定量实时 PCR 分析利什曼原虫抗锑基因表达,重点关注涉及三肽硫醇代谢和药物转运的基因。
Gene expression analysis of antimony resistance in Leishmania tropica using quantitative real-time PCR focused on genes involved in trypanothione metabolism and drug transport.
机构信息
Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran.
出版信息
Arch Dermatol Res. 2019 Jan;311(1):9-17. doi: 10.1007/s00403-018-1872-2. Epub 2018 Nov 2.
Pentavalent antimonials remain the treatment of choice for all the clinical forms of leishmaniasis. The increasing rates of antimony resistance are becoming a serious health problem in treatment of anthroponotic cutaneous leishmaniasis (ACL). Accordingly, unraveling molecular markers is crucial for improving medication strategies and monitoring of drug-resistant parasites. Different studies have suggested the importance of genes involved in trypanothione metabolism and drug transport. In this regard, present study was designed to investigate the RNA expression level of five genes including γ-GCS, ODC, TRYR (involved in trypanothione metabolism), AQP1 (acts in drug uptake) and MRPA (involved in sequestration of drug) in sensitive and resistant Leishmania tropica isolates. Seven antimony-resistant and seven antimony-sensitive L. tropica clinical isolates were collected from ACL patients. Drug sensitivity test was performed on the samples as well as reference strains; afterwards, gene expression analysis was performed on clinical isolates by quantitative real-time PCR. The results revealed that the average expression level of AQP1 gene was decreased (0.47-fold) in resistant isolates compared to sensitive ones whereas MRPA (2.45), γ-GCS (2.1) and TRYR (1.97) was upregulated in resistant isolates. The average expression of ODC (1.24-fold) gene was not different significantly between sensitive and resistant isolates. Our findings suggest that AQP1, MRPA, GSH1 and TRYR can be considered as potential molecular markers for screening of antimony resistance in some L. tropica clinical isolates.
五价锑仍然是所有临床形式利什曼病的首选治疗方法。锑耐药率的上升正在成为治疗人源皮肤利什曼病(ACL)的一个严重健康问题。因此,揭示分子标志物对于改善药物治疗策略和监测耐药寄生虫至关重要。不同的研究表明,涉及三肽硫醇代谢和药物转运的基因的重要性。在这方面,本研究旨在研究五个基因(包括 γ-GCS、ODC、TRYR(参与三肽硫醇代谢)、AQP1(参与药物摄取)和 MRPA(参与药物隔离))的 RNA 表达水平在敏感和耐药的利什曼热带菌株中。从 ACL 患者中收集了七个锑耐药和七个锑敏感的利什曼热带临床分离株。对样品和参考株进行了药物敏感性试验;随后,通过实时定量 PCR 对临床分离株进行了基因表达分析。结果表明,与敏感株相比,耐药株中 AQP1 基因的平均表达水平降低(0.47 倍),而 MRPA(2.45 倍)、γ-GCS(2.1 倍)和 TRYR(1.97 倍)在耐药株中上调。敏感株和耐药株之间 ODC(1.24 倍)基因的平均表达无显著差异。我们的研究结果表明,AQP1、MRPA、GSH1 和 TRYR 可以被认为是筛选一些利什曼热带临床分离株中锑耐药的潜在分子标志物。