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Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa

BACKGROUND: Bacteria within a biofilm are phenotypically more resistant to antibiotics, desiccation, and the host immune system, making it an important virulence factor for many microbes. Cranberry juice has long been used to prevent infections of the urinary tract, which are often related to biofil...

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Autores principales: Ulrey, Robert K, Barksdale, Stephanie M, Zhou, Weidong, van Hoek, Monique L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320558/
https://www.ncbi.nlm.nih.gov/pubmed/25511463
http://dx.doi.org/10.1186/1472-6882-14-499
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author Ulrey, Robert K
Barksdale, Stephanie M
Zhou, Weidong
van Hoek, Monique L
author_facet Ulrey, Robert K
Barksdale, Stephanie M
Zhou, Weidong
van Hoek, Monique L
author_sort Ulrey, Robert K
collection PubMed
description BACKGROUND: Bacteria within a biofilm are phenotypically more resistant to antibiotics, desiccation, and the host immune system, making it an important virulence factor for many microbes. Cranberry juice has long been used to prevent infections of the urinary tract, which are often related to biofilm formation. Recent studies have found that the A-type proanthocyanidins from cranberries have anti-biofilm properties against Escherichia coli. METHODS: Using crystal violet biofilm staining, resazurin metabolism assays, and confocal imaging, we examined the ability of A-type proanthocyanidins (PACs) to disrupt the biofilm formation of Pseudomonas aeruginosa. We used mass spectrometry to analyze the proteomic effects of PAC treatment. We also performed synergy assays and in vitro and in vivo infections to determine whether PACs, alone and in combination with gentamicin, could contribute to the killing of P. aeruginosa and the survival of cell lines and G. mellonella. RESULTS: Cranberry PACs reduced P. aeruginosa swarming motility. Cranberry PACs significantly disrupted the biofilm formation of P. aeruginosa. Proteomics analysis revealed significantly different proteins expressed following PAC treatment. In addition, we found that PACs potentiated the antibiotic activity of gentamicin in an in vivo model of infection using G. mellonella. CONCLUSIONS: Results suggest that A-type proanthocyanidins may be a useful therapeutic against the biofilm-mediated infections caused by P. aeruginosa and should be further tested. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1472-6882-14-499) contains supplementary material, which is available to authorized users.
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spelling pubmed-43205582015-02-08 Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa Ulrey, Robert K Barksdale, Stephanie M Zhou, Weidong van Hoek, Monique L BMC Complement Altern Med Research Article BACKGROUND: Bacteria within a biofilm are phenotypically more resistant to antibiotics, desiccation, and the host immune system, making it an important virulence factor for many microbes. Cranberry juice has long been used to prevent infections of the urinary tract, which are often related to biofilm formation. Recent studies have found that the A-type proanthocyanidins from cranberries have anti-biofilm properties against Escherichia coli. METHODS: Using crystal violet biofilm staining, resazurin metabolism assays, and confocal imaging, we examined the ability of A-type proanthocyanidins (PACs) to disrupt the biofilm formation of Pseudomonas aeruginosa. We used mass spectrometry to analyze the proteomic effects of PAC treatment. We also performed synergy assays and in vitro and in vivo infections to determine whether PACs, alone and in combination with gentamicin, could contribute to the killing of P. aeruginosa and the survival of cell lines and G. mellonella. RESULTS: Cranberry PACs reduced P. aeruginosa swarming motility. Cranberry PACs significantly disrupted the biofilm formation of P. aeruginosa. Proteomics analysis revealed significantly different proteins expressed following PAC treatment. In addition, we found that PACs potentiated the antibiotic activity of gentamicin in an in vivo model of infection using G. mellonella. CONCLUSIONS: Results suggest that A-type proanthocyanidins may be a useful therapeutic against the biofilm-mediated infections caused by P. aeruginosa and should be further tested. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1472-6882-14-499) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-16 /pmc/articles/PMC4320558/ /pubmed/25511463 http://dx.doi.org/10.1186/1472-6882-14-499 Text en © Ulrey et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ulrey, Robert K
Barksdale, Stephanie M
Zhou, Weidong
van Hoek, Monique L
Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa
title Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa
title_full Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa
title_fullStr Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa
title_full_unstemmed Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa
title_short Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa
title_sort cranberry proanthocyanidins have anti-biofilm properties against pseudomonas aeruginosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320558/
https://www.ncbi.nlm.nih.gov/pubmed/25511463
http://dx.doi.org/10.1186/1472-6882-14-499
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