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作 者:杨荣德[1,2] 谭福跃 邢燕[2] 刘键[2] 温艳[2] 李桓英[2]
机构地区:[1]云南省文山州皮肤病防治所,663000 [2]首都医科大学附属北京友谊医院北京热带医学研究所,北京100050
出 处:《中国麻风皮肤病杂志》2013年第7期429-432,共4页China Journal of Leprosy and Skin Diseases
基 金:李桓英基金会-2012年资助;首都医科大学热带病防治研究重点实验室开放研究课题资助
摘 要:目的:评价实时定量荧光PCR(Real-time PCR)法检测石蜡标本中麻风菌DNA的应用价值。方法:根据基因库(GenBank)发表的M.leprae的全基因组序列,以一段重复序列(repetitive element,RLEP)为扩增靶序列,合成引物和探针,构建质粒pGEMT-101作为标准品,用Real-time PCR对石蜡标本进行麻风菌DNA检测,并评价其敏感性。结果:对52例麻风患者的石蜡包埋组织标本麻风菌进行了检测,不同型别麻风(LL:8;BL:10;BT:28;TT:6)的石蜡标本检测阳性率分别为100%(8/8)、80%(8/10)、78.57%(22/28)、50%(3/6)。结论:Real-time PCR方法可在石蜡标本中快速灵敏的检测到麻风菌DNA。Objective:To assess the application of real time quantitative PCR assay for the detection of M. leprae DNA in paraffin-embedded skin biopsy specimens. Methods: Primers and prob were designed according to the repetitive sequence of M. leprae from gen Bank. The recombinant plasmid pGEMT- 101 was constructed and served as a template to prepare the standard curve for TaqMan real time PCR. The M. Lerae DNA in paraffin-embedded skin biopsy specimens was detected and the sensitivity of the results was assessed. Results: The paraffin-embedded skin biopsy specimens from 52 leprosy patients were tested. The sensitivities of the results varied in different types of the disease: LL 100% (8/8) , BL 80% (8/10), BT 78.57% (22/28) and TF 50% (3/6), respectively. Conclusion: Real-time PCR is a rapid, specific and sensitive method for the detection of M. leprae DNA in paraffin-embedded skin bioDsv snecimens.
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