Construction of gene-deleted attenuated African swine fever virus strain and application of gene-deleted attenuated African swine fever virus strain as vaccine
An African swine fever virus and gene deletion technology, which is applied in the construction and application fields of vaccines, can solve the problems of weakening the virus, and the attenuated strain cannot provide comprehensive protection for animals, and achieves the effect of good safety performance.
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Embodiment 1
[0067] Construction and purification identification of embodiment 1 attenuated African swine fever virus strain
[0068] 1. Screening expression cassette construction
[0069] To facilitate screening, an expression cassette for the selectable marker gene was constructed.
[0070] Enhanced green fluorescent protein (Enhance Green fluorescent protein, eGFP) gene screening expression cassette construction: refer to literature (O'Donnell V.African Swine Fever Virus Georgia 2007with aDeletion of Virulence-Associated Gene 9GL(B119L), when Administered at LowDoses, Leads to Virus Attenuation in Swine and Induces an EffectiveProtection against Homologous Challenge. JVirol.2015; 89(16):8556-66), amplified the p72 promoter by PCR (from -196nt upstream of the p72 gene to the sequence before +17) , standby; amplification primers are: forward primer 5'-TTATAAAACATATGTTCATAAAAAGGGTCGCCGGAGGAAAAGTC-3' (shown in SEQ ID NO.3) and reverse primer 5'-CTCCTCGCCCTTGTCCACCATATAATGTTATAAAAATAATT-3' ...
Embodiment 2
[0083] The mensuration of embodiment 2 virus titer
[0084] The titer of African swine fever virus adopts half hematosorbate amount (50% haemadsorption, HAD 50 ) means that HAD 50 For the specific operation of the experiment, please refer to the literature (BorcaMV.Development of a highly effective Africanswine fever vir us vaccine by deletion of the I177L gene results in sterile immunity against the current epi demic Eurasia strain.JVirol.2020.pii:JVI.02017-19). It is adjusted appropriately: according to approximately 1x10 in a 96-well plate 5 Cells per well were inoculated with primary PAM cells, and the recombinant virus to be tested was serially diluted 10 times, a total of 7 dilutions, each dilution was 8 wells, and the diluted virus was added to the PAM of a 96-well plate at 100 μL / well, and then added Red blood cells, a total of three replicates. Virus infection can be judged according to the rosette formed by the aggregation of red blood cells around the infected ce...
Embodiment 3
[0085] Virulence Evaluation of Example 3 Gene Deletion Attenuated African Swine Fever Virus Strain
[0086] In order to detect the virulence of the gene deletion attenuated African swine fever virus strain, this experiment used 10 4 HAD 50 The toxicity of the dose was evaluated by intramuscular injection in piglets.
[0087] In this experiment, 17 healthy Landrace piglets negative for African swine fever antigen antibody were divided into 3 groups, including 6 pigs in the gene deletion attenuated African swine fever virus strain Δ20 / 40 group, and 6 pigs in the ASFVCN / GS / 2018 isolate group. Gene deletion attenuated African swine fever virus strain Δ20 / 40 cohabitation group with 5 animals. Measure body temperature changes every day, collect peripheral blood and saliva, refer to literature (KingDP.Development of a TaqMan PCR assay with internal amplification control for the detection of African swine fever virus.J Virol Methods 107:53-61), and use fluorescence quantitative PCR ...
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