Influenza virus characterisation, Summary Europe, September 2014

Surveillance report
During the 2013–14 season, A(H1N1)pdm09, A(H3N2), B/Victoria- and B/Yamagata-lineage influenza viruses co-circulated in EU/EEA Member States. The relative prevalence has varied between countries. The WHO Collaborating Centre in London received viruses with collection dates after 31 January 2014 from 21 EU/EEA countries.

Executive Summary

Type A and type B viruses have been received at a ratio of approximately 10:1. A(H3N2) outnumbered A(H1N1)pdm09 viruses at a ratio of 1.4:1.

 

Recently circulating A(H1N1)pdm09 viruses, in Europe and worldwide, belonged to genetic subgroup 6B. Viruses in this subgroup are antigenically similar to the vaccine virus, A/California/07/2009.

 

Recently circulating A(H3N2) viruses have fallen within genetic group 3C represented by the recommended vaccine virus for the 2013–14 and 2014–15 seasons, A/Texas/50/2012. Antigenic analysis using antisera raised against cell-propagated H3N2 viruses indicates that the majority of circulating viruses are antigenically similar to those in circulation in the 2012–13 and 2013–14 influenza seasons, but those in a newly emerging genetic cluster, 3C.3a, are poorly recognised by some antisera.

 

Two genetic clades of B/Yamagata-lineage viruses continue to circulate: clade 3 represented by B/Phuket/3073/2013 and clade 2 represented by B/Massachusetts/02/2012 (the recommended vaccine component for the 2013–14 and 2014–15 influenza seasons). Viruses in clade 3 predominate in those samples collected since 31 January 2014.

 

Only two viruses of the B/Victoria-lineage were antigenically characterised since the July 2014 report. Neither was recognised well by the antiserum raised against the egg-propagated reference virus, A/Brisbane/60/2008, recommended as a component of quadrivalent influenza vaccines for 2013–14 and 2014–15 influenza seasons. Phylogenetic analysis revealed that all B/Victoria-lineage viruses received in 2014 were in genetic clade 1A, the B/Brisbane/60/2008 genetic clade.

 

In light of the emergence of antigenically distinct groups of influenza A(H3N2) and the altered prevalence of influenza B viruses, the WHO recommended composition of influenza vaccines for use in the 2015 southern hemisphere influenza season differed from that recommended for use in the 2014–15 northern hemisphere influenza season.

Publication file

Influenza virus characterisation, Summary Europe, September 2014

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