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）序对完全一致。CpnnPCR之灵敏度比传统PCR高100倍。各种呼吸系统病患儿咽拭子CpnnPCR阳性率明显高于健康儿童（P均＜0．01）。结论nPCR检测可能是Cpn感染的灵敏、特异、快速的诊断方法。
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.
出处
《中国人兽共患病杂志》
CSCD
北大核心
2000年第2期84-86,共3页
Chinese Journal of Zoonoses
基金
香港胸肺基金!A-107
