PT  - JOURNAL ARTICLE
AU  - Goldstein, Emily J.
AU  - Harvey, William T.
AU  - Wilkie, Gavin S.
AU  - Shepherd, Samantha J.
AU  - MacLean, Alasdair R.
AU  - Murcia, Pablo R.
AU  - Gunson, Rory N.
TI  - Integrating patient and whole genome sequencing data to provide insights into the epidemiology of seasonal influenza A(H3N2) viruses
AID  - 10.1101/121434
DP  - 2017 Jan 01
TA  - bioRxiv
PG  - 121434
4099  - http://biorxiv.org/content/early/2017/03/28/121434.short
4100  - http://biorxiv.org/content/early/2017/03/28/121434.full
AB  - Genetic surveillance of seasonal influenza is largely focused upon sequencing of the haemagglutinin gene. Consequently, our understanding of the contribution of the remaining seven gene segments to the evolution and epidemiological dynamics of seasonal influenza is relatively limited. The increased availability of next generation sequencing technologies allows rapid and economic whole genome sequencing (WGS). Here, 150 influenza A(H3N2) positive clinical specimens with linked epidemiological data, from the 2014/15 season in Scotland, were sequenced directly using both Sanger sequencing of the HA1 region and WGS using the Illumina MiSeq platform. Sequences generated by both methods were highly consistent and WGS provided on average >90% whole genome coverage. As reported in other European countries during 2014/15, all strains belonged to genetic group 3C, with subgroup 3C.2a predominating. Inter-subgroup reassortants were identified (9%), including three 3C.3 viruses descended from a single reassortment event, which had persisted in the population. Significant phylogenetic associations with cases of severe acute respiratory illness observed herein warrant further investigation. Severe cases were also more likely to be associated with reassortant viruses (odds ratio: 4.4 (1.3-15.5)) and occur later in the season. These results suggest that increased levels of WGS, linked to clinical and epidemiological data, could improve influenza surveillance.