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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7365468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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