畜牧兽医学报 ›› 2006, Vol. 37 ›› Issue (1): 84-90.doi:

• 研究简报 • 上一篇    下一篇

利用SYBR Green检测衣原体Real-Time PCR方法的建立

杨建民;郝永新;赵德明;何 诚   

  1. 中国农业大学动物医学院国家动物海绵状脑病实验室,北京 100094
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2006-01-25 发布日期:2006-01-25

Development of a Real-Time PCR Assay for Detection and Quantitation of Chlamydia Using SYBR Green and the Light Cycler

YANG Jian-min; HAO Yong-xin;ZHAO De-ming; HE Cheng   

  1. National Animal Transmissible Spongiform Encephalopathies Laboratory, College of Veterinary Medicine, China Agricultural University, Beijing 100094,China
  • Received:1900-01-01 Revised:1900-01-01 Online:2006-01-25 Published:2006-01-25

摘要: 利用SYBR Green建立了检测种特异性衣原体的Real-Time PCR方法。本方法应用衣原体种特异性的高度保守特异引物,能够扩增627 bp特异片段;使用定量标准基因组DNA,本方法能准确检测最少250 fg衣原体DNA。Real-Time PCR方法与免疫荧光方法的检测结果表明:检测4种衣原体临床样本,Real-Time PCR敏感性均在96%~98%;特异性均为100%;这两种方法符合率达97%以上(n=60);批内和批间重复性试验结果表明,本方法具有良好的准确性。本方法的建立对于快速、准确检测临床样本种特异性衣原体提供了一种切实有效的方法。

Abstract: Here, we presented a Chlamydiaceae-specific 23S rRNA-based real-time PCR assay for simultaneous detection and quantitation of four members of Chlamydiaceae family, C. trachomatis, C. psittaci, C. pneumoniae and C. pecorum, using SYBR Green and LightcyclerTM. The assay was characterized using plasmid constructs of the bacteria and verified on standard strains of all four species of the Chlamydiaceae and a large cohort of clinical samples collected from human and animals by comparison with fluorescence immunohistochemistry method. The results showed that the present real-time PCR assay was of high specificity and sensitivity. It was capable of detecting as few as 250 fg of chlamydial DNA (equivalent to 10-1 IFU) and was applicable to both liquid cultures and clinical samples. This assay may therefore offer a rapid, economic and reliable method for screening of the chlamydiaceae pathogens.