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The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media

Bacteria belonging to the group of ESKAPE pathogens are responsible for the majority of nosocomial infections. Due to the increase of antibiotic resistance, alternative treatment strategies are of high clinical relevance. In this context visible light as disinfection technique represents an interest...

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Autores principales: Bauer, Richard, Hoenes, Katharina, Meurle, Tobias, Hessling, Martin, Spellerberg, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714816/
https://www.ncbi.nlm.nih.gov/pubmed/34963696
http://dx.doi.org/10.1038/s41598-021-04202-x
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author Bauer, Richard
Hoenes, Katharina
Meurle, Tobias
Hessling, Martin
Spellerberg, Barbara
author_facet Bauer, Richard
Hoenes, Katharina
Meurle, Tobias
Hessling, Martin
Spellerberg, Barbara
author_sort Bauer, Richard
collection PubMed
description Bacteria belonging to the group of ESKAPE pathogens are responsible for the majority of nosocomial infections. Due to the increase of antibiotic resistance, alternative treatment strategies are of high clinical relevance. In this context visible light as disinfection technique represents an interesting option as microbial pathogens can be inactivated without adjuvants. However cytotoxic effects of visible light on host cells have also been reported. We compared the cytotoxicity of violet and blue light irradiation on monocytic THP-1 and alveolar epithelium A549 cells with the inactivation effect on ESKAPE pathogens. THP-1 cells displayed a higher susceptibility to irradiation than A549 cells with first cytotoxic effects occurring at 300 J cm(−2) (405 nm) and 400 J cm(−2) (450 nm) in comparison to 300 J cm(−2) and 1000 J cm(−2), respectively. We could define conditions in which a significant reduction of colony forming units for all ESKAPE pathogens, except Enterococcus faecium, was achieved at 405 nm while avoiding cytotoxicity. Irradiation at 450 nm demonstrated a more variable effect which was species and medium dependent. In summary a significant reduction of viable bacteria could be achieved at subtoxic irradiation doses, supporting a potential use of visible light as an antimicrobial agent in clinical settings.
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spelling pubmed-87148162022-01-05 The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media Bauer, Richard Hoenes, Katharina Meurle, Tobias Hessling, Martin Spellerberg, Barbara Sci Rep Article Bacteria belonging to the group of ESKAPE pathogens are responsible for the majority of nosocomial infections. Due to the increase of antibiotic resistance, alternative treatment strategies are of high clinical relevance. In this context visible light as disinfection technique represents an interesting option as microbial pathogens can be inactivated without adjuvants. However cytotoxic effects of visible light on host cells have also been reported. We compared the cytotoxicity of violet and blue light irradiation on monocytic THP-1 and alveolar epithelium A549 cells with the inactivation effect on ESKAPE pathogens. THP-1 cells displayed a higher susceptibility to irradiation than A549 cells with first cytotoxic effects occurring at 300 J cm(−2) (405 nm) and 400 J cm(−2) (450 nm) in comparison to 300 J cm(−2) and 1000 J cm(−2), respectively. We could define conditions in which a significant reduction of colony forming units for all ESKAPE pathogens, except Enterococcus faecium, was achieved at 405 nm while avoiding cytotoxicity. Irradiation at 450 nm demonstrated a more variable effect which was species and medium dependent. In summary a significant reduction of viable bacteria could be achieved at subtoxic irradiation doses, supporting a potential use of visible light as an antimicrobial agent in clinical settings. Nature Publishing Group UK 2021-12-28 /pmc/articles/PMC8714816/ /pubmed/34963696 http://dx.doi.org/10.1038/s41598-021-04202-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bauer, Richard
Hoenes, Katharina
Meurle, Tobias
Hessling, Martin
Spellerberg, Barbara
The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media
title The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media
title_full The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media
title_fullStr The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media
title_full_unstemmed The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media
title_short The effects of violet and blue light irradiation on ESKAPE pathogens and human cells in presence of cell culture media
title_sort effects of violet and blue light irradiation on eskape pathogens and human cells in presence of cell culture media
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714816/
https://www.ncbi.nlm.nih.gov/pubmed/34963696
http://dx.doi.org/10.1038/s41598-021-04202-x
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