Yang Wenli, Lindquist H D Alan, Cama Vitaliano, Schaefer Frank W, Villegas Eric, Fayer Ronald, Lewis Earl J, Feng Yaoyu, Xiao Lihua
National Center for Zoonotic, Vector-Borne and Enteric Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA.
Appl Environ Microbiol. 2009 Jun;75(11):3477-83. doi: 10.1128/AEM.00285-09. Epub 2009 Apr 10.
PCR techniques in combination with conventional parasite concentration procedures have potential for the sensitive and specific detection of Toxoplasma gondii oocysts in water. Three real-time PCR assays based on the B1 gene and a 529-bp repetitive element were analyzed for the detection of T. gondii tachyzoites and oocysts. Lower sensitivity and specificity were obtained with the B1 gene-based PCR than with the 529-bp repeat-based PCR. New procedures for the real-time PCR detection of T. gondii oocysts in concentrates of surface water were developed and tested in conjunction with a method for the direct extraction of inhibitor-free DNA from water. This technique detected as few as one oocyst seeded to 0.5 ml of packed pellets from water samples concentrated by Envirocheck filters. Thus, this real-time PCR may provide a detection method alternative to the traditional mouse assay and microscopy.
聚合酶链反应(PCR)技术与传统的寄生虫浓缩程序相结合,有潜力灵敏且特异地检测水中的刚地弓形虫卵囊。分析了三种基于B1基因和一个529碱基对重复元件的实时PCR检测方法,用于检测刚地弓形虫速殖子和卵囊。与基于529碱基对重复序列的PCR相比,基于B1基因的PCR敏感性和特异性较低。开发了地表水浓缩物中刚地弓形虫卵囊实时PCR检测的新程序,并结合从水中直接提取无抑制剂DNA的方法进行了测试。该技术能检测到接种到通过Envirocheck过滤器浓缩的水样0.5毫升压实沉淀中的低至一个卵囊。因此,这种实时PCR可能为传统小鼠试验和显微镜检查提供一种替代检测方法。