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

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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

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