Yang Jian-Min, Liu Hong-Xiang, Hao Yong-Xin, He Cheng, Zhao De-Ming
National Animal Transmissible Spongiform Encephalopathy Laboratory, College of Veterinary Medicine, China Agricultural University, Beijing 100094, PR China.
J Clin Virol. 2006 May;36(1):79-81. doi: 10.1016/j.jcv.2006.01.005. Epub 2006 Feb 20.
Chlamydiae are one of the causative agents of various diseases in animals and human beings, which include abortion, pneumonia, gastroenteritis, encephalomyelitis, conjunctivitis, arthritis and sexually transmitted diseases. Much work has been carried out to attempt to develop an efficient pathogen detection strategy. Here, we presented a Chlamydiaceae-specific 23S rRNA-based real-time PCR assay for simultaneous detection and quantification of four members of Chlamydiaceae family, C. trachomatis, C. psittaci, C. pneumoniae and C. pecorum, using SYBR Green and Lightcycler. 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 250fg 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 means for screening of the chlamydiaceae pathogens.
衣原体是人和动物多种疾病的病原体之一,这些疾病包括流产、肺炎、肠胃炎、脑脊髓炎、结膜炎、关节炎以及性传播疾病。为了开发一种高效的病原体检测策略,人们已经开展了大量工作。在此,我们使用SYBR Green和LightCycler技术,提出了一种基于衣原体特异性23S rRNA的实时荧光定量PCR检测方法,用于同时检测和定量衣原体科的四个成员,即沙眼衣原体、鹦鹉热衣原体、肺炎衣原体和猪衣原体。该检测方法使用细菌的质粒构建体进行表征,并通过与荧光免疫组化方法比较,在衣原体科所有四个物种的标准菌株以及从人和动物收集的大量临床样本上进行了验证。结果表明,当前的实时荧光定量PCR检测方法具有高度的特异性和敏感性。它能够检测低至250fg的衣原体DNA(相当于10(-1)IFU),并且适用于液体培养物和临床样本。因此,该检测方法可能为筛选衣原体病原体提供一种快速、经济且可靠的手段。