tetano
Editor, Senior Moderator
Virus Evol
. 2023 Apr 25;9(1):vead027.
doi: 10.1093/ve/vead027. eCollection 2023. Tracking the emergence of antigenic variants in influenza A virus epidemics in Brazil
Tara K Pillai[SUP] 1 [/SUP], Katherine E Johnson[SUP] 1 2 [/SUP], Timothy Song[SUP] 2 [/SUP], Tatiana S Gregianini[SUP] 3 [/SUP], Baccin Tatiana G[SUP] 4 5 [/SUP], Guojun Wang[SUP] 6 7 [/SUP], Rafael A Medina[SUP] 5 6 8 [/SUP], Harm Van Bakel[SUP] 9 [/SUP], Adolfo García-Sastre[SUP] 6 7 10 11 12 [/SUP], Martha I Nelson[SUP] 1 13 [/SUP], Elodie Ghedin[SUP] 1 2 [/SUP], Ana B G Veiga[SUP] 4 6 7 [/SUP]
Affiliations
Influenza A virus (IAV) circulation patterns differ in North America and South America, with influenza seasons often characterized by different subtypes and strains. However, South America is relatively undersampled considering the size of its population. To address this gap, we sequenced the complete genomes of 220 IAVs collected between 2009 and 2016 from hospitalized patients in southern Brazil. New genetic drift variants were introduced into southern Brazil each season from a global gene pool, including four H3N2 clades (3c, 3c2, 3c3, and 3c2a) and five H1N1pdm clades (clades 6, 7, 6b, 6c, and 6b1). In 2016, H1N1pdm viruses belonging to a new 6b1 clade caused a severe influenza epidemic in southern Brazil that arrived early and spread rapidly, peaking mid-autumn. Inhibition assays showed that the A/California/07/2009(H1N1) vaccine strain did not protect well against 6b1 viruses. Phylogenetically, most 6b1 sequences that circulated in southern Brazil belong to a single transmission cluster that rapidly diffused across susceptible populations, leading to the highest levels of influenza hospitalization and mortality seen since the 2009 pandemic. Continuous genomic surveillance is needed to monitor rapidly evolving IAVs for vaccine strain selection and understand their epidemiological impact in understudied regions.
Keywords: genomic surveillance; influenza A virus; phylodynamics; severe acute respiratory infection; virus evolution.
. 2023 Apr 25;9(1):vead027.
doi: 10.1093/ve/vead027. eCollection 2023. Tracking the emergence of antigenic variants in influenza A virus epidemics in Brazil
Tara K Pillai[SUP] 1 [/SUP], Katherine E Johnson[SUP] 1 2 [/SUP], Timothy Song[SUP] 2 [/SUP], Tatiana S Gregianini[SUP] 3 [/SUP], Baccin Tatiana G[SUP] 4 5 [/SUP], Guojun Wang[SUP] 6 7 [/SUP], Rafael A Medina[SUP] 5 6 8 [/SUP], Harm Van Bakel[SUP] 9 [/SUP], Adolfo García-Sastre[SUP] 6 7 10 11 12 [/SUP], Martha I Nelson[SUP] 1 13 [/SUP], Elodie Ghedin[SUP] 1 2 [/SUP], Ana B G Veiga[SUP] 4 6 7 [/SUP]
Affiliations
- PMID: 37207002
- PMCID: PMC10191192
- DOI: 10.1093/ve/vead027
Influenza A virus (IAV) circulation patterns differ in North America and South America, with influenza seasons often characterized by different subtypes and strains. However, South America is relatively undersampled considering the size of its population. To address this gap, we sequenced the complete genomes of 220 IAVs collected between 2009 and 2016 from hospitalized patients in southern Brazil. New genetic drift variants were introduced into southern Brazil each season from a global gene pool, including four H3N2 clades (3c, 3c2, 3c3, and 3c2a) and five H1N1pdm clades (clades 6, 7, 6b, 6c, and 6b1). In 2016, H1N1pdm viruses belonging to a new 6b1 clade caused a severe influenza epidemic in southern Brazil that arrived early and spread rapidly, peaking mid-autumn. Inhibition assays showed that the A/California/07/2009(H1N1) vaccine strain did not protect well against 6b1 viruses. Phylogenetically, most 6b1 sequences that circulated in southern Brazil belong to a single transmission cluster that rapidly diffused across susceptible populations, leading to the highest levels of influenza hospitalization and mortality seen since the 2009 pandemic. Continuous genomic surveillance is needed to monitor rapidly evolving IAVs for vaccine strain selection and understand their epidemiological impact in understudied regions.
Keywords: genomic surveillance; influenza A virus; phylodynamics; severe acute respiratory infection; virus evolution.