In vitro activities of ramoplanin and four glycopeptide antibiotics against clinical isolates of Clostridium difficile

Antimicrob Agents Chemother. 1991 Jan;35(1):195-7. doi: 10.1128/AAC.35.1.195.

Abstract

Seventy strains of Clostridium difficile, all isolated from symptomatic patients, were found to be uniformly susceptible to ramoplanin, a new glycolipodepsipeptide antibiotic, and to four glycopeptides (vancomycin, teicoplanin, and two semisynthetic teicoplanin derivatives). Ramoplanin is recommended for further evaluation in the treatment of C. difficile-associated disease.

MeSH terms

  • Anti-Bacterial Agents* / pharmacology*
  • Clostridioides difficile / drug effects*
  • Depsipeptides*
  • Dose-Response Relationship, Drug
  • Drug Resistance, Microbial
  • Glycopeptides / pharmacology*
  • Humans
  • Microbial Sensitivity Tests
  • Peptides, Cyclic / pharmacology
  • Ristocetin / analogs & derivatives
  • Teicoplanin
  • Vancomycin / pharmacology

Substances

  • Anti-Bacterial Agents
  • Depsipeptides
  • Glycopeptides
  • Peptides, Cyclic
  • ramoplanin
  • MDL 62873
  • Ristocetin
  • Teicoplanin
  • Vancomycin
  • teicoplanin aglycone