纪蕾, 吴晓芳, 陈莉萍, 徐德顺, 沈月华, 查赟峰, 朱晓娟. 浙江省湖州市柯萨奇病毒A组16型分离株VP1区序列测定及系统进化分析[J]. 疾病监测, 2014, 29(6): 441-444. DOI: 10.3784/j.issn.1003-9961.201.06.007
引用本文: 纪蕾, 吴晓芳, 陈莉萍, 徐德顺, 沈月华, 查赟峰, 朱晓娟. 浙江省湖州市柯萨奇病毒A组16型分离株VP1区序列测定及系统进化分析[J]. 疾病监测, 2014, 29(6): 441-444. DOI: 10.3784/j.issn.1003-9961.201.06.007
JI Lei, WU Xiao-fang, CHEN Li-ping, XU De-shun, SHEN Yue-hua, ZHA Yun-feng, ZHU Xiao-juan. Genetic characteristics of VP1 region of coxsakievirus A16 strains isolated in Huzhou, Zhejiang, 2011-2012[J]. Disease Surveillance, 2014, 29(6): 441-444. DOI: 10.3784/j.issn.1003-9961.201.06.007
Citation: JI Lei, WU Xiao-fang, CHEN Li-ping, XU De-shun, SHEN Yue-hua, ZHA Yun-feng, ZHU Xiao-juan. Genetic characteristics of VP1 region of coxsakievirus A16 strains isolated in Huzhou, Zhejiang, 2011-2012[J]. Disease Surveillance, 2014, 29(6): 441-444. DOI: 10.3784/j.issn.1003-9961.201.06.007

浙江省湖州市柯萨奇病毒A组16型分离株VP1区序列测定及系统进化分析

Genetic characteristics of VP1 region of coxsakievirus A16 strains isolated in Huzhou, Zhejiang, 2011-2012

  • 摘要: 目的 了解浙江省湖州市引起手足口病(HFMD)的柯萨奇病毒A组16型(Cox A16)分离株的VP1区基因特征。 方法 采用荧光定量反转录聚合酶链反应方法,对2011-2012年湖州市538份HFMD临床标本进行肠道病毒核酸检测;采用RD、Hep2细胞对Cox A16核酸阳性的标本进行病毒分离。选取17株具有代表性的Cox A16分离株进行VP1区的序列测定和分析。 结果 2011-2012年湖州市HFMD的主要病原为Cox A16和肠道病毒71型(EV71);湖州地区Cox A16分离株VP1区的核苷酸和氨基酸序列同源性分别为89.5%~100%和99.3%~100%。与Cox A16的B1基因亚型代表株核苷酸同源性最高,在系统进化树上与B1亚型代表株相聚在一起,并且同时存在B1a 和B1b 两个进化分支。 结论 湖州市的Cox A16分离株与国内其他地区类似,同属于B1基因亚型,并且有B1a 和B1b 两个进化分支共同进化和循环。

     

    Abstract: Objective To understand the genetic characteristics of coxsakievirus A16 (Cox A16) strains isolated in Huzhou, Zhejiang province during 2011-2012. Methods Viral nucleic acids were detected from 538 clinical specimens collected from HFMD cases in Huzhou during 2011-2012 with real-time PCR. Cox A16 RNA positive samples were used for subsequent cell culture. Sequencing and analyses of VP1 encoding gene were performed for 17 Cox A16 isolates. Results The results showed that Cox A16 and EV71 were the major pathogens of HFMD epidemic in Huzhou during 2011-2012. Sequence analysis for VP1 gene of the Cox A16 strains indicated that the viruses' nucleotides and amino acids sequences shared 89.5%-100% and 99.3%-100% homology respectively. The nucleotides sequence of the 17 strains showed a high level of identity to the B1 genotype reference strains. Phylogenetic analysis of the VP1 region showed that all the Cox A16 isolates in Huzhou were clustered within the B1a and B1b evolution branch of B1 genotype. Conclusion Like other Cox A16 strains isolated in China,the major circulating strain of Cox A16 in Huzhou during 2011-2012 belonged to B1 genotype, which could be further classified into Bla and B1b branches.

     

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