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肺炎衣原体套式聚合酶链式反应检测研究
引用本文:秦玲,糜祖煌,陆亚华. 肺炎衣原体套式聚合酶链式反应检测研究[J]. 中国人兽共患病杂志, 2000, 16(2): 84-86
作者姓名:秦玲  糜祖煌  陆亚华
作者单位:[1]无锡市克隆遗传技术研究所 [2]常州市第一人民医院儿科
基金项目:本文已被国际抗痨联盟第20届东区会议录用,并由香港胸肺基金会资助与会(A-107)。
摘    要:目的 探讨肺炎衣原体(Cpn)的套式聚合酶链式反应(nPCR)检测技术。方法 根据Campbell克隆的CpnDNA序列设计套式引物,并建立nPCR反应体系。结果 Cpn经nPCR扩增出现378bp的阳性条带,而沙眼衣原体和鹦鹉热衣原体以及其他用作特异性试验的微生物均不能扩增。3例阳性标本经DNA测序与Cpn(CWL-29株)序列完全一致。Cpn nPCR之灵敏度比传统PCR高100倍。各种呼吸系

关 键 词:肺炎衣原体 聚合酶链反应 nPCR 诊断
文章编号:1002-2694(2000)02-0084-02

DETECTION OF CHLAMYDIA PNEUMONIAEBY NESTED POLYMERASE CHAIN REACTION
QIN Ling,MI Zuhuang,LU Yahua. DETECTION OF CHLAMYDIA PNEUMONIAEBY NESTED POLYMERASE CHAIN REACTION[J]. Chinese Journal of Zoonoses, 2000, 16(2): 84-86
Authors:QIN Ling  MI Zuhuang  LU Yahua
Abstract:Aim To develop a molecular biologic technique for detection of chlamydia pneumoniae with nested polymevase chain reaction (nPCR) .Methods Nested primers were synthesized according to a cloned C.pneumoniae 474 - bp Pst Ifragmert.Results The 378be DNA fragments were amplified from C.pneuomoniae with nPCR.Nere of the C.trachomatis,C.psittaci, other organisms and etc.Strains tested were amplified by the nPCR.The sequening of 3 sample products with nPCR are quite same as C. pneumoniae (CWL - 29). The sensitivity of nPCR is higter than PCR.Conclusions This method is not only sensitive. specific and rapid but also provides an etiological basis fro diaghosis of C.pneumoniae infection.
Keywords:Chlamydia pneumoniae  Nested polymerase chain reaction
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