Preparation method for avian reovirus virus water-in-oil-in-water type inactivated vaccines
A technology of avian reovirus and water-in-oil-in-water, which is applied in the fields of biochemical equipment and methods, antiviral agents, viruses/phages, etc., can solve the problems of low feed conversion rate, high chicken waste rate, economic loss, etc. To achieve the effect of good immunogenicity, easy absorption, and avoiding side effects
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Embodiment 1
[0015] 1.1 Virus cultivation and harvest
[0016] Take 10-day-old SPF chicken embryos to prepare primary chicken embryo fibroblasts, and use 3×10 6 Inoculation amount of cells / mL The prepared cells were inoculated in M199 medium containing 8% (v / v) fetal bovine serum, and cultured overnight in shake flasks at 37°C; when the cells covered the monolayer of the medium, According to the inoculum amount of 0.2% (v / v) of the cell suspension, inoculate the cell suspension with a toxicity value ≥ 10 6.5 TCID 50 / 0.1mL of avian reovirus, control the temperature at 37°C and continue to shake the flask for 72 hours, harvest the cell culture, freeze and thaw repeatedly 3 times, and obtain the cell venom containing the supernatant;
[0017] 1.2 Inactivation of virus
[0018] Put the cell venom containing the supernatant obtained above in a sterilized container, add formaldehyde solution according to the volume of the virus liquid and adjust the final concentration of formaldehyde to 1‰ ...
Embodiment 2
[0051] 1.1 Virus cultivation and harvest
[0052] Take 11-day-old SPF chicken embryos, prepare primary chicken embryo fibroblasts, and use 3.3×10 6 Inoculation amount of cells / mL The prepared cells were inoculated in M199 medium containing 8% (v / v) fetal bovine serum, and cultured overnight in shake flasks at 37°C; when the cells covered the monolayer of the medium, According to the inoculum amount of 0.3% (v / v) of the cell suspension, inoculate the cell suspension with a toxicity value ≥ 10 6.5 TCID 50 / 0.1mL of avian reovirus, control the temperature at 37°C and continue to shake the flask for 66 hours, harvest the cell culture, freeze and thaw repeatedly 3 times, and obtain the cell venom containing the supernatant;
[0053] 1.2 Inactivation of virus
[0054] Put the cell venom containing the supernatant obtained above in a sterilized container, add formaldehyde solution according to the volume of the virus liquid and adjust the final concentration of formaldehyde to 0.8...
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