In Vitro Activities of Nontraditional Antimicrobials against Multiresistant Acinetobacter baumannii Strains Isolated in an Intensive Care Unit Outbreak

Author:

Appleman Maria D.1,Belzberg Howard2,Citron Diane M.1,Heseltine Peter N. R.3,Yellin Albert E.2,Murray James2,Berne Thomas V.2

Affiliation:

1. Departments of Pathology,1

2. Surgery,2 and

3. Medicine,3 Los Angeles County-University of Southern California Medical Center, Los Angeles, California

Abstract

ABSTRACT Fifteen multiresistant Acinetobacter baumannii isolates from patients in intensive care units and 14 nonoutbreak strains were tested to determine in vitro activities of nontraditional antimicrobials, including cefepime, meropenem, netilmicin, azithromycin, doxycycline, rifampin, sulbactam, and trovafloxacin. The latter five drugs were further tested against four of the strains for bactericidal or bacteriostatic activity by performing kill-curve studies at 0.5, 1, 2, and 4 times their MICs. In addition, novel combinations of drugs with sulbactam were examined for synergistic interactions by using a checkerboard configuration. MICs at which 90% of the isolates tested were inhibited for antimicrobials showing activity against the multiresistant A. baumannii strains were as follows (in parentheses): doxycycline (1 μg/ml), azithromycin (4 μg/ml), netilmicin (1 μg/ml), rifampin (8 μg/ml), polymyxin (0.8 U/ml), meropenem (4 μg/ml), trovafloxacin (4 μg/ml), and sulbactam (8 μg/ml). In the kill-curve studies, azithromycin and rifampin were rapidly bactericidal while sulbactam was more slowly bactericidal. Trovafloxacin and doxycycline were bacteriostatic. None of the antimicrobials tested were bactericidal against all strains tested. The synergy studies demonstrated that the combinations of sulbactam with azithromycin, rifampin, doxycycline, or trovafloxacin were generally additive or indifferent.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference15 articles.

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