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作 者:覃晓琳[1,2] 黄进梅[1,2] 薛耀华[1,2] 曾维英[1,2] 吴兴中[1,2] 欧江丽[1,2] 蓝银苑[1,2] 唐三梅 方铭恒 百顺 郑和平[1,2]
机构地区:[1]广东省皮肤性病防治中心 [2]广东省皮肤病医院,广州510091
出 处:《中国麻风皮肤病杂志》2014年第10期579-582,共4页China Journal of Leprosy and Skin Diseases
摘 要:目的:明确单管巢式实时 PCR 检测麻风杆菌的特异性、灵敏性和重复性。方法:以麻风杆菌 hsp18基因为靶基因设计引物和探针,建立单管巢式实时 PCR 方法检测麻风杆菌并与抗酸染色及普通 PCR 进行特异性和灵敏性的比较。结果:单管巢式实时 PCR 检测下限为2.1 fg 质粒 DNA,普通PCR 为21 fg 质粒 DNA,敏感性高10倍;与8种非麻风杆菌无交叉反应;批内相对标准偏差(RSD)为0.24%~1.08%,批间 RSD 为0.09%~2.8%。对比检测54例麻风疑似标本中,抗酸染色、普通 PCR 和单管巢式实时 PCR 的敏感性分别为81.3%(26/32)、87.5%(28/32)和96.9%(31/32)。结论:单管巢式实时 PCR 特异性强、敏感性高且重复性好。Objective: To detect the sensitivity of single-tube nested realtime PCR in detecting Mycobacte-rium leprae. Methods: The primers and probe were designed based on the hsp18 gene of Mycobacterium lep-rae. The single-tube nested realtime PCR was established and the sensitivity and specificity were compared with acid-fast staining and ordinary PCR. Results: The sensitivity of the single-tube nested realtime PCR for detecting Mycobacterium leprae was 2.1fg of plasmid DNA, which was 10 times more sensitive than that in the normal PCR. There was non-cross reactivity with other 8 Non-Mycobacterium leprae. Intra relative standard deviation (RSD) was 0.24%-1.08% and inter RSD was 0.09% -2.8%. The sensitivity of acid-fast staining, normal and single-tube nested PCR in detecting 54 suspected samples of leprosy was 81.3% (26/ 32), 87.5%(28/ 32) and 96.9% (31/ 32), respectively. Conclusion: The single-tube nested realtime PCR method in detecting Mycobacterium leprae is more sensitive and specific.
分 类 号:R755[医药卫生—皮肤病学与性病学]
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