A-type foot-and-mouth disease subunit vaccine as well as preparation method and application thereof
A subunit vaccine, foot-and-mouth disease technology, applied in the field of molecular biology, can solve the problems of limited value and prospects, low expression efficiency, etc., to achieve good protection, high immune efficacy, improved stability and protective efficacy.
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Embodiment 1
[0049] The preparation of embodiment 1 foot-and-mouth disease virus structural protein composition
[0050] 1. Construction of recombinant expression vector for structural protein of foot-and-mouth disease virus
[0051] (1) Design the gene sequence THS encoding the fusion tag protein composed of the following elements in series, wherein T is the nucleotide sequence of the translation initiation region, H is the nucleotide sequence encoding the histidine tag, and S is the nucleotide sequence encoding the tag containing The nucleotide sequence of Saccharomyces cerevisiae small ubiquitin-like modification protein (SUMO); the nucleotide sequence of THS is shown in SEQ ID NO:11.
[0052] (2) The above-mentioned THS gene sequence was concatenated in sequence with the structural protein genes VPO, VP3, and VP1 encoding the A / GDMM / 2013 strain, respectively, to form three fusion gene sequences THS-VPO, THS-VP3, and THS-VP1. Wherein said coding A / GDMM / 2013 strain structural protein ge...
Embodiment 2
[0075] The expression efficiency of embodiment 2 foot-and-mouth disease virus structural protein composition
[0076] Four kinds of foot-and-mouth disease virus structural protein compositions A / GDMM / 2013, Re / A / GDMM / 2013 / K3118R, Re / A / GDMM / 2013 / K1209R, Re / A / GDMM / 2013 / K3118R+K1209R was identified for prokaryotic expression, and the expression efficiency of different foot-and-mouth disease virus structural protein compositions was analyzed by SDS-PAGE. The experimental results are as follows Figure 5 As shown, neither the single gene mutation of the FMDV structural protein VP3 or VP1, nor the simultaneous mutation of the structural proteins VP3 and VP1 will significantly affect the expression efficiency of the FMDV structural protein composition.
[0077] According to the method described in Example 1, respectively to 4 kinds of foot-and-mouth disease virus structural protein compositions A / GDMM / 2013, Re / A / GDMM / 2013 / K3118R, Re / A / GDMM / 2013 / K1209R, Re / A / GDMM / 2013 / K3118R+K1209R ...
Embodiment 3
[0080] Example 3 Detection of Neutralizing Antibody Response in Animals Immunized with Foot-and-Mouth Disease Subunit Vaccine
[0081] The foot-and-mouth disease virus structural protein compositions A / GDMM / 2013, Re / A / GDMM / 2013 / K3118R, Re / A / GDMM / 2013 / K1209R, Re / A / GDMM / 2013 / K3118R+ K1209R vaccine was prepared with the same antigen dose and immunized in pigs. Blood was collected on days 0, 7, 14, 21, and 28 after immunization, and the serum was separated for detection of neutralizing antibody titers. Test results such as Figure 6As shown, the A-type foot-and-mouth disease virus structural protein composition A / GDMM / 2013, Re / A / GDMM / 2013 / K3118R, Re / A constructed with the A / GDMM / 2013 strain structural protein gene VPO, VP3, VP1 / GDMM / 2013 / K1209R, Re / A / GDMM / 2013 / K3118R+K1209R can produce higher levels of neutralizing antibodies after animal immunization, and the structural protein genes VP3 and VP1 of the A / GDMM / 2013 strain or The type A foot-and-mouth disease virus structural pr...
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Abstract
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