期刊文献+

2016-2018年长沙市人群及活禽市场环境H5N6亚型禽流感病毒监测分析 被引量:4

Analysis of surveillance results for H5N6 subtype avian influenza virus from population and live poultry market environment in Changsha city,2016-2018
原文传递
导出
摘要 目的开展2016-2018年长沙市人群感染和活禽市场(live poultry markets,LPMs)环境污染H5N6亚型禽流感病毒(avian influenza virus,AIV)监测,为防控人感染H5N6亚型AIV提供实验室数据。方法采集2016-2018年长沙市流感样病例和不明原因肺炎病例咽拭子6909份及LPMs环境样品1719份,利用实时RT-PCR进行A型、H5、H7、H9和N6亚型AIV核酸扩增,并对82份AIV核酸阳性样品进行高通量核苷酸测序,然后对测序结果进行BLAST比对和氨基酸(amino acids,aa)关键位点分析。结果从6909份病例的咽拭子样品中检出H5N6亚型AIV核酸阳性1份,从1719份LPMs环境样品中检出A型AIV核酸阳性927份(53.93%),H5N6亚型AIV核酸阳性193份(11.23%)。高通量核苷酸测序获得14株H5N6亚型AIV的基因组序列,aa关键位点分析显示病毒血凝素(hemagglutinin,HA)蛋白连接肽第338~347位出现6个碱性aa,对禽表现为高致病性的分子特征,受体结合位点(receptor binding site,RBS)第238~240位aa(对应H3型流感病毒第226~228位编码aa)为QSG或QRG,受体特征为禽源。神经氨酸酶(neuraminidase,NA)蛋白第290位耐药基因位点aa未出现R290K突变现象,对NA抑制剂(达菲/磷酸奥司他韦)敏感;病毒PB2蛋白发生E627K和D701N(I)突变,表明病毒致病力强。结论长沙市人群感染H5N6亚型AIV为偶发,LPMs环境H5N6亚型AIV污染较重,需要进一步加强LPMs环境AIV监测。 Objective To carry out the monitoring of H5N6 subtype avian influenza virus(AIV)in the population infection and live poultry markets(LPMs)environmental pollution in Changsha city from 2016 to 2018.Laboratory data were provided to prevent human infection with H5N6 subtype AIV.Methods A total of 6909 throat swab specimens from the population and 1719 environmental specimens from LPMs were collected in Changsha city from 2016 to 2018.The real-time RT-PCR method was used for the detection of influenza virus in type A,H5,H7,H9 and N6 subtypes.Eighty-two AIV nucleic acid-positive specimens were subjected to high-throughput nucleotide sequencing,and then BLAST similarity and amino acid(aa)key site analyses were performed on the sequencing results.Results One H5N6 subtype AIV nucleic acid was detected from 6909 population throat swab specimens,927(53.93%)positive specimens of A-type AIV nucleic acids and 193(11.23%)positive specimens of both H5 and N6 subtypes were detected from 1719 LPMs environmental specimens.Fourteen genomic sequences of H5N6 subtype AIV were obtained with high-throughput nucleotide sequencing,and aa key site analyses showed that there were 6 basic aa in 338-347 aa of viral HA protein-linked peptide,which was highly pathogenic to birds.Receptor binding site(RBS)238-240 aa(corresponding to H3 type influenza virus 226-228 aa)is QSG or QRG,and the receptor is characterized by avian origin.The 290th resistance gene locus of NA protein did not show R290K mutation,and was sensitive to NA inhibitor(Duffy/osoterosine phosphate).The E627K and D701N(I)mutations in the viral PB2 protein indicate that the virus is pathogenic.Conclusions Human infected with H5N6 subtype AIV in Changsha city is sporadic,and the H5N6 subtype AIV of LPMs is seriously polluted.It is necessary to further strengthen the AIV surveillance of LPMs.
作者 张如胜 陈静芳 黄政 姚栋 叶文 刘晓蕾 李灵之 欧新华 孙边成 Zhang Rusheng;Chen Jingfang;Huang Zheng;Yao Dong;Ye Wen;Liu Xiaolei;Li Lingzhi;Ou Xinhua;Sun Biancheng(Changsha Center for Disease Control and Prevention,Changsha 410007,China)
出处 《中华实验和临床病毒学杂志》 CAS CSCD 2021年第1期96-100,共5页 Chinese Journal of Experimental and Clinical Virology
基金 湖南省自然科学基金(2018JJ6084)。
关键词 流感样病例 活禽市场 禽流感病毒 H5N6亚型 基因 Influenza-like cases Live poultry market Avian influenza virus H5N6 subtype Gene
  • 相关文献

参考文献7

二级参考文献37

  • 1舒跃龙,蓝雨,温乐英,赵新生,张烨,董婕,段淑敏,聂凯,张晓光,王大燕,姚丽红,郭元吉.我国分离人H5N1禽流感病毒血凝素基因特性的研究[J].中华实验和临床病毒学杂志,2006,20(2):8-10. 被引量:6
  • 2Li C, Hatta M, Watanabe S, et al. Compatibility among polymerase subunit proteins is a restricting factor in reassortment between equine H7N7 and human H3N2 influenza viruses. J Virol, 2008, 82:11880- 11888.
  • 3Holland J, Spindler K, Horodyski F, et al. Rapid evolution of RNA genomes. Science, 1982, 215:1577-1585.
  • 4Yang H, Qiao C, Tang X, et al. Human infection from avian-like in- fluenza A (H1N1) viruses in pigs, China. Emerg Infect Dis, 2012, 18: 1144-1146.
  • 5Hoffmann E, Stech J, Guan Y, et al. Universal primer set for the full-length amplification of all influenza A viruses. Arch Virol, 2001, 146:2275-2289.
  • 6Senne D A, Panigrahy B, Kawaoka Y, et al. Survey of the hemagglu- tinin (HA) cleavage site sequence of H5 and H7 avian influenza vi- ruses: Amino acid sequence at the HA cleavage site as a marker of pathogenicity potential. Avian Dis, 1996, 40:425-437.
  • 7Subbarao K, Chen H, Swayne D, et al. Evaluation of a genetically modified reassortant H5N1 influenza a virus vaccine candidate gen- erated by plasmid-based reverse genetics. Virology, 2003, 305: 192- 200.
  • 8Zhang Y, Zhang Q, Gao Y, et al. Key molecular factors in hemagglu- tinin and PB2 contribute to efficient transmission of the 2009 H1N1 pandemic influenza virus. J Virol, 2012, 86:9666-9674.
  • 9Chen Z, Zhou H, Kim L, et al. The receptor binding specificity of the live attenuated influenza H2 and H6 vaccine viruses contributes to vaccine immunogenicity and protection in ferrets. J Virol, 2012, 86: 2780-2786.
  • 10Naeve C W, Hinshaw V S, Webster R G. Mutations in the hemagglu- tinin receptor-binding site can change the biological properties of an influenza virus. J Virol, 1984, 51:567-569.

共引文献164

同被引文献27

引证文献4

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部