杨卫红, 冯云, 章域震, 潘虹, 张云智, 韩茜, 周济华, 袁庆虹, 张海林. 2012-2015年云南省狂犬病病毒糖蛋白基因进化特征分析[J]. 疾病监测, 2018, 33(4): 300-305. DOI: 10.3784/j.issn.1003-9961.2018.04.010
引用本文: 杨卫红, 冯云, 章域震, 潘虹, 张云智, 韩茜, 周济华, 袁庆虹, 张海林. 2012-2015年云南省狂犬病病毒糖蛋白基因进化特征分析[J]. 疾病监测, 2018, 33(4): 300-305. DOI: 10.3784/j.issn.1003-9961.2018.04.010
Yang Weihong, Feng Yun, Zhang Yuzhen, Pan Hong, Zhang Yunzhi, Han Xi, Zhou Jihua, Yuan Qinghong, Zhang Hailin. Phylogenetic analysis on glycoprotein genome of rabies viruses in Yunnan,2012-2015[J]. Disease Surveillance, 2018, 33(4): 300-305. DOI: 10.3784/j.issn.1003-9961.2018.04.010
Citation: Yang Weihong, Feng Yun, Zhang Yuzhen, Pan Hong, Zhang Yunzhi, Han Xi, Zhou Jihua, Yuan Qinghong, Zhang Hailin. Phylogenetic analysis on glycoprotein genome of rabies viruses in Yunnan,2012-2015[J]. Disease Surveillance, 2018, 33(4): 300-305. DOI: 10.3784/j.issn.1003-9961.2018.04.010

2012-2015年云南省狂犬病病毒糖蛋白基因进化特征分析

Phylogenetic analysis on glycoprotein genome of rabies viruses in Yunnan,2012-2015

  • 摘要: 目的 了解云南省2012-2015年35株狂犬病病毒(RABV)糖蛋白(G)基因的进化特征及流行病学特点。方法 在云南省狂犬病流行区采集可疑犬脑组织以及狂犬病患者脑组织和唾液标本,用直接免疫荧光法进行病毒抗原检测,阳性标本提取病毒核酸,通过反转录聚合酶链式反应(RT-PCR)扩增RABV的G基因序列,用MEGA 5.0软件邻接法(NJ)进行系统进化树分析。结果 经RT-PCR和序列测定获得2012-2015年云南省35株RABV的G基因序列,并与2006-2011年获得的云南省11株RABV及邻省和东南亚地区的15株RABV的G基因序列进行系统进化分析。结果表明,云南省46株RABV中,除2006年的Tc06株属于China-Ⅵ进化群外,其他45株均属于China-Ⅰ进化群。云南省China-Ⅰ进化群流行株在2006-2015年间每年均有分布,其中,2006-2011年10株,2012-2015年35株,分布于云南省10个州(市)并与来自四川、贵州和湖南省的China-Ⅰ进化群病毒株的进化关系最为接近。China-Ⅵ(Tc06)则与缅甸、老挝和越南的东南亚进化群病毒株亲缘关系最近。结论 2012-2015年,RABV China-Ⅰ进化群在云南省狂犬病流行区广泛分布,属云南省主要进化群并具较强的传播速率,期间云南省未再发现China-Ⅱ、China-Ⅲ和China-Ⅵ等进化群病毒株的流行。

     

    Abstract: Objective To understand the molecular evolution characteristics of the glycoprotein (G) genes and epidemiological characteristics of 35 rabies virus strains isolated in Yunnan province from 2012 to 2015. Methods The brain tissue samples from sick dogs,suspected sick dogs in areas with high incidence of rabies and human brain tissue and saliva samples of rabies patients were collected in Yunnan to detect the viral antigen by using direct immunofluorescence assay(DFA). The viral RNA from positive samples was extracted. Coding region of G gene was amplified with reverse transcription polymerase chain reaction(RT-PCR)and sequenced. The phylogenetic tree was constructed by Neighbor-Joining methods of MEGA 5.0 software. Results The sequences of G genes of 35 rabies virus strains in Yunnan during this period were obtained. With the sequences of G genes of 11 rabies virus strains from Yunnan during 2006-2011 and 15 rabies virus strains from adjacent provinces and Southeast Asia countries,the phylogenetic analysis was performed. Forty-six rabies virus strains isolated in Yunnan belonged to two clades:China-Ⅰ(45 strains)and China-Ⅵ(1 strains). Clade China-Ⅰ virus circulated from 2006 to 2015. In this clade,10 strains isolated during 2006-2011 and 35 strains isolated during 2012-2015 were from 10 prefectural areas of Yunnan. The strains of clade China-Ⅰ were closely related to the strains from adjacent Sichuan,Guizhou and Hunan provinces. Clade China-Ⅵ virus was detected only in 2006,i. e. strain Tc06,which was closely related to the strains from Southeast Asia countries:Myanmar,Laos and Vietnam. Conclusion Clade China-Ⅰ rabies virus was widely distributed in rabies epidemic areas of Yunnan during 2012-2015,which was the predominant clade and had rapid spread potential. No clade China-Ⅱ,China-Ⅲ and China-Ⅵ viruses were detected again in Yunnan in recent years.

     

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