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2012-2013流感监测年度中国大陆B型流感病毒抗原性及基因特性分析
引用本文:李希妍,成艳辉,谭敏菊,王钊,黄维娟,郭俊峰,隗合江,肖宁,蓝雨.2012-2013流感监测年度中国大陆B型流感病毒抗原性及基因特性分析[J].疾病监测,2014,29(1):14-20.
作者姓名:李希妍  成艳辉  谭敏菊  王钊  黄维娟  郭俊峰  隗合江  肖宁  蓝雨
作者单位:李希妍 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 成艳辉 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 谭敏菊 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 王钊 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 黄维娟 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 郭俊峰 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 隗合江 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 肖宁 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206); 蓝雨 (中国疾病预防控制中心病毒病预防控制所国家流感中心卫生部医学病毒和病毒病重点实验室,北京,102206);
基金项目:The,study,was,funded,by,the,National,Science,and,Technology,Key,Project(项目编号:2013ZX10004-101)国家科技重大专项课题(项目编号:2013ZX10004-101)
摘    要:目的了解2012-2013流感监测年度中国大陆地区B型流感的流行状况,分析B型流感病毒的抗原性和基因变异情况。方法选择2012-2013年我国分离的B型流感病毒,利用标准雪貂抗血清进行抗原性分析。利用Sanger测序法进行病毒基因测序,采用Neighbor-Joining方法进行种系进化分析,通过基因进化树比较国内流行株与疫苗株的差异。结果 2012-2013监测年度内,B型流感病毒占所有流感病毒的9.93%,其中以B型Victoria系流感病毒为主。B型Victoria系流感病毒的抗原性与上一年度WHO推荐的疫苗株B/Brisbane/60/2008(83.5%)以及我国代表株B/Chongqing-Yuzhong/1384/2010(94.7%)的抗原性类似;而B型Yamagata系流感病毒绝大多数为WHO疫苗株B/Wisconsin/01/2010(99.3%)、WHO疫苗种子株B/Hubei-Wujiagang/158/2009(98.0%)的类似株;基因特性分析显示有1株B-Victoria系病毒发生了HA与NA基因分支间的重配,有1株B-Yamagata系病毒B/Sichuan-Gaoxin/1110/2012的NA基因位于Victoria系病毒的NA进化分支,也表明发生了种系间的基因重配。结论 2012-2013流感监测年度我国B型流感病毒活动水平较低,主要以Victoria系为主,而WHO推荐的疫苗组分是B-Yamagata系病毒,可见部分B型流感流行株与疫苗株并不匹配。

关 键 词:B型流感病毒    抗原性    基因特性
收稿时间:2013-11-21

Antigenic and genetic characteristics of influenza B virus in the mainland of China, 2012 - 2013
LI Xi-yan,CHENG Yan-hui,TAN Min-ju,WANG Zhao,HUANG Wei-juan,GUO lun-feng,WEI He-jiang,XIAO Ning,LAN Yu,ZHAO Xiang,YANG Lei,WANG Da-yan,SHU Yue-long.Antigenic and genetic characteristics of influenza B virus in the mainland of China, 2012 - 2013[J].Disease Surveillance,2014,29(1):14-20.
Authors:LI Xi-yan  CHENG Yan-hui  TAN Min-ju  WANG Zhao  HUANG Wei-juan  GUO lun-feng  WEI He-jiang  XIAO Ning  LAN Yu  ZHAO Xiang  YANG Lei  WANG Da-yan  SHU Yue-long
Institution:. Key Laboratory for Medical Virology, Chinese National Influenza Center, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China
Abstract:Objective To understand the epidemiological characteristics of influenza B and the antigenic and genetic characteristics of influenza B virus in the mainland of China during 2012 - 2013. Methods The antigenic characteristics of influenza B virus was analyzed with reference ferret anti-sera. The nucleotide sequences of the influenza B viruses were determined by Sanger dideoxy sequencing. The phylogenetic trees were constructed by neighbor-jointing method, the genetic characteristics were determined and compared the circulating influenza B virus with current vaccine strains. Results During 2012 - 2013 influenza season influenza B virus accounted for 9.93% of total influenza viruses detected, the activity of B Victoria lineage virus were stronger than B Yamagata lineage virus. Most B Victoria lineage viruses had close antigenic relation with the vaccine strain B/Brisbane/6012008 (83.5% ) recommended by WHO in previous year and the representative circulating strain B/Chongqing- Yuzhong/1384/2010 (94.7%) in the mainland of China. The majority of B Yamagata lineage viruses had closely antigenic relation with WHO recommended vaccine strain B/Wisconsin/01/2010 ( 99. 3%) and WHO vaccine seed B/Hubei-Wujiagang/158/2009 ( 98. 0% ); phylogenetic analysis on B Victoria lineage viruses indicated that one strain had intra-clade reassortants between HA and NA gene. One of the B Yamagata lineage viruses, B/Sichuan-Gaoxin/1110/2012, was confirmed to be an intra-lineage reassortant with NA gene from B Victoria lineage. Conclusion The activity of B Victoria lineage virus was stronger than Yamagata lineage virus in the mainland of China during 2012 -2013 influenza season, but only Yamagata lineage virus was included in the WHO recommended trivalent influenza vaccine for this period, which could not provide protection to B Victoria lineage virus infection.
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