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How does 'flu actually infect our cells?
(2 posts)-
Posted 2 years ago # -
Each virus particle is tiny, about 1/10,000th for the millimetre across. If you could zoom in on the surface, you’d see that it had these spikes on the surface. These spikes are a structure called haemagglutinin, which is a tiny protein resembling a molecular grappling hook. It’s viral Velcro. It gets hold of something called sialic acid, which is a chemical on the surface of the cells that line our nose and throat, and this enables the virus to grab hold of those cells and pull itself in very close.
Through this interaction the cell thinks the virus is something that it has to take inside the cell. So the cell then does something called receptor-mediated endocytosis, which basically means it pulls the virus inside the cell. Once inside the virus releases it’s genetic material and productively infects the cell.
It’s a bit like a Trojan horse actually because the Trojan horse was this juicy tidbit sitting outside the gate of Troy. The guys inside the city thought, “Wow! That looks fantastic. We’ll pull that inside because it looks good.” And it goes inside the city. And then of course, lurking inside are all these people who are then wreak havoc inside the city. And that’s basically what a flu virus does. It hijacks the cell, turns it into a virus factory and then it infects all of the cells around it and all the people around you!
Posted 2 years ago # -
Infection and replication
Influenza viruses bind through hemagglutinin onto sialic acid sugars on the surfaces of epithelial cells; typically in the nose, throat and lungs of mammals and intestines of birds (Stage 1 in infection figure).The cell imports the virus by endocytosis. In the acidic endosome, part of the hemagglutinin protein fuses the viral envelope with the vacuole's membrane, releasing the viral RNA (vRNA) molecules, accessory proteins and RNA-dependent RNA polymerase into the cytoplasm (Stage 2).[ These proteins and vRNA form a complex that is transported into the cell nucleus, where the RNA-dependent RNA polymerase begins transcribing complementary positive-sense vRNA (Steps 3a and b). The vRNA is either exported into the cytoplasm and translated (step 4), or remains in the nucleus. Newly-synthesised viral proteins are either secreted through the Golgi apparatus onto the cell surface (in the case of neuraminidase and hemagglutinin, step 5b) or transported back into the nucleus to bind vRNA and form new viral genome particles (step 5a). Other viral proteins have multiple actions in the host cell, including degrading cellular mRNA and using the released nucleotides for vRNA synthesis and also inhibiting translation of host-cell mRNAs.
Negative-sense vRNAs that form the genomes of future viruses, RNA-dependent RNA polymerase, and other viral proteins are assembled into a virion. Hemagglutinin and neuraminidase molecules cluster into a bulge in the cell membrane. The vRNA and viral core proteins leave the nucleus and enter this membrane protrusion (step 6). The mature virus buds off from the cell in a sphere of host phospholipid membrane, acquiring hemagglutinin and neuraminidase with this membrane coat (step 7).As before, the viruses adhere to the cell through hemagglutinin; the mature viruses detach once their neuraminidase has cleaved sialic acid residues from the host cell. After the release of new influenza viruses, the host cell dies.
Because of the absence of RNA proofreading enzymes, the RNA-dependent RNA polymerase makes a single nucleotide insertion error roughly every 10 thousand nucleotides, which is the approximate length of the influenza vRNA. Hence, nearly every newly-manufactured influenza virus is a mutant[49]—antigenic drift. The separation of the genome into eight separate segments of vRNA allows mixing or reassortment of vRNAs if more than one viral line has infected a single cell. The resulting rapid change in viral genetics produces antigenic shifts and allows the virus to infect new host species and quickly overcome protective immunity. This is important in the emergence of pandemics, as discussed below in the section on Epidemiology.sorry I don't know how to send you the picture.
Posted 2 years ago #
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