V292I mutation in PB2 polymerase induces increased effects of E627K on influenza H7N9 virus replication in cells

Characterization of host adaptation markers among human isolates is important for recognizing the potential for cross-species transmission in avian influenza A viruses. Here, we studied two new potential adaptive mutations, V292I and D740A, in the PB2 protein that were identified by a multi-factor regression model. The study shows that the prevalence of the PB2-V292I mutation is increased in H7N9 influenza viruses isolated from both humans and birds over the past 6 years. The phylogenetic tree showed that influenza A/H7N9 has a lineage based on the strains containing PB2-292I. Polymerase complexes containing PB2-292I/627K derived from H7N9 exhibit increased polymerase activity. PB2-292I coupled with 627K also enhances viral transcription and replication in cells, whereas PB2-292I alone did not show the same effect in the H7N9 virus. However, PB2-740A only had a limited prevalence in 2013, and the change from D to A in PB2-740A may have a negative effect on the replication of the H7N9 virus in cells.

Automated summary

The study identified an increased prevalence of the PB2-V292I mutation in H7N9 influenza viruses from both human and bird isolates over the past 6 years, with polymerase complexes containing PB2-292I showing increased activity. The PB2-740A mutation had a limited prevalence in 2013, and may have a negative effect on H7N9 virus replication in cells.