Molecular analysis of Coxsackievirus A24 variant isolates from three outbreaks of acute hemorrhagic conjunctivitis in 1988, 1994 and 2007 in Beijing, China

被引:0
|
作者
Junhan Li [1 ,2 ]
Fang Huang [3 ]
Yong Zhang [1 ,4 ]
Tianjiao Ji [1 ]
Shuangli Zhu [1 ]
Dongyan Wang [1 ]
Zhenzhi Han [1 ]
Jinbo Xiao [1 ]
Fenfen Si [1 ]
Wenbo Xu [1 ,4 ]
Dongmei Yan [1 ]
机构
[1] National Polio Laboratory, WHO WPRO Regional Polio Reference Laboratory, National Health Commission Key Laboratory for Biosecurity, National Health Commission Key Laboratory for Medical Virology, National Institute for Viral Disease Control and Prevention,
[2] Nanguan District Center for Disease Control and Prevention
[3] Beijing Center for Disease Control and Prevention
[4] Center for Biosafety Mega-Science, Chinese Academy of Sciences
基金
北京市自然科学基金;
关键词
D O I
暂无
中图分类号
R373.23 [];
学科分类号
100103 ; 100705 ;
摘要
Coxsackievirus A24 variant(CVA24v) is a major pathogen that causes continued outbreaks and pandemics of acute hemorrhagic conjunctivitis(AHC). In China, the first confirmed outbreak of CVA24v-related AHC occurred in Beijing in 1988, followed by another two significant outbreaks respectively in 1994 and 2007, which coincides with the three-stage dynamic distribution of AHC in the world after 1970s. To illustrate the genetic characteristics of CVA24v in different periods, a total of 23 strains were isolated from those three outbreaks and the whole genome of those isolations were sequenced and analyzed. Compared with the prototype strain, the 23 strains shared four nucleotide deletions in the 5’UTR except the 0744 strain isolated in 2007. And at the 98th site, one nucleotide insertion was found in all the strains collected from 2007. From 1994 to 2007, amino acid polarity in the VP1 region at the 25th and the 32nd site were changed. Both the 3C and VP1 phylogenetic tree indicated that isolates from 1988 and 1994 belonged to Genotype III(GIII), and 2007 strains to Genotype IV(GIV). According to the Bayesian analysis based on complete genome sequence, the most recent common ancestors for the isolates in1988, 1994 and 2007 were respectively estimated around October 1987, February 1993 and December 2004. The evolutionary rate of the CVA24v was estimated to be 7.45 × 10substitutions/site/year. Our study indicated that the early epidemic of CVA24v in Chinese mainland was the GIII. Point mutations and amino acid changes in different genotypes of CVA24v may generate intensity differences of the AHC outbreak. CVA24v has been evolving constantly with a relatively rapid rate.
引用
收藏
页码:168 / 176
页数:9
相关论文
共 38 条
  • [1] Molecular analysis of Coxsackievirus A24 variant isolates from three outbreaks of acute hemorrhagic conjunctivitis in 1988, 1994 and 2007 in Beijing, China
    Li, Junhan
    Huang, Fang
    Zhang, Yong
    Ji, Tianjiao
    Zhu, Shuangli
    Wang, Dongyan
    Han, Zhenzhi
    Xiao, Jinbo
    Si, Fenfen
    Xu, Wenbo
    Yan, Dongmei
    VIROLOGICA SINICA, 2022, 37 (02) : 168 - 176
  • [2] Molecular analysis of Coxsackievirus A24 variant isolates from three outbreaks of acute hemorrhagic conjunctivitis in 1988, 1994 and 2007 in Beijing, China
    Junhan Li
    Fang Huang
    Yong Zhang
    Tianjiao Ji
    Shuangli Zhu
    Dongyan Wang
    Zhenzhi Han
    Jinbo Xiao
    Fenfen Si
    Wenbo Xu
    Dongmei Yan
    Virologica Sinica, 2022, 37 (02) : 168 - 176
  • [3] Multiple outbreaks of acute hemorrhagic conjunctivitis due to a variant of coxsackievirus A24: Guangdong, China, 2007
    Wu, De
    Ke, Chang-Wen
    Mo, Yan-Ling
    Sun, Li-Mei
    Li, Hui
    Chen, Qiu-Xia
    Zou, Li-Rong
    Fang, Ling
    Huang, Ping
    Zhen, Huan-ying
    JOURNAL OF MEDICAL VIROLOGY, 2008, 80 (10) : 1762 - 1768
  • [4] Phylogenetic and molecular characterization of coxsackievirus A24 variant isolates from a 2010 acute hemorrhagic conjunctivitis outbreak in Guangdong, China
    De, Wu
    Zheng Huanying
    Hui, Li
    Corina, Monagin
    Xue, Guo
    Leng, Liu
    Zeng Hanri
    Ling, Fang
    Mo Yanling
    Zhou Huiqiong
    Huan, Zhang
    Jing, Kou
    Long Caiyun
    Yoshida, Hiromu
    Ke Changwen
    VIROLOGY JOURNAL, 2012, 9
  • [5] Phylogenetic and molecular characterization of coxsackievirus A24 variant isolates from a 2010 acute hemorrhagic conjunctivitis outbreak in Guangdong, China
    Wu De
    Zheng Huanying
    Li Hui
    Monagin Corina
    Guo Xue
    Liu Leng
    Zeng Hanri
    Fang Ling
    Mo Yanling
    Zhou Huiqiong
    Zhang Huan
    Kou Jing
    Long Caiyun
    Hiromu Yoshida
    Ke Changwen
    Virology Journal, 9
  • [6] Genetic Characteristics of the Coxsackievirus A24 Variant Causing Outbreaks of Acute Hemorrhagic Conjunctivitis in Jiangsu, China, 2010
    Wu, Bin
    Qi, Xian
    Xu, Ke
    Ji, Hong
    Zhu, Yefei
    Tang, Fenyang
    Zhou, Minghao
    PLOS ONE, 2014, 9 (01):
  • [7] Two outbreaks of acute hemorrhagic conjunctivitis in Africa due to genotype III coxsackievirus variant A24
    N. Lévêque
    I. Lahlou Amine
    G. Cartet
    A. B. Hammani
    Y. C. Khazraji
    B. Lina
    J. J. Muyembe
    H. Norder
    J. J. Chomel
    European Journal of Clinical Microbiology & Infectious Diseases, 2007, 26 : 445 - 445
  • [8] Two outbreaks of acute hemorrhagic conjunctivitis in Africa due to genotype III coxsackievirus A24 variant
    N. Lévêque
    I. L. Amine
    G. Cartet
    A. B. Hammani
    Y. C. Khazraji
    B. Lina
    J. J. Muyembe
    H. Norder
    J. J. Chomel
    European Journal of Clinical Microbiology & Infectious Diseases, 2007, 26
  • [9] Two outbreaks of acute hemorrhagic conjunctivitis in Africa due to genotype III coxsackievirus A24 variant
    Leveque, N.
    Amine, I. L.
    Cartet, G.
    Hammani, A. B.
    Khazraji, Y. C.
    Lina, B.
    Muyembe, J. J.
    Norder, H.
    Chomel, J. J.
    EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2007, 26 (03) : 199 - 202
  • [10] Rapid identification of the coxsackievirus A24 variant by molecular serotyping in an outbreak of acute hemorrhagic conjunctivitis
    Park, SW
    Lee, CS
    Jang, HC
    Kim, EC
    Oh, MD
    Choe, KW
    JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (03) : 1069 - 1071