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The serotype of IAV is determined by the HA and neuraminidase (NA) proteins expressed on its surface. [12] Neuraminidase has 11 known subtypes; hence, influenza viruses are named according to the combinations of HA and NA proteins expressed (e.g., H1N1 and H5N2). [7] Structure of influenza, showing neuraminidase marked as NA and hemagglutinin ...
These refer to hemagglutinin (H) and neuraminidase ( N), which are proteins on the surface of the virus. There are 18 different HA subtypes and 11 different NA subtypes. This makes for 198 ...
This attachment is required for efficient transfer of flu virus genes into cells, a process that can be blocked by antibodies that bind to the hemagglutinin proteins. One genetic factor in distinguishing between human flu viruses and avian flu viruses is that avian influenza HA bind to alpha 2-3 sialic acid receptors while human influenza HA ...
Two viral proteins; hemagglutinin (HA) and neuraminidase (NA), are inserted into the envelope and are exposed as spikes on the surface of the virion. Both proteins are antigenic; a host's immune system can react to them and produce antibodies in response. The M2 protein forms an ion channel in the envelope and is responsible for uncoating the ...
Viral neuraminidase cleaves terminal sialic acid residues from glycan structures on the surface of the infected cell. This promotes the release of progeny viruses and the spread of the virus from the host cell to uninfected surrounding cells. Neuraminidase also cleaves sialic acid residues from viral proteins, preventing aggregation of viruses.
Viral nonstructural proteins are proteins coded for by the genome of the virus and are expressed in infected cells. [1] However, these proteins are not assembled in the virion. [1] During the replication of viruses, some viral nonstructural proteins carry out important functions that affect the replication process itself. [1]
3D model of the flu virion. (M2 labeled in white.) The Matrix-2 (M2) protein is a proton-selective viroporin, integral in the viral envelope of the influenza A virus. The channel itself is a homotetramer (consists of four identical M2 units), where the units are helices stabilized by two disulfide bonds, and is activated by low pH.
The fact that NS1 is involved in the pathogenicity of influenza A viruses makes it a good target to attenuate these viruses. Several studies demonstrated that influenza viruses with partial deletions in NS1 proteins are attenuated and do not cause disease, but induce a protective immune response in different species including mice, [ 10 ] [ 11 ...