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Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains
Background: An unbalanced skin microbiota due to an increase in pathogenic vs. commensal bacteria can be efficiently tackled by using prebiotics. The aim of this work was to identify novel prebiotic combinations by exerting species-specific action between S. aureus and S. epidermidis strains. Method...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824076/ https://www.ncbi.nlm.nih.gov/pubmed/33374268 http://dx.doi.org/10.3390/microorganisms9010037 |
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author | Di Lodovico, Silvia Gasparri, Franco Di Campli, Emanuela Di Fermo, Paola D’Ercole, Simonetta Cellini, Luigina Di Giulio, Mara |
author_facet | Di Lodovico, Silvia Gasparri, Franco Di Campli, Emanuela Di Fermo, Paola D’Ercole, Simonetta Cellini, Luigina Di Giulio, Mara |
author_sort | Di Lodovico, Silvia |
collection | PubMed |
description | Background: An unbalanced skin microbiota due to an increase in pathogenic vs. commensal bacteria can be efficiently tackled by using prebiotics. The aim of this work was to identify novel prebiotic combinations by exerting species-specific action between S. aureus and S. epidermidis strains. Methods: First, the antimicrobial/antibiofilm effect of Xylitol-XYL and Galacto-OligoSaccharides–GOS combined with each other at different concentrations (1, 2.5, 5%) against S. aureus and S. epidermidis clinical strains was evaluated in time. Second, the most species-specific concentration was used to combine XYL with Fructo-OligoSaccharides–FOS, IsoMalto-Oligosaccharides–IMO, ArabinoGaLactan–LAG, inulin, dextran. Experiments were performed by OD(600) detection, biomass quantification and LIVE/DEAD staining. Results: 1% XYL + 1% GOS showed the best species-specific action with an immediate antibacterial/antibiofilm action against S. aureus strains (up to 34.54% ± 5.35/64.68% ± 4.77) without a relevant effect on S. epidermidis. Among the other prebiotic formulations, 1% XYL plus 1% FOS (up to 49.17% ± 21.46/37.59% ± 6.34) or 1% IMO (up to 41.28% ± 4.88/36.70% ± 10.03) or 1% LAG (up to 38.21% ± 5.31/83.06% ± 5.11) showed antimicrobial/antibiofilm effects similar to 1% XYL+1% GOS. For all tested formulations, a prevalent bacteriostatic effect in the planktonic phase and a general reduction of S. aureus biofilm formation without loss of viability were recorded. Conclusion: The combinations of 1% XYL with 1% GOS or 1% FOS or 1% IMO or 1% LAG may help to control the balance of skin microbiota, representing good candidates for topic formulations. |
format | Online Article Text |
id | pubmed-7824076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78240762021-01-24 Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains Di Lodovico, Silvia Gasparri, Franco Di Campli, Emanuela Di Fermo, Paola D’Ercole, Simonetta Cellini, Luigina Di Giulio, Mara Microorganisms Article Background: An unbalanced skin microbiota due to an increase in pathogenic vs. commensal bacteria can be efficiently tackled by using prebiotics. The aim of this work was to identify novel prebiotic combinations by exerting species-specific action between S. aureus and S. epidermidis strains. Methods: First, the antimicrobial/antibiofilm effect of Xylitol-XYL and Galacto-OligoSaccharides–GOS combined with each other at different concentrations (1, 2.5, 5%) against S. aureus and S. epidermidis clinical strains was evaluated in time. Second, the most species-specific concentration was used to combine XYL with Fructo-OligoSaccharides–FOS, IsoMalto-Oligosaccharides–IMO, ArabinoGaLactan–LAG, inulin, dextran. Experiments were performed by OD(600) detection, biomass quantification and LIVE/DEAD staining. Results: 1% XYL + 1% GOS showed the best species-specific action with an immediate antibacterial/antibiofilm action against S. aureus strains (up to 34.54% ± 5.35/64.68% ± 4.77) without a relevant effect on S. epidermidis. Among the other prebiotic formulations, 1% XYL plus 1% FOS (up to 49.17% ± 21.46/37.59% ± 6.34) or 1% IMO (up to 41.28% ± 4.88/36.70% ± 10.03) or 1% LAG (up to 38.21% ± 5.31/83.06% ± 5.11) showed antimicrobial/antibiofilm effects similar to 1% XYL+1% GOS. For all tested formulations, a prevalent bacteriostatic effect in the planktonic phase and a general reduction of S. aureus biofilm formation without loss of viability were recorded. Conclusion: The combinations of 1% XYL with 1% GOS or 1% FOS or 1% IMO or 1% LAG may help to control the balance of skin microbiota, representing good candidates for topic formulations. MDPI 2020-12-24 /pmc/articles/PMC7824076/ /pubmed/33374268 http://dx.doi.org/10.3390/microorganisms9010037 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 Di Lodovico, Silvia Gasparri, Franco Di Campli, Emanuela Di Fermo, Paola D’Ercole, Simonetta Cellini, Luigina Di Giulio, Mara Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains |
title | Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains |
title_full | Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains |
title_fullStr | Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains |
title_full_unstemmed | Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains |
title_short | Prebiotic Combinations Effects on the Colonization of Staphylococcal Skin Strains |
title_sort | prebiotic combinations effects on the colonization of staphylococcal skin strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824076/ https://www.ncbi.nlm.nih.gov/pubmed/33374268 http://dx.doi.org/10.3390/microorganisms9010037 |
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