Analysis of ahpC gene mutations in isoniazid-resistant clinical isolates of Mycobacterium tuberculosis
Author:
Affiliation:
1. Laboratory of Mycobacteria, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892, USA.
Abstract
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Link
https://journals.asm.org/doi/pdf/10.1128/AAC.41.9.2057
Reference15 articles.
1. inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis;Banerjee A.;Science,1994
2. Oxidative stress response and its role in sensitivity to isoniazid in mycobacteria: characterization and inducibility of ahpC by peroxides in Mycobacterium smegmatis and lack of expression in M. aurum and M. tuberculosis;Dhandayuthapani S.;J. Bacteriol.,1996
3. Missense mutations in the catalase-peroxidase gene, katG, are associated with isoniazid resistance in Mycobacterium tuberculosis;Heym B.;Mol. Microbiol.,1995
4. Effects of overexpression of the alkyl hydroperoxide reductase AhpC on the virulence and isoniazid resistance of Mycobacterium tuberculosis;Heym B.;Infect. Immun.,1997
5. Overexpression, purification, and characterization of the catalase-peroxidase KatG from Mycobacterium tuberculosis;Johnsson K.;J. Biol. Chem.,1997
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