A kind of recombinant prrsv virus-like particle and preparation method thereof
A recombinant baculovirus and virus-like technology, applied in the biological field, can solve the problems of late neutralizing antibody titer and virus titer decline, and achieve the effect of good immune protection, virus resistance and good immune protection effect.
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Embodiment 1
[0030] Embodiment 1: Construction of recombinant baculovirus Ac-PRRSVGP5-M
[0031] (1) Synthesis of PRRSV GP5 and M gene sequences:
[0032] Based on the sequence of PRRSV-SD16 strain (Genbank Accession No: JX087437.1), after artificial modification, the PRRSV GP5-M gene whose gene sequence is shown in SEQ ID No: 1 was obtained, and sent to Gene Synthesis Company for gene sequence synthesis , and set Bam H I and Hind III restriction sites at the 5' end and 3' end, respectively, to obtain insert fragments.
[0033] (2) Construction and identification of recombinant transfer vector:
[0034] The plasmid containing the target gene sequence GP5-M and the vector pBAC-5 (provided by Shaanxi Nuowei Lihua Biotechnology Co., Ltd., with a GFP marker gene on the vector, which can be used for fluorescence detection, see ZL201811114020.6) were subjected to Bam H I and Hind Ⅲ double enzyme digestion, after recovery and purification, use T4 ligase to perform ligation reaction, chemically ...
Embodiment 2
[0056] (1) Preparation of recombinant PRRSV virus-like particle vaccine:
[0057] The recombinant baculovirus Ac-PRRSV GP5-M prepared in Example 1 was inoculated into healthy sf9 cells at a ratio of 10%. After culturing at 27°C for 4-5 days, the cells and supernatant were collected by repeated freezing and thawing. After centrifuging for 20 minutes, collect the supernatant, then use the ammonium sulfate precipitation method to precipitate the target protein, resuspend the protein solution for 36-48 hours with binary ethyleneimine (BEI), and then use an equal amount of sodium thiosulfate Neutralize, and finally mix and emulsify the vaccine with Seppic ISA 206 adjuvant, and store it at 2-8°C for use.
[0058] In the vaccine preparation process, after the recombinant baculoviruses of Example 1 of the present invention, control group 1, control group 2 and control group 3 were cultured, they were all adjusted to a virus titer of 10 5 TCID 50 / ml, and then continue with subsequent ...
Embodiment 3
[0072] Example 3: Antibody ups and downs of vaccine immunized piglets
[0073] (1) The recombinant PRRSV virus-like particle vaccine and the vaccine of the control group 2 were prepared according to the method of Example 2, and the vaccine sample of the control group 3 (prepared by the invention patent ZL201811114020.6 was provided by Shaanxi Nuowei Lihua Biotechnology Co., Ltd. vaccine).
[0074] (2) Screen 10 one-month-old healthy piglets with double-negative PRRSV antigen and antibody, among which 1 piglet was randomly selected as the blank control group, and the remaining 9 piglets were randomly divided into 3 groups, 3 piglets in each group. The first group is immunized with the Ac-PRRSV GP5-M vaccine of the present invention (the amino acid sequence is shown in SEQ ID No: 2), the second group is immunized with the control group 2 vaccine (the amino acid sequence is shown in SEQ ID No: 6), and the third group Immune the vaccine of control group 3 (the vaccine prepared by...
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