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作 者:余毅 徐智民[1,2] 欧锡祺[1,2] 宋姗 张妙英
机构地区:[1]广东省顺德市大良医院 [2]第一军医大学南方医院全军消化内科研究所
出 处:《世界华人消化杂志》1999年第4期323-325,共3页World Chinese Journal of Digestology
摘 要:目的鞭毛是幽门螺杆菌(Hp)的重要侵袭因子,本研究拟检测Hp鞭毛素A基因的变异性,进而研究其与Hp致病性的关系.方法我们对52例胃粘膜活检标本和18株Hp临床分离株进行Hp特异的16SrRNA基因和鞭毛素A基因PCR扩增和PCRRFLP及PCRRFLPSSCP分析.结果对43例Hp(+)的flaA基因PCRRFLP(HindⅢ)大约可分7个型(变异检出率为163%),而PCRRFLPSSCP可分37个型(变异检出率为860%),两者有非常显著性差异.结论flaA基因变异性极大,PCRRFLPSSCP优于PCRRFLP,是检测其变异的有效方法.AIM To study the variability and pathogenjcity of Helicobacter pylori (Hp) . METHODS PCR was performed in fifty two biopsy specimens of gastric mucosa and 18 strains of Hp for 16S rRNA gene and flagellin A gene ( fla A). And PCR-RFLP and RFLP SSCP were also analyzed. RESULTS Seven fla A genotypes were found by PCR RFLP in 43 strains of Hp (detecting rate of variance was 16 3%), but 37 were found by PCR RFLP SSCP in the same group of cases (detecting rate of variance was 86 0%). CONCLUSION Very large variability in fla A gene of Hp was detected by PCR RFLP SSCP, which is a more effective method than PCR RFLP to identify Hp strains in human stomach.
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