In Vitro Activities of MCB3681 and Eight Comparators against Clostridium difficile Isolates with Known Ribotypes and Diverse Geographical Spread

Antimicrob Agents Chemother. 2017 Feb 23;61(3):e02077-16. doi: 10.1128/AAC.02077-16. Print 2017 Mar.

Abstract

Treatments for Clostridium difficile infection remain limited, despite the introduction of fidaxomicin, and development of new agents is necessary. We determined the in vitro susceptibilities of 199 prevalent or emerging Clostridium difficile PCR ribotypes to MCB3681, a novel investigational quinolonyl-oxazolidinone, and 8 comparators (metronidazole, vancomycin, fidaxomicin, moxifloxacin, ciprofloxacin, clindamycin, tigecycline, and linezolid). MCB3681 showed good activity against C. difficile with no evidence of MCB3681 resistance in isolates showing either moxifloxacin or linezolid resistance or both moxifloxacin and linezolid resistance.

Keywords: Clostridium difficile; MCB3681; antimicrobial susceptibility.

Publication types

  • Comparative Study

MeSH terms

  • Aminoglycosides / pharmacology
  • Anti-Bacterial Agents / pharmacology*
  • Clostridioides difficile / classification*
  • Clostridioides difficile / drug effects*
  • Clostridioides difficile / genetics
  • Clostridioides difficile / isolation & purification
  • Drug Resistance, Multiple, Bacterial / genetics
  • Enterocolitis, Pseudomembranous / microbiology
  • Fluoroquinolones / pharmacology
  • Humans
  • Linezolid / pharmacology
  • Microbial Sensitivity Tests
  • Moxifloxacin
  • Oxazolidinones / pharmacology*
  • Polymerase Chain Reaction
  • Pyrrolidines / pharmacology
  • Quinolones / pharmacology*
  • Ribotyping

Substances

  • Aminoglycosides
  • Anti-Bacterial Agents
  • Fluoroquinolones
  • MCB3681
  • Oxazolidinones
  • Pyrrolidines
  • Quinolones
  • Linezolid
  • Moxifloxacin