Department of Medical Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Molecular Dermatology Research Center, Department of Dermatology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
BMC Infect Dis. 2019 Jan 29;19(1):98. doi: 10.1186/s12879-018-3667-7.
Cutaneous leishmaniasis (CL) caused by Leishmania species, is a geographically extensive disease that infects humans and animals. CL is endemic in half of the 31 provinces of Iran, with 29,201 incidence cases reported in Fars province from 2010 to 2015. CL is polymorphic and may result in lesions characterized by different clinical features. Parasite genetic diversity is proposed to be one of the factors affecting the clinical outcome and lesion characteristics in CL patients. However, there is still very limited data regarding the genetic variation of Leishmania spp. based on the sequencing of Cytochrome b (Cyt b) gene.
All patients originated from endemic regions in Fars province. The amplification of the Cyt b gene from isolates of 100 patients with disparate clinical forms of CL was accomplished using Nested-PCR. Sequence analysis of the amplified Cyt b was used to scrutinize the genetic variations among Leishmania isolates and connect the results with clinical pictures. The clinical demonstrations were basically of two types, typical and atypical lesions. Molecular phylogenetic tree was constructed using the Neighbor-Joining method, with species/strains from this study compared to species/strains from other geographical regions.
Leishmania major was identified as the predominant infecting Leishmania spp. (86% of cases), with the remainder of cases being infected by Leishmania tropica. Clinical examination of patients revealed 12 different clinical CL forms. Among Leishmania samples analyzed, five distinct haplotypes were recognized: three in L. major and two in L. tropica. We found a correlation between clinical outcomes and Cyt b sequence variation of Leishmania spp. involved. Moreover, we observed a higher presence of polymorphisms in L. major compared with L. tropica. This difference may be due to the different eco-epidemiologies of both species, with L. tropica being an anthroponosis compared to L. major, which is a zoonosis.
The sequence analysis of Cyt b gene from 25 L. major and L. tropica strains demonstrated genetic variability of L. major and L. tropica causing CL in southern Iran, and a feasible connection amid the genetic heterogeneity of the parasite, geographical source and clinical appearance of the disease in human was detected.
由利什曼原虫引起的皮肤利什曼病(CL)是一种广泛流行的疾病,可感染人类和动物。伊朗 31 个省份中有一半存在 CL 地方性流行,2010 年至 2015 年法尔斯省报告了 29201 例发病病例。CL 呈多态性,可能导致具有不同临床特征的病变。寄生虫遗传多样性被认为是影响 CL 患者临床结果和病变特征的因素之一。然而,基于细胞色素 b(Cyt b)基因测序,关于利什曼原虫属的遗传变异的信息仍然非常有限。
所有患者均来自法尔斯省的地方性流行区。采用巢式 PCR 从 100 例临床表型不同的 CL 患者的分离物中扩增 Cyt b 基因。对扩增的 Cyt b 进行序列分析,以检查利什曼原虫分离株之间的遗传变异,并将结果与临床图片联系起来。临床表现基本上有两种类型,即典型和非典型病变。采用邻接法构建分子系统发育树,将本研究中的种/株与来自其他地理区域的种/株进行比较。
鉴定出利什曼原虫是主要的感染利什曼原虫属(86%的病例),其余病例由利什曼热带菌感染。对患者的临床检查显示出 12 种不同的临床 CL 形式。在所分析的利什曼样本中,识别出 5 种不同的单倍型:3 种在利什曼原虫中,2 种在利什曼热带菌中。我们发现利什曼属的临床结果与 Cyt b 序列变异有关。此外,我们观察到利什曼原虫中的多态性比利什曼热带菌更高。这种差异可能是由于两种物种不同的生态流行病学所致,利什曼热带菌是一种人源传染病,而利什曼原虫则是一种动物源传染病。
对来自伊朗南部 25 株利什曼原虫和利什曼热带菌的 Cyt b 基因序列分析表明,利什曼原虫和利什曼热带菌引起的 CL 存在遗传变异性,并且在寄生虫的遗传异质性、地理来源和人类疾病的临床表现之间检测到了可行的联系。