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Science ; 263(5144): 227-30, 1994 Jan 14.
Article in English | MEDLINE | ID: mdl-8284673

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.


Subject(s)
Bacterial Proteins/genetics , Drug Resistance, Microbial/genetics , Ethionamide/pharmacology , Genes, Bacterial , Isoniazid/pharmacology , Mycobacterium tuberculosis/genetics , Oxidoreductases , Amino Acid Sequence , Bacterial Proteins/chemistry , Base Sequence , Cloning, Molecular , Ethionamide/metabolism , Isoniazid/metabolism , Molecular Sequence Data , Mutation , Mycobacterium/drug effects , Mycobacterium/genetics , Mycobacterium bovis/drug effects , Mycobacterium bovis/genetics , Mycobacterium tuberculosis/chemistry , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/metabolism , Mycolic Acids/metabolism , Open Reading Frames , Sequence Alignment
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