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Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection

Emerging pharmacological strategies that target major virulence factors of antibiotic-resistant Mycobacterium tuberculosis (Mtb) are presented and discussed. This review is divided into three parts corresponding to structures and functions important for Mtb pathogenicity: the cell wall, the lipoarab...

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Autores principales: Italia, Alice, Shaik, Mohammed Monsoor, Peri, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296423/
https://www.ncbi.nlm.nih.gov/pubmed/37371579
http://dx.doi.org/10.3390/biom13060999
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author Italia, Alice
Shaik, Mohammed Monsoor
Peri, Francesco
author_facet Italia, Alice
Shaik, Mohammed Monsoor
Peri, Francesco
author_sort Italia, Alice
collection PubMed
description Emerging pharmacological strategies that target major virulence factors of antibiotic-resistant Mycobacterium tuberculosis (Mtb) are presented and discussed. This review is divided into three parts corresponding to structures and functions important for Mtb pathogenicity: the cell wall, the lipoarabinomannan, and the secretory proteins. Within the cell wall, we further focus on three biopolymeric sub-components: mycolic acids, arabinogalactan, and peptidoglycan. We present a comprehensive overview of drugs and drug candidates that target cell walls, envelopes, and secretory systems. An understanding at a molecular level of Mtb pathogenesis is provided, and potential future directions in therapeutic strategies are suggested to access new drugs to combat the growing global threat of antibiotic-resistant Mtb infection.
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spelling pubmed-102964232023-06-28 Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection Italia, Alice Shaik, Mohammed Monsoor Peri, Francesco Biomolecules Review Emerging pharmacological strategies that target major virulence factors of antibiotic-resistant Mycobacterium tuberculosis (Mtb) are presented and discussed. This review is divided into three parts corresponding to structures and functions important for Mtb pathogenicity: the cell wall, the lipoarabinomannan, and the secretory proteins. Within the cell wall, we further focus on three biopolymeric sub-components: mycolic acids, arabinogalactan, and peptidoglycan. We present a comprehensive overview of drugs and drug candidates that target cell walls, envelopes, and secretory systems. An understanding at a molecular level of Mtb pathogenesis is provided, and potential future directions in therapeutic strategies are suggested to access new drugs to combat the growing global threat of antibiotic-resistant Mtb infection. MDPI 2023-06-16 /pmc/articles/PMC10296423/ /pubmed/37371579 http://dx.doi.org/10.3390/biom13060999 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Italia, Alice
Shaik, Mohammed Monsoor
Peri, Francesco
Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection
title Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection
title_full Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection
title_fullStr Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection
title_full_unstemmed Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection
title_short Emerging Extracellular Molecular Targets for Innovative Pharmacological Approaches to Resistant Mtb Infection
title_sort emerging extracellular molecular targets for innovative pharmacological approaches to resistant mtb infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296423/
https://www.ncbi.nlm.nih.gov/pubmed/37371579
http://dx.doi.org/10.3390/biom13060999
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