Correlation of penicillin-induced lysis of Enterococcus faecium with saturation of essential penicillin-binding proteins and release of lipoteichoic acid

Antimicrob Agents Chemother. 1990 Oct;34(10):1901-7. doi: 10.1128/AAC.34.10.1901.

Abstract

Clinical isolates of Enterococcus faecium that had a range of susceptibilities to penicillin were found to differ significantly in their responses to the antibiotic. In the penicillin-susceptible group (MIC, less than or equal to 4 micrograms/ml), the cessation of growth (bacteriostasis) at 10 x the MIC of penicillin appeared to correlate with the inhibition of penicillin-binding protein (PBP) 5*, whereas the onset of lysis (bactericidal effect) at higher antibiotic concentrations (100 x the MIC) was concomitant with the inhibition of the lower-affinity PBP 5. In contrast, in the resistant (MIC, greater than or equal to 8 micrograms/ml) group (in which most of the strains did not contain PBP 5*), the degree of saturation of PBP 5 seemed to determine the physiological response to the antibiotic: low levels of saturation caused growth inhibition, whereas almost complete saturation correlated with lysis. The penicillin-induced cell lysis of both penicillin-susceptible and -resistant strains was attributed, at least in part, to the extensive loss of acylated lipoteichoic acid into the growth medium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins*
  • Carrier Proteins / analysis
  • Carrier Proteins / metabolism*
  • Enterobacter / drug effects*
  • Enterobacter / metabolism
  • Hexosyltransferases*
  • Lipopolysaccharides / metabolism*
  • Microbial Sensitivity Tests
  • Muramoylpentapeptide Carboxypeptidase / analysis
  • Muramoylpentapeptide Carboxypeptidase / metabolism*
  • Penicillin Resistance
  • Penicillin-Binding Proteins
  • Penicillins / pharmacology*
  • Peptidyl Transferases*
  • Phenotype
  • Teichoic Acids / metabolism*

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • Lipopolysaccharides
  • Penicillin-Binding Proteins
  • Penicillins
  • Teichoic Acids
  • lipoteichoic acid
  • Peptidyl Transferases
  • Hexosyltransferases
  • Muramoylpentapeptide Carboxypeptidase