A kind of anti-foot-and-mouth disease vaccine composition and its preparation method and application
A vaccine composition and foot-and-mouth disease technology, applied to medical preparations containing active ingredients, pharmaceutical formulas, antiviral agents, etc., can solve the problems of easy mutation of foot-and-mouth disease virus, decreased vaccine protection, and weak immunogenicity
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Embodiment 1
[0086] Preparation of Type O Foot-and-Mouth Disease Virus Ⅰ Virus-like Particles (VP4, VP2, VP3, VP1)
[0087] 1. Synthesize the full length of the gene shown in the amino acid sequence of O-type foot-and-mouth disease virus I VP4, VP2, VP3, and VP1 shown in SEQ ID NO.1, 2, 3, and 4 by Sangon Bioengineering (Shanghai) Co., Ltd. The full lengths of the synthesized gene fragments were 255bp, 654bp, 660bp, 639bp, respectively. The foot-and-mouth disease gene template of the present invention is prepared on the basis of the artificially synthesized foot-and-mouth disease gene fragment.
[0088] 2. Construction of foot-and-mouth disease gene expression vector
[0089] For the foot-and-mouth disease gene template synthesized in the previous step, primers were designed respectively (see Table 1), and the O-type foot-and-mouth disease virus I VP4, VP2, VP3, and VP1 genes were amplified.
[0090] Table 1 O-type foot-and-mouth disease virus Ⅰ primer list
[0091]
[0092] Perform ...
Embodiment 2
[0103] Preparation of Type O Foot-and-Mouth Disease Virus Ⅰ Virus-like Particles (VPO, VP3, VP1)
[0104] Referring to the method in Example 1, primers were respectively designed according to the gene sequences of type O foot-and-mouth disease virus I structural proteins VPO, VP3, and VP1 for tandem expression to prepare virus-like particles. The collected bacteria were resuspended according to the ratio of 1 g of bacteria to 10 ml of lysate, and the bacteria were crushed 4 times with a homogenizer at a pressure of 800 bar. Centrifuge at 13500rpm for 40min, save the supernatant, and detect by 15% SDS-PAGE electrophoresis. At this time, the expression level of the three serially expressed proteins in the supernatant is about 20%. Ammonium sulfate fractional precipitation was used for crude protein purification, followed by chromatographic purification. The purified protein was subjected to SDS-PAGE electrophoresis, which showed that the target protein was purified and enriched....
Embodiment 3
[0107] Preparation of Asian Foot-and-Mouth Disease Type 1 Virus-like Particles (VP0, VP3, VP1)
[0108] The genes shown in the amino acid sequences of Asian type 1 foot-and-mouth disease virus VPO, VP3, and VP1 shown in SEQ ID NO.21, 22, and 23 were respectively designed according to the method of Example 1 and expressed in tandem to prepare virus-like particles.
[0109] Negative staining with phosphotungstic acid and electron microscope observation showed that the FMD protein had formed virus-like particles, and the formed virus-like particles were plump, with high assembly efficiency and no aggregation. After placing the foot-and-mouth disease virus-like particles at 4°C for 4 months, negative staining with phosphotungstic acid and electron microscope observation showed that the virus-like particles were still full without aggregation. It shows that the foot-and-mouth disease protein prepared according to the three-stage expression of the screened sequence of the present in...
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