p -糖蛋白A、g -谷氨酰半胱氨酸合成酶1和甘油oporin 1基因在未愈合的人畜共患皮肤利什曼病中的表达研究

S. Hejazi, S. Saberi, R. Arjmand, S. Soleimanifard
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引用次数: 0

摘要

背景与目的:针对临床越来越多的耐锑利什曼病,了解耐药原因是有帮助的。本研究旨在发现耐药相关基因p -糖蛋白A (PgpA)、g -谷氨酰半胱氨酸合成酶1 (Gsh1)和水甘酯oporin 1 (Aqp1)在临床耐药菌株中的表达水平。方法:对10例未愈合的利什曼病溃疡患者进行标本分离,采用巢式聚合酶链反应(巢式PCR)法进行菌种鉴定。体外实验采用J774细胞系无尾巨噬细胞模型,体内实验采用动物模型Balb/c小鼠。最后,采用定量反转录(q-RT)实时PCR法测定基因表达量,并与非耐药利什曼原虫(MRHO/IR/75/ER)进行比较。结果:分子鉴定表明,分离的原生动物均为L. major。临床耐药患者分离标本耐药基因表达无升高(P>0.05)。最后,发现患者缺乏改善与耐药基因表达增加无关。结论:总的来说,在测试样本中没有观察到固有的抗性,也没有发现病变愈合与基因表达水平之间的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The study of P-glycoprotein A, G-glutamylcysteine synthetase 1, and aquaglyceroporin 1 genes expression in non-healing zoonotic cutaneous leishmaniasis cases
Background and aims: Regarding the increasing numbers of clinical antimonial-resistant Leishmaniasis, understanding the reasons for drug resistance is helpful. This study aimed to find the expression level of the genes related to resistance, P-glycoprotein A (PgpA), G-glutamylcysteine synthetase 1 (Gsh1), and aquaglyceroporin 1 (Aqp1) in antimonial-resistant clinical isolates. Methods: Samples were isolated from leishmaniasis ulcers of 10 non-healing patients and the species were identified by the nested-polymerase chain reaction (PCR) method. In vitro experiments were performed using the amastigote-macrophage model by J774 cell line, and in vivo studies were conducted by animal model, the Balb/c mice. Finally, the values of genes expression were determined by quantitative-reverse transcription (q-RT) real-time PCR method and then compared with non-resistant Leishmania major (MRHO/IR/75/ER). Results: Molecular identification showed that all isolated protozoa were L. major. The isolated samples from clinical resistant patients represented no increase in expression in the tested resistance genes (P>0.05). Finally, it was found that the lack of improvements in patients was not associated with the increased expression of resistance genes. Conclusion: In general, no inherent resistance was observed in the tested samples neither a correlation between the healing of lesions and the level of genes expression.
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