Porcine pseudorabies virus vaccine
A porcine pseudorabies and vaccine technology, applied in antiviral agents, antibody medical ingredients, medical preparations containing active ingredients, etc., can solve the problems that vaccines cannot completely protect PRV, economic losses of immune pig farms, etc., and achieve good commercial development Prospect, effective immune protection, effect on genetic stabilization
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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 gene deletion strain
specific Embodiment approach
[0017] The DNA of the isolated strain was extracted from the isolated porcine pseudorabies virus (CGMCC No.10266), the virulence gene TK gene of the isolated strain was deleted by the method of genetic engineering, and the cell was rescued and named as PRV / TK - , Toxic, after adding a protective agent as a seed poison. The specific implementation is as follows:
[0018] 1 PCR primer
[0019] Referring to the whole genome sequence of PRV (BK001744), a series of primers were synthesized by ourselves, which were used to amplify the left and right homology arms of the TK gene, amplify the EGFP and EGFP eukaryotic expression cassettes, and primers used to identify the deletion of the TK gene. The primer sequences and expected PCR product sizes are listed in Table 1.
[0020] Table 1: Primers used in this study
[0021]
[0022]
[0023] Construction of 2TK gene transfer vector
[0024] Using the PRV QD strain genome as a template, using primers TKLF / TKLR and TKRF / TKRR, ...
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