Pretreatment with the protegrin IB-367 affects Gram-positive biofilm and enhances the therapeutic efficacy of linezolid in animal models of central venous catheter infection

JPEN J Parenter Enteral Nutr. 2007 Nov-Dec;31(6):463-8. doi: 10.1177/0148607107031006463.

Abstract

Background: Biofilms play an important role in the pathogenesis of several chronic infections and nosocomial infections related to indwelling medical devices.

Methods: To assess the efficacy of IB-367 and linezolid (LZD) in the treatment of central venous catheter (CVC) infections using the antibiotic-lock technique, in vitro and in vivo studies were performed. The in vitro antibiotic susceptibility assay for Staphylococcus aureus and Enterococcus faecalis biofilms developed on 96-well polystyrene tissue culture plates was performed to determine the activity of the compounds. Efficacy studies were performed in rat models of Gram-positive CVC infection. Silastic catheters were implanted into the superior cava of adult male Wistar rats. Twenty-four hours after implantation, the catheters were pretreated by filling with IB-367. Thirty minutes later, rats were challenged via the CVC with 1.0 x 10(6) CFU (colony forming units) of S aureus strain diffuse Smith and clinical isolate of slime-producing E faecalis. Administration of LZD into the CVC at a concentration equal to the minimum bacteriocidal concentration observed using adherent cells or at a much higher concentration (1024 microg/mL) began 24 hours later.

Results: Both for S aureus and E faecalis, the killing activities of LZD against adherent bacteria were at least 4-fold to 8-fold lower than that against freely growing cells. For both strains, in IB-367-pretreated wells, LZD strongly increases its activity. The in vivo studies showed that when CVCs were pretreated with IB-367, Gram-positive biofilm bacterial load was further decreased to 10(1) CFU/mL and bacteremia was not detected.

Conclusions: IB-367 has potential as an adjunctive agent to LZD in the treatment of Gram-positive biofilm infections such as CVC infections.

MeSH terms

  • Acetamides / pharmacology*
  • Animals
  • Anti-Infective Agents / pharmacology*
  • Antimicrobial Cationic Peptides
  • Biofilms* / drug effects
  • Biofilms* / growth & development
  • Catheterization, Central Venous / adverse effects
  • Colony Count, Microbial
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Enterococcus faecalis / drug effects
  • Enterococcus faecalis / physiology
  • Gram-Positive Bacterial Infections / prevention & control*
  • Linezolid
  • Male
  • Microbial Sensitivity Tests
  • Oxazolidinones / pharmacology*
  • Peptides / pharmacology*
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Staphylococcal Infections / prevention & control*
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / physiology
  • Treatment Outcome

Substances

  • Acetamides
  • Anti-Infective Agents
  • Antimicrobial Cationic Peptides
  • Oxazolidinones
  • Peptides
  • Linezolid
  • antimicrobial peptide IB-367