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通过半胱氨酸蛋白酶B基因的特异性聚合酶链反应扩增和快速试纸条检测鉴定旧大陆利什曼原虫属。

Identification of Old World Leishmania spp. by specific polymerase chain reaction amplification of cysteine proteinase B genes and rapid dipstick detection.

作者信息

Laurent Thierry, Van der Auwera Gert, Hide Mallorie, Mertens Pascal, Quispe-Tintaya Wilber, Deborggraeve Stijn, De Doncker Simonne, Leclipteux Thierry, Bañuls Anne-Laure, Büscher Philippe, Dujardin Jean-Claude

机构信息

Department of Parasitology, Institute of Tropical Medicine Antwerp, 2000 Antwerp, Belgium.

出版信息

Diagn Microbiol Infect Dis. 2009 Feb;63(2):173-81. doi: 10.1016/j.diagmicrobio.2008.10.015. Epub 2008 Dec 18.

Abstract

We used the cysteine proteinase B (cpb) gene family of the trypanosomatid genus Leishmania as a target to develop rapid, specific, and easy-to-use polymerase chain reaction (PCR) tests to discriminate Leishmania infantum, Leishmania donovani, Leishmania tropica, Leishmania aethiopica, and Leishmania major. Identification of all 5 Old World species and validation of intraspecies variability are features lacking in other species-specific PCRs. Amplicon analysis was done on agarose gels and was further simplified by using an oligochromatography dipstick to detect L. infantum and L. donovani products. Because the analytical sensitivity is lower than that of certain other species- and genus-specific PCRs, our assays are especially valuable for use on cultured isolates or directly on cryostabilates. As such, they can be implemented by research and health centers having access to culturing, DNA isolation, and PCR.

摘要

我们以利什曼原虫属的半胱氨酸蛋白酶B(cpb)基因家族为靶点,开发快速、特异且易于使用的聚合酶链反应(PCR)检测方法,以区分婴儿利什曼原虫、杜氏利什曼原虫、热带利什曼原虫、埃塞俄比亚利什曼原虫和硕大利什曼原虫。鉴定所有5种旧世界利什曼原虫物种以及验证种内变异性是其他物种特异性PCR所缺乏的特性。扩增子分析在琼脂糖凝胶上进行,并通过使用寡色谱试纸条检测婴儿利什曼原虫和杜氏利什曼原虫的产物而进一步简化。由于分析灵敏度低于某些其他物种和属特异性PCR,我们的检测方法对于培养的分离株或直接对冷冻稳定物特别有价值。因此,有培养、DNA分离和PCR条件的研究和卫生中心都可以采用这些方法。

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