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深圳市HIV-1 E亚型感染毒株的分子流行病学分析
引用本文:冯铁建,邵一鸣,李良成. 深圳市HIV-1 E亚型感染毒株的分子流行病学分析[J]. 中华实验和临床病毒学杂志, 2000, 14(4): 330-332
作者姓名:冯铁建  邵一鸣  李良成
作者单位:[1]深圳市卫生防疫站 [2]卫生部艾滋病预防控制中心参比实验室
摘    要:目的 了解人类免疫缺陷病毒1型E亚型毒株在深圳市不同人群中流行传播情况、流行时间和传播规律。方法 应用聚合酶链反应(PCR)方法对1996年深圳市检出的3份人类免疫缺陷病毒1型(HIV-1)感染者外周血单个核细胞样本进行扩增,获得HIV-1膜蛋白(env)基因片段,并对C2-V3及其邻区350~450个核苷酸序列进行测定和分析。结果 这3份血样为HIV-1E亚型毒株感染(sz-E),彼此间的基因离散率为2.6%;与A-E国际参考亚型及国内部分地区流行的BE型代表株比较,sz-E与A-D参考亚型共享序列及国内B亚型代表株间的基因离散率均大于24%,而与主要代表泰国E亚型(Econ)间的基因离散率仅为6.2%。系统树分析显示,sz-E与Econ聚集在一起,远离其他国际亚型毒株序列。结论 HIV-1E亚型在深圳的流行

关 键 词:HIV-1 病毒基因 聚合酶链反应 分子流行病学

Molecular epidemiology analysis of HIV-1 subtype E strains found in Shenzhen
FENG Tiejian ,SHAO Yiming,Li Liangcheng,et al.. Molecular epidemiology analysis of HIV-1 subtype E strains found in Shenzhen[J]. Chinese journal of experimental and clinical virology, 2000, 14(4): 330-332
Authors:FENG Tiejian   SHAO Yiming  Li Liangcheng  et al.
Affiliation:Shenzhen Hygiene and Anti-epidemic Station, Shenzhen 518020, China.
Abstract:Objective To investigate the prevalent status of HIV 1 subtype E epidemic among different populations in Shenzhen. Methods HIV 1 proviral DNA. from peripheral blood mononuclear cells (PBMCs) of 3 HIV infected individuals found in Shenzhen was amplified by nested PCR. The C2 V3 and its flanking region (350 450 nucleotides) of HIV 1 env gene were sequenced directly from the PCR products and analysed.Results These 3 cases were confirmed to be infected with HIV 1 subtype E strain (sz E). The innergroups distance of sz E was 2.6%. In comparison with the consesus sequence of intenational A E subgroups and some of subtype B epidemic in China, the genetic distances among sz E and each of A D subgroups and some of subtype B were more than 24%. Furthermore, the phylogenetic tree analysis showed that sz E clustered closely to Econ.Conclusion These findings suggested that the epidemic time for HIV 1 subtype E , which was mainly prevalent among IDUs population and some professional blood donors, had been about 2 3 years in Shenzhen.
Keywords:HIV-1  Gene   viral  Polymerase chain reaction
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