Construction of attenuated African swine fever virus strain with e184l gene deletion and its application as a vaccine
An African swine fever virus, E184L technology, applied in the field of construction of E184L gene deletion attenuated African swine fever virus strains, can solve the problems of large differences in weakening effect, incomplete deletion, loss of protective effect of attenuated strains, etc. Social value, high safety, effect of reducing immunosuppressive activity and pathogenicity
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Embodiment 1
[0077] Example 1 Detection of immunosuppressive activity of E184L protein
[0078] 1. Detection of E184L protein inhibiting poly(dA:dT)-induced IFN-β, ISRE and NF-κB promoter activity
[0079] Construction of E184L expression plasmid: the African swine fever virus E184L protein coding sequence was amplified by RT-PCR to construct the E184L expression plasmid. The forward primer is 5'-TTTTGCGGCCGCGATGTTGGTGATCTTCTTGGGAATT-3' (shown in SEQ ID NO: 3); the reverse primer is 5'-TTTCGTCGACTTAACTATTATTTTCTTTCCACTCT- 3' (shown in SEQ ID NO: 4); digested by NotI and SalI respectively The amplified fragment and the FLAG-CMV-7.1 vector were purified and recovered and ligated with T4 ligase, and the E184L coding sequence was constructed into the FLAG-CMV-7.1 vector to obtain the E184L expression plasmid. Plasmid DNA was extracted with an endotoxin-free plasmid extraction kit, the concentration was measured, and stored at -20°C for later use. According to gene sequence determination, the...
Embodiment 2
[0101] Example 2 Construction and purification identification of attenuated African swine fever virus strain with loss of function of E184L gene-encoded protein
[0102] Primary porcine alveolar macrophages (PAM) and primary bone marrow macrophages (BMDM) used in the present invention are obtained from 2-4 month old healthy pigs (purchased from the Animal Center of Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences), and the cells are aseptically collected Afterwards, red blood cells were removed with erythrocyte lysate (purchased from Biosharp), after low-speed centrifugation, the supernatant was discarded, and the cells were resuspended in RPMI 1640 complete medium (purchased from Gibco) containing 10% FBS (purchased from PAN) in 37°C, 5% CO 2 cultured in an incubator. BMDM cell culture requires an additional 10ng / mL final concentration of recombinant porcine GM-CSF (purchased from R&D Systems) in RPMI 1640 complete medium, placed at 37°C, 5% CO...
Embodiment 3
[0114] Example 3 Virus titer determination of attenuated African swine fever virus strain ASFVΔE184L in PAM cells
[0115] The titration of African swine fever virus adopts half hematosorbate amount (50% haemadsorption, HAD 50 ) in two ways. Dilute the above-mentioned recombinant virus by 10 times, take 100 μl and inoculate the porcine primary PAM cells in 96 wells that have been laid in advance to form a single layer, add 25 μl of 1% red blood cell suspension to each well, the virus infection can be based on the accumulation of red blood cells around the infected cells The formed rosettes are judged, and the plate can be read for the first time after 12-16 hours of culture, and the observation is continued for 7 days, and the half hemasorbed dose (HAD) is calculated according to the Reed and Muench method. 50 ). The results showed that: 48 hours after infection, the average titer of the attenuated African swine fever virus strain ASFVΔE184L was 10 4.5 / mL, while the averag...
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