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Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma
Bacterial biofilms are three-dimensional structures containing bacterial cells enveloped in a protective polymeric matrix, which renders them highly resistant to antibiotics and the human immune system. Therefore, the capacity to make biofilms is considered as a major virulence factor for pathogenic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319976/ https://www.ncbi.nlm.nih.gov/pubmed/28275584 http://dx.doi.org/10.3389/fcimb.2017.00043 |
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author | Helgadóttir, Saga Pandit, Santosh Mokkapati, Venkata R. S. S. Westerlund, Fredrik Apell, Peter Mijakovic, Ivan |
author_facet | Helgadóttir, Saga Pandit, Santosh Mokkapati, Venkata R. S. S. Westerlund, Fredrik Apell, Peter Mijakovic, Ivan |
author_sort | Helgadóttir, Saga |
collection | PubMed |
description | Bacterial biofilms are three-dimensional structures containing bacterial cells enveloped in a protective polymeric matrix, which renders them highly resistant to antibiotics and the human immune system. Therefore, the capacity to make biofilms is considered as a major virulence factor for pathogenic bacteria. Cold Atmospheric Plasma (CAP) is known to be quite efficient in eradicating planktonic bacteria, but its effectiveness against biofilms has not been thoroughly investigated. The goal of this study was to evaluate the effect of exposure of CAP against mature biofilm for different time intervals and to evaluate the effect of combined treatment with vitamin C. We demonstrate that CAP is not very effective against 48 h mature bacterial biofilms of several common opportunistic pathogens: Staphylococcus epidermidis, Escherichia coli, and Pseudomonas aeruginosa. However, if bacterial biofilms are pre-treated with vitamin C for 15 min before exposure to CAP, a significantly stronger bactericidal effect can be obtained. Vitamin C pretreatment enhances the bactericidal effect of cold plasma by reducing the viability from 10 to 2% in E. coli biofilm, 50 to 11% in P. aeruginosa, and 61 to 18% in S. epidermidis biofilm. Since it is not feasible to use extended CAP treatments in medical practice, we argue that the pre-treatment of infectious lesions with vitamin C prior to CAP exposure can be a viable route for efficient eradication of bacterial biofilms in many different applications. |
format | Online Article Text |
id | pubmed-5319976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53199762017-03-08 Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma Helgadóttir, Saga Pandit, Santosh Mokkapati, Venkata R. S. S. Westerlund, Fredrik Apell, Peter Mijakovic, Ivan Front Cell Infect Microbiol Microbiology Bacterial biofilms are three-dimensional structures containing bacterial cells enveloped in a protective polymeric matrix, which renders them highly resistant to antibiotics and the human immune system. Therefore, the capacity to make biofilms is considered as a major virulence factor for pathogenic bacteria. Cold Atmospheric Plasma (CAP) is known to be quite efficient in eradicating planktonic bacteria, but its effectiveness against biofilms has not been thoroughly investigated. The goal of this study was to evaluate the effect of exposure of CAP against mature biofilm for different time intervals and to evaluate the effect of combined treatment with vitamin C. We demonstrate that CAP is not very effective against 48 h mature bacterial biofilms of several common opportunistic pathogens: Staphylococcus epidermidis, Escherichia coli, and Pseudomonas aeruginosa. However, if bacterial biofilms are pre-treated with vitamin C for 15 min before exposure to CAP, a significantly stronger bactericidal effect can be obtained. Vitamin C pretreatment enhances the bactericidal effect of cold plasma by reducing the viability from 10 to 2% in E. coli biofilm, 50 to 11% in P. aeruginosa, and 61 to 18% in S. epidermidis biofilm. Since it is not feasible to use extended CAP treatments in medical practice, we argue that the pre-treatment of infectious lesions with vitamin C prior to CAP exposure can be a viable route for efficient eradication of bacterial biofilms in many different applications. Frontiers Media S.A. 2017-02-22 /pmc/articles/PMC5319976/ /pubmed/28275584 http://dx.doi.org/10.3389/fcimb.2017.00043 Text en Copyright © 2017 Helgadóttir, Pandit, Mokkapati, Westerlund, Apell and Mijakovic. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Helgadóttir, Saga Pandit, Santosh Mokkapati, Venkata R. S. S. Westerlund, Fredrik Apell, Peter Mijakovic, Ivan Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma |
title | Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma |
title_full | Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma |
title_fullStr | Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma |
title_full_unstemmed | Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma |
title_short | Vitamin C Pretreatment Enhances the Antibacterial Effect of Cold Atmospheric Plasma |
title_sort | vitamin c pretreatment enhances the antibacterial effect of cold atmospheric plasma |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319976/ https://www.ncbi.nlm.nih.gov/pubmed/28275584 http://dx.doi.org/10.3389/fcimb.2017.00043 |
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