Cell envelope lipids in the pathophysiology of Mycobacterium tuberculosis

Author:

Singh Parul12,Rameshwaram Nagender Rao1,Ghosh Sudip3,Mukhopadhyay Sangita1

Affiliation:

1. Laboratory of Molecular Cell Biology, Centre for DNA Fingerprinting & Diagnostics (CDFD), Inner Ring Road, Uppal, Hyderabad, 500 039, India

2. Graduate Studies, Manipal Academy of Higher Education, Manipal, Karnataka, 576 104, India

3. Molecular Biology Division, National Institute of Nutrition (ICMR), Jamai-Osmania PO, Hyderabad, 500 007, India

Abstract

Mycobacterium tuberculosis is an intracellular bacterium that persists and replicates inside macrophages. The bacterium possesses an unusual lipid-rich cell envelope that provides a hydrophobic impermeable barrier against many environmental stressors and allows it to survive extremely hostile intracellular surroundings. Since the lipid-rich envelope is crucial for M. tuberculosis virulence, the components of the cell wall lipid biogenesis pathways constitute an attractive target for the development of vaccines and antimycobacterial chemotherapeutics. In this review, we provide a detailed description of the mycobacterial cell envelope lipid components and their contributions to the physiology and pathogenicity of mycobacteria. We also discussed the current status of the antimycobacterial drugs that target biosynthesis, export and regulation of cell envelope lipids.

Publisher

Future Medicine Ltd

Subject

Microbiology (medical),Microbiology

Reference214 articles.

1. Mycobacterium tuberculosis Pathogenesis and Molecular Determinants of Virulence

2. World Health Organization. Global tuberculosis report – 2016. WHO, Geneva. http://apps.who.int/iris/bitstream/10665/137094/1/9789241564809_eng.pdf.

3. World Health Organization. Latent TB infection fact sheet (2014). www.who.int/tb/challenges/ltbi_factsheet_2014.pdf?ua=1.

4. The Global Burden of Latent Tuberculosis Infection: A Re-estimation Using Mathematical Modelling

5. Pathogenesis in tuberculosis: transcriptomic approaches to unraveling virulence mechanisms and finding new drug targets

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