Recombinant Newcastle disease LaSota low virulent vaccine strain expressing bird flu virus H5 subtype HA protein
A technology of avian influenza virus and attenuated vaccine, which is applied in the field of recombinant Newcastle disease LaSota attenuated vaccine strain expressing H5 subtype HA protein of avian influenza virus, which can solve the problems of inconvenient use, high manufacturing cost, and lack of wide application
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Embodiment 1
[0038] Example 1 Construction of recombinant Newcastle disease LaSota attenuated vaccine strain expressing wild-type or mutant avian influenza virus H5 subtype hemagglutinin (HA) protein
[0039] cells and viruses
[0040] BHK-21 cells (milk hamster kidney cells ATCC CCL-10), culture medium is DMEM (Dulbecco's modified Eagle's medium) containing 10% fetal bovine serum (Hyclone) and 1 μg / ml G418; NDV Lasota vaccine Strain AV1615 (purchased from China Center for Veterinary Culture Collection (CVCC)). The allantoic cavity of 9-10-day-old SPF chicken embryos was inoculated and frozen at -70°C for later use; chicken anti-NDV hyperimmune serum was prepared by our laboratory (Chu, H.P., G.Snell, D.J.Alexander, and G.C.Schild.1982 .Avian Pathol 11:227-234); SPF chicken embryos and SPF chicks were provided by the SPF Experimental Animal Center of Harbin Veterinary Research Institute. H5 subtype highly pathogenic avian influenza virus (HPAIV) A / Goose / Guangdong / 96 / 1 / H5N1 isolate [GD / 1 / ...
Embodiment 2
[0049] Example 2 Recombinant NDV expresses AVIHA protein indirect immunofluorescence assay (IFA) test
[0050] The NDV LaSota vaccine strain can transiently infect mammalian cells cultured in vitro. In order to prove the replication of rLasota-H5wtHA and rLasota-H5mutHA viruses in BHK-21 cells and the expression of virus antigens, the two allantoxins infected about 70-80% of monolayer BHK-21 cells with MOI as 1 virus load ( Figure 3A and B), while using the NDV wild-type LaSota vaccine strain infected cells as a control (Figure 3C), 20 hours after the infection, the cells showed early CPE (cytopathic) phenomenon, and immediately used the NDV high immune SPF chicken positive serum as the detection antibody. Indirect immunofluorescence staining, the results of the three virus-infected cells under a fluorescence microscope observed a strong positive reaction (Figure 3A, B and C) More specifically, the experimental steps are as follows:
[0051] Chicken embryos were inoculated wi...
Embodiment 3
[0053] Example 3 Western-Blot identification of recombinant NDV expressing AVI HA protein
[0054]Take virus-infected chicken embryo fibroblast (CEF) lysate (after discarding the culture medium, add 1 / 10 volume of PBS, suspend the cells, add an equal volume of 2×SDS lysis buffer to lyse in boiling water for 10 min, centrifuge at 12000 g for 10 min , harvest the supernatant) or virus-inoculated SPF chicken embryo allantoic stock solution, carry out SDS-PAGE (Bio-Rad). Protein electrotransfer (Bio-Rad) to nylon membrane (Ameresco), 10% skimmed milk blocked overnight, PBST (0.05% Tween20) was added after washing, 1:50 diluted DNA was added for immunization to prepare chicken anti-H5 subtype avian influenza virus HA Antigen hyperimmune serum was the primary antibody, horseradish peroxidase (HRP)-labeled rabbit anti-chicken goat anti-mouse IgG (Sigma) was the secondary antibody, diluted 1:2500 times in PBST, DAB (diaminobenzidine, Sigma) After 3-5 minutes, the reaction was termina...
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