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Aerosolization and recovery of viable murine norovirus in an experimental setup
Noroviruses are the major cause for viral acute gastroenteritis in the world. Despite the existing infection prevention strategies in hospitals, the disease continues to spread and causes extensive and numerous outbreaks. Hence, there is a need to investigate the possibility of airborne transmission...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525472/ https://www.ncbi.nlm.nih.gov/pubmed/32994471 http://dx.doi.org/10.1038/s41598-020-72932-5 |
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author | Alsved, Malin Widell, Anders Dahlin, Henrik Karlson, Sara Medstrand, Patrik Löndahl, Jakob |
author_facet | Alsved, Malin Widell, Anders Dahlin, Henrik Karlson, Sara Medstrand, Patrik Löndahl, Jakob |
author_sort | Alsved, Malin |
collection | PubMed |
description | Noroviruses are the major cause for viral acute gastroenteritis in the world. Despite the existing infection prevention strategies in hospitals, the disease continues to spread and causes extensive and numerous outbreaks. Hence, there is a need to investigate the possibility of airborne transmission of norovirus. In this study, we developed an experimental setup for studies on the infectivity of aerosolized murine norovirus (MNV), a model for the human norovirus. Two aerosol generation principles were evaluated: bubble bursting, a common natural aerosolization mechanism, and nebulization, a common aerosolization technique in laboratory studies. The aerosolization setup was characterized by physical and viral dilution factors, generated aerosol particle size distributions, and the viral infectivity after aerosolization. We found a lower physical dilution factor when using the nebulization generator than with the bubble bursting generator. The viral dilution factor of the system was higher than the physical dilution; however, when comparing the physical and viral dilution factors, bubble bursting generation was more efficient. The infectivity per virus was similar using either generation principle, suggesting that the generation itself had a minor impact on MNV infectivity and that instead, the effect of drying in air could be a major reason for infectivity losses. |
format | Online Article Text |
id | pubmed-7525472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75254722020-10-01 Aerosolization and recovery of viable murine norovirus in an experimental setup Alsved, Malin Widell, Anders Dahlin, Henrik Karlson, Sara Medstrand, Patrik Löndahl, Jakob Sci Rep Article Noroviruses are the major cause for viral acute gastroenteritis in the world. Despite the existing infection prevention strategies in hospitals, the disease continues to spread and causes extensive and numerous outbreaks. Hence, there is a need to investigate the possibility of airborne transmission of norovirus. In this study, we developed an experimental setup for studies on the infectivity of aerosolized murine norovirus (MNV), a model for the human norovirus. Two aerosol generation principles were evaluated: bubble bursting, a common natural aerosolization mechanism, and nebulization, a common aerosolization technique in laboratory studies. The aerosolization setup was characterized by physical and viral dilution factors, generated aerosol particle size distributions, and the viral infectivity after aerosolization. We found a lower physical dilution factor when using the nebulization generator than with the bubble bursting generator. The viral dilution factor of the system was higher than the physical dilution; however, when comparing the physical and viral dilution factors, bubble bursting generation was more efficient. The infectivity per virus was similar using either generation principle, suggesting that the generation itself had a minor impact on MNV infectivity and that instead, the effect of drying in air could be a major reason for infectivity losses. Nature Publishing Group UK 2020-09-29 /pmc/articles/PMC7525472/ /pubmed/32994471 http://dx.doi.org/10.1038/s41598-020-72932-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Alsved, Malin Widell, Anders Dahlin, Henrik Karlson, Sara Medstrand, Patrik Löndahl, Jakob Aerosolization and recovery of viable murine norovirus in an experimental setup |
title | Aerosolization and recovery of viable murine norovirus in an experimental setup |
title_full | Aerosolization and recovery of viable murine norovirus in an experimental setup |
title_fullStr | Aerosolization and recovery of viable murine norovirus in an experimental setup |
title_full_unstemmed | Aerosolization and recovery of viable murine norovirus in an experimental setup |
title_short | Aerosolization and recovery of viable murine norovirus in an experimental setup |
title_sort | aerosolization and recovery of viable murine norovirus in an experimental setup |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525472/ https://www.ncbi.nlm.nih.gov/pubmed/32994471 http://dx.doi.org/10.1038/s41598-020-72932-5 |
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