inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis
- PMID: 8284673
- DOI: 10.1126/science.8284673
inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis
Abstract
Isoniazid (isonicotinic acid hydrazide, INH) is one of the most widely used antituberculosis drugs, yet its precise target of action on Mycobacterium tuberculosis is unknown. A missense mutation within the mycobacterial inhA gene was shown to confer resistance to both INH and ethionamide (ETH) in M. smegmatis and in M. bovis. The wild-type inhA gene also conferred INH and ETH resistance when transferred on a multicopy plasmid vector to M. smegmatis and M. bovis BCG. The InhA protein shows significant sequence conservation with the Escherichia coli enzyme EnvM, and cell-free assays indicate that it may be involved in mycolic acid biosynthesis. These results suggest that InhA is likely a primary target of action for INH and ETH.
Comment in
-
Unveiling a tuberculosis drug target.Science. 1994 Jan 14;263(5144):172. doi: 10.1126/science.8284668. Science. 1994. PMID: 8284668 No abstract available.
Similar articles
-
Overexpression of inhA, but not kasA, confers resistance to isoniazid and ethionamide in Mycobacterium smegmatis, M. bovis BCG and M. tuberculosis.Mol Microbiol. 2002 Oct;46(2):453-66. doi: 10.1046/j.1365-2958.2002.03162.x. Mol Microbiol. 2002. PMID: 12406221
-
The mabA gene from the inhA operon of Mycobacterium tuberculosis encodes a 3-ketoacyl reductase that fails to confer isoniazid resistance.Microbiology (Reading). 1998 Oct;144 ( Pt 10):2697-2704. doi: 10.1099/00221287-144-10-2697. Microbiology (Reading). 1998. PMID: 9802011
-
Comparative analysis of mycobacterial NADH pyrophosphatase isoforms reveals a novel mechanism for isoniazid and ethionamide inactivation.Mol Microbiol. 2011 Dec;82(6):1375-91. doi: 10.1111/j.1365-2958.2011.07892.x. Epub 2011 Nov 3. Mol Microbiol. 2011. PMID: 22026918 Free PMC article.
-
Resistance to Isoniazid and Ethionamide in Mycobacterium tuberculosis: Genes, Mutations, and Causalities.Microbiol Spectr. 2014 Aug;2(4):MGM2-0014-2013. doi: 10.1128/microbiolspec.MGM2-0014-2013. Microbiol Spectr. 2014. PMID: 26104204 Free PMC article. Review.
-
The mechanism of isoniazid killing: clarity through the scope of genetics.Annu Rev Microbiol. 2007;61:35-50. doi: 10.1146/annurev.micro.61.111606.122346. Annu Rev Microbiol. 2007. PMID: 18035606 Review.
Cited by
-
A Long Residence Time Enoyl-Reductase Inhibitor Explores an Extended Binding Region with Isoenzyme-Dependent Tautomer Adaptation and Differential Substrate-Binding Loop Closure.ACS Infect Dis. 2021 Apr 9;7(4):746-758. doi: 10.1021/acsinfecdis.0c00437. Epub 2021 Mar 12. ACS Infect Dis. 2021. PMID: 33710875 Free PMC article.
-
Platforms for antibiotic discovery.Nat Rev Drug Discov. 2013 May;12(5):371-87. doi: 10.1038/nrd3975. Nat Rev Drug Discov. 2013. PMID: 23629505 Review.
-
REMap: Operon map of M. tuberculosis based on RNA sequence data.Tuberculosis (Edinb). 2016 Jul;99:70-80. doi: 10.1016/j.tube.2016.04.010. Epub 2016 Apr 29. Tuberculosis (Edinb). 2016. PMID: 27450008 Free PMC article.
-
Comparative genomic analysis of mycobacteriophage Tweety: evolutionary insights and construction of compatible site-specific integration vectors for mycobacteria.Microbiology (Reading). 2007 Aug;153(Pt 8):2711-2723. doi: 10.1099/mic.0.2007/008904-0. Microbiology (Reading). 2007. PMID: 17660435 Free PMC article.
-
Direct detection of rifampin- and isoniazid-resistant Mycobacterium tuberculosis in auramine-rhodamine-positive sputum specimens by real-time PCR.J Clin Microbiol. 2004 Apr;42(4):1585-9. doi: 10.1128/JCM.42.4.1585-1589.2004. J Clin Microbiol. 2004. PMID: 15071008 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
