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通过实时聚合酶链反应检测法快速鉴定利什曼原虫复合体

Rapid identification of Leishmania complexes by a real-time PCR assay.

作者信息

Wortmann Glenn, Hochberg Lisa, Houng Huo-Hsu, Sweeney Colleen, Zapor Michael, Aronson Naomi, Weina Peter, Ockenhouse Christian F

机构信息

Infectious Disease Service, Walter Reed Army Medical Center, Washington, DC 20307-5001, USA.

出版信息

Am J Trop Med Hyg. 2005 Dec;73(6):999-1004.

Abstract

A real-time PCR assay for the detection of four Leishmania complexes (L. Viannia, L. mexicana, L. donovani/infantum, and L. major) was developed and evaluated. The assay was developed to detect the glucosephosphate isomerase gene and capitalizes on DNA sequence variability within that gene for Leishmania complex identification. Primer/probe sets were created and tested against a panel of 21 known negative controls and on DNA extracted from cultured promastigotes or from tissue biopsies from patients with cutaneous leishmaniasis. The assay was highly specific, as no amplification products were detected in the negative control samples while simultaneously retaining a high degree of complex-specific diagnostic accuracy for cultured organisms and patient clinical samples. Real-time PCR offers rapid (within hours) identification of Leishmania to the complex level and provides a useful molecular tool to assist both epidemiologists and clinicians.

摘要

开发并评估了一种用于检测四种利什曼原虫复合体(维氏利什曼原虫、墨西哥利什曼原虫、杜氏/婴儿利什曼原虫和硕大利什曼原虫)的实时PCR检测方法。该检测方法旨在检测葡萄糖磷酸异构酶基因,并利用该基因内的DNA序列变异性来鉴定利什曼原虫复合体。创建了引物/探针组,并针对一组21个已知阴性对照以及从培养的前鞭毛体或皮肤利什曼病患者的组织活检中提取的DNA进行了测试。该检测方法具有高度特异性,因为在阴性对照样品中未检测到扩增产物,同时对培养的生物体和患者临床样品保持高度的复合体特异性诊断准确性。实时PCR能够在数小时内快速将利什曼原虫鉴定到复合体水平,并为流行病学家和临床医生提供了一种有用的分子工具。

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