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Viruses enter host cells using a variety of mechanisms, including the endocytic and non-endocytic routes. [4] They can also fuse at the plasma membrane and can spread within the host via fusion or cell-cell fusion. [5] Viruses attach to proteins on the host cell surface known as cellular receptors or attachment factors to aid entry. [6]
Once inside the cell, the virus leaves the host vesicle by which it was taken up and thus gains access to the cytoplasm. Examples of viruses that enter this way include the poliovirus, hepatitis C virus, [14] and foot-and-mouth disease virus. [15] Many enveloped viruses, such as SARS-CoV-2, also enter the cell through endocytosis. Entry via the ...
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 ...
Hemagglutinins are small proteins that extend from the surface of the virus membrane as spikes that are 135 Angstroms (Å) in length and 30-50 Å in diameter. [19] Each spike is composed of three identical monomer subunits, making the protein a homotrimer.
To enter the cells, proteins on the surface of the virus interact with proteins of the cell. Attachment, or adsorption, occurs between the viral particle and the host cell membrane. A hole forms in the cell membrane, then the virus particle or its genetic contents are released into the host cell, where replication of the viral genome may commence.
Dr. Davis emphasizes that valve damage is not only caused by poor dietary habits, explaining, “Diet is often talked about in connection to heart disease, but valve damage has different causes.
Hemagglutinin, neuraminidase, and M2 protein in the influenza virus; gp160, composed of subunits gp120 and gp41, in the human immunodeficiency virus (HIV). [1] Viral glycoproteins play a critical role in virus-to-cell fusion. Virus-to-cell fusion is initiated when viral glycoproteins bind to cellular receptors. [5]
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