Alizadeh R, Hooshyar H, Bandehpor M, Arbabi M, Kazemi F, Talari A, Kazemi B
Department of Parasitology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Iran Red Crescent Med J. 2011 Dec;13(12):863-7. Epub 2011 Dec 1.
Cutaneous leishmaniasis is still a health problem in many rural and urban regions of Iran and drug resistance has emerged as a major impediment in the treatment of leishmaniasis. This study aims to determine the drug resistance gene in cutaneous leishmaniasis by PCR in some endemic areas of Iran.
Ninety seven samples were collected from ulcers of leishmaniasis patients from some endemic areas of Iran. The Giemsa stained samples were examined microscopically and cultured in NNN and RPMI 1640 mediums for parasite detection. After DNA extraction, PCR was done by a pair of specific primers. For detection of mutation in DNA, first PCR products were electrophoresed on CSGE gel. The suspected samples were compared by sequencing and RFLP results were demonstrated. Comparison of DNA derived from a wild type cell and mutant cell was undertaken by CSGE and sequencing methods.
Among 90 isolates (92.8%) examined for detection of mutation in gene with CSGE and RFLP, 10 (11.1%) revealed a disorder in sequencing selection for unresponsive to drug.
Drug resistance in cutaneous leishmaniasis to sodium stiboglocanat is probably due to a mutation in a genome. A field study is needed to determine the distribution of drug resistance and other gene mutations involved in unresponsiveness to drugs in leishmaniasis endemic areas of Iran.
皮肤利什曼病在伊朗的许多城乡地区仍是一个健康问题,耐药性已成为利什曼病治疗的主要障碍。本研究旨在通过聚合酶链反应(PCR)确定伊朗一些流行地区皮肤利什曼病的耐药基因。
从伊朗一些流行地区的利什曼病患者溃疡处采集97份样本。对吉姆萨染色的样本进行显微镜检查,并在NNN和RPMI 1640培养基中培养以检测寄生虫。DNA提取后,用一对特异性引物进行PCR。为检测DNA中的突变,首先将PCR产物在变性梯度凝胶电泳(CSGE)凝胶上进行电泳。通过测序对疑似样本进行比较,并展示限制性片段长度多态性(RFLP)结果。采用CSGE和测序方法对野生型细胞和突变细胞的DNA进行比较。
在通过CSGE和RFLP检测基因突变的90株分离株(92.8%)中,10株(11.1%)显示对药物无反应的测序选择出现紊乱。
皮肤利什曼病对葡萄糖酸锑钠的耐药性可能是由于基因组中的突变。需要进行一项实地研究,以确定伊朗利什曼病流行地区耐药性的分布以及与药物无反应相关的其他基因突变情况。