Rifamycin antibiotics and the mechanisms of their failure

J Antibiot (Tokyo). 2021 Nov;74(11):786-798. doi: 10.1038/s41429-021-00462-x. Epub 2021 Aug 16.

Abstract

Rifamycins are a class of antibiotics that were first discovered in 1957 and are known for their use in treating tuberculosis (TB). Rifamycins exhibit bactericidal activity against many Gram-positive and Gram-negative bacteria by inhibiting RNA polymerase (RNAP); however, resistance is prevalent and the mechanisms range from primary target modification and antibiotic inactivation to cytoplasmic exclusion. Further, phenotypic resistance, in which only a subpopulation of bacteria grow in concentrations exceeding their minimum inhibitory concentration, and tolerance, which is characterized by reduced rates of bacterial cell death, have been identified as additional causes of rifamycin failure. Here we summarize current understanding and recent developments regarding this critical antibiotic class.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antibiotics, Antitubercular / pharmacology
  • Antibiotics, Antitubercular / therapeutic use*
  • Drug Resistance, Microbial
  • Humans
  • Mycobacterium tuberculosis
  • Rifamycins / pharmacology
  • Rifamycins / therapeutic use*
  • Treatment Failure
  • Tuberculosis / drug therapy*

Substances

  • Antibiotics, Antitubercular
  • Rifamycins