Ahmadian Salman, Eslami Gilda, Fatahi Ali, Hosseini Saeede Sadat, Vakili Mahmoud, Ajamein Fahadan Vahid, Elloumi Mourad
1Research Center for Food Hygiene and Safety, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
2Department of Parasitology and Mycology, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
J Parasit Dis. 2019 Mar;43(1):39-45. doi: 10.1007/s12639-018-1052-5. Epub 2018 Nov 20.
Cutaneous leishmaniasis (CL) is a major disease in many parts of the world. Since no vaccine has been developed, treatment is the best way to control it. In most areas, antimonial resistance whose mechanisms have not been completely understood has been reported. The main aim of this study is gene expression assessing of - and - in clinical isolates. The patients with CL from central and north Iran were considered for this study. The samples were transferred in RNAlater solution and stored in - 20 °C. RNA extraction and cDNA synthesis were performed. The gene expression analysis was done with SYBR Green real-time PCR using ∆∆CT. Written informed consent forms were filled out by patients, and then, information forms were filled out based on the Helsinki Declaration. Statistical analysis was done with SPSS (16.0; SPSS Inc, Chicago) using independent test, Shapiro-Wilk, and Pearson's and Spearman's rank correlation coefficients. ≤ 0.05 was considered significant. The gene expression of and had no relation with sex and age. The gene expression was high in sensitive isolates obtained from north of the country. The gene expression was significant in sensitive and no response-antimonial isolates from the north, but no significant differences were detected in sensitive and resistant isolates from central Iran. Differential gene expression of and in various clinical resistances isolates in different geographical areas shows multifactorial ways of developing resistance in different isolates.
皮肤利什曼病(CL)是世界许多地区的一种主要疾病。由于尚未研发出疫苗,治疗是控制该病的最佳方法。在大多数地区,已报告了抗锑性,但其机制尚未完全明确。本研究的主要目的是评估临床分离株中[具体基因名称未给出]的基因表达。本研究纳入了来自伊朗中部和北部的CL患者。样本在RNA Later溶液中转运,并储存在-20°C。进行了RNA提取和cDNA合成。使用ΔΔCT通过SYBR Green实时PCR进行基因表达分析。患者填写了书面知情同意书,然后根据《赫尔辛基宣言》填写了信息表。使用SPSS(16.0;SPSS公司,芝加哥)进行统计分析,采用独立样本t检验、Shapiro-Wilk检验以及Pearson和Spearman等级相关系数。P≤0.05被认为具有统计学意义。[具体基因名称未给出]的基因表达与性别和年龄无关。在该国北部获得的敏感分离株中[具体基因名称未给出]的基因表达较高。在北部的敏感和无抗锑反应的分离株中[具体基因名称未给出]的基因表达有显著差异,但在伊朗中部的敏感和耐药分离株中未检测到显著差异。不同地理区域不同临床耐药分离株中[具体基因名称未给出]的差异基因表达显示了不同分离株产生耐药性的多因素方式。