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Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols

Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen responsible for a wide range of clinical conditions, from mild infections to life-threatening nosocomial biofilm-associated diseases, which are particularly severe in susceptible individuals. The aim of this in vitro study was to as...

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Autores principales: Meto, Aida, Colombari, Bruna, Meto, Agron, Boaretto, Giorgia, Pinetti, Diego, Marchetti, Lucia, Benvenuti, Stefania, Pellati, Federica, Blasi, Elisabetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074903/
https://www.ncbi.nlm.nih.gov/pubmed/32059431
http://dx.doi.org/10.3390/microorganisms8020243
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author Meto, Aida
Colombari, Bruna
Meto, Agron
Boaretto, Giorgia
Pinetti, Diego
Marchetti, Lucia
Benvenuti, Stefania
Pellati, Federica
Blasi, Elisabetta
author_facet Meto, Aida
Colombari, Bruna
Meto, Agron
Boaretto, Giorgia
Pinetti, Diego
Marchetti, Lucia
Benvenuti, Stefania
Pellati, Federica
Blasi, Elisabetta
author_sort Meto, Aida
collection PubMed
description Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen responsible for a wide range of clinical conditions, from mild infections to life-threatening nosocomial biofilm-associated diseases, which are particularly severe in susceptible individuals. The aim of this in vitro study was to assess the effects of an Albanian propolis on several virulence-related factors of P. aeruginosa, such as growth ability, biofilm formation, extracellular DNA (eDNA) release and phenazine production. To this end, propolis was processed using three different solvents and the extracted polyphenolic compounds were identified by means of high performance liquid chromatography coupled to electrospray ionization mass spectrometry (HPLC-ESI-MS) analysis. As assessed by a bioluminescence-based assay, among the three propolis extracts, the ethanol (EtOH) extract was the most effective in inhibiting both microbial growth and biofilm formation, followed by propylene glycol (PG) and polyethylene glycol 400 (PEG 400) propolis extracts. Furthermore, Pseudomonas exposure to propolis EtOH extract caused a decrease in eDNA release and phenazine production. Finally, caffeic acid phenethyl ester (CAPE) and quercetin decreased upon propolis EtOH extract exposure to bacteria. Overall, our data add new insights on the anti-microbial properties of a natural compound, such as propolis against P. aeruginosa. The potential implications of these findings will be discussed.
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spelling pubmed-70749032020-03-20 Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols Meto, Aida Colombari, Bruna Meto, Agron Boaretto, Giorgia Pinetti, Diego Marchetti, Lucia Benvenuti, Stefania Pellati, Federica Blasi, Elisabetta Microorganisms Article Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen responsible for a wide range of clinical conditions, from mild infections to life-threatening nosocomial biofilm-associated diseases, which are particularly severe in susceptible individuals. The aim of this in vitro study was to assess the effects of an Albanian propolis on several virulence-related factors of P. aeruginosa, such as growth ability, biofilm formation, extracellular DNA (eDNA) release and phenazine production. To this end, propolis was processed using three different solvents and the extracted polyphenolic compounds were identified by means of high performance liquid chromatography coupled to electrospray ionization mass spectrometry (HPLC-ESI-MS) analysis. As assessed by a bioluminescence-based assay, among the three propolis extracts, the ethanol (EtOH) extract was the most effective in inhibiting both microbial growth and biofilm formation, followed by propylene glycol (PG) and polyethylene glycol 400 (PEG 400) propolis extracts. Furthermore, Pseudomonas exposure to propolis EtOH extract caused a decrease in eDNA release and phenazine production. Finally, caffeic acid phenethyl ester (CAPE) and quercetin decreased upon propolis EtOH extract exposure to bacteria. Overall, our data add new insights on the anti-microbial properties of a natural compound, such as propolis against P. aeruginosa. The potential implications of these findings will be discussed. MDPI 2020-02-12 /pmc/articles/PMC7074903/ /pubmed/32059431 http://dx.doi.org/10.3390/microorganisms8020243 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Meto, Aida
Colombari, Bruna
Meto, Agron
Boaretto, Giorgia
Pinetti, Diego
Marchetti, Lucia
Benvenuti, Stefania
Pellati, Federica
Blasi, Elisabetta
Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols
title Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols
title_full Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols
title_fullStr Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols
title_full_unstemmed Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols
title_short Propolis Affects Pseudomonas aeruginosa Growth, Biofilm Formation, eDNA Release and Phenazine Production: Potential Involvement of Polyphenols
title_sort propolis affects pseudomonas aeruginosa growth, biofilm formation, edna release and phenazine production: potential involvement of polyphenols
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074903/
https://www.ncbi.nlm.nih.gov/pubmed/32059431
http://dx.doi.org/10.3390/microorganisms8020243
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