tetano
Editor, Senior Moderator
- Erik de Vries[SUP]1[/SUP] , Cornelis AM de Haan[SUP]1[/SUP]
The authors focused on the amino acid substitution T271A in polymerase subunit PB2, which is known to enhance polymerase activity of influenza A virus (IAV) in mammalian host cells similar to the seminal PB2 E627K mutation. They also show that the only substitution in haemagglutinin (HA) in comparison with closely related avian strains is I390M. This mutation is in the stem region of HA and might be associated with altered HA stability and transmissibility but as of yet has no known biological relevance. Mutations previously associated with increased human-type alpha 2,6-linked sialic acid receptor binding and/or airborne transmission in ferrets [2] were still limited to the lack of a glycosylation site at position 158. Substitutions F74S and V163L in neuraminidase (NA), which are located at sites of unknown functional importance, also distinguished the viruses in minks from closely related avian viruses. Remarkably, all four viruses from minks contained a methionine at position 396 located in the second sialic acid binding site (2SBS) in NA (for a review on the 2SBS, see [3]). Influenza A(H5N1) viruses predominantly carry an isoleucine at this position, which is critical for efficient binding of sialic acid to the 2SBS [3,4].
Phylogenetic analysis using Nextstrain (https://nextstrain.org, accessed: 1 Feb 2023 [5]) indicated that the I396M substitution, seldom observed in other H5N1 viruses, was acquired in an avian host immediately before emergence of the H5N1 virus in mink. The analysis moreover showed that substitution S369I, which is at the position of a sialic acid contact residue in the 2SBS, was obtained immediately before the acquisition of I396M. Substitution of residues at positions 369 and 396 has been shown to negatively affect N1 activity [3,4], herein referred to as residues 372 and 400. A functional 2SBS promotes NA activity, presumably by bringing multivalent sialic acid substrates in closer proximity of the catalytic site. A functional 2SBS, which specifically binds to alpha 2,3-linked sialic acid receptors, has been lost in all human (pandemic) viruses and in several other viruses adapted to mammalian host species. Notably, whereas a 2SBS is conserved in nearly all avian IAVs [3], it is disrupted in some avian influenza A(H7N9) and A(H9N2) isolates. This preceded the acquisition of mutations in HA that decreased binding to avian-type alpha 2,3-linked sialic acid receptors. It is possible that this concerted evolution of NA and HA is driven by the need to preserve an optimal HA-NA balance. At the same time, such compensatory mutations may also increase binding to human-type receptors [3], as was recently demonstrated for H5N1 viruses [6].
Disruption of the 2SBS in H5N1 viruses in minks is thus far an unreported feature that they have in common with human-adapted influenza A viruses. Loss of the 2SBS may drive selection for changes in the receptor binding properties of HA, possibly resulting in increased binding to human-type receptors. Such changes in HA are expected to promote replication and transmission in mammalian hosts, including humans. Preservation or loss of the 2SBS is likely a viral host range determinant and could be an early adaptation signal that should be included in analysis of the pandemic potential of emerging IAVs.
https://www.eurosurveillance.org/con...#html_fulltext