Kumar Rajesh, Bumb Ram Avtar, Ansari Nasim A, Mehta Rajesh D, Salotra Poonam
Institute of Pathology (ICMR), Safdarjung Hospital Campus, New Delhi, India.
Am J Trop Med Hyg. 2007 May;76(5):896-901.
Identification of new foci of cutaneous leishmaniasis (CL), along with reports of Leishmania donovani causing the disease, is an issue of concern. Clinico-epidemiologic analysis of 98 cases in the endemic regions of Rajasthan state, India, suggested the preponderance of infection in men (62.24%) compared with women (37.75%). Species characterization by internal transcribed spacer 1 (ITS1) polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP), kDNA-PCR, and immunofluorescence assay established L. tropica as the causative organism. When applied directly to 32 clinical samples, kDNA PCR had a sensitivity of 96.6%, whereas ITS1 PCR had a sensitivity of 82.75%, thus facilitating diagnosis and species identification. Either parasite culture or direct microscopy alone detected 48.2% and 65.5% of the positive samples, respectively, whereas culture and microscopy together improved overall sensitivity to 89.3% (25/28). Except for the kDNA PCR, all other assays were 100% specific. This study provides the first comprehensive molecular and immunologic studies of CL in India.
发现皮肤利什曼病(CL)新病灶以及杜氏利什曼原虫引发该病的报告令人担忧。对印度拉贾斯坦邦流行地区的98例病例进行临床流行病学分析表明,男性感染率(62.24%)高于女性(37.75%)。通过内转录间隔区1(ITS1)聚合酶链反应(PCR)-限制性片段长度多态性(RFLP)、kDNA-PCR和免疫荧光试验进行的物种鉴定确定热带利什曼原虫为病原体。直接应用于32份临床样本时,kDNA PCR的灵敏度为96.6%,而ITS1 PCR的灵敏度为82.75%,从而有助于诊断和物种鉴定。单独的寄生虫培养或直接显微镜检查分别检测出48.2%和65.5%的阳性样本,而培养和显微镜检查相结合将总体灵敏度提高到89.3%(25/28)。除kDNA PCR外,所有其他检测方法的特异性均为100%。本研究首次对印度的CL进行了全面的分子和免疫学研究。