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A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid

Baloxavir acid (BXA), the active compound in baloxavir marboxil (BXM), reduces the propagation of influenza A and B viruses by inhibiting the cap-dependent endonuclease activity of the polymerase acidic (PA) subunit. Although BXM has been used to treat influenza virus infections, recently, there has...

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Autores principales: Takizawa, Naoki, Momose, Fumitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069958/
https://www.ncbi.nlm.nih.gov/pubmed/35511288
http://dx.doi.org/10.1007/s00705-022-05456-0
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author Takizawa, Naoki
Momose, Fumitaka
author_facet Takizawa, Naoki
Momose, Fumitaka
author_sort Takizawa, Naoki
collection PubMed
description Baloxavir acid (BXA), the active compound in baloxavir marboxil (BXM), reduces the propagation of influenza A and B viruses by inhibiting the cap-dependent endonuclease activity of the polymerase acidic (PA) subunit. Although BXM has been used to treat influenza virus infections, recently, there has been general concern about the emergence of viruses with low susceptibility to BXA. Here, we identified a novel PA subunit substitution, PA E198K, that reduced susceptibility to BXA. The IC(50) of BXA toward influenza A viruses containing PA E198K increased approximately 2- to 6-fold. These findings help to understand the mechanism by which PA substitutions reduce susceptibility to BXA.
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spelling pubmed-90699582022-05-04 A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid Takizawa, Naoki Momose, Fumitaka Arch Virol Brief Report Baloxavir acid (BXA), the active compound in baloxavir marboxil (BXM), reduces the propagation of influenza A and B viruses by inhibiting the cap-dependent endonuclease activity of the polymerase acidic (PA) subunit. Although BXM has been used to treat influenza virus infections, recently, there has been general concern about the emergence of viruses with low susceptibility to BXA. Here, we identified a novel PA subunit substitution, PA E198K, that reduced susceptibility to BXA. The IC(50) of BXA toward influenza A viruses containing PA E198K increased approximately 2- to 6-fold. These findings help to understand the mechanism by which PA substitutions reduce susceptibility to BXA. Springer Vienna 2022-05-05 2022 /pmc/articles/PMC9069958/ /pubmed/35511288 http://dx.doi.org/10.1007/s00705-022-05456-0 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Brief Report
Takizawa, Naoki
Momose, Fumitaka
A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid
title A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid
title_full A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid
title_fullStr A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid
title_full_unstemmed A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid
title_short A novel E198K substitution in the PA gene of influenza A virus with reduced susceptibility to baloxavir acid
title_sort novel e198k substitution in the pa gene of influenza a virus with reduced susceptibility to baloxavir acid
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069958/
https://www.ncbi.nlm.nih.gov/pubmed/35511288
http://dx.doi.org/10.1007/s00705-022-05456-0
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