Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 May-Jun;52(3):435-450.
doi: 10.7868/S0026898418030060.

[Molecular Mechanisms of Drug Tolerance in Mycobacterium tuberculosis]

[Article in Russian]
Affiliations
Free article
Review

[Molecular Mechanisms of Drug Tolerance in Mycobacterium tuberculosis]

[Article in Russian]
A V Antonova et al. Mol Biol (Mosk). 2018 May-Jun.
Free article

Abstract

A dramatic increase in drug-resistant forms of tuberculosis (TB) stimulates a search for novel anti-TB drugs and studies of the drug resistance acquisition. One of the possible causes is a phenotypic resistance or drug tolerance which is not associated with genomic changes. The majority of anti-TB drugs eliminate 99% of MTB cells in 3-5 days, but the remaining subpopulation becomes unsusceptible to treatment and capable for long-term persistence with ability to resuscitate once the external adverse factor is removed. This evasion of the stress factor facilitates selection of resistant forms, thus warranting long-term treatment with at least four antibacterial drugs in TB. The review considers the main mechanisms of bacterial tolerance that are due to alterations in the cell wall, activation of efflux pumps, induction of transcriptional regulons, changes in metabolic flows, and modification of molecular machineries.

Keywords: Mycobacterium tuberculosis; drug tolerance; efflux pumps; phenotypic resistance; regulation of gene expression.

PubMed Disclaimer

MeSH terms

Substances

LinkOut - more resources