Gookin Jody L, Birkenheuer Adam J, Breitschwerdt Edward B, Levy Michael G
Departments of Molecular Biomedical Sciences. Clinical Sciences. Food Animal and Health Resource Management, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina 27606, USA.
J Clin Microbiol. 2002 Nov;40(11):4126-30. doi: 10.1128/JCM.40.11.4126-4130.2002.
Tritrichomonas foetus, a venereal pathogen of cattle, was recently identified as an inhabitant of the large intestine in young domestic cats with chronic diarrhea. Recognition of the infection in cats has been mired by unfamiliarity with T. foetus in cats as well as misdiagnosis of the organisms as Pentatrichomonas hominis or Giardia sp. when visualized by light microscopy. The diagnosis of T. foetus presently depends on the demonstration of live organisms by direct microscopic examination of fresh feces or by fecal culturing. As T. foetus organisms are fastidious and fragile, routine flotation techniques and delayed examination and refrigeration of feces are anticipated to preclude the diagnosis in numerous cases. The objective of this study was to develop a sensitive and specific PCR test for the diagnosis of feline T. foetus infection. A single-tube nested PCR was designed and optimized for the detection of T. foetus in feline feces by using a combination of novel (TFITS-F and TFITS-R) and previously described (TFR3 and TFR4) primers. The PCR is based on the amplification of a conserved portion of the T. foetus internal transcribed spacer (ITS) region (ITS1 and ITS2) and the 5.8S rRNA gene. The absolute detection limit of the single-tube nested PCR was 1 organism, while the practical detection limit was 10 organisms per 200 mg of feces. Specificity was examined by using P. hominis, Giardia lamblia, and feline genomic DNA. Our results demonstrate that the single-tube nested PCR is ideally suited for (i) diagnostic testing of feline fecal samples that are found negative by direct microscopy and culturing and (ii) definitive identification of microscopically observable or cultivated organisms.
胎儿三毛滴虫是牛的一种性传播病原体,最近被鉴定为患有慢性腹泻的幼年家猫大肠中的一种寄居菌。由于对猫体内的胎儿三毛滴虫不熟悉,以及在光学显微镜下观察时将这些生物体误诊为人五毛滴虫或贾第虫属,猫感染的识别一直受到困扰。目前,胎儿三毛滴虫的诊断依赖于通过直接显微镜检查新鲜粪便或粪便培养来证明活的生物体。由于胎儿三毛滴虫生物体挑剔且脆弱,常规的漂浮技术以及粪便的延迟检查和冷藏预计会在许多情况下排除诊断。本研究的目的是开发一种灵敏且特异的PCR检测方法,用于诊断猫的胎儿三毛滴虫感染。通过使用新型引物(TFITS-F和TFITS-R)和先前描述的引物(TFR3和TFR4)的组合,设计并优化了一种单管巢式PCR,用于检测猫粪便中的胎儿三毛滴虫。该PCR基于胎儿三毛滴虫内部转录间隔区(ITS)区域(ITS1和ITS2)以及5.8S rRNA基因保守部分的扩增。单管巢式PCR的绝对检测限为1个生物体,而实际检测限为每200毫克粪便中有10个生物体。通过使用人五毛滴虫、蓝氏贾第鞭毛虫和猫基因组DNA来检测特异性。我们的结果表明,单管巢式PCR非常适合(i)对直接显微镜检查和培养呈阴性的猫粪便样本进行诊断测试,以及(ii)对显微镜下可观察到或培养出的生物体进行明确鉴定。