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A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition

Bacterial efflux pumps are active transport proteins responsible for resistance to selected biocides and antibiotics. It has been shown that production of efflux pumps is up-regulated in a number of highly pathogenic bacteria, including methicillin resistant Staphylococcus aureus. Thus, the identifi...

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Autores principales: Brown, Adam R., Ettefagh, Keivan A., Todd, Daniel, Cole, Patrick S., Egan, Joseph M., Foil, Daniel H., Graf, Tyler N., Schindler, Bryan D., Kaatz, Glenn W., Cech, Nadja B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427306/
https://www.ncbi.nlm.nih.gov/pubmed/25961825
http://dx.doi.org/10.1371/journal.pone.0124814
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author Brown, Adam R.
Ettefagh, Keivan A.
Todd, Daniel
Cole, Patrick S.
Egan, Joseph M.
Foil, Daniel H.
Graf, Tyler N.
Schindler, Bryan D.
Kaatz, Glenn W.
Cech, Nadja B.
author_facet Brown, Adam R.
Ettefagh, Keivan A.
Todd, Daniel
Cole, Patrick S.
Egan, Joseph M.
Foil, Daniel H.
Graf, Tyler N.
Schindler, Bryan D.
Kaatz, Glenn W.
Cech, Nadja B.
author_sort Brown, Adam R.
collection PubMed
description Bacterial efflux pumps are active transport proteins responsible for resistance to selected biocides and antibiotics. It has been shown that production of efflux pumps is up-regulated in a number of highly pathogenic bacteria, including methicillin resistant Staphylococcus aureus. Thus, the identification of new bacterial efflux pump inhibitors is a topic of great interest. Existing assays to evaluate efflux pump inhibitory activity rely on fluorescence by an efflux pump substrate. When employing these assays to evaluate efflux pump inhibitory activity of plant extracts and some purified compounds, we observed severe optical interference that gave rise to false negative results. To circumvent this problem, a new mass spectrometry-based method was developed for the quantitative measurement of bacterial efflux pump inhibition. The assay was employed to evaluate efflux pump inhibitory activity of a crude extract of the botanical Hydrastis Canadensis, and to compare the efflux pump inhibitory activity of several pure flavonoids. The flavonoid quercetin, which appeared to be completely inactive with a fluorescence-based method, showed an IC(50) value of 75 μg/mL with the new method. The other flavonoids evaluated (apigenin, kaempferol, rhamnetin, luteolin, myricetin), were also active, with IC(50) values ranging from 19 μg/mL to 75 μg/mL. The assay described herein could be useful in future screening efforts to identify efflux pump inhibitors, particularly in situations where optical interference precludes the application of methods that rely on fluorescence.
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spelling pubmed-44273062015-05-21 A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition Brown, Adam R. Ettefagh, Keivan A. Todd, Daniel Cole, Patrick S. Egan, Joseph M. Foil, Daniel H. Graf, Tyler N. Schindler, Bryan D. Kaatz, Glenn W. Cech, Nadja B. PLoS One Research Article Bacterial efflux pumps are active transport proteins responsible for resistance to selected biocides and antibiotics. It has been shown that production of efflux pumps is up-regulated in a number of highly pathogenic bacteria, including methicillin resistant Staphylococcus aureus. Thus, the identification of new bacterial efflux pump inhibitors is a topic of great interest. Existing assays to evaluate efflux pump inhibitory activity rely on fluorescence by an efflux pump substrate. When employing these assays to evaluate efflux pump inhibitory activity of plant extracts and some purified compounds, we observed severe optical interference that gave rise to false negative results. To circumvent this problem, a new mass spectrometry-based method was developed for the quantitative measurement of bacterial efflux pump inhibition. The assay was employed to evaluate efflux pump inhibitory activity of a crude extract of the botanical Hydrastis Canadensis, and to compare the efflux pump inhibitory activity of several pure flavonoids. The flavonoid quercetin, which appeared to be completely inactive with a fluorescence-based method, showed an IC(50) value of 75 μg/mL with the new method. The other flavonoids evaluated (apigenin, kaempferol, rhamnetin, luteolin, myricetin), were also active, with IC(50) values ranging from 19 μg/mL to 75 μg/mL. The assay described herein could be useful in future screening efforts to identify efflux pump inhibitors, particularly in situations where optical interference precludes the application of methods that rely on fluorescence. Public Library of Science 2015-05-11 /pmc/articles/PMC4427306/ /pubmed/25961825 http://dx.doi.org/10.1371/journal.pone.0124814 Text en © 2015 Brown et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Brown, Adam R.
Ettefagh, Keivan A.
Todd, Daniel
Cole, Patrick S.
Egan, Joseph M.
Foil, Daniel H.
Graf, Tyler N.
Schindler, Bryan D.
Kaatz, Glenn W.
Cech, Nadja B.
A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition
title A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition
title_full A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition
title_fullStr A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition
title_full_unstemmed A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition
title_short A Mass Spectrometry-Based Assay for Improved Quantitative Measurements of Efflux Pump Inhibition
title_sort mass spectrometry-based assay for improved quantitative measurements of efflux pump inhibition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427306/
https://www.ncbi.nlm.nih.gov/pubmed/25961825
http://dx.doi.org/10.1371/journal.pone.0124814
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