高分辨熔融法筛选结核分枝杆菌katG、inhA和rpoB基因对异烟肼和利福平耐药相关突变的基因分型

Z. Tavakkoli, A. Nazemi
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引用次数: 3

摘要

简介:结核病是传染病之一,在世界上造成300万人死亡,这是由于耐药结核病患者的增加而增加的。因此,检测结核病患者的耐药性似乎至关重要。利福平和异烟肼是治疗结核病的两种基本药物。与结核病患者的传统方法相比,新的高分辨率熔化方法简单、快速和廉价,可用于检测导致这些耐药性的突变。材料与方法:对2年内转诊至伊朗治疗中心的疑似肺结核患者采集痰液样本2500份,其中结核分枝杆菌涂片阳性样本1650份。从样品中提取基因组DNA后,根据SY -9的颜色对样品采用高分辨率熔化法,并对PCR产物进行测序以验证突变。结果:1650份阳性涂片样本中,有116份因katG和inhA基因突变对异烟肼产生耐药性,其中inhA基因突变20份,katG基因突变96份。65份样品对利福平耐药,rpoB基因突变。结论:高分辨率熔融法快速、简便、经济,不浪费培养时间和PCR后处理时间,可用于结核病临床样品的耐药诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genotyping of Related Mutations to Drug Resistance in Isoniazid and Rifampin by Screening of katG, inhA and rpoB Genes in Mycobacterium tuberculosis by High Resolution Melting Method
Introduction: Tuberculosis is one of the infectious diseases and this is responsible for 3 million mortalities in the world which is increased by the rise of drug-resistant tuberculosis patients. Thus, it seems essential to detect the drug resistances in tuberculosis patients. Rifampin and isoniazid are two essential drugs for treatment of tuberculosis patients. The new High Resolution Melting method is simple, rapid and inexpensive for detection of these mutations responsible for these resistances compared to conventional methods in tuberculosis patients. Materials and methods: 2500 sputum samples were collected from patients with suspected tuberculosis referred to Iran Remedial Center over a period of 2 years in which, 1650 samples had positive smear for Mycobacterium tuberculosis. After extraction of genomic DNA from samples, High resolution melting method was used for samples based on the color of SY to-9 and PCR product were sequenced to verify the mutation. Results: Our findings showed that, 116 out of 1650 positive smear samples, were resistant to isoniazid due to mutations in katG and inhA genes, which this resistance is created by mutation of 20 samples in inhA gene and 96 samples in katG gene. Whist 65 samples had resistance to rifampin with mutation in rpoB gene. Conclusion: High resolution melting method is quick, easy and affordable without wasting time for culturing and Post PCR processes for diagnosing these resistances in tuberculosis clinical samples.
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