TB Research

Application of Mycobacterium smegmatis as a surrogate to evaluate drug leads against Mycobacterium tuberculosis

Lelovic N, Mitachi K, Yang J, Lemieux MR, Ji Y, Kurosu M

The Journal of antibiotics · 2020-05

Abstract

Discovery of new anti-tuberculosis (TB) drugs is a time-consuming process due to the slow-growing nature of Mycobacterium tuberculosis (Mtb). A requirement of biosafety level 3 (BSL-3) facility for performing research associated with Mtb is another limitation for the development of TB drug discovery. In our screening of BSL-1 Mycobacterium spp. against a battery of TB drugs, M. smegmatis (ATCC607) exhibits good agreement with its drug susceptibility against the TB drugs under a low-nutrient culture medium (0.5% Tween 80 in Middlebrook 7H9 broth). M. smegmatis (ATCC607) enters its dormant form in 14 days under a nutrient-deficient condition (a PBS buffer), and shows resistance to a majority of TB drugs, but shows susceptibility to amikacin, capreomycin, ethambutol, and rifampicin (with high concentrations) whose activities against non-replicating (or dormant) Mtb were previously validated.

MeSH terms

  • Mycobacterium smegmatis
  • Mycobacterium tuberculosis
  • DNA-Directed RNA Polymerases
  • RNA, Ribosomal, 16S
  • Antitubercular Agents
  • Microbial Sensitivity Tests
  • Drug Evaluation
  • Sequence Alignment
  • Drug Resistance, Bacterial
  • Amino Acid Sequence
  • Structure-Activity Relationship
  • Genes, Bacterial
  • Drug Discovery