Castilho Tiago Moreno, Camargo Luís Marcelo Aranha, McMahon-Pratt Diane, Shaw Jeffrey Jon, Floeter-Winter Lucile Maria
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06510, USA.
Am J Trop Med Hyg. 2008 Jan;78(1):122-32.
A real-time polymerase chain reaction (PCR) test was developed on the basis of the Leishmania glucose-6-phosphate dehydrogenase locus that enables identification and quantification of parasites. Using two independent pairs of primers in SYBR-Green assays, the test identified etiologic agents of cutaneous leishmaniasis belonging to both subgenera, Leishmania (Viannia) and Leishmania (Leishmania) in the Americas. Furthermore, use of TaqMan probes enables distinction between L. (V.) braziliensis or L. (V.) peruviania from the other L. (Viannia) species. All assays were negative with DNA of related trypanosomatids, humans, and mice. The parasite burden was estimated by normalizing the number of organisms per total amount of DNA in the sample or per host glyceraldehyde-3-phosphate dehydrogenase copies. The real-time PCR assay for L. (Leishmania) subgenus showed a good linear correlation with quantification on the basis of a limiting dilution assay in experimentally infected mice. The test successfully identifies and quantifies Leishmania in human biopsy specimens and represents a new tool to study leishmaniasis.
基于利什曼原虫葡萄糖-6-磷酸脱氢酶基因座开发了一种实时聚合酶链反应(PCR)检测方法,该方法能够鉴定和定量寄生虫。在SYBR-绿染法中使用两对独立的引物,该检测方法可鉴定美洲地区属于利什曼原虫(维扬亚属)和利什曼原虫(利什曼亚属)这两个亚属的皮肤利什曼病的病原体。此外,使用TaqMan探针能够区分巴西利什曼原虫(维扬亚属)或秘鲁利什曼原虫(维扬亚属)与其他利什曼原虫(维扬亚属)物种。所有检测对相关锥虫、人类和小鼠的DNA均呈阴性。通过将样本中每单位总DNA量的生物体数量或每宿主甘油醛-3-磷酸脱氢酶拷贝数进行标准化来估计寄生虫负荷。针对利什曼原虫(利什曼亚属)的实时PCR检测与在实验感染小鼠中基于有限稀释法的定量分析显示出良好的线性相关性。该检测方法成功地鉴定和定量了人类活检标本中的利什曼原虫,是研究利什曼病的一种新工具。