» Articles » PMID: 12118524

Variations in the Occurrence of the S315T Mutation Within the KatG Gene in Isoniazid-resistant Clinical Mycobacterium Tuberculosis Isolates from Kuwait

Overview
Publisher Mary Ann Liebert
Date 2002 Jul 18
PMID 12118524
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

The worldwide threat of drug-resistant tuberculosis (TB) to human health has led to the development of molecular methods for rapidly determining the resistance of clinical Mycobacterium tuberculosis isolates to the two front-line antituberculous drugs, isoniazid and rifampin. The prevalence of the S315T mutation within the katG gene, which confers clinically significant resistance to isoniazid, was determined in isoniazid-resistant clinical M. tuberculosis isolates recovered from TB patients in Kuwait. A total of 67 isoniazid-resistant and 18 susceptible clinical M. tuberculosis isolates were tested. The mutation S315T was found in 46 (69%) of the 67 resistant strains, whereas none of the susceptible strains contained this mutation. The prevalence of this mutation was highest (32 of 40, 80%) in isolates recovered from patients of South Asian origin and lowest in isolates from patients of Middle Eastern origin (8 of 18, 44%). The genotyping performed on isolates carrying the S315T mutation showed that the isolates belong to several different types as they exhibited unique DNA banding patterns. The results point to a varying prevalence of the S315T mutation within the katG gene in clinical M. tuberculosis isolates recovered from patients of different ethnic groupings within the same country. The results also suggest that detection of the S315T mutation in the katG gene may be used as a rapid screening method for identifying isoniazid-resistant clinical M. tuberculosis isolates recovered from majority of patients in some ethnic groupings.

Citing Articles

First insights into the phylogenetic diversity of Mycobacterium tuberculosis in Kuwait and evaluation of REBA MTB-MDR assay for rapid detection of MDR-TB.

Al-Mutairi N, Ahmad S, Mokaddas E, Al-Hajoj S PLoS One. 2022; 17(10):e0276487.

PMID: 36264939 PMC: 9584360. DOI: 10.1371/journal.pone.0276487.


Deciphering Isoniazid Drug Resistance Mechanisms on Dimeric KatG via Post-molecular Dynamics Analyses Including Combined Dynamic Residue Network Metrics.

Barozi V, Musyoka T, Sheik Amamuddy O, Tastan Bishop O ACS Omega. 2022; 7(15):13313-13332.

PMID: 35474779 PMC: 9025985. DOI: 10.1021/acsomega.2c01036.


Molecular characterization of multidrug-resistant Mycobacterium tuberculosis (MDR-TB) isolates identifies local transmission of infection in Kuwait, a country with a low incidence of TB and MDR-TB.

Al-Mutairi N, Ahmad S, Mokaddas E Eur J Med Res. 2019; 24(1):38.

PMID: 31806020 PMC: 6894303. DOI: 10.1186/s40001-019-0397-2.


Occurrence of disputed rpoB mutations among Mycobacterium tuberculosis isolates phenotypically susceptible to rifampicin in a country with a low incidence of multidrug-resistant tuberculosis.

Al-Mutairi N, Ahmad S, Mokaddas E, Eldeen H, Joseph S BMC Infect Dis. 2019; 19(1):3.

PMID: 30606116 PMC: 6318973. DOI: 10.1186/s12879-018-3638-z.


A Chip for Detecting Tuberculosis Drug Resistance Based on Polymerase Chain Reaction (PCR)-Magnetic Bead Molecule Platform.

Lyu J, Wu W, Cheng P, Liu X, Luo F, Zhang Z Front Microbiol. 2018; 9:2106.

PMID: 30258420 PMC: 6143819. DOI: 10.3389/fmicb.2018.02106.