Verweij Jaco J, Ten Hove Robert, Brienen Eric A T, van Lieshout Lisette
Department of Parasitology, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands.
Diagn Microbiol Infect Dis. 2007 Feb;57(2):163-7. doi: 10.1016/j.diagmicrobio.2006.08.009. Epub 2006 Oct 3.
A multiplex real-time polymerase chain reaction (PCR) method was developed for the simultaneous detection of Enterocytozoon bieneusi (n = 30) and Encephalitozoon spp. (n = 3) in stool samples. The multiplex PCR also included an internal control to detect inhibition of the amplification by fecal constituents in the sample. The assay was performed on species-specific DNA controls (n = 22) and a range of well-defined stool samples (n = 140), and it achieved 100% specificity and sensitivity. The use of this assay in a diagnostic laboratory offers the possibility of introducing DNA detection as a feasible technique in the routine diagnosis of intestinal microsporidian infections.
开发了一种多重实时聚合酶链反应(PCR)方法,用于同时检测粪便样本中的微小隐孢子虫(n = 30)和脑炎微孢子虫属(n = 3)。该多重PCR还包括一个内部对照,以检测样本中粪便成分对扩增的抑制作用。该检测方法在物种特异性DNA对照(n = 22)和一系列明确的粪便样本(n = 140)上进行,其特异性和灵敏度均达到100%。在诊断实验室中使用该检测方法,为在肠道微孢子虫感染的常规诊断中引入DNA检测作为一种可行技术提供了可能性。