Department of Zoology, Bethune College, Bidhan Sarani, Kolkata, India.
Acta Trop. 2012 Dec;124(3):229-34. doi: 10.1016/j.actatropica.2012.08.017. Epub 2012 Aug 31.
Visceral Leishmaniasis or Kala-azar (KA) is a serious health concern in India. In the present study, Restriction Fragment Length Polymorphism (RFLP) of three genetic markers viz., Internal Transcribed Spacer (ITS), ITS1 and heat shock protein 70 (hsp70) have been employed for typing the clinical isolates [n=15] of KA and post Kala-azar Dermal Leishmaniosis (PKDL) collected from India and Bangladesh in the period of 2006-2010. Experimentally, ITS, ITS1 and hsp70 regions of genomes of all the clinical isolates were separately amplified by PCR and then digested with restriction enzymes: ITS with Alu1, EcoR1 and Msp1, ITS1 with Hae III and Rsa1 and hsp70 with Hae III. The resultant fragments were analyzed by agarose gel electrophoresis and the RFLP profiles of the clinical isolates were compared with that of the WHO reference strains for Leishmania donovani (DD8) and Leishmania tropica (K27), respectively. Also, the ITS1 regions of all the clinical isolates along with the two WHO reference strains were sequenced and a phylogram was constructed to ascertain the extent of similarity or dissimilarity. Interestingly, the RFLP profiles of one of the isolates showed a significant homology with K27 and the phylogram revealed its closeness with the same putting credence to our earlier typing of isolates by RAPD method. This observation also supported an earlier report claiming that both the species are responsible for KA in India and thus, emphasizes urgent need for thorough systematic characterization of the clinical isolates of Indian KA as appropriate treatment regime relies primarily on proper diagnosis.
内脏利什曼病或黑热病(KA)是印度严重的健康问题。在本研究中,采用限制性片段长度多态性(RFLP)分析了三个遗传标记,即内部转录间隔区(ITS)、ITS1 和热休克蛋白 70(hsp70),对 2006 年至 2010 年间从印度和孟加拉国收集的 15 株 KA 临床分离株和黑热病后皮肤利什曼病(PKDL)进行了分型。实验中,分别通过 PCR 扩增所有临床分离株的 ITS、ITS1 和 hsp70 区基因组,然后用限制酶 Alu1、EcoR1 和 Msp1 消化 ITS,用 Hae III 和 Rsa1 消化 ITS1,用 Hae III 消化 hsp70。用琼脂糖凝胶电泳分析所得片段,并将临床分离株的 RFLP 图谱与 WHO 利什曼原虫参考株(DD8)和利什曼原虫热带株(K27)进行比较。此外,对所有临床分离株的 ITS1 区以及这两个 WHO 参考株进行测序,并构建系统发育树以确定其相似性或相异性的程度。有趣的是,其中一个分离株的 RFLP 图谱与 K27 具有显著的同源性,系统发育树显示其与 K27 非常接近,这进一步证实了我们之前通过 RAPD 方法对分离株的分型。这一观察结果也支持了早些时候的一份报告,该报告声称这两个物种都可能是印度 KA 的原因,因此,强调迫切需要对印度 KA 的临床分离株进行彻底的系统特征描述,因为适当的治疗方案主要依赖于正确的诊断。