4.5 Article

Detection and characterization of mutations in genes related to isoniazid resistance in Mycobacterium tuberculosis clinical isolates from Iran

Journal

MOLECULAR BIOLOGY REPORTS
Volume 49, Issue 7, Pages 6135-6143

Publisher

SPRINGER
DOI: 10.1007/s11033-022-07404-2

Keywords

Iran; Mycobacterium tuberculosis; Isoniazid resistance; katG; inhA; kasA; furA; oxyR-ahpC; ndh

Funding

  1. Ahvaz Jundishapur University of Medical Sciences (AJUMS), Ahvaz, Iran [OG-9930]

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This study investigated mutations in gene loci associated with isoniazid (INH) resistance in Mycobacterium tuberculosis (M.tb) clinical isolates from southwestern Iran. The study found that mutations in katG and inhA can serve as predictive molecular markers for INH resistance, and the co-detection of these mutations can identify a significant proportion of INH-resistant isolates.
Background The global rise in drug-resistant Mycobacterium tuberculosis (M.tb), and especially the significant prevalence of isoniazid (INH)-resistance constitute a significant challenge to global health. Therefore, the present study aimed to investigate mutations in prevalent gene loci-involved in INH-resistance phenotype-among M.tb clinical isolates from southwestern Iran. Methods Drug susceptibility testing (DST) was performed using the conventional proportional method on confirmed 6620 M.tb clinical isolates, and in total, 15 INH-resistant and 18 INH-susceptible isolates were included in the study. Fragments of six genetic loci most related to INH-resistance (katG, inhA promoter, furA, kasA, ndh, oxyR-ahpC intergenic region) were PCR-amplified and sequenced. Mutations were explored by pairwise alignment with the M.tb H37Rv genome. Results The analysis of gene loci revealed 13 distinct mutations in INH-resistant isolates. 60% (n = 9) of the INH-resistant isolates had mutations in katG, with codon 315 predominately (53.3%, n = 8). Mutation at InhA - 15 was found in 20% (n = 3) of resistant isolates. 26.7% (n = 4) of the INH-resistant isolates had kasA mutations, of which G269S substitution was the most common (20%, n = 3). The percentage of mutations in furA, oxyR-ahpC and ndh was 6.7% (n = 1), 46.7% (n = 7), and 20% (n = 3), respectively. Of the mutations detected in ndh and oxyR-ahpC, 5 were also observed in INH-susceptible isolates. This study revealed seven novel mutations, four of which were exclusively in resistant isolates. Conclusions This study supports the usefulness of katG and inhA mutations as a predictive molecular marker for INH resistance. Co-detection of katG S315 and inhA-15 mutations identified 73.3% (11 out of 15 isolates) of INH-resistant isolates.

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