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使用实时荧光定量聚合酶链反应对粪便样本中的微小隐孢子虫和脑炎微孢子虫属进行多重检测。

Multiplex detection of Enterocytozoon bieneusi and Encephalitozoon spp. in fecal samples using real-time PCR.

作者信息

Verweij Jaco J, Ten Hove Robert, Brienen Eric A T, van Lieshout Lisette

机构信息

Department of Parasitology, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands.

出版信息

Diagn Microbiol Infect Dis. 2007 Feb;57(2):163-7. doi: 10.1016/j.diagmicrobio.2006.08.009. Epub 2006 Oct 3.

Abstract

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.

摘要

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。

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