Sophie Mariam, Hameed Abdul, Muneer Akhtar, Samdani Azam J, Saleem Saima, Azhar Abid
Karachi Institute of Biotechnology & Genetic Engineering (KIBGE), University of Karachi, Karachi, 75270, Pakistan.
Institute of Biomedical and Genetic Engineering (IBGE), 24-Mauve Area, G- 9/1, Islamabad, Pakistan.
Parasit Vectors. 2017 Jan 7;10(1):12. doi: 10.1186/s13071-016-1934-2.
The vector-borne cutaneous leishmaniasis (CL) is endemic in several regions of Pakistan mainly affecting poor populations. Host genetic factors, particularly SLC11A1 (solute carrier transmembrane protein) within macrophages, play a crucial role in disease pathology and susceptibility. Association of SLC11A1 with cutaneous leishmaniasis, a neglected tropical disease, is not well established. Inconsistencies have been observed within different populations worldwide with respect to genetic susceptibility. This study was designed to investigate genetic variation(s) in SLC11A1 and to assess possible association with cutaneous leishmaniasis in Pakistan.
Eight polymorphisms (rs2276631, rs3731864, rs2290708, rs2695342, rs201565523, rs17215556, rs17235409, rs17235416) were genotyped across SLC11A1 in 274 patients and 119 healthy controls. Six polymorphisms were studied by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and sequencing. Two single nucleotide polymorphisms were analyzed with newly designed semi-nested PCR assays. Case-control analysis showed no association between selected polymorphisms in SLC11A1 and cutaneous leishmaniasis. No significant difference was observed in the distribution of alleles between leishmaniasis patients and healthy individuals. Strong pairwise linkage disequilibrium was observed between rs2276631 and rs2290708 (r = 64); and rs17235409 and rs17235416 (r = 78).
This study shows that genetic variations in the candidate gene SLC11A1 do not affect susceptibility to cutaneous leishmaniasis in the sample population from Pakistan.
媒介传播的皮肤利什曼病(CL)在巴基斯坦的多个地区呈地方性流行,主要影响贫困人口。宿主遗传因素,尤其是巨噬细胞内的溶质载体跨膜蛋白11A1(SLC11A1),在疾病病理和易感性中起关键作用。SLC11A1与被忽视的热带病皮肤利什曼病之间的关联尚未完全明确。在全球不同人群中,关于遗传易感性存在不一致的观察结果。本研究旨在调查SLC11A1的遗传变异,并评估其与巴基斯坦皮肤利什曼病的可能关联。
对274例患者和119名健康对照者的SLC11A1基因进行了8个多态性位点(rs2276631、rs3731864、rs2290708、rs2695342、rs201565523、rs17215556、rs17235409、rs17235416)的基因分型。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和测序研究了6个多态性位点。使用新设计的半巢式PCR检测分析了2个单核苷酸多态性。病例对照分析显示,SLC11A1中所选多态性与皮肤利什曼病之间无关联。利什曼病患者和健康个体之间的等位基因分布未观察到显著差异。在rs2276631和rs2290708(r = 64)以及rs17235409和rs17235416(r = 78)之间观察到强成对连锁不平衡。
本研究表明,候选基因SLC11A1的遗传变异不影响来自巴基斯坦样本人群对皮肤利什曼病的易感性。