In Vitro Synergistic Activity of Antimicrobial Agents in Combination against Clinical Isolates of Colistin-Resistant Acinetobacter baumannii

Antimicrob Agents Chemother. 2016 Oct 21;60(11):6774-6779. doi: 10.1128/AAC.00839-16. Print 2016 Nov.

Abstract

Emerging resistance to colistin in clinical Acinetobacter baumannii isolates is of growing concern. Since current treatment options for these strains are extremely limited, we investigated the in vitro activities of various antimicrobial combinations against colistin-resistant A. baumannii Nine clinical isolates (8 from bacteremia cases and 1 from a pneumonia case) of colistin-resistant A. baumannii were collected in Asan Medical Center, Seoul, South Korea, between January 2010 and December 2012. To screen for potential synergistic effects, multiple combinations of two antimicrobials among 12 commercially available agents were tested using the multiple-combination bactericidal test (MCBT). Checkerboard tests were performed to validate these results. Among the 9 colistin-resistant strains, 6 were pandrug resistant and 3 were extensively drug resistant. With MCBT, the most effective combinations were colistin-rifampin and colistin-teicoplanin; both combinations showed synergistic effect against 8 of 9 strains. Colistin-aztreonam, colistin-meropenem, and colistin-vancomycin combinations showed synergy against seven strains. Colistin was the most common constituent of antimicrobial combinations that were active against colistin-resistant A. baumannii Checkerboard tests were then conducted in colistin-based combinations. Notably, colistin-rifampin showed synergism against all nine strains (100%). Both colistin-vancomycin and colistin-teicoplanin showed either synergy or partial synergy. Colistin combined with another β-lactam agent (aztreonam, ceftazidime, or meropenem) showed a relatively moderate effect. Colistin combined with ampicillin-sulbactam, tigecycline, amikacin, azithromycin, or trimethoprim-sulfamethoxazole demonstrated limited synergism. Using MCBT and checkerboard tests, we found that only colistin-based combinations, particularly those with rifampin, glycopeptides, or β-lactams, may confer therapeutic benefits against colistin-resistant A. baumannii.

MeSH terms

  • Acinetobacter Infections / microbiology
  • Acinetobacter Infections / pathology
  • Acinetobacter baumannii / drug effects*
  • Acinetobacter baumannii / growth & development
  • Acinetobacter baumannii / isolation & purification
  • Anti-Bacterial Agents / pharmacology*
  • Aztreonam / pharmacology
  • Bacteremia / microbiology
  • Bacteremia / pathology
  • Ceftazidime / pharmacology
  • Colistin / pharmacology*
  • Drug Combinations
  • Drug Resistance, Multiple, Bacterial / drug effects*
  • Drug Synergism
  • Humans
  • Meropenem
  • Microbial Sensitivity Tests
  • Pneumonia, Bacterial / microbiology
  • Pneumonia, Bacterial / pathology
  • Retrospective Studies
  • Rifampin / pharmacology*
  • Teicoplanin / pharmacology*
  • Thienamycins / pharmacology
  • Vancomycin / pharmacology

Substances

  • Anti-Bacterial Agents
  • Drug Combinations
  • Thienamycins
  • Teicoplanin
  • Vancomycin
  • Ceftazidime
  • Meropenem
  • Aztreonam
  • Rifampin
  • Colistin

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.