Detection of Mutation in Codon ۳۱۵ katG Gene as a Gene Marker Associated with Isoniazid Resistance, in Mycobacterium tuberculosis Strains Isolated from Patients in Isfahan and Tehran by PCR-RFLP Method

Publish Year: 1388
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:

JR_ZUMS-17-66_004

تاریخ نمایه سازی: 11 اردیبهشت 1400

Abstract:

Background and Objective: Drug resistance to tuberculosis is continuously increasing and is a significant threat to tuberculosis control programs because afew effective drugs are present against Mycobacterium tuberculosis. Although isoniazid (INH) is the most effective drug against tuberculosis, resistance to this drug also develops readily. Mutations in katG, specially the Ser۳۱۵Thr substitution, are responsible for isoniazid resistance in a large proportion of patients with tuberculosis. However, the frequency of the katG Ser۳۱۵Thr substitution varies among population samples. This study provided molecular characterization of isoniazid resistance of M. tuberculosis strains and extended our knowledge about molecular basis of M. tuberculosis drug resistance that is widely applicable for rapid drug resistance detection. Materials and Methods: Using ۱% proportional method, the sensitivity of ۱۲۶ strains isolated from patients in Isfahan and Tehran to isoniazid was determined. The katG mutations in codon ۳۱۵ associated with isoniazid resistance among isoniazid resistant isolates was determined by PCR-RFLP. In this way, ۳۵۵ bp PCR products were digested by MspI. Results: Out of ۱۲۶ isolates of M. tuberculosis, ۳۲ (۲۵.۴%) strains were determined as INH resistant. Resistance rate was ۲۲.۶% (۱۹ strains) in Isfahan and ۳۱% (۱۳ strains) in Tehran. Overall, ۷۲% of isoniazid-resistant isolates could be identified by analysis of just katG ۳۱۵ loci. Conclusion: The PCR-RFLP using MspI restriction enzyme that detects katG Ser۳۱۵Thr substitution could be identified in ۷۲% of isoniazid-resistant strains. Elucidation of the molecular characterization of isoniazid resistance in M. tuberculosis has led to the development of different genotypic approaches to the rapid detection of isoniazid resistant in clinical isolates.

Keywords:

Key words: Mycobacterium Tuberculosis , Isoniazid , PCR-RFLP , KatG , Isfahan , Tehran

Authors

پرویز مهاجری

Dept. of Microbiology, Faculty of Medicine, Kermanshah University of Medical Science, Kermanshah, Iran

اکبر توکلی

Dept. of Microbiology, Faculty of Medicine, Kermanshah University of Medical Science, Kermanshah, Iran

شراره مقیم

Dept. of Bacteriology, Faculty of Medicine, Isfahan University of Medical Science, Isfahan, Iran