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Article: Baloxavir marboxil susceptibility of influenza viruses from the Asia-Pacific, 2012–2018

TitleBaloxavir marboxil susceptibility of influenza viruses from the Asia-Pacific, 2012–2018
Authors
KeywordsInfluenza
Susceptibility
Baloxavir marboxil
Resistance
Antiviral activity
Issue Date2019
Citation
Antiviral Research, 2019, v. 164, p. 91-96 How to Cite?
Abstract© 2019 The Authors Baloxavir Marboxil (BXM) is an influenza polymerase inhibitor antiviral that binds to the endonuclease region in the PA subunit of influenza A and B viruses. To establish the baseline susceptibility of viruses circulating prior to licensure of BXM and to monitor for susceptibility post-BXM use, a cell culture-based focus reduction assay was developed to determine the susceptibility of 286 circulating seasonal influenza viruses, A(H1N1)pdm09, A(H3N2), B (Yamagata/Victoria) lineage viruses, including neuraminidase inhibitor (NAI) resistant viruses, to Baloxavir Acid (BXA), the active metabolic form of BXM. BXA was effective against all influenza subtypes tested with mean EC 50 values (minimum-maximum) of 0.7 ± 0.5 nM (0.1–2.1 nM), 1.2 ± 0.6 nM (0.1–2.4), 7.2 ± 3.5 nM (0.7–14.8), and 5.8 ± 4.5 nM (1.8–15.5) obtained for A(H1N1)pdm09, A(H3N2), B(Victoria lineage), and B(Yamagata lineage) influenza viruses, respectively. Using reverse genetics, amino acid substitutions known to alter BXA susceptibility were introduced into the PA protein resulting in EC 50 fold change increases that ranged from 2 to 65. Our study demonstrates that currently circulating viruses are susceptible to BXA and that the newly developed focus reduction assay is well suited to susceptibility monitoring in reference laboratories.
Persistent Identifierhttp://hdl.handle.net/10722/288590
ISSN
2021 Impact Factor: 10.103
2020 SCImago Journal Rankings: 2.052
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKoszalka, Paulina-
dc.contributor.authorTilmanis, Danielle-
dc.contributor.authorRoe, Merryn-
dc.contributor.authorVijaykrishna, Dhanasekaran-
dc.contributor.authorHurt, Aeron C.-
dc.date.accessioned2020-10-12T08:05:21Z-
dc.date.available2020-10-12T08:05:21Z-
dc.date.issued2019-
dc.identifier.citationAntiviral Research, 2019, v. 164, p. 91-96-
dc.identifier.issn0166-3542-
dc.identifier.urihttp://hdl.handle.net/10722/288590-
dc.description.abstract© 2019 The Authors Baloxavir Marboxil (BXM) is an influenza polymerase inhibitor antiviral that binds to the endonuclease region in the PA subunit of influenza A and B viruses. To establish the baseline susceptibility of viruses circulating prior to licensure of BXM and to monitor for susceptibility post-BXM use, a cell culture-based focus reduction assay was developed to determine the susceptibility of 286 circulating seasonal influenza viruses, A(H1N1)pdm09, A(H3N2), B (Yamagata/Victoria) lineage viruses, including neuraminidase inhibitor (NAI) resistant viruses, to Baloxavir Acid (BXA), the active metabolic form of BXM. BXA was effective against all influenza subtypes tested with mean EC 50 values (minimum-maximum) of 0.7 ± 0.5 nM (0.1–2.1 nM), 1.2 ± 0.6 nM (0.1–2.4), 7.2 ± 3.5 nM (0.7–14.8), and 5.8 ± 4.5 nM (1.8–15.5) obtained for A(H1N1)pdm09, A(H3N2), B(Victoria lineage), and B(Yamagata lineage) influenza viruses, respectively. Using reverse genetics, amino acid substitutions known to alter BXA susceptibility were introduced into the PA protein resulting in EC 50 fold change increases that ranged from 2 to 65. Our study demonstrates that currently circulating viruses are susceptible to BXA and that the newly developed focus reduction assay is well suited to susceptibility monitoring in reference laboratories.-
dc.languageeng-
dc.relation.ispartofAntiviral Research-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectInfluenza-
dc.subjectSusceptibility-
dc.subjectBaloxavir marboxil-
dc.subjectResistance-
dc.subjectAntiviral activity-
dc.titleBaloxavir marboxil susceptibility of influenza viruses from the Asia-Pacific, 2012–2018-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1016/j.antiviral.2019.02.007-
dc.identifier.pmid30771405-
dc.identifier.scopuseid_2-s2.0-85061619800-
dc.identifier.volume164-
dc.identifier.spage91-
dc.identifier.epage96-
dc.identifier.eissn1872-9096-
dc.identifier.isiWOS:000463303700008-
dc.identifier.issnl0166-3542-

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