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Intranasal antisepsis to reduce influenza virus transmission in an animal model

BACKGROUND: Seasonal influenza annually causes significant morbidity and mortality, and unpredictable respiratory virus zoonoses, such as the current COVID‐19 pandemic, can threaten the health and lives of millions more. Molecular iodine (I(2)) is a broad‐spectrum, pathogen‐nonspecific antiseptic ag...

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Autores principales: Gaaloul ben Hnia, Nassima, Komen, Mathew Kipkemboi, Wlaschin, Katie F., Parthasarathy, Ranjani V., Landgrebe, Kevin D., Bouvier, Nicole M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835424/
https://www.ncbi.nlm.nih.gov/pubmed/36225128
http://dx.doi.org/10.1111/irv.13035
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author Gaaloul ben Hnia, Nassima
Komen, Mathew Kipkemboi
Wlaschin, Katie F.
Parthasarathy, Ranjani V.
Landgrebe, Kevin D.
Bouvier, Nicole M.
author_facet Gaaloul ben Hnia, Nassima
Komen, Mathew Kipkemboi
Wlaschin, Katie F.
Parthasarathy, Ranjani V.
Landgrebe, Kevin D.
Bouvier, Nicole M.
author_sort Gaaloul ben Hnia, Nassima
collection PubMed
description BACKGROUND: Seasonal influenza annually causes significant morbidity and mortality, and unpredictable respiratory virus zoonoses, such as the current COVID‐19 pandemic, can threaten the health and lives of millions more. Molecular iodine (I(2)) is a broad‐spectrum, pathogen‐nonspecific antiseptic agent that has demonstrated antimicrobial activity against a wide range of bacteria, virus, and fungi. METHODS: We investigated a commercially available antiseptic, a non‐irritating formulation of iodine (5% povidone‐iodine) with a film‐forming agent that extends the duration of the iodine's antimicrobial activity, for its ability to prevent influenza virus transmission between infected and susceptible animals in the guinea pig model of influenza virus transmission. RESULTS: We observed that a once‐daily topical application of this long‐lasting antiseptic to the nares of either the infected virus‐donor guinea pig or the susceptible virus‐recipient guinea pig, or to the nares of both animals, prior to virus inoculation effectively reduced transmission of a highly transmissible influenza A virus, even when the donor and recipient guinea pigs shared the same cage. Daily treatment of the recipient guinea pig starting 1 day after initial exposure to an infected donor guinea pig in the same cage was similarly effective in preventing detectable influenza virus infection in the recipient animal. CONCLUSIONS: We conclude that a daily application of this antiseptic formulation is efficacious in reducing the transmission of influenza A virus in the guinea pig model, and further study in this and other preclinical models is warranted.
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spelling pubmed-98354242023-01-17 Intranasal antisepsis to reduce influenza virus transmission in an animal model Gaaloul ben Hnia, Nassima Komen, Mathew Kipkemboi Wlaschin, Katie F. Parthasarathy, Ranjani V. Landgrebe, Kevin D. Bouvier, Nicole M. Influenza Other Respir Viruses Original Articles BACKGROUND: Seasonal influenza annually causes significant morbidity and mortality, and unpredictable respiratory virus zoonoses, such as the current COVID‐19 pandemic, can threaten the health and lives of millions more. Molecular iodine (I(2)) is a broad‐spectrum, pathogen‐nonspecific antiseptic agent that has demonstrated antimicrobial activity against a wide range of bacteria, virus, and fungi. METHODS: We investigated a commercially available antiseptic, a non‐irritating formulation of iodine (5% povidone‐iodine) with a film‐forming agent that extends the duration of the iodine's antimicrobial activity, for its ability to prevent influenza virus transmission between infected and susceptible animals in the guinea pig model of influenza virus transmission. RESULTS: We observed that a once‐daily topical application of this long‐lasting antiseptic to the nares of either the infected virus‐donor guinea pig or the susceptible virus‐recipient guinea pig, or to the nares of both animals, prior to virus inoculation effectively reduced transmission of a highly transmissible influenza A virus, even when the donor and recipient guinea pigs shared the same cage. Daily treatment of the recipient guinea pig starting 1 day after initial exposure to an infected donor guinea pig in the same cage was similarly effective in preventing detectable influenza virus infection in the recipient animal. CONCLUSIONS: We conclude that a daily application of this antiseptic formulation is efficacious in reducing the transmission of influenza A virus in the guinea pig model, and further study in this and other preclinical models is warranted. John Wiley and Sons Inc. 2022-10-12 /pmc/articles/PMC9835424/ /pubmed/36225128 http://dx.doi.org/10.1111/irv.13035 Text en © 2022 The Authors. Influenza and Other Respiratory Viruses published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Gaaloul ben Hnia, Nassima
Komen, Mathew Kipkemboi
Wlaschin, Katie F.
Parthasarathy, Ranjani V.
Landgrebe, Kevin D.
Bouvier, Nicole M.
Intranasal antisepsis to reduce influenza virus transmission in an animal model
title Intranasal antisepsis to reduce influenza virus transmission in an animal model
title_full Intranasal antisepsis to reduce influenza virus transmission in an animal model
title_fullStr Intranasal antisepsis to reduce influenza virus transmission in an animal model
title_full_unstemmed Intranasal antisepsis to reduce influenza virus transmission in an animal model
title_short Intranasal antisepsis to reduce influenza virus transmission in an animal model
title_sort intranasal antisepsis to reduce influenza virus transmission in an animal model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835424/
https://www.ncbi.nlm.nih.gov/pubmed/36225128
http://dx.doi.org/10.1111/irv.13035
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