Antisense RNA to ahpC, an oxidative stress defence gene involved in isoniazid resistance, indicates that AhpC of Mycobacterium bovis has virulence properties
- 1 October 1998
- journal article
- Published by Microbiology Society in Microbiology
- Vol. 144 (10) , 2687-2695
- https://doi.org/10.1099/00221287-144-10-2687
Abstract
SUMMARY: Antisense RNA is a versatile tool for reducing gene expression. It was used to determine if ahpC, a gene that is involved in defence against oxidative stress and isoniazid (INH) resistance, is important for virulence of Mycobacterium bovis, a member of the Mycobecterium tuberculosis complex. Antisense RNA constructs of ahpC were made using different strength promoters in front of a reversed coding sequence of ahpC. These constructs were electroporated into a virulent wild-type M. bowis strain and a moderately virulent INH-resistant M. bo wis strain that was cata lase/peroxi dase-negat ive. Down- regulation of protein synthesis occurred and this was visualized by immunoblotting. All strains containing antisense RNA were markedly less virulent than their parent strains in guinea pigs. M. bowis with an up-regulated ahpC gene was more resistant to cumene hydroperoxide than its parent strain, which had a wild- type ahpC promoter. These results agree with a model of INH resistance in which overexpression of AhpC compensates in some INH-resistant strains for loss of catalase/peroxidase by maintaining the ability to defend against oxidative stress mediated through organic peroxides. In addition, normal expression of AhpC is crucial for maintaining the virulence of wild-type M. bovis, which has normal catalase/peroxidase levels.Keywords
This publication has 28 references indexed in Scilit:
- Kinetics of Inactivation of WT and C243S Mutant of Mycobacterium tuberculosis Enoyl Reductase by Activated IsoniazidJournal of the American Chemical Society, 1996
- Biochemical and Genetic Data Suggest that InhA Is Not the Primary Target for Activated Isoniazid in Mycobacterium tuberculosisThe Journal of Infectious Diseases, 1996
- 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. tuberculosisJournal of Bacteriology, 1996
- Mycobacterium tuberculosis is a natural mutant with an inactivated oxidative‐stress regulatory gene:implications for sensitivity to isoniazidMolecular Microbiology, 1995
- Mutation of the principal sigma factor causes loss of virulence in a strain of the Mycobacterium tuberculosis complex.Proceedings of the National Academy of Sciences, 1995
- Crystal Structure and Function of the Isoniazid Target of Mycobacterium tuberculosisScience, 1995
- Missense mutations in the catalase‐peroxidase gene, katG, are associated with isoniazid resistance in Mycobacterium tuberculosisMolecular Microbiology, 1995
- Mechanistic Studies of the Oxidation of Isoniazid by the Catalase Peroxidase from Mycobacterium tuberculosisJournal of the American Chemical Society, 1994
- inhA , a Gene Encoding a Target for Isoniazid and Ethionamide in Mycobacterium tuberculosisScience, 1994
- Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimuriumCell, 1985