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幽门螺杆菌临床分离株的REP-PCR分析
引用本文:彭颖,吕建新,叶嗣颖,黄庆华.幽门螺杆菌临床分离株的REP-PCR分析[J].遗传,2002,24(6):684-686.
作者姓名:彭颖  吕建新  叶嗣颖  黄庆华
作者单位:1.温州医学院 细胞与分子医学研究所,浙江 温州 325027; 2.华中科技大学同济医学院微生物学教研室,武汉 430030
基金项目:卫生部科学研究基金(No.98-1-123)资助
摘    要:应用REP-PCR对来自20例单纯性胃炎和20例消化性溃疡病人的幽门螺杆菌菌株进行基因分型,并运用SAS软件进行聚类分析。结果显示这些菌株按照基因型被分为两大类,但两种来源的菌株在两大类中的比例无明显差异(P>0.1),提示幽门螺杆菌临床分离株REP-PCR基因型与致病性之间不存在明显相关性。 REP-PCR Analysis of Helicobacter pylori Clinical Strains PENG Ying1,LU Jian-xin1,YE Si-ying2,HUANG Qing-hua2 1.Institute of Cellular and Molecular Medicine,Wenzhou Medical College,Wenzhou,Zhejiang 325027,China; 2.Department of Microbiology,Tongji Medical College,Wuhan 430030,China Abstract:Helicobacter pylori strains isolated from 20 gastritis patients and 20 peptic ulcer patients was genotyped by REP-PCR and was clustered with SAS software.These strains are devided into two categories according to their genotype.But the rate of the two sources of strain in the two categories shows no apparent difference(P>0.1),indicating that there is no significant close relationship between the genotype and the pathogenicity. Key words:Helicobacter pylori;REP-PCR;genotype

关 键 词:幽门螺杆菌  REP-PCR  基因分型  
文章编号:0253-9772(2002)06-0684-03
修稿时间:2001年12月4日

REP-PCR Analysis of Helicobacter pylori Clinical Strains
Ying Peng,Jian-xin Lu,Si-ying Ye,Qing-hua Huang.REP-PCR Analysis of Helicobacter pylori Clinical Strains[J].Hereditas,2002,24(6):684-686.
Authors:Ying Peng  Jian-xin Lu  Si-ying Ye  Qing-hua Huang
Institution:Institute of Cellular and Molecular Medicine, Wenzhou Medical College, Wenzhou, Zhejiang 325027, China.
Abstract:Helicobacter pylori strains isolated from 20 gastritis patients and 20 peptic ulcer patients was genotyped by REP-PCR and was clustered with SAS software. These strains are divided into two categories according to their genotype. But the rate of the two sources of strain in the two categories shows no apparent difference(P approximately 0.1), indicating that there is no significant close relationship between the genotype and the pathogenicity.
Keywords:REP-PCR
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