In vitro susceptibility of Mycobacterium tuberculosis isolates to an oral carbapenem alone or in combination with β-lactamase inhibitors

Antimicrob Agents Chemother. 2014 Nov;58(11):7010-4. doi: 10.1128/AAC.03539-14. Epub 2014 Sep 15.

Abstract

We evaluated the antituberculosis (anti-TB) activity of five β-lactams alone or in combination with β-lactamase inhibitors against 41 clinical isolates of Mycobacterium tuberculosis, including multidrug-resistant and extensively drug-resistant strains. Of those, tebipenem, an oral carbapenem, showed the most potent anti-TB activity against clinical isolates, with a MIC range of 0.125 to 8 μg/ml, which is achievable in the human blood. More importantly, in the presence of clavulanate, MIC values of tebipenem declined to 2 μg/ml or less.

MeSH terms

  • Antitubercular Agents / pharmacology*
  • Carbapenems / pharmacology*
  • Drug Combinations
  • Drug Resistance, Multiple, Bacterial
  • Humans
  • Microbial Sensitivity Tests
  • Mycobacterium tuberculosis / drug effects*
  • Mycobacterium tuberculosis / isolation & purification
  • Tuberculosis, Multidrug-Resistant / drug therapy
  • Tuberculosis, Multidrug-Resistant / microbiology
  • Tuberculosis, Pulmonary / drug therapy
  • Tuberculosis, Pulmonary / microbiology
  • beta-Lactamase Inhibitors / pharmacology*

Substances

  • Antitubercular Agents
  • Carbapenems
  • Drug Combinations
  • beta-Lactamase Inhibitors
  • tebipenem