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Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm

We investigated the in vitro and in vivo activities of epigallocatechin-3-gallate (EGCg), a green tea component, against Stenotrophomonas maltophilia (Sm) isolates from cystic fibrosis (CF) patients. In vitro effects of EGCg and the antibiotic colistin (COL) on growth inhibition, survival, and also...

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Autores principales: Vidigal, Pedrina G., Müsken, Mathias, Becker, Katrin A., Häussler, Susanne, Wingender, Jost, Steinmann, Eike, Kehrmann, Jan, Gulbins, Erich, Buer, Jan, Rath, Peter Michael, Steinmann, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972220/
https://www.ncbi.nlm.nih.gov/pubmed/24690894
http://dx.doi.org/10.1371/journal.pone.0092876
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author Vidigal, Pedrina G.
Müsken, Mathias
Becker, Katrin A.
Häussler, Susanne
Wingender, Jost
Steinmann, Eike
Kehrmann, Jan
Gulbins, Erich
Buer, Jan
Rath, Peter Michael
Steinmann, Jörg
author_facet Vidigal, Pedrina G.
Müsken, Mathias
Becker, Katrin A.
Häussler, Susanne
Wingender, Jost
Steinmann, Eike
Kehrmann, Jan
Gulbins, Erich
Buer, Jan
Rath, Peter Michael
Steinmann, Jörg
author_sort Vidigal, Pedrina G.
collection PubMed
description We investigated the in vitro and in vivo activities of epigallocatechin-3-gallate (EGCg), a green tea component, against Stenotrophomonas maltophilia (Sm) isolates from cystic fibrosis (CF) patients. In vitro effects of EGCg and the antibiotic colistin (COL) on growth inhibition, survival, and also against young and mature biofilms of S. maltophilia were determined. Qualitative and quantitative changes on the biofilms were assessed by confocal laser scanning microscopy (CLSM). Further, in vivo effects of nebulized EGCg in C57BL/6 and Cftr mutant mice during acute Sm lung infection were evaluated. Subinhibitory concentrations of EGCg significantly reduced not only biofilm formation, but also the quantity of viable cells in young and mature biofilms. CLSM showed that EGCg-exposed biofilms exhibited either a change in total biofilm biovolume or an increase of the fraction of dead cells contained within the biofilm in a dose depended manner. Sm infected wild-type and Cftr mutant mice treated with 1,024 mg/L EGCg by inhalation exhibited significantly lower bacterial counts than those undergoing no treatment or treated with COL. EGCg displayed promising inhibitory and anti-biofilm properties against CF Sm isolates in vitro and significantly reduced Sm bacterial counts in an acute infection model with wild type and CF mice. This natural compound may represent a novel therapeutic agent against Sm infection in CF.
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spelling pubmed-39722202014-04-04 Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm Vidigal, Pedrina G. Müsken, Mathias Becker, Katrin A. Häussler, Susanne Wingender, Jost Steinmann, Eike Kehrmann, Jan Gulbins, Erich Buer, Jan Rath, Peter Michael Steinmann, Jörg PLoS One Research Article We investigated the in vitro and in vivo activities of epigallocatechin-3-gallate (EGCg), a green tea component, against Stenotrophomonas maltophilia (Sm) isolates from cystic fibrosis (CF) patients. In vitro effects of EGCg and the antibiotic colistin (COL) on growth inhibition, survival, and also against young and mature biofilms of S. maltophilia were determined. Qualitative and quantitative changes on the biofilms were assessed by confocal laser scanning microscopy (CLSM). Further, in vivo effects of nebulized EGCg in C57BL/6 and Cftr mutant mice during acute Sm lung infection were evaluated. Subinhibitory concentrations of EGCg significantly reduced not only biofilm formation, but also the quantity of viable cells in young and mature biofilms. CLSM showed that EGCg-exposed biofilms exhibited either a change in total biofilm biovolume or an increase of the fraction of dead cells contained within the biofilm in a dose depended manner. Sm infected wild-type and Cftr mutant mice treated with 1,024 mg/L EGCg by inhalation exhibited significantly lower bacterial counts than those undergoing no treatment or treated with COL. EGCg displayed promising inhibitory and anti-biofilm properties against CF Sm isolates in vitro and significantly reduced Sm bacterial counts in an acute infection model with wild type and CF mice. This natural compound may represent a novel therapeutic agent against Sm infection in CF. Public Library of Science 2014-04-01 /pmc/articles/PMC3972220/ /pubmed/24690894 http://dx.doi.org/10.1371/journal.pone.0092876 Text en © 2014 Vidigal 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
Vidigal, Pedrina G.
Müsken, Mathias
Becker, Katrin A.
Häussler, Susanne
Wingender, Jost
Steinmann, Eike
Kehrmann, Jan
Gulbins, Erich
Buer, Jan
Rath, Peter Michael
Steinmann, Jörg
Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm
title Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm
title_full Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm
title_fullStr Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm
title_full_unstemmed Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm
title_short Effects of Green Tea Compound Epigallocatechin-3-Gallate against Stenotrophomonas maltophilia Infection and Biofilm
title_sort effects of green tea compound epigallocatechin-3-gallate against stenotrophomonas maltophilia infection and biofilm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972220/
https://www.ncbi.nlm.nih.gov/pubmed/24690894
http://dx.doi.org/10.1371/journal.pone.0092876
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