Multidrug efflux inhibition in Acinetobacter baumannii: comparison between 1-(1-naphthylmethyl)-piperazine and phenyl-arginine-beta-naphthylamide

J Antimicrob Chemother. 2006 May;57(5):970-4. doi: 10.1093/jac/dkl081. Epub 2006 Mar 10.

Abstract

Objectives: 1-(1-Naphthylmethyl)-piperazine (NMP) has been shown to reverse multidrug resistance (MDR) in Escherichia coli overexpressing RND-type efflux pumps but there are no data on its activity in non-fermenters like Acinetobacter.

Methods: Antimicrobial susceptibility in the absence and presence of NMP and, for comparison, phenyl-arginine-beta-naphthylamide (PAbetaN), another putative efflux pump inhibitor (EPI), was tested in laboratory and mutant strains with differing intracellular dye accumulation and expression of adeB, and in clinical isolates of Acinetobacter baumannii.

Results: Based on a 4-fold or greater MIC reduction, the effects of both EPIs at low concentrations (25 mg/L) were limited. PAbetaN had a highly selective action on the reduction in the MIC of rifampicin and clarithromycin. At a higher concentration of the putative EPIs (100 mg/L), NMP was more active than PAbetaN. This effect was not limited to strains with adeB overexpression, but affected the susceptibility to linezolid, chloramphenicol and tetracycline most, and was enhanced in clinical isolates with reduced fluoroquinolone susceptibility.

Conclusion: NMP can partially reverse MDR in A. baumannii and differs substantially in its activity from that of PAbetaN.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acinetobacter baumannii / drug effects*
  • Acinetobacter baumannii / isolation & purification
  • Acinetobacter baumannii / metabolism
  • Anti-Bacterial Agents / pharmacology*
  • Bacterial Proteins / antagonists & inhibitors*
  • Bacterial Proteins / biosynthesis
  • Dipeptides / pharmacology*
  • Drug Resistance, Multiple, Bacterial / drug effects*
  • Membrane Transport Proteins / biosynthesis
  • Microbial Sensitivity Tests
  • Piperazines / pharmacology*

Substances

  • 1-(1-naphthylmethyl)piperazine
  • AdeA protein, Acinetobacter baumannii
  • AdeB protein, Acinetobacter baumannii
  • AdeC protein, Acinetobacter baumannii
  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Dipeptides
  • Membrane Transport Proteins
  • Piperazines
  • phenylalanine arginine beta-naphthylamide