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New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination

The requirement for novel decontamination technologies for use in hospitals is ever present. One such system uses 405 nm visible light to inactivate microorganisms via ROS-generated oxidative damage. Although effective for bacterial and fungal inactivation, little is known about the virucidal effect...

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Autores principales: Tomb, Rachael M., Maclean, Michelle, Coia, John E., Graham, Elizabeth, McDonald, Michael, Atreya, Chintamani D., MacGregor, Scott J., Anderson, John G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429381/
https://www.ncbi.nlm.nih.gov/pubmed/28040848
http://dx.doi.org/10.1007/s12560-016-9275-z
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author Tomb, Rachael M.
Maclean, Michelle
Coia, John E.
Graham, Elizabeth
McDonald, Michael
Atreya, Chintamani D.
MacGregor, Scott J.
Anderson, John G.
author_facet Tomb, Rachael M.
Maclean, Michelle
Coia, John E.
Graham, Elizabeth
McDonald, Michael
Atreya, Chintamani D.
MacGregor, Scott J.
Anderson, John G.
author_sort Tomb, Rachael M.
collection PubMed
description The requirement for novel decontamination technologies for use in hospitals is ever present. One such system uses 405 nm visible light to inactivate microorganisms via ROS-generated oxidative damage. Although effective for bacterial and fungal inactivation, little is known about the virucidal effects of 405 nm light. Norovirus (NoV) gastroenteritis outbreaks often occur in the clinical setting, and this study was designed to investigate potential inactivation effects of 405 nm light on the NoV surrogate, feline calicivirus (FCV). FCV was exposed to 405 nm light whilst suspended in minimal and organically-rich media to establish the virucidal efficacy and the effect biologically-relevant material may play in viral susceptibility. Antiviral activity was successfully demonstrated with a 4 Log(10) (99.99%) reduction in infectivity when suspended in minimal media evident after a dose of 2.8 kJ cm(−2). FCV exposed in artificial faeces, artificial saliva, blood plasma and other organically rich media exhibited an equivalent level of inactivation using between 50–85% less dose of the light, indicating enhanced inactivation when the virus is present in organically-rich biologically-relevant media. Further research in this area could aid in the development of 405 nm light technology for effective NoV decontamination within the hospital environment.
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spelling pubmed-54293812017-05-30 New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination Tomb, Rachael M. Maclean, Michelle Coia, John E. Graham, Elizabeth McDonald, Michael Atreya, Chintamani D. MacGregor, Scott J. Anderson, John G. Food Environ Virol Original Paper The requirement for novel decontamination technologies for use in hospitals is ever present. One such system uses 405 nm visible light to inactivate microorganisms via ROS-generated oxidative damage. Although effective for bacterial and fungal inactivation, little is known about the virucidal effects of 405 nm light. Norovirus (NoV) gastroenteritis outbreaks often occur in the clinical setting, and this study was designed to investigate potential inactivation effects of 405 nm light on the NoV surrogate, feline calicivirus (FCV). FCV was exposed to 405 nm light whilst suspended in minimal and organically-rich media to establish the virucidal efficacy and the effect biologically-relevant material may play in viral susceptibility. Antiviral activity was successfully demonstrated with a 4 Log(10) (99.99%) reduction in infectivity when suspended in minimal media evident after a dose of 2.8 kJ cm(−2). FCV exposed in artificial faeces, artificial saliva, blood plasma and other organically rich media exhibited an equivalent level of inactivation using between 50–85% less dose of the light, indicating enhanced inactivation when the virus is present in organically-rich biologically-relevant media. Further research in this area could aid in the development of 405 nm light technology for effective NoV decontamination within the hospital environment. Springer US 2016-12-31 2017 /pmc/articles/PMC5429381/ /pubmed/28040848 http://dx.doi.org/10.1007/s12560-016-9275-z Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Tomb, Rachael M.
Maclean, Michelle
Coia, John E.
Graham, Elizabeth
McDonald, Michael
Atreya, Chintamani D.
MacGregor, Scott J.
Anderson, John G.
New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination
title New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination
title_full New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination
title_fullStr New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination
title_full_unstemmed New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination
title_short New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination
title_sort new proof-of-concept in viral inactivation: virucidal efficacy of 405 nm light against feline calicivirus as a model for norovirus decontamination
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429381/
https://www.ncbi.nlm.nih.gov/pubmed/28040848
http://dx.doi.org/10.1007/s12560-016-9275-z
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