PRRSV and PCV2 co-infection mouse disease model
A disease model, mouse technology, applied in antiviral agents, biochemical equipment and methods, medical raw materials derived from viruses/phages, etc., can solve the problems of time-consuming, labor-intensive and inapplicable
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[0064] 1PCV2, PRRSV reproduction
[0065] (1) Reproduction of PCV2
[0066] When the PK15 cells in the culture flask are 40%-50% confluent, add 1 mL / bottle of virus solution, absorb for 1 hour, discard the virus solution, wash twice with PBS, add new 10% MEM medium, and incubate at 37°C. Cultivate in a 5% CO2 incubator, subculture when the cells cover the bottom of the bottle, and collect one bottle for each generation of cells for detection of cell proliferation, and use D-glucosamine treatment group as a control.
[0067] (2) Propagation of PRRSV
[0068] When the Marc-145 cells in the culture flask are 50%-60% confluent, add 1 mL / bottle of virus solution, absorb for 1 hour, discard the virus solution, wash twice with PBS, add new 10% MEM medium, and Cultivate in an incubator with 5% CO2 at 37°C, collect the cells when the bottom of the flask is covered, and freeze at -80°C for later use.
[0069]2 Preparation of pathological slides
[0070] (1) Production of slices
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