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Ultraviolet A light effectively reduces bacteria and viruses including coronavirus

Antimicrobial-resistant and novel pathogens continue to emerge, outpacing efforts to contain and treat them. Therefore, there is a crucial need for safe and effective therapies. Ultraviolet-A (UVA) phototherapy is FDA-approved for several dermatological diseases but not for internal applications. We...

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Autores principales: Rezaie, Ali, Leite, Gabriela G. S., Melmed, Gil Y., Mathur, Ruchi, Villanueva-Millan, Maria Jesus, Parodi, Gonzalo, Sin, Jon, Germano, Juliana F., Morales, Walter, Weitsman, Stacy, Kim, Seung Young, Park, Jae Ho, Sakhaie, Siamak, Pimentel, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365468/
https://www.ncbi.nlm.nih.gov/pubmed/32673355
http://dx.doi.org/10.1371/journal.pone.0236199
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author Rezaie, Ali
Leite, Gabriela G. S.
Melmed, Gil Y.
Mathur, Ruchi
Villanueva-Millan, Maria Jesus
Parodi, Gonzalo
Sin, Jon
Germano, Juliana F.
Morales, Walter
Weitsman, Stacy
Kim, Seung Young
Park, Jae Ho
Sakhaie, Siamak
Pimentel, Mark
author_facet Rezaie, Ali
Leite, Gabriela G. S.
Melmed, Gil Y.
Mathur, Ruchi
Villanueva-Millan, Maria Jesus
Parodi, Gonzalo
Sin, Jon
Germano, Juliana F.
Morales, Walter
Weitsman, Stacy
Kim, Seung Young
Park, Jae Ho
Sakhaie, Siamak
Pimentel, Mark
author_sort Rezaie, Ali
collection PubMed
description Antimicrobial-resistant and novel pathogens continue to emerge, outpacing efforts to contain and treat them. Therefore, there is a crucial need for safe and effective therapies. Ultraviolet-A (UVA) phototherapy is FDA-approved for several dermatological diseases but not for internal applications. We investigated UVA effects on human cells in vitro, mouse colonic tissue in vivo, and UVA efficacy against bacteria, yeast, coxsackievirus group B and coronavirus-229E. Several pathogens and virally transfected human cells were exposed to a series of specific UVA exposure regimens. HeLa, alveolar and primary human tracheal epithelial cell viability was assessed after UVA exposure, and 8-Oxo-2'-deoxyguanosine was measured as an oxidative DNA damage marker. Furthermore, wild-type mice were exposed to intracolonic UVA as an in vivo model to assess safety of internal UVA exposure. Controlled UVA exposure yielded significant reductions in Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Enterococcus faecalis, Clostridioides difficile, Streptococcus pyogenes, Staphylococcus epidermidis, Proteus mirabilis and Candida albicans. UVA-treated coxsackievirus-transfected HeLa cells exhibited significantly increased cell survival compared to controls. UVA-treated coronavirus-229E-transfected tracheal cells exhibited significant coronavirus spike protein reduction, increased mitochondrial antiviral-signaling protein and decreased coronavirus-229E-induced cell death. Specific controlled UVA exposure had no significant effect on growth or 8-Oxo-2'-deoxyguanosine levels in three types of human cells. Single or repeated in vivo intraluminal UVA exposure produced no discernible endoscopic, histologic or dysplastic changes in mice. These findings suggest that, under specific conditions, UVA reduces various pathogens including coronavirus-229E, and may provide a safe and effective treatment for infectious diseases of internal viscera. Clinical studies are warranted to further elucidate the safety and efficacy of UVA in humans.
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spelling pubmed-73654682020-08-11 Ultraviolet A light effectively reduces bacteria and viruses including coronavirus Rezaie, Ali Leite, Gabriela G. S. Melmed, Gil Y. Mathur, Ruchi Villanueva-Millan, Maria Jesus Parodi, Gonzalo Sin, Jon Germano, Juliana F. Morales, Walter Weitsman, Stacy Kim, Seung Young Park, Jae Ho Sakhaie, Siamak Pimentel, Mark PLoS One Research Article Antimicrobial-resistant and novel pathogens continue to emerge, outpacing efforts to contain and treat them. Therefore, there is a crucial need for safe and effective therapies. Ultraviolet-A (UVA) phototherapy is FDA-approved for several dermatological diseases but not for internal applications. We investigated UVA effects on human cells in vitro, mouse colonic tissue in vivo, and UVA efficacy against bacteria, yeast, coxsackievirus group B and coronavirus-229E. Several pathogens and virally transfected human cells were exposed to a series of specific UVA exposure regimens. HeLa, alveolar and primary human tracheal epithelial cell viability was assessed after UVA exposure, and 8-Oxo-2'-deoxyguanosine was measured as an oxidative DNA damage marker. Furthermore, wild-type mice were exposed to intracolonic UVA as an in vivo model to assess safety of internal UVA exposure. Controlled UVA exposure yielded significant reductions in Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Enterococcus faecalis, Clostridioides difficile, Streptococcus pyogenes, Staphylococcus epidermidis, Proteus mirabilis and Candida albicans. UVA-treated coxsackievirus-transfected HeLa cells exhibited significantly increased cell survival compared to controls. UVA-treated coronavirus-229E-transfected tracheal cells exhibited significant coronavirus spike protein reduction, increased mitochondrial antiviral-signaling protein and decreased coronavirus-229E-induced cell death. Specific controlled UVA exposure had no significant effect on growth or 8-Oxo-2'-deoxyguanosine levels in three types of human cells. Single or repeated in vivo intraluminal UVA exposure produced no discernible endoscopic, histologic or dysplastic changes in mice. These findings suggest that, under specific conditions, UVA reduces various pathogens including coronavirus-229E, and may provide a safe and effective treatment for infectious diseases of internal viscera. Clinical studies are warranted to further elucidate the safety and efficacy of UVA in humans. Public Library of Science 2020-07-16 /pmc/articles/PMC7365468/ /pubmed/32673355 http://dx.doi.org/10.1371/journal.pone.0236199 Text en © 2020 Rezaie et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rezaie, Ali
Leite, Gabriela G. S.
Melmed, Gil Y.
Mathur, Ruchi
Villanueva-Millan, Maria Jesus
Parodi, Gonzalo
Sin, Jon
Germano, Juliana F.
Morales, Walter
Weitsman, Stacy
Kim, Seung Young
Park, Jae Ho
Sakhaie, Siamak
Pimentel, Mark
Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
title Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
title_full Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
title_fullStr Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
title_full_unstemmed Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
title_short Ultraviolet A light effectively reduces bacteria and viruses including coronavirus
title_sort ultraviolet a light effectively reduces bacteria and viruses including coronavirus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365468/
https://www.ncbi.nlm.nih.gov/pubmed/32673355
http://dx.doi.org/10.1371/journal.pone.0236199
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