Department of Microbiology and Molecular Genetics, IMRIC, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
PLoS Negl Trop Dis. 2013;7(1):e2031. doi: 10.1371/journal.pntd.0002031. Epub 2013 Jan 24.
BACKGROUND/OBJECTIVES: Visceral leishmaniasis (VL) caused by Leishmania donovani is a major health problem in Ethiopia. Parasites in disparate regions are transmitted by different vectors, and cluster in distinctive genotypes. Recently isolated strains from VL and HIV-VL co-infected patients in north and south Ethiopia were characterized as part of a longitudinal study on VL transmission.
METHODOLOGY/PRINCIPAL FINDINGS: Sixty-three L. donovani strains were examined by polymerase chain reaction (PCR) targeting three regions: internal transcribed spacer 1 (ITS1), cysteine protease B (cpb), and HASPB (k26). ITS1- and cpb--PCR identified these strains as L. donovani. Interestingly, the k26--PCR amplicon size varied depending on the patient's geographic origin. Most strains from northwestern Ethiopia (36/40) produced a 290 bp product with a minority (4/40) giving a 410 bp amplicon. All of the latter strains were isolated from patients with HIV-VL co-infections, while the former group contained both VL and HIV-VL co-infected patients. Almost all the strains (20/23) from southwestern Ethiopia produced a 450 bp amplicon with smaller products (290 or 360 bp) only observed for three strains. Sudanese strains produced amplicons identical (290 bp) to those found in northwestern Ethiopia; while Kenyan strains gave larger PCR products (500 and 650 bp). High-resolution melt (HRM) analysis distinguished the different PCR products. Sequence analysis showed that the k26 repeat region in L. donovani is comprised of polymorphic 13 and 14 amino acid motifs. The 13 amino acid peptide motifs, prevalent in L. donovani, are rare in L. infantum. The number and order of the repeats in L. donovani varies between geographic regions.
CONCLUSIONS/SIGNIFICANCE: HASPB repeat region (k26) shows considerable polymorphism among L. donovani strains from different regions in East Africa. This should be taken into account when designing diagnostic assays and vaccines based on this antigen.
背景/目的:由利什曼原虫引起的内脏利什曼病(VL)是埃塞俄比亚的一个主要健康问题。不同地区的寄生虫由不同的媒介传播,并聚集在不同的基因型中。最近从埃塞俄比亚北部和南部 VL 和 HIV-VL 合并感染患者中分离出的菌株作为 VL 传播的纵向研究的一部分进行了特征描述。
方法/主要发现:对 63 株利什曼原虫进行聚合酶链反应(PCR)检测,针对三个区域:内部转录间隔区 1(ITS1)、半胱氨酸蛋白酶 B(cpb)和 HASPB(k26)。ITS1-PCR 和 cpb-PCR 鉴定这些菌株为利什曼原虫。有趣的是,k26-PCR 扩增子的大小取决于患者的地理位置。来自埃塞俄比亚西北部的大多数菌株(36/40)产生 290 bp 的产物,少数(4/40)产生 410 bp 的扩增子。后者的所有菌株均分离自 HIV-VL 合并感染患者,而前者则包含 VL 和 HIV-VL 合并感染患者。来自埃塞俄比亚西南部的几乎所有菌株(20/23)都产生 450 bp 的扩增子,只有 3 个菌株产生较小的产物(290 或 360 bp)。苏丹菌株产生与西北部埃塞俄比亚相同的扩增子(290 bp);而肯尼亚菌株则产生更大的 PCR 产物(500 和 650 bp)。高分辨率熔解(HRM)分析可区分不同的 PCR 产物。序列分析表明,利什曼原虫 k26 重复区由多态性 13 和 14 个氨基酸基序组成。在利什曼原虫中普遍存在的 13 个氨基酸肽基序在利什曼原虫婴儿中很少见。利什曼原虫中重复的数量和顺序在不同的地理区域有所不同。
结论/意义:来自东非不同地区的利什曼原虫菌株的 HASPB 重复区(k26)显示出相当大的多态性。在基于该抗原设计诊断检测和疫苗时应考虑这一点。