Department of Parasitology, Faculty of Veterinary Medicine, University of Ankara, 06110 Diskapi, Ankara, Turkey.
Parasitol Res. 2010 Feb;106(3):683-7. doi: 10.1007/s00436-010-1737-x. Epub 2010 Jan 28.
In this study, the sensitivity and specificity of different previously described primer sets for Cryptosporidium parvum detection by polymerase chain reaction (PCR) was evaluated. For this purpose, the primer sets defined by Cacciò et al. (FEMS Microbiol Lett 170(1):173-179, 1999) (tub), Widmer et al. (Appl Environ Microbiol 64(11):4477-4481, 1998) (btub) and Rochelle et al. (Appl Environ Microbiol 63:2029-2037, 1997) (cphsp), respectively, were used. Deoxyribonucleic acid (DNA) was isolated from three different sample materials: (1) from the faeces of an experimentally C. parvum-infected calf, (2) from purified C. parvum oocysts, and (3) from C. parvum-infected HCT-8 cell cultures. The DNA samples were subjected to PCR reactions with each of the three given primer sets to investigate sensitivity and suitability for routine use. The primers described by Cacciò et al. (FEMS Microbiol Lett 170(1):173-179, 1999) (TUB) were superior regarding sensitivity and specificity in terms of detection of C. parvum in faeces, in purified oocysts and also in cell culture, and may thus be applied for routine diagnostic use in common sample materials.
在这项研究中,评估了先前描述的不同引物组用于聚合酶链反应 (PCR) 检测微小隐孢子虫的敏感性和特异性。为此,使用了 Cacciò 等人定义的引物组 (FEMS Microbiol Lett 170(1):173-179, 1999) (tub)、Widmer 等人 (Appl Environ Microbiol 64(11):4477-4481, 1998) (btub) 和 Rochelle 等人 (Appl Environ Microbiol 63:2029-2037, 1997) (cphsp)。脱氧核糖核酸 (DNA) 从三种不同的样品材料中分离出来:(1) 来自实验性微小隐孢子虫感染小牛的粪便,(2) 来自纯化的微小隐孢子虫卵囊,和 (3) 来自微小隐孢子虫感染的 HCT-8 细胞培养物。用三种给定的引物组对 DNA 样品进行 PCR 反应,以研究敏感性和常规使用的适用性。Cacciò 等人描述的引物 (FEMS Microbiol Lett 170(1):173-179, 1999) (TUB) 在检测粪便、纯化卵囊和细胞培养物中的微小隐孢子虫方面具有较高的敏感性和特异性,因此可应用于常见样品材料的常规诊断。