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Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus

Staphylococcus aureus is a Gram-positive opportunistic human pathogen responsible for severe infections and thousands of deaths annually, mostly due to its multidrug-resistant (MDR) variants. The cell membrane has emerged as a promising new therapeutic target, and lipophilic molecules, such as biosu...

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Autores principales: Buonocore, Carmine, Giugliano, Rosa, Della Sala, Gerardo, Palma Esposito, Fortunato, Tedesco, Pietro, Folliero, Veronica, Galdiero, Massimiliano, Franci, Gianluigi, de Pascale, Donatella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958974/
https://www.ncbi.nlm.nih.gov/pubmed/36840022
http://dx.doi.org/10.3390/pharmaceutics15020700
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author Buonocore, Carmine
Giugliano, Rosa
Della Sala, Gerardo
Palma Esposito, Fortunato
Tedesco, Pietro
Folliero, Veronica
Galdiero, Massimiliano
Franci, Gianluigi
de Pascale, Donatella
author_facet Buonocore, Carmine
Giugliano, Rosa
Della Sala, Gerardo
Palma Esposito, Fortunato
Tedesco, Pietro
Folliero, Veronica
Galdiero, Massimiliano
Franci, Gianluigi
de Pascale, Donatella
author_sort Buonocore, Carmine
collection PubMed
description Staphylococcus aureus is a Gram-positive opportunistic human pathogen responsible for severe infections and thousands of deaths annually, mostly due to its multidrug-resistant (MDR) variants. The cell membrane has emerged as a promising new therapeutic target, and lipophilic molecules, such as biosurfactants, are currently being utilized. Herein, we evaluated the antimicrobial activity of a rhamnolipids mixture produced by the Antarctic marine bacterium Pseudomonas gessardii M15. We demonstrated that our mixture has bactericidal activity in the range of 12.5–50 µg/mL against a panel of clinical MDR isolates of S. aureus, and that the mixture eradicated the bacterial population in 30 min at MIC value, and in 5 min after doubling the concentration. We also tested abilities of RLs to interfere with biofilm at different stages and determined that RLs can penetrate biofilm and kill the bacteria at sub-MICs values. The mixture was then used to functionalize a cotton swab to evaluate the prevention of S. aureus proliferation. We showed that by using 8 µg of rhamnolipids per swab, the entire bacterial load is eradicated, and just 0.5 µg is sufficient to reduce the growth by 99.99%. Our results strongly indicate the possibility of using this mixture as an additive for wound dressings for chronic wounds.
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spelling pubmed-99589742023-02-26 Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus Buonocore, Carmine Giugliano, Rosa Della Sala, Gerardo Palma Esposito, Fortunato Tedesco, Pietro Folliero, Veronica Galdiero, Massimiliano Franci, Gianluigi de Pascale, Donatella Pharmaceutics Article Staphylococcus aureus is a Gram-positive opportunistic human pathogen responsible for severe infections and thousands of deaths annually, mostly due to its multidrug-resistant (MDR) variants. The cell membrane has emerged as a promising new therapeutic target, and lipophilic molecules, such as biosurfactants, are currently being utilized. Herein, we evaluated the antimicrobial activity of a rhamnolipids mixture produced by the Antarctic marine bacterium Pseudomonas gessardii M15. We demonstrated that our mixture has bactericidal activity in the range of 12.5–50 µg/mL against a panel of clinical MDR isolates of S. aureus, and that the mixture eradicated the bacterial population in 30 min at MIC value, and in 5 min after doubling the concentration. We also tested abilities of RLs to interfere with biofilm at different stages and determined that RLs can penetrate biofilm and kill the bacteria at sub-MICs values. The mixture was then used to functionalize a cotton swab to evaluate the prevention of S. aureus proliferation. We showed that by using 8 µg of rhamnolipids per swab, the entire bacterial load is eradicated, and just 0.5 µg is sufficient to reduce the growth by 99.99%. Our results strongly indicate the possibility of using this mixture as an additive for wound dressings for chronic wounds. MDPI 2023-02-19 /pmc/articles/PMC9958974/ /pubmed/36840022 http://dx.doi.org/10.3390/pharmaceutics15020700 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Buonocore, Carmine
Giugliano, Rosa
Della Sala, Gerardo
Palma Esposito, Fortunato
Tedesco, Pietro
Folliero, Veronica
Galdiero, Massimiliano
Franci, Gianluigi
de Pascale, Donatella
Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus
title Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus
title_full Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus
title_fullStr Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus
title_full_unstemmed Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus
title_short Evaluation of Antimicrobial Properties and Potential Applications of Pseudomonas gessardii M15 Rhamnolipids towards Multiresistant Staphylococcus aureus
title_sort evaluation of antimicrobial properties and potential applications of pseudomonas gessardii m15 rhamnolipids towards multiresistant staphylococcus aureus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958974/
https://www.ncbi.nlm.nih.gov/pubmed/36840022
http://dx.doi.org/10.3390/pharmaceutics15020700
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