Patent Grant
11952400
This application claims priority to Chinese Patent Application No. 2020106380052, filed with the Chinese Patent Office on Jul. 6, 2020, entitled “Bovine Rotavirus Fusion Protein and Calf Diarrhea Multivalent Vaccine”, which is incorporated herein by reference in its entirety.
This disclosure references a Sequence Listing submitted as an ASCII text file, entitled “17232952 SEQ LISTING” originally created on Apr. 16, 2021 and revised on Jun. 25, 2021, having a size of 27 KB, the contents of which is incorporated herein by reference in its entirety.
The present disclosure relates to the technical field of molecular biology, in particular to a bovine rotavirus fusion protein and calf diarrhea multivalent vaccine.
The calf diarrhea, as one of the most common clinical diseases in a cattle farm, is common to calves of 7-15 days, has high morbidity and mortality, thus not only causing significant economic loss to the cattle farm, but also affecting the growth and development of the calves and the lactation performance in adulthood. Among the pathogenic factors, bovine rotavirus (BRV), bovine coronavirus and toxigenic E. coli are three main pathogens that cause the calf diarrhea, wherein BRV caused calf diarrhea has the highest incidence, accounting for about 46% of calf diarrhea cases.
After bovine rotavirus infection, the clinical characteristics are lethargy, anorexia, vomiting, diarrhea and dehydration, and weight loss. The bovine coronavirus is one of the other main pathogens that cause newborn calf diarrhea, clinically mainly characterized by hemorrhagic diarrhea, depression of sick cattle, reduction or stopping of milk intake, serious features such as fever, dehydration, blood concentration, and death may occur in a few cattle. Bovine colibacillosis is an infectious disease caused by pathogenic E. coli, and mainly affects calves. When the newborn calves have insufficient resistance or digestive disorder, they may be attacked. The incubation period of disease for calf is very short, the sick cattle often appear in the forms of diarrhea, septicemia and the like, the body temperature may rise to 40° C., and symptoms such as pneumonia and arthritis appear when the course of disease is prolonged. Calf diarrhea caused by pathogenic E. coli may occur all the year round, and is mostly caused in the period of drylot feeding in winter and spring. The disease is in locally endemic or sporadic form when attacking to the bovine, and great harm is brought to the breeding industry all over the world.
The calf diarrhea has the problem of cross infection, the rotavirus infection facilitates attachment and mixed infection of other pathogens such as pathogenic E. coli, then the calf diarrhea is more severe, the mortality is higher, and when there is mixed infection of coronavirus, the condition is more severe, and the mortality of the sick calves can be as high as 50%-100%. Due to the existence of reasons of cross infection and repeated attack of diarrhea, pathogens are extremely difficult to purify, and vaccine immunization becomes an important means for preventing and treating calf diarrhea. At present, no commercial mature vaccine capable of preventing and controlling calf diarrhea caused by a variety of pathogens exists in the market.
In view of this, the present disclosure is specifically proposed.
According to one aspect of the present disclosure, the present disclosure provides a bovine rotavirus fusion protein, which contains a VP6 fragment, wherein the VP6 fragment contains an amino acid sequence as represented by SEQ ID NO: 4, and at least one loop region of the following (a)˜(c) in the amino acid sequence as represented by SEQ ID NO: 4 is substituted with a fragment of an antigenic epitope derived from bovine coronavirus and/or an antigenic epitope derived from E. coli:
According to one aspect of the present disclosure, the present disclosure provides a nucleic acid encoding the bovine rotavirus fusion protein.
According to one aspect of the present disclosure, the present disclosure provides a virus-like particle assembled from the bovine rotavirus fusion protein.
According to one aspect of the present disclosure, the present disclosure provides a method for preparing the virus-like particle, including expressing genes encoding the bovine rotavirus fusion protein in a host.
According to one aspect of the present disclosure, the present disclosure provides a host expressing the bovine rotavirus fusion protein or the virus-like particle.
According to one aspect of the present disclosure, the present disclosure provides calf diarrhea multivalent vaccine, which contains the bovine rotavirus fusion protein, the nucleic acid or the virus-like particles.
In order to more clearly illustrate technical solutions in the embodiments of the present disclosure or the prior art, accompanying drawings which need to be used in the description of the embodiments or the prior art will be introduced briefly below. Apparently, the accompanying drawings in the description below are for some embodiments of the present disclosure. A person ordinarily skilled in the art still could obtain other accompanying drawings in light of these accompanying drawings, without using creative efforts.
Technical solutions of the present disclosure will be described below clearly and comprehensively in connection with examples. Apparently, the described examples are only a part of examples of the present disclosure, rather than all examples. All of other examples, obtained by those ordinarily skilled in the art based on the examples in the present disclosure without using any creative efforts, shall fall into the scope of protection of the present disclosure.
A first objective of the present disclosure is to provide a bovine rotavirus fusion protein, which contains a plurality of antigenic epitopes, and can enable a host to generate a plurality of antibodies after immunizing the host.
A second objective of the present disclosure is to provide a virus-like particle assembled from the above bovine rotavirus fusion protein.
A third objective of the present disclosure is to provide calf diarrhea multivalent vaccine.
In order to solve the above technical problems, the present disclosure specifically adopts following technical solutions.
According to one aspect of the present disclosure, the present disclosure provides a bovine rotavirus fusion protein, which contains a VP6 fragment, wherein the VP6 fragment contains an amino acid sequence as represented by SEQ ID NO: 4, and at least one loop region of the following (a)˜(c) in the amino acid sequence as represented by SEQ ID NO: 4 is substituted with a fragment of an antigenic epitope derived from bovine coronavirus and/or an antigenic epitope derived from E. coli:
Preferably, in the VP6 fragment, at least one loop region in (a)˜(c) is substituted with at least one antigenic epitope in (d)˜(f) below:
Preferably, the amino acid sequence of the VP6 fragment is represented by SEQ ID NO: 8 and/or SEQ ID NO: 13.
Preferably, the bovine rotavirus fusion protein further contains at least one of a VP2 fragment, a VP4 fragment and a VP7 fragment;
Preferably, the bovine rotavirus fusion protein contains the VP6 fragment and the VP2 fragment.
According to one aspect of the present disclosure, the present disclosure provides a nucleic acid encoding the bovine rotavirus fusion protein.
Preferably, a nucleotide sequence encoding the VP6 fragment is represented by SEQ ID NO: 9 or SEQ ID NO: 15.
According to one aspect of the present disclosure, the present disclosure provides a virus-like particle assembled from the bovine rotavirus fusion protein.
According to one aspect of the present disclosure, the present disclosure provides a method for preparing the virus-like particle, including expressing genes encoding the bovine rotavirus fusion protein in a host;
According to one aspect of the present disclosure, the present disclosure provides a host expressing the bovine rotavirus fusion protein or the virus-like particle.
According to one aspect of the present disclosure, the present disclosure provides calf diarrhea multivalent vaccine, which contains the bovine rotavirus fusion protein, the nucleic acid or the virus-like particles;
Compared with the prior art, the present disclosure has the following beneficial effects:
The virus-like particles provided in the present disclosure are formed after soluble expression of the genes encoding the bovine rotavirus fusion protein using the exogenous expression system through the genetic engineering technology, displays the main antigenic epitopes of the bovine coronavirus and/or the E. coli on the surfaces of the chimeric virus-like particles, has quite good immunogenicity against the bovine rotavirus, the bovine coronavirus and/or the pathogenic E. coli. After the virus-like particles are used as immunogen to immunize animals, the animals can generate relatively strong immune protection against the various pathogens.
The calf diarrhea multivalent vaccine provided in the present disclosure chimerizes antigens derived from a plurality of pathogens and capable of inducing organisms to produce specific antibodies, thereby expanding the preventing and controlling scope for disease, saving the labor, and improving the working efficiency. Moreover, the calf diarrhea multivalent vaccine is multivalent subunit vaccine prepared using the genetic engineering technology, has the characteristics such as no toxin dispersion and no toxicity increasing, may be used for pregnant cows and newborn calves, can be quickly served to the market, and has wide application prospects.
According to one aspect of the present disclosure, the present disclosure provides a bovine rotavirus fusion protein, which contains a VP6 fragment, wherein the VP6 fragment contains an amino acid sequence as represented by SEQ ID NO: 4, and at least one loop region of the following (a)˜(c) in the amino acid sequence as represented by SEQ ID NO: 4 is substituted with a fragment of an antigenic epitope derived from bovine coronavirus and/or an antigenic epitope derived from E. coli:
The rotavirus belongs to rotavirus genus of reoviridae, an outer capsid of the virus particles is composed of two layers, i.e. glycoproteins VP7 and VP4, and a middle layer is composed of VP6, where a main antigenic epitope region exists on VP6 protein, and can trigger neutralizing antibody activity. The VP6 protein determines the genotype of the virus, and is highly conserved among different species, and is the main antigen in rotavirus vaccine research and development. The bovine coronavirus is spherical virus particles with a diameter of about 80-120 nm and belonging to the coronavirus of Coronaviridae, the virus particles are externally wrapped with an aliphatic membrane, and spike protein (S) in three kinds of glycoproteins on the surface of the membrane is a main receptor binding site and a main antigen site. Pathogenic E. coli constitutes a variety of serotypes by 173 thallus (0) antigens, 80 surface (K) antigens and 56 flagella (H) antigens, wherein the most common serotypes are K88 and K99. The bovine rotavirus fusion protein provided in the present disclosure contains the bovine rotavirus antigen, the bovine coronavirus antigen and/or the antigen of E. coli, and enables animals to generate relatively strong immune protection against various pathogens after immunizing the animals as an immunogen, thus having the application value for preparing the multivalent vaccine.
It should be noted that the antigenic epitopes derived from the same kind of pathogen may include a plurality of antigenic epitopes, and specific examples include, but are not limited to, antigenic epitopes located in different proteins or domains in the same pathogen and having different sequences; or homologous identical antigenic epitopes of the same pathogen but different subtypes; or antigenic epitopes of the same pathogen but located in different proteins or domains in different subtypes, with different sequences. For example, antigenic epitopes derived from E. coli include K88 antigenic epitopes and K99 antigenic epitopes derived from main B cell epitope of pathogenic E. coli. At least one loop region of (a)˜(c) is substituted with other antigenic epitopes, and specific examples include, but are not limited to, that one of (a), (b) or (c) is substituted; (a) and (b) are substituted; (c) and (b) are substituted; (a) and (c) are substituted; or (a), (b) and (c) are all substituted and so on. Antigenic epitopes for substituting different loop regions may be the same or different, and specific examples include, but are not limited to, that all of (a), (b) and (c) are substituted with an antigenic epitope derived from bovine coronavirus or an antigenic epitope derived from E. coli; or (a) and (b) are substituted with an antigenic epitope derived from E. coli, and (c) is substituted with an antigenic epitope derived from bovine coronavirus.
In some preferred embodiments, in the VP6 fragment of the bovine rotavirus fusion protein, at least one loop region of (a)˜(c) is substituted with at least one antigenic epitope in (d)˜(f) below;
In some optional embodiments, in the VP6 fragment, the amino acid residues of sites 168-177 of the VP6 fragment are substituted with an antigenic epitope of the E. coli K88 having an amino acid sequence represented by SEQ ID NO: 6; the amino acid residues of sites 194-205 of the VP6 fragment are substituted with an antigenic epitope of the E. coli K99 having an amino acid sequence represented by SEQ ID NO: 7; and the amino acid residues of sites 296-316 of the VP6 fragment are substituted with a coronavirus antigenic epitope having an amino acid sequence represented by SEQ ID NO: 5. The amino acid sequence of the VP6 fragment obtained after the substitution is represented by SEQ ID NO: 8.
In some optional embodiments, the amino acid residues of sites 168-177 of the VP6 fragment are substituted with an antigenic epitope of the E. coli K99 having an amino acid sequence represented by SEQ ID NO: 7; the amino acid residues of sites 194-205 of the VP6 fragment are substituted with an antigenic epitope of the E. coli K88 having an amino acid sequence represented by SEQ ID NO: 6; and the amino acid residues of sites 296-316 of the VP6 fragment are substituted with a coronavirus antigenic epitope having an amino acid sequence represented by SEQ ID NO: 11. The amino acid sequence of the VP6 fragment obtained after the substitution is represented by SEQ ID NO: 13.
In some preferred embodiments, the bovine rotavirus fusion protein further may contain at least one of a VP2 fragment, a VP4 fragment and a VP7 fragment, and the bovine rotavirus fusion protein preferably consists of the VP6 fragment and the VP2 fragment.
According to another aspect of the present disclosure, the present disclosure further provides a nucleic acid encoding the above bovine rotavirus fusion protein. In the above, “nucleic acid” refers to a polymeric form of nucleotide with any length, wherein the nucleotide includes ribonucleotides and/or deoxyribonucleotides. Examples of nucleic acid include, but are not limited to, single-stranded, double-stranded or multi-stranded DNA or RNA, genomic DNA, cDNA, DNA-RNA hybrids or polymers containing purine and pyrimidine bases or other natural, chemical or biochemical modifications, non-natural or derived nucleotide bases.
The bovine rotavirus fusion protein provided in the present disclosure may be obtained by expression of a chimeric gene, and also may be obtained by co-expression after introducing a plurality of nucleic acids encoding different regions of the bovine rotavirus fusion protein into the host cell, therefore, the nucleic acid encoding the above bovine rotavirus fusion protein provided in the present disclosure may be an independent nucleic acid molecule containing a chimeric gene, and also may be a set of a plurality of nucleic acid molecules containing independent genes for encoding each part of the bovine rotavirus fusion protein, for example, a set of nucleic acids composed of nucleic acids that encode the VP6 fragment, and encode at least one of the VP2 fragment, VP4 fragment and VP7 fragment, respectively. It may be understood that the nucleic acid may also contain fragments encoding other functional units such as promoters, enhancers, tags and vectors, which are not limited in the present disclosure. Preferably, the nucleic acid encoding the bovine rotavirus fusion protein is subjected to codon optimization, and the nucleic acid sequence encoding the VP6 protein fragment part in the nucleic acid is preferably represented by SEQ ID NO: 9, and it encodes the VP6 fragment having an amino acid sequence represented by SEQ ID NO: 8; or the nucleic acid sequence encoding the VP6 protein fragment part in the nucleic acid is preferably represented by SEQ ID NO: 15, and it encodes the VP6 fragment having an amino acid sequence represented by SEQ ID NO: 13.
According to another aspect of the present disclosure, the present disclosure further provides a virus-like particle assembled from the bovine rotavirus fusion protein. VLP is formed by autonomously assembling one or several structural proteins of virus, and mimic natural viral particles in size, morphology and composition, without viral genome, without infectivity, and having advantages in immunogenicity, antigen stability and production. VLP combines the best advantages of whole viruses and subunit antigens. The chimeric virus-like particles can be formed after soluble expression of the genes encoding the bovine rotavirus fusion protein using the exogenous expression system through the genetic engineering technology, displays the main antigenic epitopes of the bovine coronavirus and/or the E. coli on the surfaces of the chimeric virus-like particles, has quite good immunogenicity against the bovine rotavirus, the bovine coronavirus and/or the pathogenic E. coli. After the VLP is used as immunogen to immunize animals, the animals can generate relatively strong immune protection against various pathogens.
According to another aspect of the present disclosure, the present disclosure further provides a method for preparing the above virus-like particles, which method includes: expressing genes encoding the bovine rotavirus fusion protein in a host. The genes encoding the bovine rotavirus fusion proteins may be located in the same nucleic acid fragment, and also may be located in different nucleic acid fragments, and the genes located in different nucleic acid fragments are co-expressed in a host, so that the host expresses the virus-like particles. The genes encoding the bovine rotavirus fusion protein preferably are subjected to rare codon optimization firstly.
The host includes E. coli, yeast, insect cells, plant or mammalian cells, preferably including yeast. The yeast expression system may be subjected to post-translation modification, such as glycosylation or phosphorylation, meanwhile the expression amount of the target protein is increased, and the production cost is reduced. At the same time, preferably, the host capable of expressing the genes encoding the bovine rotavirus fusion protein is monoclonal after screening under selection pressure, so as to increase the amount of the protein expressed by the host, preferably with high concentration antibiotics as screening pressure. When the genes encoding the bovine rotavirus fusion protein are located in different nucleic acid fragments, genes encoding a part of the bovine rotavirus fusion proteins may be first introduced into the host, to screen out highly expressed monoclonals, and then genes encoding the remaining part of the bovine rotavirus fusion proteins are introduced into the monoclonals, so as to further increase the expression amount of target proteins.
In some optional embodiments, taking the yeast acting as the host cell as an example, the method includes steps of preparing genes, constructing recombinant vector, cell transfection, screening highly expressed strains and obtaining recombinant proteins, specifically including: firstly linearizing the obtained vectors, then subjecting the yeast competent cells to electrotransformation, expressing the fusion protein, and purifying the obtained fusion protein, then, selecting a suitable buffer solution to perform viroid particle assembly on the purified fusion protein, and identifying the assembly effect using an electron microscope. The vectors preferably are pPIC3.5K vectors. After the linearized vectors are subjected to electrotransformation into the yeast competent cells, the yeast competent cells are preferably directly coated on a high antibiotic concentration plate, and highly expressed monoclonal strains are selected using a relatively high selection pressure. The electrotransformation is preferably performed multiple times, that is, on the basis of the first highly expressed strain, the expression vectors containing other part of target protein genes are again integrated.
According to another aspect of the present disclosure, the present disclosure further provides a host expressing the bovine rotavirus fusion protein or expressing the virus-like particles. The host provided in the present disclosure is a recombinant cell or recombinant microorganism obtained by introducing a nucleic acid encoding the bovine rotavirus fusion protein into a host. In some preferred embodiments, the nucleic acid is introduced into the host through a vector, the host preferably includes yeast, and the vector preferably is pPIC3.5K.
According to another aspect of the present disclosure, the present disclosure further provides calf diarrhea multivalent vaccine, which contains the bovine rotavirus fusion protein, the nucleic acid or the virus-like particle encoding the bovine rotavirus fusion protein. The multivalent vaccine prepared by chimerizing a plurality of antigens, i.e. the bovine rotavirus, and the bovine coronavirus and/or the E. coli that pathogenically induce organisms to generate specific antibodies expands the disease control range, saves the labor, and improves the working efficiency. Moreover, the calf diarrhea multivalent vaccine is multivalent subunit vaccine prepared using the genetic engineering technology, has the characteristics such as no toxin dispersion and no toxicity increasing, may be used for pregnant cows and newborn calves, can be quickly served to the market, and has wide application prospects.
In some preferred embodiments, the bovine diarrhea multivalent vaccine includes virus-like particles assembled from bovine rotavirus fusion proteins and an adjuvant. The virus-like particles are taken as immunogen, the antigens are highly concentrated, and the chimeric antigenic epitopes have a certain spatial structure, and have a better immune effect. The adjuvant may be a conventional adjuvant in the art, which is not limited in the present disclosure, and the ISA206 adjuvant is preferably used.
The technical solutions and beneficial effects of the present disclosure are further described below in connection with preferred examples.
Expression of Fusion Protein by Pichia pastoris Expression System:
the bovine rotavirus VP6 protein structure was analyzed by means of structural biology, and the antigenic epitopes of the bovine coronavirus and pathogenic E. coli were embedded onto the bovine rotavirus VP6 protein backbone, with a sequence named VP6-S-K88/K99, and a specific amino acid sequence represented by SEQ ID NO: 8;
the fusion protein VP6-S-K88/K99 was subjected to a Pichia pastoris expression system codon optimization, and the nucleotide sequence was represented by SEQ ID NO: 9.
The genes encoding the VP6-S-K88/K99 fusion protein were synthesized by means of genetic engineering, the target genes were inserted into the pPIC3.5k vectors via Bam HI and Age I, and the positive recombinant vectors were screened out through enzymatic identification and sequencing, transformed into E. Coli DH5a competent cells for amplification, and the plasmids were extracted in large quantity, named as pPIC3.5K-VP6-S-K88/K99.
After the pPIC3.5K-VP6-S-K88/K99 plasmids were subjected to linearize restriction enzyme digestion with Pme I restriction endonuclease, the linear expression plasmids were recovered, and measured for the purity and concentration thereof.
The competent cells subjected to electrotransformation of Pichia pastoris X33 strains were prepared, and the linearized pPIC3.5K-VP6-S-K88/K99 vectors and the competent cells were mixed and placed and then subjected to electrotransformation, and the bacterial solution after the electrotransformation was directly coated on a high concentration G418 antibiotic plate for screening.
The monoclonal strains grown on the plates were subjected to shaking culture, amplification and expression, and fermented bacteria were crushed and subjected to SDS-PAGE detection and Western blot detection, the strains with positive detection results were Pichia pastoris X33-VP6-S-K88/K99 engineered bacteria that can express the VP6-S-K88/K99 fusion protein. The SDS-PAGE detection results are as shown in
The X33-VP6-S-K88/K99 engineered bacteria were activated in BMGY medium at 30° C. for 24 h; the activated culture bacterial solution was inoculated in BMGY medium at a ratio of 1:400 for fermentation, and cultured at 30° C. for 24 h, then changed into BMMY medium for continued induction of expression, and methanol was added once every 24 h so that the final concentration of methanol was 0.5%, and the bacteria were collected 72 h after induction of expression.
Expression of Multilayer Chimeric VLP Particles by Pichia pastoris Expression System:
The genes encoding VP2-N93 protein were synthesized by means of genetic engineering, and the amino acid sequence was represented by SEQ ID NO: 10. The target genes were inserted into the pPICZ A vectors via Bst BI and Age I, and the positive recombinant vectors were screened out through enzymatic identification and sequencing, transformed into E. Coli DH5a competent cells for amplification, and the plasmids were extracted in large quantity, named as pPICZ A-VP2-N93.
After the pPICZ A-VP2-N93 plasmids were subjected to linearize restriction enzyme digestion with Pme I restriction endonuclease, the linear expression plasmids were recovered, and measured for the purity and concentration thereof.
The competent cells subjected to electrotransformation of Pichia pastoris X33-VP6-S-K88/K99 strains were prepared, and the linearized pPICZ A-VP2-N93 vectors and the competent cells were mixed and placed and then subjected to electrotransformation, and the bacterial solution after the electrotransformation was directly coated on a high concentration Zeocin antibiotic (2 mg/ml) plate for screening.
The monoclonal strains grown on the plates were subjected to shaking culture, amplification and expression, and fermented bacteria were crushed and subjected to SDS-PAGE detection, the strains with positive detection results were Pichia pastoris X33-VP2-N93-VP6-S-K88/K99 engineered bacteria that can co-express the VP6-S-K88/K99 fusion protein and the VP2-N93 protein. The SDS-PAGE detection results are as shown in
The engineered bacteria were activated in BMGY medium at 30° C. for 24 h; the activated culture bacterial solution was inoculated in BMGY medium at a ratio of 1:400 for fermentation, and cultured at 30° C. for 24 h, then changed into BMMY medium for continued induction of expression, and methanol was added once every 24 h so that the final concentration of methanol was 0.5%, and the bacteria were collected 72 h after induction of expression.
Purification of VP6-S-K88/K99 Fusion Protein and VP2-N93-VP6-S-K88/K99 Fusion Protein and Assembly of VLP:
Buffer A (20 mM HEPES, 300 mM NaCl, pH 7.3) was added to the thallus of the X33-VP6-S-K88/K99 engineered bacteria and the X33-VP2-N93-VP6-S-K88/K99 engineered bacteria in a mass volume ratio of 1:10, respectively, and the bacteria were crushed by a high pressure crushing method;
the crushed cells were centrifuged at 4° C., 12000 rpm for 60 min, after the supernatant from the centrifugation was precipitated with 30% ammonium sulfate at 4° C. for 1 h, the precipitate was resuspended again with buffer A for crude purification.
The above purified target proteins were subjected to secondary purification by gel filtration chromatography, and the target proteins were collected. The VP6-S-K88/K99 target proteins were switched into buffer B (50 mM sodium citrate, 300 mM NaCl, pH 4.82) and then placed at 4° C. for assembly, and the particle size and uniformity thereof were detected with an electron microscope, and the results are as shown in
Expression of Fusion Protein by Pichia pastoris Expression System:
the bovine rotavirus VP6 protein structure was analyzed by means of structural biology, and the antigenic epitopes of the bovine coronavirus and pathogenic E. coli were embedded onto the bovine rotavirus VP6 protein backbones, wherein two sequences were designed, named as VP6-S-K88/K99-test1 and VP6-S-K88/K99-test2, respectively, and the specific amino acid sequences are represented by SEQ ID NO: 12 and SEQ ID NO: 13;
the fusion proteins VP6-S-K88/K99-test1 and VP6-S-K88/K99-test2 were subjected to Pichia pastoris expression system optimization, respectively, and the nucleotide sequences are represented by SEQ ID NO: 14 and SEQ ID NO: 15.
Genes encoding the VP6-S-K88/K99-test1 and VP6-S-K88/K99-test2 fusion proteins were synthesized by means of genetic engineering, the target genes were inserted into the pPIC3.5k vectors via Bam HI and Age I, and the positive recombinant vectors were screened out through enzymatic identification and sequencing, transformed into E. Coli DH5a competent cells for amplification, and the plasmids were extracted in large quantity, named as pPIC3.5K-VP6-S-K88/K99-test1 and pPIC3.5K-VP6-S-K88/K99-test2.
After the pPIC3.5K-VP6-S-K88/K99-test1, pPIC3.5K-VP6-S-K88/K99-test2 plasmids were subjected to linearized restriction enzyme digestion with Pme I restriction endonuclease, the linear expression plasmids were recovered, and measured for the purity and concentration thereof.
The competent cells subjected to electrotransformation of Pichia pastoris X33 strains were prepared, and the linearized pPIC3.5K-VP6-S-K88/K99-test1 and pPIC3.5K-VP6-S-K88/K99-test2 vectors and the competent cells were mixed and placed and then subjected to electrotransformation, and the bacterial solution after the electrotransformation was directly coated on a high concentration G418 antibiotic plate for screening.
The monoclonal strains grown on the plates were subjected to shaking culture, amplification and expression, and fermented bacteria were crushed and subjected to SDS-PAGE detection and Western blot detection, the strains with positive detection results were Pichia pastoris X33-VP6-S-K88/K99-test1 engineered bacteria that can express the VP6-S-K88/K99-test1 fusion protein and Pichia pastoris X33-VP6-S-K88/K99-test2 engineered bacteria that can express the VP6-S-K88/K99-test2 fusion protein. The SDS-PAGE detection results are as shown in
The X33-VP6-S-K88/K99-test1 and X33-VP6-S-K88/K99-test2 engineered bacteria were activated in BMGY medium at 30° C. for 24 h; the activated culture bacterial solution was inoculated in BMGY medium at a ratio of 1:400 for fermentation, and cultured at 30° C. for 24 h, then changed into BMMY medium for continued induction of expression, and methanol was added once every 24 h so that the final concentration of methanol was 0.5%, and the bacteria were collected 72 h after induction of expression.
Purification of VP6-S-K88/K99-Test1 Fusion Protein and VP6-S-K88/K99-Test2 Fusion Protein and Assembly of VLP:
Buffer A (20 mM HEPES, 300 mM NaCl, pH 7.3) was added to the thallus of the X33-VP6-S-K88/K99-test1 engineered bacteria and the X33-VP6-S-K88/K99-test2 engineered bacteria in a mass volume ratio of 1:10, respectively, and the bacteria were crushed by a high pressure crushing method;
the crushed cells were centrifuged at 4° C., 12000 rpm for 60 min, the supernatant from the centrifugation and the precipitate from the centrifugation were was subjected to SDS-PAGE identification, and SDS-PAGE detection results are as shown in
In the above, the majority of VP6-S-K88/K99-test1 was present in insoluble form, which did not comply with the expectation, and no purification and electron microscopy experiments were performed.
In the above, the supernatant from centrifugation of VP6-S-K88/K99-test2 was first precipitated with 30% ammonium sulfate at 4° C. for 1 h, and the precipitate was resuspended again with buffer A for crude purification.
The above purified target proteins were subjected to secondary purification by gel filtration chromatography, and the target proteins were collected. The VP6-S-K88/K99-test2 target proteins were switched into buffer B (50 mM sodium citrate, 300 mM NaCl, pH 4.82) and then placed at 4° C. for assembly, and the particle size and uniformity thereof were detected with an electron microscope, and the results are as shown in
Preparation of Calf Diarrhea Multivalent Vaccine and Antibody Evaluation:
Vaccine Preparation:
The VP6-S-K88/K99 VLP described above was diluted to different concentrations using PBS solution, and the diluted fusion protein solution and the SEPPIC ISA206 adjuvant were mixed together in a ratio of 1:1 of antigen component to adjuvant, and the final concentration was 100 μg/mL. The vaccine was subjected to aseptic inspection, viscosity measurement, and stability measurement according to the requirements of annexes of the Veterinary Pharmacopoeia of PRC (current edition), and then placed at 4° C. for later use.
Mouse Immunization:
6-week old female Balb/c mice were randomly grouped, 10 mice in each group and 2 groups in total, one group was not injected with vaccine (control group), and the other group was an experimental group, and injected with the prepared VLP vaccine at the dose of 0.1 mL per mouse (antigen protein content 10 μg). Two days before immunization, 100 μL of submaxillary blood was collected intravenously as a pre-immunization control. The blood collected was placed in a 1.5 mL EP tube, placed in a 37° C. water bath for 1 h, 4° C. for 2 h, 3000 rpm, centrifuged at 4° C. for 3 min, and the supernatant was separated and stored at −20° C. after partitioning. 21 days after the first time of immunization, 100 μL of blood was collected, and subjected to serum separation with the same method as the above; then secondary immunization was performed with an immunization dose of 0.1 mL per mouse (antigen protein content 10 μg). 14 days after the secondary immunization, 100 μL of blood was collected, and subjected to serum separation with the same method as the above.
Bovine Rotavirus Antibody Detection:
(1) Establishment of Bovine Rotavirus Detection Method
The separated bovine rotavirus was diluted with 50 mM phosphate buffer at pH 7.6 and then coated in the enzyme plate, 100 μL/well, 4° C. overnight. The next day the coating liquid was discarded, and the enzyme plate was washed 3 times with PBST, 200 μL/well. 2% bovine serum albumin (BSA) was added as blocking liquid, 100 μL/well, 37° C. 1 h. The blocking liquid was discarded, and after three times of washing, the negative and positive serum was diluted with 1% bovine serum albumin (BSA) in proportions and added to the enzyme plate, 100 μL/well, at 37° C. for 1 h. The liquid in the plate was discarded, and after five times of washing, HRP-labeled goat anti-bovine IgG diluted by 1% bovine serum albumin (BSA) at 1:2500 was added, 100 μL/well, at 37° C. for 1 h. The liquid in the plate was discarded, and after five times of washing, TMB developing solution was added, 100 μL/well, followed by light shielding color development at 37° C. for 15 min, and then 2 mol/L H2SO4 was added to terminate the reaction, 100 μL/well. The OD450 nm value was read on ELIASA.
(2) Bovine Rotavirus Antibody Detection
14 days after the secondary immunization of mice, antibody levels of all mice in the immunization group turned to be positive (S/N value>2.1), indicating that the vaccine prepared can induce the mice to generate anti-bovine rotavirus specific antibody, and the specific detection results are as shown in Table 1.
Mouse Challenging Experiments with E. coli K88, K99:
(1) Preparation of Bacterial Solution for Challenging
The challenging strains K88 and K99 used in the test were purchased from China institute for veterinary medicine, before challenging, the rejuvenated E. coli standard strains were respectively inoculated into conical flasks with 50 mL of LB liquid culture medium, and cultured at 37° C. for 16˜20 hours under the condition of 200 rmp, and the concentration of the bacterial solution is 1×108 CFU/L. The bacterial solution was diluted by 1000 times with sterile LB liquid medium, two bacterial solutions were mixed in equal proportion, and stored at 4° C. for later use.
(2) Challenging
For the mice immunized above, 15 days after the secondary immunization, five mice in the control group were intraperitoneally injected with 0.2 mL of sterile normal saline; and the other five mice were intraperitoneally injected with 0.2 mL of the bacterial solution prepared above for challenging. The ten mice in the immunization experimental group were intraperitoneally injected with 0.2 mL of the bacterial solution for challenging. After challenging, the mice were observed every 3 hours, and the diarrhea, death and other conditions of the mice were recorded.
(3) Results
3 hours after the challenging, the challenged mice in the control group began to die, and 45 hours after the challenging, all of the five challenged mice in the control group died. For the mice injected with saline, all of the five mice survived 48 hours after injection. For the mice in the immunization group, nine mice survived and were healthy 48 hours after the challenging, and one mouse died of diarrhea 24 hours after challenging. The test results show that the protection rate of the prepared vaccine against pathogenic E. coli in the immunization group is 90%.
Finally, it should be noted that various examples above are merely used for illustrating the technical solutions of the present disclosure, rather than limiting the present disclosure. While the detailed description is made to the present disclosure with reference to the preceding examples, those ordinarily skilled in the art should understand that they still could modify the technical solutions recited in the preceding examples, or make equivalent substitutions to some or all of the technical features therein. These modifications or substitutions do not make the corresponding technical solutions essentially depart from the scope of the technical solutions of the various examples of the present disclosure.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202010638005.2 | Jul 2020 | CN | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20160185826 | Lin | Jun 2016 | A1 |
| Entry |
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| Gonzalez DD, et al. Evaluation of a bovine rotavirus VP6 vaccine efficacy in the calf model of infection and disease. Vet Immunol Immunopathol. Sep. 15, 2010;137(1-2):155-60. doi: 10.1016/j.vetimm.2010.04.015. Epub Apr. 29, 2010. PMID: 20546933. 2010. |
| Number | Date | Country | |
|---|---|---|---|
| 20220002350 A1 | Jan 2022 | US |
