Molecular bases of the interaction of M. tuberculosis complex and anti-tuberculosis drugs: the current state of the problem and its epidemiological significance

Yu. S. Khomyakov, D. D. Zvyagintseva, T. Khomyakova
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Abstract

According to the WHO Global Tuberculosis Report, published in 2022, tuberculosis and its drug-resistant forms are on the rise for the first time in lasted years. The ability to become immune to anti-tuberculosis drugs is a fundamental feature of the TB agent. In some cases, it develops a transient resistance to antibacterial drugs based on a combination of adaptive biological properties of mycobacterium without altering the genetic apparatus. This phenomenon is called drug-induced tolerance. Its development is associated with the slowing or altering of bacterial metabolism, increasing the thickness of the cell wall, activation of specific molecular pumps, removing medicinal substances from the cell outside the cell. The same and some other mechanisms are involved in the development of another phenomenon - drug resistance, which is associated with inherited changes in the genetic apparatus of mycobacterium. The review is devoted to the consideration of the molecular bases of mycobacterium tuberculosis interaction with anti-tuberculosis drugs and its epidemiological significance.
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结核分枝杆菌复合体与抗结核药物相互作用的分子基础:问题现状及其流行病学意义
根据世卫组织2022年发布的《全球结核病报告》,结核病及其耐药形式多年来首次出现上升趋势。对抗结核药物产生免疫的能力是结核病药物的一个基本特征。在某些情况下,它在不改变遗传装置的情况下,基于分枝杆菌的适应性生物学特性的组合,对抗菌药物产生短暂的耐药性。这种现象被称为药物诱导耐受性。它的发展与细菌代谢的减慢或改变、细胞壁厚度的增加、特定分子泵的激活、从细胞外的细胞中清除药物物质有关。同样的机制和其他一些机制也涉及到另一种现象的发展-耐药性,这与分枝杆菌遗传装置的遗传变化有关。本文就结核分枝杆菌与抗结核药物相互作用的分子基础及其流行病学意义作一综述。
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