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A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones
Sufficient concentration of antibiotics close to their target is key for antimicrobial action. Among the tools exploited by bacteria to reduce the internal concentration of antibiotics, multidrug efflux pumps stand out for their ability to capture and expel many unrelated compounds out of the cell....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537517/ https://www.ncbi.nlm.nih.gov/pubmed/36203030 http://dx.doi.org/10.1038/s42003-022-04024-1 |
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author | Vergalli, Julia Chauvet, Hugo Oliva, Francesco Pajović, Jelena Malloci, Giuliano Vargiu, Attilio Vittorio Réfrégiers, Matthieu Ruggerone, Paolo Pagès, Jean-Marie |
author_facet | Vergalli, Julia Chauvet, Hugo Oliva, Francesco Pajović, Jelena Malloci, Giuliano Vargiu, Attilio Vittorio Réfrégiers, Matthieu Ruggerone, Paolo Pagès, Jean-Marie |
author_sort | Vergalli, Julia |
collection | PubMed |
description | Sufficient concentration of antibiotics close to their target is key for antimicrobial action. Among the tools exploited by bacteria to reduce the internal concentration of antibiotics, multidrug efflux pumps stand out for their ability to capture and expel many unrelated compounds out of the cell. Determining the specificities and efflux efficiency of these pumps towards their substrates would provide quantitative insights into the development of antibacterial strategies. In this light, we developed a competition efflux assay on whole cells, that allows measuring the efficacy of extrusion of clinically used quinolones in populations and individual bacteria. Experiments reveal the efficient competitive action of some quinolones that restore an active concentration of other fluoroquinolones. Computational methods show how quinolones interact with the multidrug efflux transporter AcrB. Combining experiments and computations unveils a key molecular mechanism acting in vivo to detoxify bacterial cells. The developed assay can be generalized to the study of other efflux pumps. |
format | Online Article Text |
id | pubmed-9537517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95375172022-10-08 A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones Vergalli, Julia Chauvet, Hugo Oliva, Francesco Pajović, Jelena Malloci, Giuliano Vargiu, Attilio Vittorio Réfrégiers, Matthieu Ruggerone, Paolo Pagès, Jean-Marie Commun Biol Article Sufficient concentration of antibiotics close to their target is key for antimicrobial action. Among the tools exploited by bacteria to reduce the internal concentration of antibiotics, multidrug efflux pumps stand out for their ability to capture and expel many unrelated compounds out of the cell. Determining the specificities and efflux efficiency of these pumps towards their substrates would provide quantitative insights into the development of antibacterial strategies. In this light, we developed a competition efflux assay on whole cells, that allows measuring the efficacy of extrusion of clinically used quinolones in populations and individual bacteria. Experiments reveal the efficient competitive action of some quinolones that restore an active concentration of other fluoroquinolones. Computational methods show how quinolones interact with the multidrug efflux transporter AcrB. Combining experiments and computations unveils a key molecular mechanism acting in vivo to detoxify bacterial cells. The developed assay can be generalized to the study of other efflux pumps. Nature Publishing Group UK 2022-10-06 /pmc/articles/PMC9537517/ /pubmed/36203030 http://dx.doi.org/10.1038/s42003-022-04024-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Vergalli, Julia Chauvet, Hugo Oliva, Francesco Pajović, Jelena Malloci, Giuliano Vargiu, Attilio Vittorio Réfrégiers, Matthieu Ruggerone, Paolo Pagès, Jean-Marie A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones |
title | A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones |
title_full | A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones |
title_fullStr | A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones |
title_full_unstemmed | A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones |
title_short | A framework for dissecting affinities of multidrug efflux transporter AcrB to fluoroquinolones |
title_sort | framework for dissecting affinities of multidrug efflux transporter acrb to fluoroquinolones |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537517/ https://www.ncbi.nlm.nih.gov/pubmed/36203030 http://dx.doi.org/10.1038/s42003-022-04024-1 |
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