H7N9 subtype avian influenza virus-like particle vaccine preparation as well as preparation and application thereof
A bird flu virus and granule technology, which is applied in the direction of antiviral agents, double-stranded DNA viruses, antisense single-stranded RNA viruses, etc., to achieve the effect of facilitating large-scale production, increasing the cost of use, and inhibiting the detoxification of chickens
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Embodiment 1
[0045] The preparation of embodiment 1 avian influenza virus-like particles (H7N9-VLP)
[0046] (1) Construction of HA, NA, and M1 gene recombination transfer plasmids
[0047] (1) In this embodiment, the nucleotide sequences of the HA, NA, and M1 genes of the avian influenza virus have been codon-optimized, biased towards insect cell expression, and 6x his tags are added to the C-terminals of the HA, NA, and M1 genes; Artificially synthesized to obtain the nucleotide sequences of the codon-optimized HA, NA, and M1 genes, and respectively link them into the PUC57 vector to obtain the corresponding recombinant plasmids (Beijing Liuhe Huada Gene Technology Co., Ltd.); wherein, the codon-optimized The nucleotide and amino acid sequences of the HA gene, NA gene, and M1 gene are shown below.
[0048] Nucleotide sequence of HA gene after codon optimization:
[0049] ATGAACACTCAGATCCTGGTCTTCGCTCTGATCGCTATCATCCCCACTAACGCCGACAAGATCTGCCTGGGTCACCACGCTGTGAGCAACGGCACTAAGGTCAACACTCTGACTGA...
Embodiment 2
[0078] Example 2 Construction of Recombinant Baculovirus Plasmid Bacmid-HMN
[0079] (1) The present embodiment designs a recombinant chimeric protein HMN (amino acid sequence such as SEQ ID NO: 9) based on the conservative epitope of the avian influenza virus. The recombinant chimeric protein HMN is expressed by the conservative antigenic epitope of the avian influenza virus The conserved antigenic epitope of avian influenza virus includes amino acid residues 76-130 of hemagglutinin protein HA2 (HA2 76-130), matrix protein M2 Amino acid residues 2-24 of the extracellular domain (M2e 2-24) and amino acid residues 55-69 of the nucleoprotein NP (NP 55-69), the amino acid sequences of which are shown in SEQ ID NO: 1-3 , the amino acid sequence of bee venom signal peptide and 6x-His tag protein is shown in SEQ ID NO: 4-5; wherein, M2e 2-24 has four copies of tandem repeats, and each copy is connected by a flexible linker linker1 ; NP 55-69 has eight copies of tandem repeats, each...
Embodiment 3
[0088] The acquisition of embodiment 3 recombinant baculovirus BV-HMN
[0089] (1) Using the conventional liposome-mediated transfection method, the recombinant bacmid-HMN prepared in Example 2 was transfected into sf9 insect cells (Invitrogen). The specific steps of transfection are:
[0090] ①Confirm that the Sf9 cells in the six-well plate to be treated are in the logarithmic phase (1.0~2.5×10 6 cell / mL), and the cell viability is higher than 95%;
[0091] ② Take 1 μL of recombinant bacmid Bacmid-HMN (concentration above 1000ng / μL) and dilute it in 100 μL of Grace’s solution (Thermo Fisher Scientific), mix gently; mix before use II liposome, draw 6-8 μL into 100 μL Grace’s solution, briefly vortex and mix well; mix the diluted recombinant baculovirus plasmid Bacmid-HMN with the diluted II mix (total volume about 210μL), mix gently and incubate at room temperature for 15-30min to obtain DNA-liposome mixture;
[0092] ③ Pipette 800 μL of Grace's solution to the DNA-lipo...
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