Duck SBDS (Short Beak and Dwarfism Syndrome) vaccine and preparation method thereof
A syndrome and dwarf technology, applied in the fields of microorganisms and veterinary biopharmaceuticals, can solve the problems of IL-2 research lag, achieve good immune and preventive effects, good safety, and facilitate large-scale production
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Embodiment 1
[0023] Example 1 Preparation and identification of goose parvovirus virus-like particles with duck short beak dwarf syndrome
[0024] The VP2 sequence was obtained by sequencing the goose parvovirus M15 strain isolated from the Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Sciences, and the VP2 sequence was changed to the classic ATG start. a. Then optimize it according to the preference of Sf9 cells, and send it to the company for gene synthesis. The optimized sequence of duck short beak dwarf syndrome goose parvovirus VP2 is shown in SEQ ID NO.3.
[0025] For the optimized sequence, use primers (shown in SEQ ID NO.4-5) to amplify the VP2 gene, connect it into the pH MCS of the pFastBac Dual vector through PstI-HindIII, and then introduce IL- 2 gene sequence, its nucleotide sequence is shown in SEQ ID NO.6. The IL-VP2 gene was amplified by PCR (primers are as shown in SEQ ID NO.7-8), ligated into p10MCS using SmaI-XhoI, and finally o...
Embodiment 2
[0027] Embodiment 2 Duckling immunity test
[0028] The duck short beak dwarf syndrome goose parvovirus virus-like particles prepared in Example 1 were diluted with PBS so that the latex agglutination titer was 1:2 4 , adding thimerosal at a final concentration of 0.005%, mixing the antigen and oil adjuvant at a ratio of 1:1.5, emulsifying to make a virus-like particle vaccine, and storing at 4°C. Antigen (latex agglutination titer is 1:2) prepared after inactivation of duck embryo allantoic fluid 4 ) and oil adjuvant at a ratio of 1:1.5, emulsified to make a virus-like particle vaccine, and stored at 4°C.
[0029] 18 8-day-old ducklings were randomly divided into 3 groups, with 6 ducks in each group. Group A was immunized with virus-like particle vaccine 0.3ml / feather, group B was immunized with whole virus inactivated vaccine group 0.3ml / feather, and group C was the control Group is not immune. Blood was collected before immunization, 14 days, 21 days, and 28 days after i...
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