Duck viral hepatitis and duck reovirus disease bivalent inactivated vaccine and preparation method thereof
A dual inactivated vaccine and reovirus disease technology, applied to biochemical equipment and methods, viruses, vaccines, etc., can solve problems such as duck lameness and economic losses in duck farming
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Embodiment 1
[0078] Example 1—Isolation and Identification of Type 3 Duck Hepatitis Virus
[0079] Disease material treatment Collect the liver and follicle tissues of diseased ducks from the breeding duck flocks that have experienced egg production decline, cut the liver and follicle membranes, add sterilized saline at a ratio of 1:3, grind to make a tissue suspension, freeze and thaw, Centrifuge at 12000r / min for 5min. The supernatant was collected, sterilized by filtration, and set aside.
[0080] Disease material inoculation Inoculate 5 susceptible duck embryos 10-11 days old with the above-mentioned filtrate through the allantoic cavity, 0.2ml / embryo, and continue to hatch at 37°C. Duck embryos that died within 24 hours were discarded, and then the embryos were photographed twice a day, observed continuously until the fifth day, the allantoic fluid of duck embryos that died within 24 to 120 hours was aseptically harvested, and the lesions of duck embryos were observed. The collected...
Embodiment 2
[0087] Example 2—Isolation and identification of type 1 duck hepatitis virus
[0088] Disease material treatment Collect the liver and follicle tissues of diseased ducks from the breeding duck flocks that have experienced egg production decline, cut the liver and follicle membranes, add sterilized saline at a ratio of 1:3, grind to make a tissue suspension, freeze and thaw, Centrifuge at 12000r / min for 5min. The supernatant was collected, sterilized by filtration, and set aside.
[0089] Disease material inoculation Inoculate 5 9-10-day-old SPF chicken embryos with the above-mentioned filtrate through the allantoic cavity, 0.2ml / embryo, and continue to hatch at 37°C. Duck embryos that died within 24 hours were discarded, and the embryos were photographed twice a day thereafter, observed continuously until the fifth day, the allantoic fluid of dead chicken embryos was aseptically harvested within 24 to 120 hours, and the lesions of the chicken embryos were observed. The colle...
Embodiment 3
[0096] Example 3—Isolation and identification of novel duck reovirus
[0097] Disease material treatment Collect the spleen tissue of diseased ducks from the Cherry Valley duck group with spleen necrosis, cut it into pieces, add sterilized saline at a ratio of 1:3, grind to make a tissue suspension, freeze-thaw, and centrifuge at 12000r / min for 5min . The supernatant was collected, sterilized by filtration, and set aside.
[0098] Disease material inoculation Inoculate 5 6-7 day-old susceptible chicken embryos with the above-mentioned filtrate through the yolk sac, 0.2ml / embryo, and continue to hatch at 37°C. Duck embryos that died within 24 hours were discarded, and the embryos were photographed twice a day thereafter, observed continuously until the fifth day, the allantoic fluid of dead chicken embryos was aseptically harvested within 24 to 120 hours, and the lesions of the chicken embryos were observed. The collected allantoic fluid is poisonous and cryopreserved.
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