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SEN病毒部分基因的克隆及序列测定
引用本文:詹林盛,孟庆华,贾帅争,孙红琰,杜芝燕,王全立. SEN病毒部分基因的克隆及序列测定[J]. 军事医学科学院院刊, 2001, 25(2): 88-90
作者姓名:詹林盛  孟庆华  贾帅争  孙红琰  杜芝燕  王全立
作者单位:1. 军事医学科学院野战输血研究所,
2. 北京佑安医院肝病三科,
摘    要:目的:了解我国人群中是否存在SEN病毒(SENV)感染,并分析SENV国内分离株的部分基因序列,方法:在SENV的保守区设计引物,建立巢式PCR方法检测血清中SENV DNA,并对PCR产物进行克隆,测序,结果,7例非甲-非瘐型肝炎,且输血传播病毒(TTV)阴性患者中,2例SENV阳性,其中一株的序列与意大利SENV-D株(AX-25730)相对应位置核苷酸序列同源性为90%,结论:本研究证初了我国存在SENV感染,建立了检测SENV的PCR方法,并对SENV部分基因进行了克隆及测序,对进一步开展SENV诊断和流行病学调查具有重要意义。

关 键 词:SEN病毒 肝炎病毒 非甲-非瘐型肝炎 聚合酶链反应 序列排列
文章编号:1000-5501(2001)02-0088-03
修稿时间:2001-03-09

Cloning and sequencing of partial gene from SENV isolate in China
ZHAN LinSheng,MENG Qinghua,JIA ShuaiZheng,Sun Hongyan,DU ZhiYan,Wang Quanli. Cloning and sequencing of partial gene from SENV isolate in China[J]. Bulletin of the Academy of Military Medical Sciences, 2001, 25(2): 88-90
Authors:ZHAN LinSheng  MENG Qinghua  JIA ShuaiZheng  Sun Hongyan  DU ZhiYan  Wang Quanli
Affiliation:ZHAN Lin Sheng 1,MENG Qing Hua 2,JIA Shuai Zheng 1,SUN Hong Yan 1,DU Zhi Yan 1,WANG Quan Li 1
Abstract:Objective:To investigate the presence of SENV infection among patients in China,and analyze partial nucleotide sequence of SENV isolated from a patient with non A-G hepatitis.Methods:A nested polymerase chain reaction (PCR) assay with primers from ORF1 of SENV genome was established to detect SENV DNA.The PCR product was cloned and sequenced.Results:SENV DNA was positive in 2 of 7 patients with non A-G hepatitis and TTV negative.Partial gene of a SENV isolate was compared with the corresponding region of SENV isolate(AX025730)from Italy and was found that the nucleotide homology was 90%.Conclusions:The results of this study confirmed the presence of SENV infection in China.The development of a PCR assay for SENV DNA detection and the cloning,sequencing of the SENV isolate have important implication for the diagnosis and epidemiological investigation on SENV infection. [
Keywords:SENV  hepatitis viruses  non A-G hepatitis  polymerase chain reaction  sequencing alignment
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