Laboratory for Poliomyelitis and National Health Commission Key Laboratory of Biosafety, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China 2. Shandong Center for Disease Control and Prevention, Jinan 250014, China 3. Laboratory of Virology, Beijing Key Laboratory of Etiology of Viral Diseases in Children, Capital Institute of Pediatrics, Beijing 102206, China 4. Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan 430071, China
Abstract
The aim of this study was to determine the global genetic diversity and transmission dynamics of coxsackievirus B4 (CVB4) and to propose future directions for disease surveillance. Next-generation sequencing was performed to obtain the complete genome sequence of CVB4, and the genetic diversity and transmission dynamics of CVB4 worldwide were analyzed using bioinformatics methods such as phylogenetic analysis, evolutionary dynamics, and phylogeographic analysis. Forty complete genomes of CVB4 were identified from asymptomatic infected individuals and hand, foot, and mouth disease (HFMD) patients. Frequent recombination between CVB4 and EV-B multiple serotypes in the 3Dpol region was found and formed 12 recombinant patterns (A-L). Among these, the CVB4 isolated from asymptomatic infected persons and HFMD patients belonged to lineages H and I, respectively. Transmission dynamics analysis based on the VP1 region revealed that CVB4 epidemics in countries outside China were dominated by the D genotype, whereas the E genotype was dominant in China, and both genotypes evolved at a rate of > 6.50 × 10−3 substitutions/site/year. CVB4 spreads through the population unseen, with the risk of disease outbreaks persisting as susceptible individuals accumulate. Our findings add to publicly available CVB4 genomic sequence data and deepen our understanding of CVB4 molecular epidemiology.
Funder
National Key Research and Development Program of China Natural Science Foundation of Beijing
Subject
Virology,Infectious Diseases
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