Gosling plague virus originated from muscovy ducks
A technology of gosling plague virus and Muscovy duck, which is applied in the field of Muscovy duck-origin gosling plague virus, can solve the problems such as the reduction of vaccine potency, and achieve good safety and the effect of preventing the infection of gosling plague virus in young Muscovy ducks
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Embodiment 1
[0010] Embodiment 1, the screening of YBGPV-M strain
[0011] In 2013, a disease characterized by diarrhea and embolism due to the shedding of some duck intestinal mucosa appeared in a group of young muscovy ducks in a duck farm in Fujian Province. The incidence rate was 50% to 80%, and the fatality rate was 45% to 70%. The use of antibiotics, Muscovy duck parvovirus vaccine and Muscovy duck parvovirus hyperimmune yolk antibody could not control the disease. The inventor aseptically collected the liver, spleen and pancreas of dying ducks, homogenized the liver, spleen and pancreas with sterile normal saline to make a 20% suspension, centrifuged at 3000r / min for 15min, took the bacteria from the upper part and passed through the allantoic cavity Inoculate 11-day-old muscovy duck embryos, hatch for 168 hours, collect the allantoic fluid and embryo body tissue of the dead embryos after 24 hours, homogenize, freeze and thaw three times, and take the supernatant for freezing. Afte...
Embodiment 2
[0014] Embodiment 2 prepares vaccine
[0015] 1. Preparation of virus liquid for seedling production Dilute the YBGPV-M strain 100 times with sterile saline, inoculate 11-12 day-old susceptible Muscovy duck embryos in the allantoic cavity, 0.2ml per embryo, and incubate at 37°C , according to embryo inspection 2 times a day. Select duck embryos that died within 48 to 168 hours after inoculation, place them at 2 to 8°C for 4 to 12 hours, open the air chamber under sterile conditions, and pick out embryos with extensive hemorrhage, hair follicle hemorrhage, liver degeneration and necrosis, and chorioallantois For embryos with mild edema, take the embryo body (remove the head and limbs) and put it into a tissue grinder to crush, collect allantoic fluid and amniotic fluid, homogenate with embryo fluid, take the crushed tissue and add it at a ratio of 1:3 Physiological saline was mixed, freeze-thawed 3 times, centrifuged at 4000r / min for 30min, the supernatant was taken and mixed ...
Embodiment 3
[0039] 1. Preparation of antigens for seedling production
[0040] 1. Preparation of virus liquid for seedling production Dilute the YBGPV-M strain 100 times with sterile saline, inoculate 11-12 day-old susceptible Muscovy duck embryos in the allantoic cavity, 0.2ml per embryo, and incubate at 37°C , according to embryo inspection 2 times a day. Select duck embryos that died within 48 to 168 hours after inoculation, place them at 2 to 8°C for 4 to 12 hours, open the air chamber under sterile conditions, and pick out embryos with extensive hemorrhage, hair follicle hemorrhage, liver degeneration and necrosis, and chorioallantois For embryos with mild edema, take the embryo body (remove the head and limbs) and put it into a tissue grinder to crush, collect allantoic fluid and amniotic fluid, homogenate with embryo fluid, take the crushed tissue and add it at a ratio of 1:3 Physiological saline was mixed, freeze-thawed 3 times, centrifuged at 4000r / min for 30min, the supernatant...
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