Selective inhibition of the accumulation of extracellular proteases of Pseudomonas aeruginosa by gentamicin and tobramycin

Antimicrob Agents Chemother. 1985 Apr;27(4):468-72. doi: 10.1128/AAC.27.4.468.

Abstract

Gentamicin and tobramycin inhibited the accumulation of extracellular proteases secreted by Pseudomonas aeruginosa. The secretion of protease was inhibited at concentrations of these drugs that were below the level required to inhibit general protein synthesis. Neither magnesium ions nor high ionic strength antagonized the ability of the aminoglycosides to block secretion of the proteases. Under these culture conditions magnesium ions were shown to antagonize the effects of the aminoglycosides on protein synthesis and aminoglycoside-mediated lysozyme lysis of P. aeruginosa. These results suggested that the drugs blocked secretion of the proteases by acting at the level of the outer membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Culture Media
  • Enzyme-Linked Immunosorbent Assay
  • Gentamicins / pharmacology*
  • Magnesium / pharmacology
  • Peptide Hydrolases / metabolism*
  • Protease Inhibitors / metabolism
  • Protease Inhibitors / pharmacology*
  • Pseudomonas aeruginosa / enzymology*
  • Pseudomonas aeruginosa / metabolism
  • Time Factors
  • Tobramycin / pharmacology*

Substances

  • Culture Media
  • Gentamicins
  • Protease Inhibitors
  • Peptide Hydrolases
  • Magnesium
  • Tobramycin