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Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model
Influenza antivirals are important tools in our fight against annual influenza epidemics and future influenza pandemics. Combinations of antivirals may reduce the likelihood of drug resistance and improve clinical outcomes. Previously, two hospitalised immunocompromised influenza patients, who recei...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9517990/ https://www.ncbi.nlm.nih.gov/pubmed/36171475 http://dx.doi.org/10.1038/s42003-022-04005-4 |
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author | Stannard, Harry L. Mifsud, Edin J. Wildum, Steffen Brown, Sook Kwan Koszalka, Paulina Shishido, Takao Kojima, Satoshi Omoto, Shinya Baba, Keiko Kuhlbusch, Klaus Hurt, Aeron C. Barr, Ian G. |
author_facet | Stannard, Harry L. Mifsud, Edin J. Wildum, Steffen Brown, Sook Kwan Koszalka, Paulina Shishido, Takao Kojima, Satoshi Omoto, Shinya Baba, Keiko Kuhlbusch, Klaus Hurt, Aeron C. Barr, Ian G. |
author_sort | Stannard, Harry L. |
collection | PubMed |
description | Influenza antivirals are important tools in our fight against annual influenza epidemics and future influenza pandemics. Combinations of antivirals may reduce the likelihood of drug resistance and improve clinical outcomes. Previously, two hospitalised immunocompromised influenza patients, who received a combination of a neuraminidase inhibitor and baloxavir marboxil, shed influenza viruses resistant to both drugs. Here-in, the replicative fitness of one of these A(H1N1)pdm09 virus isolates with dual resistance mutations (NA-H275Y and PA-I38T) was similar to wild type virus (WT) in vitro, but reduced in the upper respiratory tracts of challenged ferrets. The dual-mutant virus transmitted well between ferrets in an airborne transmission model, but was outcompeted by the WT when the two viruses were co-administered. These results indicate the dual-mutant virus had a moderate loss of viral fitness compared to the WT virus, suggesting that while person-to-person transmission of the dual-resistant virus may be possible, widespread community transmission is unlikely. |
format | Online Article Text |
id | pubmed-9517990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95179902022-09-29 Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model Stannard, Harry L. Mifsud, Edin J. Wildum, Steffen Brown, Sook Kwan Koszalka, Paulina Shishido, Takao Kojima, Satoshi Omoto, Shinya Baba, Keiko Kuhlbusch, Klaus Hurt, Aeron C. Barr, Ian G. Commun Biol Article Influenza antivirals are important tools in our fight against annual influenza epidemics and future influenza pandemics. Combinations of antivirals may reduce the likelihood of drug resistance and improve clinical outcomes. Previously, two hospitalised immunocompromised influenza patients, who received a combination of a neuraminidase inhibitor and baloxavir marboxil, shed influenza viruses resistant to both drugs. Here-in, the replicative fitness of one of these A(H1N1)pdm09 virus isolates with dual resistance mutations (NA-H275Y and PA-I38T) was similar to wild type virus (WT) in vitro, but reduced in the upper respiratory tracts of challenged ferrets. The dual-mutant virus transmitted well between ferrets in an airborne transmission model, but was outcompeted by the WT when the two viruses were co-administered. These results indicate the dual-mutant virus had a moderate loss of viral fitness compared to the WT virus, suggesting that while person-to-person transmission of the dual-resistant virus may be possible, widespread community transmission is unlikely. Nature Publishing Group UK 2022-09-28 /pmc/articles/PMC9517990/ /pubmed/36171475 http://dx.doi.org/10.1038/s42003-022-04005-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Stannard, Harry L. Mifsud, Edin J. Wildum, Steffen Brown, Sook Kwan Koszalka, Paulina Shishido, Takao Kojima, Satoshi Omoto, Shinya Baba, Keiko Kuhlbusch, Klaus Hurt, Aeron C. Barr, Ian G. Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
title | Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
title_full | Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
title_fullStr | Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
title_full_unstemmed | Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
title_short | Assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
title_sort | assessing the fitness of a dual-antiviral drug resistant human influenza virus in the ferret model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9517990/ https://www.ncbi.nlm.nih.gov/pubmed/36171475 http://dx.doi.org/10.1038/s42003-022-04005-4 |
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