动粒体
内脏利什曼病
生物
聚合酶链反应
杜氏利什曼原虫
利什曼病
核糖体RNA
利什曼原虫
DNA
计算生物学
免疫学
遗传学
寄生虫寄主
基因
计算机科学
万维网
作者
Grégoire Pasquier,Quentin Andreotti,Christophe Ravel,Yvon Sterkers
标识
DOI:10.1128/spectrum.02154-23
摘要
PCR revolutionized the direct diagnosis of infectious diseases, especially protozooses, where the infectious load is usually low. Commercial PCR methods are available and offer many advantages, including convenience and batch tracking as part of a quality system. For most parameters, the performance of commercial methods is at least as good as that of finely optimized methods developed in expert laboratories. This comparison work has not been done for the molecular diagnosis of visceral leishmaniasis. Leishmania sp. has a unique organelle, the kinetoplast, which corresponds to the mitochondrial DNA. It is organized into a large number of minicircles, which has made it a target for the development of diagnostic PCR. The quanty Leishmaniae, Clonit kit targeting ribosomal DNA was compared to a widely used laboratory-developed method based on kinetoplast DNA. This reference method gave significantly better results, probably due to the difference in the number of repeats of the PCR targets.
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