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Chemical Basis of Combination Therapy to Combat Antibiotic Resistance

[Image: see text] The antimicrobial resistance crisis is a global health issue requiring discovery and development of novel therapeutics. However, conventional screening of natural products or synthetic chemical libraries is uncertain. Combination therapy using approved antibiotics with inhibitors t...

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Autores principales: Si, Zhangyong, Pethe, Kevin, Chan-Park, Mary B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975838/
https://www.ncbi.nlm.nih.gov/pubmed/36873689
http://dx.doi.org/10.1021/jacsau.2c00532
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author Si, Zhangyong
Pethe, Kevin
Chan-Park, Mary B.
author_facet Si, Zhangyong
Pethe, Kevin
Chan-Park, Mary B.
author_sort Si, Zhangyong
collection PubMed
description [Image: see text] The antimicrobial resistance crisis is a global health issue requiring discovery and development of novel therapeutics. However, conventional screening of natural products or synthetic chemical libraries is uncertain. Combination therapy using approved antibiotics with inhibitors targeting innate resistance mechanisms provides an alternative strategy to develop potent therapeutics. This review discusses the chemical structures of effective β-lactamase inhibitors, outer membrane permeabilizers, and efflux pump inhibitors that act as adjuvant molecules of classical antibiotics. Rational design of the chemical structures of adjuvants will provide methods to impart or restore efficacy to classical antibiotics for inherently antibiotic-resistant bacteria. As many bacteria have multiple resistance pathways, adjuvant molecules simultaneously targeting multiple pathways are promising approaches to combat multidrug-resistant bacterial infections.
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spelling pubmed-99758382023-03-02 Chemical Basis of Combination Therapy to Combat Antibiotic Resistance Si, Zhangyong Pethe, Kevin Chan-Park, Mary B. JACS Au [Image: see text] The antimicrobial resistance crisis is a global health issue requiring discovery and development of novel therapeutics. However, conventional screening of natural products or synthetic chemical libraries is uncertain. Combination therapy using approved antibiotics with inhibitors targeting innate resistance mechanisms provides an alternative strategy to develop potent therapeutics. This review discusses the chemical structures of effective β-lactamase inhibitors, outer membrane permeabilizers, and efflux pump inhibitors that act as adjuvant molecules of classical antibiotics. Rational design of the chemical structures of adjuvants will provide methods to impart or restore efficacy to classical antibiotics for inherently antibiotic-resistant bacteria. As many bacteria have multiple resistance pathways, adjuvant molecules simultaneously targeting multiple pathways are promising approaches to combat multidrug-resistant bacterial infections. American Chemical Society 2023-01-31 /pmc/articles/PMC9975838/ /pubmed/36873689 http://dx.doi.org/10.1021/jacsau.2c00532 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Si, Zhangyong
Pethe, Kevin
Chan-Park, Mary B.
Chemical Basis of Combination Therapy to Combat Antibiotic Resistance
title Chemical Basis of Combination Therapy to Combat Antibiotic Resistance
title_full Chemical Basis of Combination Therapy to Combat Antibiotic Resistance
title_fullStr Chemical Basis of Combination Therapy to Combat Antibiotic Resistance
title_full_unstemmed Chemical Basis of Combination Therapy to Combat Antibiotic Resistance
title_short Chemical Basis of Combination Therapy to Combat Antibiotic Resistance
title_sort chemical basis of combination therapy to combat antibiotic resistance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975838/
https://www.ncbi.nlm.nih.gov/pubmed/36873689
http://dx.doi.org/10.1021/jacsau.2c00532
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