scholarly journals Isoniazid resistance and the point mutation of codon 463 of katG gene of Mycobacterium tuberculosis

1997 ◽  
Vol 12 (2) ◽  
pp. 92 ◽  
Author(s):  
T S Shim ◽  
C G Yoo ◽  
S K Han ◽  
Y S Shim ◽  
Y W Kim
2018 ◽  
Vol 16 (2) ◽  
pp. 353-360
Author(s):  
Nghiem Minh Ngoc ◽  
Nguyen Thi Hoai Thu

Infection of Mycobacterium tuberculosis (MTB) is one of the most common infections in humans. However, the detection rate is only 37% of estimated patients. Currently, Tuberculosic bacteria (TB) are becoming more serious with many TB strains developing multi-drug resistance, and particularly, in case of co-infection with TB and HIV/AIDS. The izoniazid resistant TB strains (INH) also resistant to the other anti-TB antibiotics. The molecular biology methods have allowed rapid and accurate diagnosis of patients infected with drug-resistant TB bacteria. In this study, we used primers katG-F and katG-R designed for amplication of a fragment of 684 bp in katG gene in 7 strains of TB bacteria collected in Pham Ngoc Thach - Ho Chi Minh city and Hue Central hospitals. Sequence analysis of the katG gene fragments showed that 5 samples had substitution mutations at codon 315 (point mutation G to C), leading to the change of amino acid from Serine to Threonine (S315T). In the 5th sample there appeared another mutation at codon 324, changing amino acid Aspartic (D) to Glycine (G) (D324G). In the sample DA1, no mutation has been found in any codon in the katG gene fragment studied. The results obtained in this study may have important implications in changing the treatment regimen and control of tuberculosis in a country with high number of TB patients as in Vietnam.


1996 ◽  
Vol 40 (4) ◽  
pp. 1053-1056 ◽  
Author(s):  
H Ohno ◽  
H Koga ◽  
S Kohno ◽  
T Tashiro ◽  
K Hara

We analyzed the relationship between rifampin MICs and rpoB mutations of 40 clinical isolates of Mycobacterium tuberculosis. A point mutation in either codon 516, 526, or 531 was found in 13 strains requiring MICs of > or = 64 micrograms/ml, while 21 strains requiring MICs of < or = 1 microgram/ml showed no alteration in these codons. However, 3 of these 21 strains contained a point mutation in either codon 515 or 533. Of the other six strains requiring MICs between 2 and 32 micrograms/ml, three contained a point mutation in codon 516 or 526, while no alteration was detected in the other three. Our results indicate that the sequencing analysis of a 69-bp fragment in the rpoB gene is useful in predicting rifampin-resistant phenotypes.


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