<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(3)</volume><submitter>Gubareva LV</submitter><pubmed_abstract>The anti-influenza therapeutic baloxavir targets cap-dependent endonuclease activity of polymerase acidic (PA) protein. We monitored baloxavir susceptibility in the United States with next generation sequencing analysis supplemented by phenotypic one-cycle infection assay. Analysis of PA sequences of 6,891 influenza A and B viruses collected during 2016/17 and 2017/18 seasons showed amino acid substitutions: I38L (two A(H1N1)pdm09 viruses), E23G (two A(H1N1)pdm09 viruses) and I38M (one A(H3N2) virus); conferring 4-10-fold reduced susceptibility to baloxavir.</pubmed_abstract><journal>Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6344838</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Assessing baloxavir susceptibility of influenza viruses circulating in the United States during the 2016/17 and 2017/18 seasons.</pubmed_title><pmcid>PMC6344838</pmcid><pubmed_authors>Patel MC</pubmed_authors><pubmed_authors>Wentworth DE</pubmed_authors><pubmed_authors>Barnes J</pubmed_authors><pubmed_authors>Mishin VP</pubmed_authors><pubmed_authors>Nguyen HT</pubmed_authors><pubmed_authors>Fry AM</pubmed_authors><pubmed_authors>Gubareva LV</pubmed_authors><pubmed_authors>Sinner M</pubmed_authors><pubmed_authors>Katz JM</pubmed_authors><pubmed_authors>Chesnokov A</pubmed_authors><pubmed_authors>Reid H</pubmed_authors><pubmed_authors>Spencer S</pubmed_authors><pubmed_authors>Garten R</pubmed_authors><pubmed_authors>Campbell AP</pubmed_authors><pubmed_authors>De La Cruz J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Assessing baloxavir susceptibility of influenza viruses circulating in the United States during the 2016/17 and 2017/18 seasons.</name><description>The anti-influenza therapeutic baloxavir targets cap-dependent endonuclease activity of polymerase acidic (PA) protein. We monitored baloxavir susceptibility in the United States with next generation sequencing analysis supplemented by phenotypic one-cycle infection assay. Analysis of PA sequences of 6,891 influenza A and B viruses collected during 2016/17 and 2017/18 seasons showed amino acid substitutions: I38L (two A(H1N1)pdm09 viruses), E23G (two A(H1N1)pdm09 viruses) and I38M (one A(H3N2) virus); conferring 4-10-fold reduced susceptibility to baloxavir.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-25T23:29:02.113Z</modification><creation>2019-03-26T22:53:12Z</creation></dates><accession>S-EPMC6344838</accession><cross_references><pubmed>30670144</pubmed><doi>10.2807/1560-7917.ES.2019.24.3.1800666</doi></cross_references></HashMap>