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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 ...
Examples of class II viral fusion proteins include the dengue virus E protein, and the west nile virus E protein. [5] [6] Class III: Structural conformation is a combination of features from Class I and Class II viral membrane fusion proteins. An example of a Class III viral fusion protein is the rabies virus glycoprotein, G. [6]
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 ...
Influenza viruses A and B are estimated to have diverged from a single ancestor around 4,000 years ago, while the ancestor of influenza viruses A and B and the ancestor of influenza virus C are estimated to have diverged from a common ancestor around 8,000 years ago. [40] Outbreaks of influenza-like disease can be found throughout recorded history.
Influenza A viruses are further classified, based on the viral surface proteins hemagglutinin (HA or H) and neuraminidase (NA or N). 18 HA subtypes (or serotypes) and 11 NA subtypes of influenza A virus have been isolated in nature. Among these, the HA subtype 1-16 and NA subtype 1-9 are found in wild waterfowl and shorebirds and the HA ...
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.
The capsid is made from proteins encoded by the viral genome and its shape serves as the basis for morphological distinction. [41] [42] Virally-coded protein subunits will self-assemble to form a capsid, in general requiring the presence of the virus genome. Complex viruses code for proteins that assist in the construction of their capsid.
It does this by making the cell copy the virus's DNA or RNA, making viral proteins, which all assemble to form new virus particles. [37] There are six basic, overlapping stages in the life cycle of viruses in living cells: [38] Attachment is the binding of the virus to specific molecules on the surface of the cell. This specificity restricts ...