Giant salamander iridescent virus vaccine, preparation method and application
A giant salamander iridescent virus and vaccine technology, applied in the biological field, can solve the problems of difficult exogenous genes and efficient expression of heterogeneous biological cells, and achieve the effects of simple cultivation, high expression, and quality control
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Embodiment 1
[0056] Obtaining of truncated optimized recombinant protein JDMCP:
[0057] 1. Truncated region screening
[0058] The antigenic region, hydrophilic region and surface display probability of the giant salamander iridescent virus MCP gene were analyzed, and the hydrophilic sequence with concentrated antigenic determinants and strong antigenicity was selected as the proposed expression gene.
[0059] 2. Codon optimization
[0060] According to the yeast codon preference, codon optimization was performed on the proposed expression gene sequence, and the GC content was kept moderate, and the optimized sequence was synthesized. Compared with the original sequence (MCP), the optimized MCP sequence has 20%-30% bases optimized and the low-frequency codons of Pichia pastoris are all replaced by high-frequency or sub-high-frequency codons.
[0061] 3. Amplification of MCP truncation-optimized genes
[0062] 3.1 Design of PCR primers for MCP truncated optimized gene
[0063] Accordin...
Embodiment 2
[0107] A preparation method of giant salamander iridescent virus disease vaccine, the steps are as follows:
[0108] Pick the Pichia pastoris Km71 / GSIV-MCP strain, inoculate it into 100mL BMGY medium, and culture it at 30°C and 250r / min shaking until OD 600 When the value reaches about 6, centrifuge at room temperature at 1500g for 5min, resuspend the bacteria in 20mL of BMMY medium, transfer the obtained bacterial solution into a 100mL shake flask, seal the bottle, add 100% methanol to a final concentration of 0.5%, and store at 30°C, 250r / The culture was induced under the condition of 1 min, and methanol was added every 24 hours to maintain the concentration of methanol at 0.5%. After continuous induction for 3 days, the yeast in the induction solution was removed by centrifugation (removing the precipitate and leaving the supernatant), and the Bradford protein analysis method was used to calculate the content of the target protein (recombinant protein JDMCP) in the origina...
Embodiment 3
[0112] A kind of application of giant salamander iridescent virus disease vaccine in preparation giant salamander iridescent virus vaccine, its application process is as follows:
[0113] The recombinant protein JDMCP prepared in Example 2 was used to immunize giant salamanders (70 ± 5 grams) with substantially no difference in body weight, good mental condition, and giant salamander iridescent virus negative, and a positive control and a normal saline control (100 microliters of each giant salamander intramuscularly injected, The specific concentration is shown in Table 1), after 15 days, the immunization was boosted with the same dose, and after the antibody was detected by the ELISA kit, the giant salamander iridescent virus strain was used for the challenge experiment, and 500 microliters of 1×10 per fish were injected intraperitoneally. 6.5 TCID 50 / ml giant salamander iridescent virus (CCTCC NO: V201134) to detect whether the antibodies produced have protective power (Ta...
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