Muscovy duck parvovirus and application thereof
A technology of Muscovy duck parvovirus and microbial strains, applied in antiviral agents, virus/bacteriophage, antiviral immunoglobulin, etc., can solve the problems of reduced vaccine potency, achieve high immunogenicity, low toxicity, prevent Effects of parvovirus infection in ducklings
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[0014] 2. Preparation of antigens for seedling production
[0015] 1. Preparation of virus liquid for seedling production Inoculate 12-14-day-old susceptible muscovy duck embryos into the allantoic cavity of the virus species YBMDV strain for production, 0.2ml per embryo, incubate at 36-37°C, and inspect the embryos twice a day . Select embryos that died within 48 to 120 hours after inoculation, and embryo bodies with extensive hemorrhage, hair follicle hemorrhage, liver degeneration and necrosis, and mild edema of choriourinium, and put the allantoic fluid and embryo bodies into a tissue masher Crush, take the crushed tissue and mix it with saline at a ratio of 1:2; place it at 2-8°C for 4-12 hours, collect allantoic fluid, amniotic fluid and embryo body (remove the head and limbs). Homogenize with embryo fluid, freeze-thaw 3 times, centrifuge at 4000r / min for 30min, take supernatant and mix it in a sterile container, store at 2-8°C.
[0016] 2. Inactivation Put the YBMDV s...
Embodiment 1
[0039]1. Preparation of antigens for seedling production
[0040] 1. Preparation of virus liquid for seedling production Inoculate 12-14-day-old susceptible muscovy duck embryos into the allantoic cavity of the virus species YBMDV strain for production, 0.2ml per embryo, incubate at 36-37°C, and inspect the embryos twice a day . Muscovy duck embryos that died within 48 to 120 hours after inoculation, and embryo bodies with extensive hemorrhage, hair follicle hemorrhage, liver degeneration and necrosis, and chorioallantoic membrane with mild edema were selected, and the allantoic fluid and Muscovy duck embryo bodies were put into Crush the tissue in a masher, take the crushed tissue and mix it with normal saline at a ratio of 1:2; place it at 2-8°C for 4-12 hours, and collect the allantoic fluid, amniotic fluid, and embryo body (remove the head and limbs). Homogenize with embryo fluid, freeze-thaw 3 times, centrifuge at 4000r / min for 30min, take supernatant and mix it in a ste...
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