A recombinant porcine pseudorabies virus tk/ge/gi triple gene deletion strain
A technology for porcine pseudorabies and virus strains, which is applied in the directions of antiviral agents, inactivation/attenuation, medical preparations containing active ingredients, etc. Prospects for commercial development, effective immune protection, and genetically stable effects
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Embodiment 1
[0011] Embodiment 1: Breeding of porcine pseudorabies virus strain
[0012] In recent years, pseudorabies has occurred in many pig farms in my country, most of which are breeding pig farms, and the infected pigs have been injected with pseudorabies vaccine before, and it is speculated that the infected virus has mutated; Screening for porcine pseudorabies virus.
[0013] Obtain samples of internal organs of sick pigs, including: heart, liver, lungs, spleen, tonsils and lymph nodes. Homogenate the visceral sample and PBS (0.1M, pH7.2) at V / V1:5, freeze-thaw 3 times, centrifuge at 3000r / min for 15min, add double antibody to the supernatant, incubate at 37°C for 1h, Sterilize by filtration through a 0.22 μm membrane filter. Take 1ml of the virus filtrate and inoculate the Vero cells grown into a single layer, pass three generations blindly, and observe the cytopathic changes (CPE). The cell culture medium with CPE was plaque-purified, and the purified virus was subpackaged and ...
Embodiment 2
[0016] Embodiment 2: Construction of recombinant porcine pseudorabies virus TK / gE / gI double gene deletion strain
specific Embodiment approach
[0017] The DNA of the isolated strain was extracted from the isolated porcine pseudorabies virus (CGMCC No.10266), and the virulence genes TK, gE and gI genes of the isolated strain were deleted by genetic engineering, and rescued on the cells Designated as PRV / TK - / gE - / gI - , Toxic, after adding a protective agent as a seed poison. The specific implementation is as follows:
[0018] 1 PCR primer
[0019] Referring to the complete PRV genome sequence (BK001744), a series of primers were synthesized by ourselves, which were used to amplify the left and right homology arms of the TK gene, and the homology arms located on both sides of the US7 (gI) gene and US8 (gE) gene (including part of the gI and gE genes). Left arm fragment (L) and right arm fragment (R) available for homologous recombination. In addition, primers were designed to amplify EGFP and EGFP eukaryotic expression cassettes, as well as primers for identifying gene deletions. The primer sequences and expect...
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