In vitro activity of N-formimidoyl thienamycin against 98 clinical isolates of Brucella melitensis compared with those of cefoxitin, rifampin, tetracycline, and co-trimoxazole

Antimicrob Agents Chemother. 1982 Mar;21(3):501-3. doi: 10.1128/AAC.21.3.501.

Abstract

IN vitro susceptibilities of 98 isolates of Brucella melitensis to N-formimidoyl thienamycin, tetracycline, co-trimoxazole, rifampin, and cefoxitin were determined. N-Formimidoyl thienamycin showed good activity which was similar to those of tetracycline and rifampin and different from that of the other beta-lactam antibiotic tested (cefoxitin), which showed poor activity. Co-trimoxazole showed good activity.

Publication types

  • Comparative Study

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Brucella / drug effects*
  • Brucellosis / microbiology
  • Cefoxitin / pharmacology
  • Drug Combinations / pharmacology
  • Humans
  • Imipenem
  • Lactams / pharmacology
  • Microbial Sensitivity Tests
  • Rifampin / pharmacology
  • Sulfamethoxazole / pharmacology
  • Tetracycline / pharmacology
  • Trimethoprim / pharmacology
  • Trimethoprim, Sulfamethoxazole Drug Combination

Substances

  • Anti-Bacterial Agents
  • Drug Combinations
  • Lactams
  • Cefoxitin
  • Imipenem
  • Trimethoprim, Sulfamethoxazole Drug Combination
  • Trimethoprim
  • Tetracycline
  • Sulfamethoxazole
  • Rifampin