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Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance
Fluoroquinolones (FQs) are arguably among the most successful antibiotics of recent times. They have enjoyed over 30 years of clinical usage and become essential tools in the armoury of clinical treatments. FQs target the bacterial enzymes DNA gyrase and DNA topoisomerase IV, where they stabilise a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730664/ https://www.ncbi.nlm.nih.gov/pubmed/33271787 http://dx.doi.org/10.3390/molecules25235662 |
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author | Bush, Natassja G. Diez-Santos, Isabel Abbott, Lauren R. Maxwell, Anthony |
author_facet | Bush, Natassja G. Diez-Santos, Isabel Abbott, Lauren R. Maxwell, Anthony |
author_sort | Bush, Natassja G. |
collection | PubMed |
description | Fluoroquinolones (FQs) are arguably among the most successful antibiotics of recent times. They have enjoyed over 30 years of clinical usage and become essential tools in the armoury of clinical treatments. FQs target the bacterial enzymes DNA gyrase and DNA topoisomerase IV, where they stabilise a covalent enzyme-DNA complex in which the DNA is cleaved in both strands. This leads to cell death and turns out to be a very effective way of killing bacteria. However, resistance to FQs is increasingly problematic, and alternative compounds are urgently needed. Here, we review the mechanisms of action of FQs and discuss the potential pathways leading to cell death. We also discuss quinolone resistance and how quinolone treatment can lead to resistance to non-quinolone antibiotics. |
format | Online Article Text |
id | pubmed-7730664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77306642020-12-12 Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance Bush, Natassja G. Diez-Santos, Isabel Abbott, Lauren R. Maxwell, Anthony Molecules Review Fluoroquinolones (FQs) are arguably among the most successful antibiotics of recent times. They have enjoyed over 30 years of clinical usage and become essential tools in the armoury of clinical treatments. FQs target the bacterial enzymes DNA gyrase and DNA topoisomerase IV, where they stabilise a covalent enzyme-DNA complex in which the DNA is cleaved in both strands. This leads to cell death and turns out to be a very effective way of killing bacteria. However, resistance to FQs is increasingly problematic, and alternative compounds are urgently needed. Here, we review the mechanisms of action of FQs and discuss the potential pathways leading to cell death. We also discuss quinolone resistance and how quinolone treatment can lead to resistance to non-quinolone antibiotics. MDPI 2020-12-01 /pmc/articles/PMC7730664/ /pubmed/33271787 http://dx.doi.org/10.3390/molecules25235662 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bush, Natassja G. Diez-Santos, Isabel Abbott, Lauren R. Maxwell, Anthony Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance |
title | Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance |
title_full | Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance |
title_fullStr | Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance |
title_full_unstemmed | Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance |
title_short | Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance |
title_sort | quinolones: mechanism, lethality and their contributions to antibiotic resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730664/ https://www.ncbi.nlm.nih.gov/pubmed/33271787 http://dx.doi.org/10.3390/molecules25235662 |
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