Rapid identification of a point mutation of the Mycobacterium tuberculosis catalase-peroxidase (katG) gene associated with isoniazid resistance

J Infect Dis. 1995 Jan;171(1):240-5. doi: 10.1093/infdis/171.1.240.

Abstract

The complete catalase-peroxidase (katG) gene DNA sequence was determined for 15 strains of Mycobacterium tuberculosis with a wide range of susceptibility to isoniazid. Five of 9 strains with isoniazid MICs > or = 1.0 microgram/mL had one or more missense mutations and all 5 strains had a common G-->T transversion in codon 463, causing the replacement of arginine with leucine and the loss of an NciI or MspI restriction site. None of 6 strains with an isoniazid MIC < 1.0 microgram/mL had mutations affecting codon 463. Restriction analysis of 43 strains with isoniazid MICs > or = 1.0 microgram/mL showed that 19 (44.2%) had lost the NciI-MspI restriction site at the locus of codon 463 while only 1 of 32 strains with isoniazid MICs < or = 1.0 microgram/L had this restriction polymorphism. These results indicate that the mutation arginine-->leucine in codon 463 of the catalase-peroxidase gene occurs in a significant fraction (44.2%) of M. tuberculosis strains with isoniazid MICs > or = 1.0 microgram/mL.

MeSH terms

  • Bacterial Proteins*
  • Base Sequence
  • Catalase / genetics
  • Catalase / metabolism
  • DNA Primers
  • Drug Resistance, Microbial
  • Genes, Bacterial
  • Humans
  • Isoniazid / pharmacology*
  • Molecular Sequence Data
  • Mycobacterium tuberculosis / drug effects
  • Mycobacterium tuberculosis / enzymology
  • Mycobacterium tuberculosis / genetics*
  • Peroxidases / genetics*
  • Peroxidases / metabolism
  • Point Mutation*
  • Tuberculosis, Pulmonary / microbiology

Substances

  • Bacterial Proteins
  • DNA Primers
  • Peroxidases
  • Catalase
  • catalase HPI
  • Isoniazid