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作 者:张彩萍[1,2] 丁克云[2] 王洪生[1] 冯雨苗[1] 林麟[1] 崔盘根[1] 陈敏[1] 吴勤学[1]
机构地区:[1]中国医学科学院皮肤病研究所,南京210042 [2]江苏大学附属人民医院皮肤科
出 处:《中国麻风皮肤病杂志》2013年第3期158-161,共4页China Journal of Leprosy and Skin Diseases
摘 要:目的:评价分枝杆菌热休克蛋白65(Hsp65)基因检测分枝杆菌皮肤感染标本的敏感性和特异性。方法:多聚酶链反应-限制性片段长度多态性(PCR-砒LP)的10%非变性聚丙烯酰胺凝胶法直接检测Hsp65基因,PCR-RFLP检测阳性的标本再经Hsp65基因和16S rRNA DNA基因测序验证。结果:与培养法相比,PCR-RFLP法检测临床分枝杆菌皮肤感染的敏感性为30%(3/10),特异性为100%(10/10)。结论:分枝杆菌PCR-RFLP的10%非变性聚丙烯酰胺凝胶法可用于分枝杆菌皮肤感染的临床检测。Objective: To assess the sensitivity and specificity of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP)based on hsp65 by 10% non-denaturizing polyacrylamide gel in the detection of mycobacterium infections of skin. Methods: Twenty clinical skin specimens suspected of mycobacterium infections were detected and identified by culture and PCR- RFLP directly and confirmed by sequencing of hsp65 and 16S rRNA DNA genes. Results: Compared with culture method, the sensitivity and the specificity of PCR- RFLP were 30% (3/10) and 100% (10/10). Conclusion: PCR- RFLP based on hsp65 with 10% polyacrylamide gel can be clinically applied in the detection of mycobacterium infections of skin.
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