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Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli

Medicinal plants are an important source for the therapeutic remedies of various diseases including urinary tract infections. This prompted us to perform research in this area. We decided to focus on medicinal plants species used in urinary tract infections prevention. The aim of our study was to de...

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Autores principales: Wojnicz, Dorota, Kucharska, Alicja Z., Sokół-Łętowska, Anna, Kicia, Marta, Tichaczek-Goska, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495101/
https://www.ncbi.nlm.nih.gov/pubmed/22915095
http://dx.doi.org/10.1007/s00240-012-0499-6
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author Wojnicz, Dorota
Kucharska, Alicja Z.
Sokół-Łętowska, Anna
Kicia, Marta
Tichaczek-Goska, Dorota
author_facet Wojnicz, Dorota
Kucharska, Alicja Z.
Sokół-Łętowska, Anna
Kicia, Marta
Tichaczek-Goska, Dorota
author_sort Wojnicz, Dorota
collection PubMed
description Medicinal plants are an important source for the therapeutic remedies of various diseases including urinary tract infections. This prompted us to perform research in this area. We decided to focus on medicinal plants species used in urinary tract infections prevention. The aim of our study was to determine the influence of Betula pendula, Equisetum arvense, Herniaria glabra, Galium odoratum, Urtica dioica, and Vaccinium vitis-idaea extracts on bacterial survival and virulence factors involved in tissue colonization and biofilm formation of the uropathogenic Escherichia coli rods. Qualitative and quantitative analysis of plant extracts were performed. Antimicrobial assay relied on the estimation of the colony forming unit number. Hydrophobicity of cells was established by salt aggregation test. Using motility agar, the ability of bacteria to move was examined. The erythrocyte hemagglutination test was used for fimbriae P screening. Curli expression was determined using YESCA agar supplemented with congo red. Quantification of biofilm formation was carried out using a microtiter plate assay and a spectrophotometric method. The results of the study indicate significant differences between investigated extracts in their antimicrobial activities. The extracts of H. glabra and V. vitis-idaea showed the highest growth-inhibitory effects (p < 0.05). Surface hydrophobicity of autoaggregating E. coli strain changed after exposure to all plant extracts, except V. vitis-idaea (p > 0.05). The B. pendula and U. dioica extracts significantly reduced the motility of the E. coli rods (p < 0.05). All the extracts exhibited the anti-biofilm activity.
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spelling pubmed-34951012012-11-14 Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli Wojnicz, Dorota Kucharska, Alicja Z. Sokół-Łętowska, Anna Kicia, Marta Tichaczek-Goska, Dorota Urol Res Original Paper Medicinal plants are an important source for the therapeutic remedies of various diseases including urinary tract infections. This prompted us to perform research in this area. We decided to focus on medicinal plants species used in urinary tract infections prevention. The aim of our study was to determine the influence of Betula pendula, Equisetum arvense, Herniaria glabra, Galium odoratum, Urtica dioica, and Vaccinium vitis-idaea extracts on bacterial survival and virulence factors involved in tissue colonization and biofilm formation of the uropathogenic Escherichia coli rods. Qualitative and quantitative analysis of plant extracts were performed. Antimicrobial assay relied on the estimation of the colony forming unit number. Hydrophobicity of cells was established by salt aggregation test. Using motility agar, the ability of bacteria to move was examined. The erythrocyte hemagglutination test was used for fimbriae P screening. Curli expression was determined using YESCA agar supplemented with congo red. Quantification of biofilm formation was carried out using a microtiter plate assay and a spectrophotometric method. The results of the study indicate significant differences between investigated extracts in their antimicrobial activities. The extracts of H. glabra and V. vitis-idaea showed the highest growth-inhibitory effects (p < 0.05). Surface hydrophobicity of autoaggregating E. coli strain changed after exposure to all plant extracts, except V. vitis-idaea (p > 0.05). The B. pendula and U. dioica extracts significantly reduced the motility of the E. coli rods (p < 0.05). All the extracts exhibited the anti-biofilm activity. Springer-Verlag 2012-08-23 2012 /pmc/articles/PMC3495101/ /pubmed/22915095 http://dx.doi.org/10.1007/s00240-012-0499-6 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Wojnicz, Dorota
Kucharska, Alicja Z.
Sokół-Łętowska, Anna
Kicia, Marta
Tichaczek-Goska, Dorota
Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli
title Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli
title_full Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli
title_fullStr Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli
title_full_unstemmed Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli
title_short Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli
title_sort medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic escherichia coli
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495101/
https://www.ncbi.nlm.nih.gov/pubmed/22915095
http://dx.doi.org/10.1007/s00240-012-0499-6
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