In vitro activity of teicoplanin, vancomycin, A16686, clindamycin, erythromycin and fusidic acid against anaerobic bacteria

Singapore Med J. 1990 Feb;31(1):56-8.

Abstract

The in vitro activity of teicoplanin and A16686, two new glycopeptide antibiotics was determined against 196 isolates of anaerobic bacteria. The activity of teicoplanin and A16686, in comparison with that of vancomycin, clindamycin, erythromycin and fusidic acid was 2 to 16 times higher against the gram positive anaerobes, namely, Propionibacterium acnes, Clostridium perfringens, Clostridium difficile, Clostridium species, Peptococcus species and Peptostreptococcus species. However, Bacteroides fragilis was resistant to teicoplanin and A16686 while Bacteroides melaninogenicus and Bacteroides bivius were found to be sensitive.

MeSH terms

  • Anti-Bacterial Agents* / pharmacology*
  • Bacteria, Anaerobic / drug effects*
  • Clindamycin / pharmacology
  • Depsipeptides*
  • Drug Resistance, Microbial
  • Fusidic Acid / pharmacology
  • Glycopeptides / pharmacology
  • Microbial Sensitivity Tests
  • Peptides, Cyclic*
  • Teicoplanin
  • Vancomycin / pharmacology

Substances

  • Anti-Bacterial Agents
  • Depsipeptides
  • Glycopeptides
  • Peptides, Cyclic
  • ramoplanin
  • Clindamycin
  • Fusidic Acid
  • Teicoplanin
  • Vancomycin