Development of resistance during antimicrobial therapy caused by insertion sequence interruption of porin genes

Antimicrob Agents Chemother. 1999 Apr;43(4):937-9. doi: 10.1128/AAC.43.4.937.

Abstract

We have demonstrated by using an in vitro approach that interruption of the OmpK36 porin gene by insertion sequences (ISs) is a common type of mutation that causes loss of porin expression and increased resistance to cefoxitin in Klebsiella pneumoniae. This mechanism also operates in vivo: of 13 porin-deficient cefoxitin-resistant clinical isolates of K. pneumoniae, 4 presented ISs in their ompK36 gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins*
  • Cefoxitin / pharmacology
  • Cephamycins / pharmacology
  • DNA Transposable Elements / genetics
  • Drug Resistance, Microbial / genetics
  • Humans
  • Klebsiella pneumoniae / drug effects
  • Klebsiella pneumoniae / genetics*
  • Klebsiella pneumoniae / metabolism
  • Mutagenesis, Insertional
  • Porins / biosynthesis
  • Porins / genetics*

Substances

  • Bacterial Proteins
  • Cephamycins
  • DNA Transposable Elements
  • OmpK36 protein, Klebsiella pneumoniae
  • Porins
  • Cefoxitin