Pseudorabies virus and application of pseudorabies virus
A porcine pseudorabies and virus technology, applied in antiviral agents, virus/bacteriophage, inactivation/attenuation, etc., can solve the problems that vaccines cannot completely protect PRV and economic losses of immunized pig farms, and achieve high protection rate and safety Good results
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Embodiment 1
[0009] Embodiment 1: Isolation of porcine pseudorabies virus
[0010] In recent years, pseudorabies has occurred in many pig farms in my country, most of which are breeding pig farms, and the affected pigs have been injected with pseudorabies vaccine before, and it is speculated that the infected virus has mutated; Screening for porcine pseudorabies virus.
[0011] The visceral samples of sick pigs were taken, including: heart, liver, lung, spleen, tonsil, 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 stored at...
Embodiment 2
[0012] Embodiment 2: the breeding and identification of the porcine pseudorabies virus of screening
[0013] 1. Cultivation The porcine pseudorabies virus that was screened was named PRV QD strain, which was identified as virulent by PCR, domesticated by Vero cell culture, and the virus content reached 10 7.0 TCID 50 / More than 0.1ml. The virus was deposited on March 6, 2015 at the General Microbiology Center of the China Committee for the Collection of Microbial Cultures at the Institute of Microbiology, Chinese Academy of Sciences, No. 3, No. 1, Beichen West Road, Chaoyang District, Beijing, and the preservation number is CGMCC No.10266.
[0014] 2. Identification
[0015] 2.1 Primer design Referring to the published PRV gE gene fragments, a pair of primers were designed using Oligo 7.0 to amplify the full length:
[0016] F1: 5'-ATGCGGCCCTTTCTGCTGCGCGCC-3';
[0017] F2: 5'-TTAAGCGGGGCGGGACATCAACAGGC-3'.
[0018] 2.2 Identification results PCR detection was performed on...
Embodiment 3
[0024] Embodiment 3: Preparation of antigen for seedling production
[0025] The DNA of the isolated strain was extracted from the clinically isolated porcine pseudorabies virus, and the virulence genes TK, gE and gI genes of the isolated strain were sequentially deleted by genetic engineering methods, and named PRV / TK - / gE - / gI - Poisonous seeds, multiplied and poisonous, can be used as seed poison after adding protective agent.
[0026] PRV / TK - / gE - / gI - Virus seed safety test: Dilute the antigen 10 times with PBS, inoculate four 100g mice intramuscularly, 0.2mL each, observe for 14 days, no more than two of them react or die. The results showed that the vaccine was safe for mice, had no pseudorabies-specific symptoms, and did not affect growth and development.
[0027] The above-mentioned virus seed safety test result illustrates that the porcine pseudorabies virus gene deletion vaccine (PRV / TK) of the present invention's transformation - / gE - / gI - ) is sa...
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