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.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Bacterial Proteins / chemistry
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Bacterial Proteins / genetics*
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Base Sequence
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Cloning, Molecular
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Drug Resistance, Microbial / genetics*
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Ethionamide / metabolism
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Ethionamide / pharmacology*
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Genes, Bacterial*
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Isoniazid / metabolism
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Isoniazid / pharmacology*
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Molecular Sequence Data
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Mutation
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Mycobacterium / drug effects
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Mycobacterium / genetics
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Mycobacterium bovis / drug effects
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Mycobacterium bovis / genetics
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Mycobacterium tuberculosis / chemistry
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Mycobacterium tuberculosis / drug effects
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Mycobacterium tuberculosis / genetics*
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Mycobacterium tuberculosis / metabolism
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Mycolic Acids / metabolism
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Open Reading Frames
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Oxidoreductases*
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Sequence Alignment
Substances
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Bacterial Proteins
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Mycolic Acids
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Oxidoreductases
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InhA protein, Mycobacterium
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Ethionamide
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Isoniazid
Associated data
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GENBANK/U02492
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GENBANK/U02530