Metabolic Rewiring of Mycobacterium tuberculosis upon Drug Treatment and Antibiotics Resistance

Author:

Singha Biplab1,Murmu Sumit2,Nair Tripti3,Rawat Rahul Singh4,Sharma Aditya Kumar5ORCID,Soni Vijay6ORCID

Affiliation:

1. Department of Microbiology and Physiological Systems, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA

2. Regional Centre of Biotechnology, Faridabad 121001, India

3. Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089, USA

4. Eukaryotic Gene Expression Laboratory, National Institute of Immunology, New Delhi 110067, India

5. Department of Pathology, College of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA

6. Division of Infectious Diseases, Weill Department of Medicine, Weill Cornell Medicine, New York, NY 10021, USA

Abstract

Tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb), remains a significant global health challenge, further compounded by the issue of antimicrobial resistance (AMR). AMR is a result of several system-level molecular rearrangements enabling bacteria to evolve with better survival capacities: metabolic rewiring is one of them. In this review, we present a detailed analysis of the metabolic rewiring of Mtb in response to anti-TB drugs and elucidate the dynamic mechanisms of bacterial metabolism contributing to drug efficacy and resistance. We have discussed the current state of AMR, its role in the prevalence of the disease, and the limitations of current anti-TB drug regimens. Further, the concept of metabolic rewiring is defined, underscoring its relevance in understanding drug resistance and the biotransformation of drugs by Mtb. The review proceeds to discuss the metabolic adaptations of Mtb to drug treatment, and the pleiotropic effects of anti-TB drugs on Mtb metabolism. Next, the association between metabolic changes and antimycobacterial resistance, including intrinsic and acquired drug resistance, is discussed. The review concludes by summarizing the challenges of anti-TB treatment from a metabolic viewpoint, justifying the need for this discussion in the context of novel drug discovery, repositioning, and repurposing to control AMR in TB.

Publisher

MDPI AG

Reference204 articles.

1. World Health Organization (2022). Global Tuberculosis Report 2022, World Health Organization. Available online: https://iris.who.int/bitstream/handle/10665/363752/9789240061729-eng.pdf?sequence=1.

2. Treatment of latent tuberculosis infection: An update;Lobue;Respirology,2010

3. Rifamycins—Obstacles and opportunities;Aristoff;Tuberculosis,2010

4. Rifampin;Schonell;Can. Med. Assoc. J.,1972

5. Pyrazinamide-induced hyperuricemia;Pham;Pharm. Ther.,2014

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Key challenges in TB drug discovery: A perspective;Bioorganic & Medicinal Chemistry Letters;2024-09

2. Alternative therapeutics to control antimicrobial resistance: a general perspective;Frontiers in Drug Discovery;2024-07-17

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3