Patent Application
20220265804
The sequence listing provided in the file entitled C6351-056_2022-04-08_SQL.txt, which is an ASCII text file that was created on Apr. 8, 2022, and which comprises 42,385 bytes, is hereby incorporated by reference in its entirety.
The present invention relates to a fusion protein capable of self-assembling into a protein nanoparticle and application thereof, which belongs to the field of biomedicine.
Vaccines play a vital role in the prevention of pathogenic bacterial infections. The new generation of vaccine products (subunit vaccines) have a more single and clear composition, which makes their products safer. However, these vaccines often have a relatively low immunogenicity, and will be rapidly diluted by body fluids and quickly degraded after being injected into the body. Therefore some adjuvants and suitable delivery systems are often required to promote the maximum immune response. In recent years, extensive research has found that nanoscale vaccines can significantly improve immunological effect. Particularly, nano-carrier vaccines have been continuously used. The main features are that the nano-carrier vaccines can replace adjuvants, and concurrently trigger cellular immunity and humoral immunity, and yield ideal immunological effect especially for relatively weak epitopes, thereby providing a good direction for future vaccine development.
Polysaccharide conjugate vaccines are formed by covalently linking immunogenic polysaccharides to appropriate substrate proteins, and thus the polysaccharide antigens are transformed from T-cell-independent antigens to T-cell-dependent antigens, which enables a long-lasting protective effect in the body. Effective antibodies are produced especially for the elderly, infants and young children. Therefore, polysaccharide conjugate vaccines are considered to be one of the most successful forms of vaccines because of the simultaneous triggering T-cell-dependent and T-cell-independent immune responses. However, polysaccharide conjugate vaccines prepared by the current technology still show weak immune response ability against certain bacteria, which needs to be further improved.
Therefore, on the basis of the current vaccines, if the carrier proteins in the polysaccharide conjugate vaccines can be replaced by protein nanoparticles, the immunological effect will be further improved.
The present inventors have carried out a fusion expression of a known carrier protein naturally present in prokaryotes with a peptide fragment capable of forming a trimer, and further used the glycosylation system to link bacterial polysaccharides therein, to successfully obtain nano level glycoproteins. Animal experiments showed that the nano level glycoproteins have significantly improved the antibody level, bactericidal activity and protective effects compared to single polysaccharide and polysaccharide conjugate vaccine with only pentameric protein. This shows that more promising nanoscale polysaccharide conjugate vaccines can be prepared by biological methods, which provides a direction for the next step of the development of polysaccharide conjugate vaccines.
Fusion Protein
Therefore, in the first aspect, the present invention provides a fusion protein capable of self-assembling into a protein nanoparticle. The fusion protein includes an AB5 toxin B subunit (hereinafter also referred to as B5 or B5 protein) capable of forming a pentamer and a trimerization domain sequence (hereinafter also referred to as Tri or Tri sequence) capable of forming a trimer structure.
For convenience, the fusion protein described above is named B5Tri, where B5 is the B subunit in AB5 toxin from bacteria and can form a pentamer. In some embodiments, the B5 protein is selected from cholera toxin B subunit (CTB), Shiga toxin B subunit (StxB), Escherichia coli heat-labile enterotoxin B subunit (LTB), and Bacillus subtilis toxin B subunit (SubB). In some embodiments, the CTB has an amino acid sequence shown in SEQ ID No. 1, and a nucleotide sequence shown in SEQ ID No. 2; the StxB has an amino acid sequence shown in SEQ ID No. 3, and a nucleotide sequence shown in SEQ ID No. 4; the LTB has an amino acid sequence shown in SEQ ID No. 5, and a nucleotide sequence shown in SEQ ID No. 6; and the SubB has an amino acid sequence shown in SEQ ID No. 7, and a nucleotide sequence shown in SEQ ID No. 8.
AB5 toxin is a common form of microbial toxins in nature, mainly composed of an A subunit and B subunits. These five B subunits form a cyclic pentamer, which is responsible for binding to the surface of a host cell and catalyzing the destruction of the host cell by the A subunit.
CTB is the cholera toxin B subunit, which can specifically bind to the ganglioside GM1 on the surface of most mammals' cells, promote the antigenic protein connected thereto to pass through the mucosal barrier, and at the same time enhance the antigen presentation by dendritic cells (DCs) and other antigen-presenting cells. As such, CTB is a good carrier protein.
StxB is the Shiga toxin B subunit, which possesses powerful immunomodulatory properties, enables identification of exogenous antigens by major histocompatibility complex class I (MHC-I) in antigen-presenting cells, and thus mediates cellular immune response. Therefore, StxB is a very promising non-active and non-toxic vaccine carrier and has been proven to have anti-tumor protective immunity in mice. Furthermore, the ability of StxB to induce cell-mediated immunity also indicates its potential use in the immunoprophylaxis and treatment of infectious diseases.
LTB is the B subunit of Escherichia coli heat-labile enterotoxin, having structure and function similar to CTB. Both can promote immune response through the GM1 receptor. In addition, LTB can also bind to some glycolipids or glycoproteins on the cell surface to promote antigen identification and presentation.
SubB is the Bacillus subtilis toxin B subunit, similar to cholera toxin and heat-labile enterotoxin. SubB can also trigger immune response, promote T cell activation, and facilitate the release of inflammatory factors.
Tri in the B5Tri fusion protein refers to a polypeptide sequence that can form a trimer structure. In some embodiments, the Tri has an amino acid sequence shown in SEQ ID No. 9, and a nucleotide sequence shown in SEQ ID No. 10. This sequence is artificially designed, has no homology with human protein sequence, and can form a trimer under natural conditions.
The present inventors surprisingly found that pentameric proteins in AB5 toxin such as cholera toxin B subunit (CTB), Shiga toxin B subunit (StxB), Escherichia coli heat-labile enterotoxin B subunit (LTB), and Bacillus subtilis toxin B subunit (SubB), when subjected to a fusion expression with Tri sequence, can self-assemble into 10-20 nm fusion protein particles. The fusion protein particles each are composed of a pentamer of B5 carrier protein and a trimer of Tri. Due to the characteristics that pentamer and trimer can be formed concurrently, multiple monomeric proteins can spatially self-assemble into a higher polymer, forming 10-20 nm spherical particles.
In some embodiments, the fusion protein contains the AB5 toxin B subunit and the trimerization domain sequence from N terminus to C terminus.
In some exemplary embodiments, the fusion protein contains an amino acid sequence selected from:
(1) an amino acid sequence consisting of amino acid residues at positions 20 to 172 from the N terminus of the sequence shown in SEQ ID NO. 21;
(2) an amino acid sequence consisting of amino acid residues at positions 20 to 157 from the N terminus of the sequence shown in SEQ ID NO. 23;
(3) an amino acid sequence consisting of amino acid residues at positions 20 to 172 from the N terminus of the sequence shown in SEQ ID NO. 25; and
(4) an amino acid sequence consisting of amino acid residues at positions 20 to 209 from the N terminus of the sequence shown in SEQ ID NO. 27.
Preparing polysaccharide conjugate vaccines by biological methods mainly relies on the relaxed substrate specificity of glycosyltransferases, where the glycosyltransferases, bacterial surface polysaccharides and substrate proteins are subjected to a co-expression in bacteria (generally Escherichia coli), so that the polysaccharides are transferred to the substrate proteins under the catalysis of the glycosyltransferases, and the glycoproteins can be obtained after one step of purification. Specifically, the glycosyltransferase PglL of Neisseria meningitidis has been widely used because it has relaxed substrate specificity and can recognize almost all glycans. Therefore, the fusion protein of the present invention can be further fused with a sequence containing glycosylation sites, as a result, by co-expression with glycosyltransferases, bacterial polysaccharides can be linked to the fusion protein of the present invention to prepare nanoscale polysaccharide conjugate vaccines.
In this regard, in the second aspect, the present invention also provides a fusion protein, which comprises the fusion protein described in the first aspect and a glycosylation sequence containing an O-glycosylation site. The glycosylation sequence can serve as the substrate protein of the glycosyltransferase (such as PglL) in the O-glycosylation system, and the bacterial O-polysaccharide can be transferred to the glycosylation site contained in the glycosylation sequence under the action of the glycosyltransferase.
In some embodiments, the glycosylation sequence is selected from the peptide fragment containing O-glycosylation site of the pilin protein PilE of Neisseria meningitidis. In some embodiments, the O-glycosylation site is the serine at position 63 from the N terminus of PilE. In some embodiments, the peptide fragment containing O-glycosylation site of the pilin protein PilE of Neisseria meningitidis includes at least the serine at position 63 from the N terminus of PilE. In some embodiments, the peptide fragment containing O-glycosylation site of the pilin protein PilE of Neisseria meningitidis is a peptide fragment containing at least the amino acid residues at positions 45 to 73 from the N terminus.
In some embodiments, the glycosylation sequence contains a peptide fragment consisting of amino acid residues at positions 45 to 73 from the N terminus of PilE.
In some embodiments, the glycosylation sequence contains the sequence shown in SEQ ID NO. 29.
In some embodiments, the fusion protein, from N terminus to C terminus, contains the AB5 toxin B subunit, the trimerization domain sequence, and the glycosylation sequence.
In some exemplary embodiments, the fusion protein contains an amino acid sequence selected from:
(1) an amino acid sequence consisting of amino acid residues at positions 20 to 205 from the N terminus of the sequence shown in SEQ ID NO. 21;
(2) an amino acid sequence consisting of amino acid residues at positions 20 to 190 from the N terminus of the sequence shown in SEQ ID NO. 23;
(3) an amino acid sequence consisting of amino acid residues at positions 20 to 205 from the N terminus of the sequence shown in SEQ ID NO. 25; and
(4) an amino acid sequence consisting of amino acid residues at positions 20 to 242 from the N terminus of the sequence shown in SEQ ID NO. 27.
In some embodiments, any two adjacent domains (e.g., AB5 toxin B subunit and trimerization domain sequence, trimerization domain sequence and glycosylation sequence) contained in the fusion protein described in the first or second aspect are optionally linked by peptide linkers. In some embodiments, the peptide linkers include, but not limited to, KK (lysine-lysine), GP (glycine-proline), GPGP (glycine-proline-glycine-proline), GGS (glycine-glycine-serine), GGGS, GGGGS their repetitions and various combinations thereof. In some embodiments, the peptide linker is a flexible amino acid linker containing glycine (G) and serine (S). In some embodiments, the peptide linker is composed of 1-20 amino acids (e.g., 1-15 amino acids, 1-8 amino acids, 2-6 amino acids, or about 4 amino acids). In some exemplary embodiments, the peptide linker has the sequence shown in SEQ ID NO. 30.
In some embodiments, the fusion protein of the first or second aspect may further include a signal peptide, thereby facilitating a secretory expression of the fusion protein of the present invention in a host cell. In some embodiments, the fusion protein of the present invention contains a signal peptide at its N terminus.
The signal peptide inherently possessed by AB5 toxin B subunit can be integrally fused into the fusion protein of the present invention. Alternatively, the signal peptide can be removed, and replaced with a signal peptide of a protein derived from a prokaryotic cell, such as a signal peptide of a secreted protein (for example, outer membrane protein or periplasmic protein (e.g., DsbA)) from Escherichia coli.
In some exemplary embodiments, the signal peptide has the sequence shown in SEQ ID NO. 31.
In some exemplary embodiments, the fusion protein contains an amino acid sequence selected from:
(1) an amino acid sequence consisting of amino acid residues at positions 1 to 205 from the N terminus of the sequence shown in SEQ ID NO. 21;
(2) an amino acid sequence consisting of amino acid residues at positions 1 to 190 from the N terminus of the sequence shown in SEQ ID NO. 23;
(3) an amino acid sequence consisting of amino acid residues at positions 1 to 205 from the N terminus of the sequence shown in SEQ ID NO. 25; and
(4) an amino acid sequence consisting of amino acid residues at positions 1 to 242 from the N terminus of the sequence shown in SEQ ID NO. 27.
In some embodiments, the fusion protein of the first or second aspect may further include a protein tag. Such protein tag is well known in the art, examples of which include, but are not limited to, His, Flag, GST, MBP, HA, Myc, etc., and those skilled in the art know how to select a proper protein tag according to a desired purpose (for example, purification, detection or tracing). In some exemplary embodiments, the fusion protein of the present invention contains a His tag. In some embodiments, the fusion protein of the present invention contains a protein tag at its C terminus.
In some exemplary embodiments, the fusion protein includes the amino acid sequence shown in SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, or SEQ ID NO.
27.
Protein Nanoparticles and Preparation Thereof
The fusion protein of the present invention can self-assemble into nanoparticles after being expressed in cells. The protein nanoparticles have an average particle size of about 10-20 nm, and each of the protein nanoparticles contains or is composed of a pentamer of B5 protein and a trimer of Tri sequence.
Therefore, in another aspect, the present invention further relates to a protein nanoparticle which is obtained by expressing the fusion protein in a host cell containing a nucleotide sequence encoding the fusion protein of the first aspect.
In another aspect, the present invention provides an isolated nucleic acid molecule which contains a nucleotide sequence encoding the fusion protein of the first aspect.
In another aspect, the present invention provides a vector (such as a cloning vector or an expression vector), which contains the isolated nucleic acid molecule as described above. In some embodiments, the vector is, for example, a plasmid, a cosmid, a bacteriophage, and the like.
In another aspect, the present invention provides a host cell, which contains the isolated nucleic acid molecule or the vector as described above. Such host cells include, but are not limited to, prokaryotic cells such as E. coli cells, eukaryotic cells such as yeast cells, insect cells, plant cells, and animal cells (such as mammalian cells, e.g., mouse cells, human cells, etc.). In some embodiments, the host cell is a prokaryotic cell (such as bacterial cells, e.g., E. coli cells).
In another aspect, a method for preparing the fusion protein of the first aspect is provided, including culturing the host cell as described above under conditions that allow protein expression, and recovering the fusion protein from the cultured host cell culture. The fusion protein exists in the form of nanoparticles.
In another aspect, a method for preparing the protein nanoparticles is provided, which includes culturing the host cell as described above, under conditions that allow protein expression, and recovering the nanoparticles from the cultured host cell culture.
Glycoprotein Nanoparticles
When the fusion protein of the present invention contains a glycosylation sequence, by co-expression with glycosyltransferases in bacterial cells, the glycosyltransferases can transfer bacterial polysaccharides to the fusion protein of the present invention, thereby obtaining glycoprotein nanoparticles.
Therefore, in the third aspect, the present invention provides a method for preparing glycoprotein nanoparticles, which includes the following steps:
(1) provide bacterial host cells lacking O-antigen ligase, wherein the deletion of endogenous O-antigen ligase can prevent O-antigen polysaccharides from being catalyzed and transferred by O-antigen ligase to lipid A core polysaccharide to form lipopolysaccharides, as a result, free O-antigen polysaccharide can be produced; and
(2) express the fusion protein and the glycosyltransferase PglL described in the second aspect in the bacterial host cell, thereby producing the target glycoprotein nanoparticle.
In some embodiments, the method further includes: (3) purifying the target glycoprotein nanoparticles. In some embodiments, the target glycoprotein nanoparticles are purified by affinity chromatography and/or molecular sieve. In some embodiments, when the fusion protein contains a protein tag, the method may further include the step of detecting the target glycoprotein nanoparticle by using an antibody specific for the protein tag.
In some embodiments, in step (1), the bacterial host cell lacking O-antigen ligase is provided by knocking out the endogenous O-antigen ligase gene in the bacterial host cell. Herein, “knocking out” in the context of a gene means that a host cell carrying the knockout does not produce a functional protein product of the gene.
Knockout can be performed in a variety of ways including removing all or part of coding sequences, introducing frameshift mutations so that no functional protein (truncated or nonsense sequence) is produced, removing or changing regulatory components (e.g., promoters) so that no gene transcription occurs, and preventing translation by binding to mRNA, and so on. Generally, knockout is carried out at the level of genomic DNA, so that cell progeny also permanently carry the knockout.
In some embodiments, the O-antigen ligase gene is a waaL gene.
In some embodiments, the bacterial host cell is a pathogenic bacterial cell. In some embodiments, the bacterial host cell is a pathogenic gram-negative bacterial (gram-negative pathogenic bacterial) cell. In some embodiments, the bacterial host cell is selected from Shigella, Escherichia coli, Shigella dysenteriae, Salmonella paratyphi A, and Vibrio cholerae.
In some embodiments, the fusion protein and PglL of the second aspect are co-expressed in the same bacterial host cell. The co-expression is optionally performed by expressing each protein on the same or different expression vectors. The bacterial host cell can be co-transfected with two expression vectors, where the first vector encodes the fusion protein and the second vector encodes the PglL. Alternatively, a single vector that can respectively encode and express the fusion protein and the PglL can be used.
In some embodiments, step (2) includes the following steps:
(2a) introducing a first nucleotide sequence encoding the fusion protein of the second aspect and a second nucleotide sequence encoding the PglL into the bacterial host cell, wherein the first nucleotide sequence and the second nucleoside sequence are provided on the same or different expression vectors (for example, prokaryotic expression vector);
(2b) culturing the bacterial host cell (for example, under a condition that allows protein expression); and
(2c) recovering the target glycoprotein nanoparticles from a cell culture (such as a cell lysate).
In the fourth aspect, the present invention provides a glycoprotein nanoparticle, which includes a protein-polysaccharide conjugate. The conjugate is formed by coupling a bacterial O-polysaccharide and the fusion protein described in the second aspect, and the bacterial O-polysaccharide is coupled to the fusion protein of the second aspect through the O-glycosylation site in the glycosylation sequence of the fusion protein.
In some embodiments, the bacterial O-polysaccharide is selected from pathogenic bacteria O-polysaccharide.
In some embodiments, the bacterial O-antigen polysaccharide is selected from Shigella O polysaccharide, Escherichia coli O157O polysaccharide, Shigella dysenteriae O polysaccharide, Salmonella paratyphi A O polysaccharide, and Vibrio cholerae O polysaccharide.
In some embodiments, in the glycoprotein nanoparticle, the AB5 toxin B subunit in the fusion protein exists in a form of pentamer, and the trimerization domain sequence in the fusion protein exists in a form of trimer.
In some embodiments, the average particle size of the glycoprotein nanoparticle is about 25-50 nm.
In some embodiments, the glycoprotein nanoparticle is prepared by the method described in the third aspect.
Application of Glycoprotein Nanoparticles
In the fifth aspect, the present invention provides an immunogenic composition or vaccine, including: (i) an immunologically effective dose of the glycoprotein nanoparticle described in the fourth aspect, or (ii) an immunologically effective dose of a mixture including the fusion protein described in the first or second aspect or the protein nanoparticle formed by the fusion protein, and a bacterial polysaccharide (for example, bacterial O-polysaccharide). Preferably, the immunogenic composition or vaccine does not contain an adjuvant.
In some embodiments, the immunogenic composition or vaccine is used to induce an immune response (such as an antibody response) to a bacterial O-polysaccharide in a subject, and/or to prevent and/or treat bacterial infections (such as infections caused by bacteria expressing O-polysaccharides).
In some embodiments, the bacteria are pathogenic bacteria. In some embodiments, the bacteria are gram-negative bacteria. In some embodiments, the bacteria are pathogenic gram-negative bacteria (gram-negative pathogenic bacteria). In some embodiments, the bacteria are selected from Shigella, Escherichia coli, Shigella dysenteriae, Salmonella paratyphi A, and Vibrio cholerae.
In some embodiments, the bacterial O-polysaccharide is selected from pathogenic bacteria O-polysaccharide. In some embodiments, the bacterial O-antigen polysaccharide is selected from Shigella O polysaccharide, Escherichia coli O157O polysaccharide, Shigella dysenteriae O polysaccharide, Salmonella paratyphi A O polysaccharide, and Vibrio cholerae O polysaccharide.
In some embodiments, the immunogenic composition or vaccine further includes a pharmaceutically acceptable carrier and/or excipient.
The glycoprotein nanoparticle, or the immunogenic composition or vaccine of the present invention can be in any form known in the medical field, for example, it can be tablet, pill, suspension, emulsion, solution, gel, capsule, powder, granule, elixir, lozenge, suppository, injection (including injection solutions, freeze-dried powders), inhalant, spray and other forms. A skilled person should understand that a preferred dosage form depends on a desired method of administration and therapeutic use. In some embodiments, the glycoprotein nanoparticle, or the immunogenic composition or vaccine of the present invention is an injection preparation, such as an injection solution, a sterile powder for injection, or a concentrated solution for injection.
The glycoprotein nanoparticle, or the immunogenic composition or vaccine of the present invention can be administered by any suitable method known in the art, including but not limited to oral, rectal, parenteral or topical administration. In some embodiments, the glycoprotein nanoparticle, or the immunogenic composition or vaccine of the present invention is parenterally administered, for example, subcutaneous injection, intravenous injection, intraperitoneal injection, intramuscular injection, intrasternal injection and introduction. The dosage form for parenteral administration may be an injection preparation, including an injection solution, a sterile powder for injection, or a concentrated solution for injection. In addition to active ingredients, the injection preparation may contain a pharmaceutically acceptable carrier such as sterile water, Ringer's solution and isotonic sodium chloride solution. Furthermore, appropriate additives such as an antioxidant, a buffering agent and a bacteriostatic agent can be added based on the properties of drugs.
In addition, other carrier materials and administration methods known in the pharmaceutical field can also be used. The glycoprotein nanoparticle, or the immunogenic composition or vaccine of the present invention can be prepared by any known pharmaceutical process, such as effective preparation and administration method.
In the sixth aspect, the present invention provides a use of the glycoprotein nanoparticle of the fourth aspect or the immunogenic composition or vaccine of the fifth aspect in preparing a product for inducing a specific immune response (for example, an antibody response) to a bacterial O-polysaccharide in a subject and/or for a prevention and/or treatment of bacterial infections (for example, infections caused by bacteria expressing O-polysaccharides). In some embodiments, the product is a vaccine.
In some embodiments, the bacteria are pathogenic bacteria. In some embodiments, the bacteria are gram-negative bacteria. In some embodiments, the bacteria are pathogenic gram-negative bacteria (gram-negative pathogenic bacteria). In some embodiments, the bacteria are selected from Shigella, Escherichia coli, Shigella dysenteriae, Salmonella paratyphi A, and Vibrio cholerae.
In some embodiments, the bacterial O-polysaccharide is selected from pathogenic bacteria O-polysaccharide. In some embodiments, the bacterial O-antigen polysaccharide is selected from Shigella O polysaccharide, Escherichia coli O157O polysaccharide, Shigella dysenteriae O polysaccharide, Salmonella paratyphi A O polysaccharide, and Vibrio cholerae O polysaccharide.
In the seventh aspect, the present invention further provides a method for inducing a specific immune response (such as an antibody response) to bacterial O-polysaccharides in a subject and/or for preventing and/or treating bacterial infections (such as infections caused by bacteria expressing O-polysaccharides), which includes: administering a subject in need with an immunologically effective dose of the glycoprotein nanoparticle according to the fourth aspect or the immunogenic composition or vaccine according to the fifth aspect.
In some embodiments, the bacteria are pathogenic bacteria. In some embodiments, the bacteria are gram-negative bacteria. In some embodiments, the bacteria are pathogenic gram-negative bacteria (gram-negative pathogenic bacteria). In some embodiments, the bacteria are selected from Shigella, Escherichia coli, Shigella dysenteriae, Salmonella paratyphi A, and Vibrio cholerae.
In some embodiments, the bacterial O-polysaccharide is selected from pathogenic bacteria O-polysaccharide. In some embodiments, the bacterial O-antigen polysaccharide is selected from Shigella O polysaccharide, Escherichia coli O157O polysaccharide, Shigella dysenteriae O polysaccharide, Salmonella paratyphi A O polysaccharide, and Vibrio cholerae O polysaccharide.
In some embodiments, the subject is a mammal, such as human.
The present invention further includes the following exemplary embodiments:
Item 1. A fusion protein capable of self-assembling into a protein nanoparticle. The fusion protein includes a bacterium-derived carrier protein B5 capable of forming a pentamer and a polypeptide sequence Tri capable of forming a trimer structure.
Item 2. The fusion protein according to the item 1, where the B5 protein is selected from cholera toxin B subunit (CTB), Shiga toxin B subunit (StxB), Escherichia coli heat-labile enterotoxin B subunit (LTB), and Bacillus subtilis toxin B subunit (SubB). Preferably, the CTB has an amino acid sequence shown in SEQ ID No. 1, and a nucleotide sequence shown in SEQ ID No. 2; the StxB has an amino acid sequence shown in SEQ ID No. 3, and a nucleotide sequence shown in SEQ ID No. 4; the LTB has an amino acid sequence shown in SEQ ID No. 5, and a nucleotide sequence shown in SEQ ID No. 6; and the SubB has an amino acid sequence shown in SEQ ID No. 7, and a nucleotide sequence shown in SEQ ID No. 8.
Item 3. The fusion protein according to the item 1 or 2, where the Tri is a polypeptide sequence capable of forming a trimer structure. Preferably, the Tri has an amino acid sequence shown in SEQ ID No. 9, and a nucleotide sequence shown in SEQ ID No. 10.
Item 4. The fusion protein according to any one of the items 1-3 has an amino acid sequence shown at positions 20 to 172 of SEQ ID No. 12, positions 20 to 157 of SEQ ID No. 14, positions 20 to 172 of SEQ ID No. 16, or positions 20 to 209 of SEQ ID No. 18.
Item 5. The fusion protein according to any one of the items 1-4 can self-assemble into a 10-20 nm nanoparticle after being expressed, and is composed of a pentamer of B5 protein and a trimer of Tri.
Item 6. The fusion protein according to any one of the items 1-4 further includes a peptide fragment containing O-glycosylation site of the pilin protein PilE of Neisseria meningitidis. Preferably, the peptide fragment is a peptide fragment of PilE starting from the serine at position 45 (S45) of the N terminal to the lysine at position 73 (K73). Preferably, the amino acid sequence of the fusion protein is shown in SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, or SEQ ID NO. 21.
Item 7. A glycoprotein nanoparticle includes a protein-polysaccharide conjugate. The conjugate is formed by coupling a bacterial O-polysaccharide and the fusion protein described in the item 6, and the bacterial polysaccharide is coupled to the fusion protein of the item 6 through the glycosylation site 4573. Preferably, the bacterial O-antigen polysaccharide is selected from Shigella O polysaccharide, Escherichia coli O157O polysaccharide, Shigella dysenteriae O polysaccharide, Salmonella paratyphi A O polysaccharide, and Vibrio cholerae O polysaccharide.
Item 8. The glycoprotein nanoparticle according to item 7 has a size of about 25-50 nm.
Item 9. A method for preparing the glycoprotein nanoparticle according to the item 7 or 8 includes the following steps:
1) constructing a host bacterium lacking O-antigen ligase;
2) construct a co-expression vector of the fusion protein described in the item 6 and glycosyltransferase PglL, and transferring into the above host bacterium to induce expression; and
3) purifying the target glycoprotein nanoparticle, preferably, purifying the target glycoprotein nanoparticle by affinity chromatography and molecular sieve.
Item 10. Application of the glycoprotein nanoparticle according to the item 7 or 8 in a product for producing a specific antibody to a bacterial polysaccharide in an animal. Preferably, the product is a vaccine.
Item 11. An immunogenic composition for inducing an immune response to a bacterial polysaccharide, where the immunogenic composition includes an immunologically effective dose of the glycoprotein nanoparticle according to the item 7 or 8. Preferably, the immunogenic composition does not contain an adjuvant.
Item 12. A vaccine for inducing an immune response to a bacterial polysaccharide, where the vaccine includes an immunologically effective dose of the fusion protein according to any one of the items 1-6 and a bacterial polysaccharide, or the glycoprotein nanoparticle according to the item 7 or 8. Preferably, the vaccine does not contain an adjuvant.
In the present invention, unless otherwise specified, the scientific and technical terms used herein have the meanings commonly understood by those skilled in the art. In addition, the microbiology, the operating steps adopted herein associated with microbiology, immunology, biochemistry, nucleic acid chemistry and the like are all routine steps widely used in the corresponding fields. At the same time, in order to better understand the present invention, definitions and explanations of related terms are provided below.
As used herein, the term “O-polysaccharide” refers to the outermost part of lipopolysaccharide, which is composed of dozens of identical oligosaccharide units. O-polysaccharide has antigenic properties, so it is also called O-antigen. O-antigen is a bacterial antigen of the specific polysaccharide of gram-negative bacteria.
As used herein, the term “AB5 toxin B subunit” can be used interchangeably with “B5” or “B5 protein”. AB5 toxin produced by bacteria is a proteinaceous exotoxin produced by toxin-producing bacteria and secreted out of bacterial cells. AB5 toxin is composed of one toxic active subunit (A subunit) and five binding subunits (B subunit) with cell binding activity. AB5 toxin B subunit can self-assemble into a pentamer.
As used herein, the term “vector” refers to a nucleic acid delivery vehicle into which a polynucleotide can be inserted. When the vector enables an expression of the protein encoded by the inserted polynucleotide, the vector is called an expression vector. The vector can be introduced into a host cell through transformation, transduction or transfection, so that genetic material elements that are carried can be expressed in the host cell. The vector is well known to those skilled in the art, including but not limited to: plasmids; phagemids; cosmids; artificial chromosomes, such as yeast artificial chromosomes (YAC), bacterial artificial chromosomes (BAC) or P1-derived artificial chromosomes (PAC); bacteriophages such as lambda (λ) phages or M13 phages and animal viruses. Animal viruses that can be used as a vector include, but are not limited to, retroviruses (including lentiviruses), adenoviruses, adeno-associated viruses, herpes viruses (such as herpes simplex virus), poxviruses, baculoviruses, papillomavirus, and papovaviruses (such as SV40). A vector can contain a variety of elements that control expression, including but not limited to promoter sequences, transcription initiation sequences, enhancer sequences, selection elements, and reporter genes. In addition, the vector may also contain a replication origin.
As used herein, the term “host cell” refers to a cell where a vector can be introduced, which includes, but is not limited to, prokaryotic cells such as Escherichia coli or Bacillus subtilis, fungal cells such as yeast cells or Aspergillus, insect cells such as Drosophila S2 cells or Spodoptera frugiperda (Sf9), or animal cells such as fibroblasts, Chinese hamster ovary (CHO) cells, COS cells, NSO cells, HeLa cells, BHK cells, HEK 293 cells or human cells.
The twenty conventional amino acids involved herein are written in a common manner, referring to, for example, Immunology-A Synthesis (2nd Edition, E. S. Golub and D. R. Gren, Eds., Sinauer Associates, Sunderland, Mass. (1991)), which is incorporated herein by reference. In the present invention, the terms “polypeptide” and “protein” have the same meaning and can be used interchangeably. Moreover, in the present invention, amino acids are usually represented by one-letter and three-letter abbreviations that are well known in the art. For example, alanine can be represented as A or Ala.
As used herein, the term “pharmaceutically acceptable carrier and/or excipient” refers to a carrier and/or excipient that is pharmacologically and/or physiologically compatible with a subject and an active ingredient, which is well known in the art (see, for example, Remington's Pharmaceutical Sciences. Edited by Gennaro A R, 19th ed. Pennsylvania: Mack Publishing Company, 1995), and includes, but is not limited to: pH adjusters, surfactants, ionic strength enhancers, agents for maintaining osmotic pressure, agents for delaying absorption, diluents, preservatives, stabilizers, etc. For example, the pH adjusters include, but are not limited to, a phosphate buffer solution. The surfactants include, but are not limited to, cationic, anionic or nonionic surfactants, such as Tween-80. The ionic strength enhancers include, but are not limited to, sodium chloride. The agents for maintaining osmotic pressure include, but are not limited to, sugar, NaCl and analogues thereof. The Agents for delaying absorption include, but are not limited to, monostearate and gelatin. The diluents include, but are not limited to, water, aqueous buffers (such as buffered saline), alcohols and polyols (such as glycerol), etc. The preservatives include, but are not limited to, various antibacterial agents and antifungal agents, such as thimerosal, 2-phenoxyethanol, paraben, chlorobutanol, phenol, sorbic acid and the like. The stabilizers have the meaning commonly understood by those skilled in the art, which can stabilize the desired activity of the active ingredient in a drug, and include, but are not limited to, sodium glutamate, gelatin, SPGA, sugars (such as sorbitol, mannitol, starch, sucrose, lactose, dextran, or glucose), amino acids (such as glutamic acid, glycine), proteins (such as dried whey, albumin or casein) or their degradation products (such as lactalbumin hydrolysate), etc.
As used herein, the term “immunologically effective dose” is an amount that is sufficient to provide a protective immune response to bacterial infections (for example, infections caused by gram-negative pathogenic bacteria) or to induce the body to produce a protective immune response to antigens (for example, bacterial polysaccharide antigen). In some embodiments, the amount should be sufficient to significantly prevent the likelihood or reduce the severity of bacterial infections (for example, infections caused by gram-negative pathogenic bacteria). The immunologically effective dose of the glycoprotein nanoparticle, or the immunogenic composition or vaccine of the present invention may vary with the overall state of a patient's own immune system, the patient's general conditions (such as age, weight, and gender), the method of drug administration, other concurrently used treatments and other factors.
Beneficial Effects
The present inventors discovered for the first time that nanoscale glycoprotein can be obtained by subjecting B5 toxin B subunit and a peptide capable of forming a trimer to a fusion expression and linking a bacterial polysaccharide therein by a glycosylation system. The nanoscale glycoprotein is significantly superior to a single polysaccharide antigen and a polysaccharide conjugate vaccine that only binds to the B5 toxin B subunit carrier protein in terms of the level of antibody induced, bactericidal activity and protective effect. Therefore, the nanoscale glycoprotein of the present invention is particularly suitable for inducing a specific immune response to bacterial O-polysaccharides, and for preventing and/or treating bacterial infections, possessing great clinical value.
Sequence Information
The experimental methods in the following embodiments, unless otherwise specified, are all conventional methods. The materials, reagents, etc. used in the following embodiments are commercially available unless otherwise specified.
The non-toxic Shigella flexneri 301DWP lacking O-antigen ligase gene waal in the following embodiments was obtained by modifying the wild strain of Shigella flexneri 2a 301 (S. flexneri 2a 301) (Jin Q et al. Nucleic Acids Res. 2002 Oct. 15; 30(20):4432-41). The public can reach it from the Institute of Bioengineering, Academy of Military Medicine, PLA Academy of Military Sciences. The biological material was only used for repeating the relevant experiments of the present invention, and cannot be used for other purposes.
pET28a(+) in the following embodiments was purchased from Novagen.
HRP-labeled Anti-His antibody in the following embodiments was an Abmart product, with a product number of M20020.
Rabbit-derived Freund's type II serum in the following embodiments was a product of Denka Seiken Co., Ltd., with a number of 210227.
HRP-labeled goat anti-rabbit in the following embodiments was a product of TransGen Biotech Co., LTD, with a number of HS-101-01.
HRP-labeled donkey anti-mouse IgG, goat anti-mouse IgG1, IgG2a, IgG2b, and IgG3 in the following embodiments were purchased from Abcam, with numbers of ab6820, ab97240, ab97245, ab97250, and ab97260, respectively.
Aluminum hydroxide adjuvant Rehydragel LV in the following embodiments was purchased from General Chemical Company, with a number of 203120070602.
Complement in the following embodiments was purchased from Pel-Freez LLC, with a number of 31061-3.
1) Construction of B5Tri Fusion Protein Expression Vector
In the present embodiment, a vector for expressing the fusion protein (B5Tri) including B5 protein and Tri sequence was constructed, where the B5 protein included cholera toxin B subunit (CTB), Shiga toxin B subunit (StxB), Escherichia coli heat-labile enterotoxin B subunit (LTB), and Bacillus subtilis toxin B subunit (SubB), and the Tri sequence was shown in SEQ ID NO. 9. The construction method was as follows:
CTBTri expression vector construction: According to the amino acid sequence of cholera toxin B subunit (X76390.1) published by GeneBack, a signal peptide (first 21 amino acids) was replaced with a DsbA signal peptide (SEQ ID NO. 31), and Tri sequence was fused at the C terminus of CTB to construct CTB fusion protein CTBTri. In the CTBTri expression cassette, the expression of CTBTri was initiated by the tac promoter. The expression cassette was named tacCTBTri, and had a nucleotide sequence shown in SEQ ID No. 11, wherein the nucleotides at positions 103 to 131 were the tac promoter sequence, the nucleotides at positions 178 to 729 were the coding sequence of CTBTri (CTBTri protein sequentially included DsbA signal peptide, CTB, Tri and His tag from N terminal to C terminal). Specifically from the 5′ end, the nucleotides at positions 178 to 234 were the signal peptide sequence, the nucleotides at positions 235 to 543 were the CTB coding sequence, and the nucleotides at positions 556 to 693 were the Tri sequence. The amino acid sequence of the CTBTri protein was shown in SEQ ID No. 12, in which from the N terminus, the nucleotides at positions 1 to 19 were the DsbA signal peptide sequence, the nucleotides at positions 20 to 122 were the CTB amino acid sequence, and the nucleotides at positions 123 to 126 were a flexible linker, and the nucleotides at positions 127 to 172 were the Tri sequence.
StxBTri expression vector construction: In the StxBTri expression cassette, the expression of StxBTri was initiated by the tac promoter. The expression cassette was named tacStxBTri, and had a nucleotide sequence shown in SEQ ID No. 13, wherein the nucleotides at positions 103 to 131 were the tac promoter sequence, and the nucleotides at positions 178 to 684 were the coding sequence of StxBTri (StxBTri protein sequentially included DsbA signal peptide, StxB, Tri, and His tag from N terminal to C terminal). Specifically from the 5′ end, the nucleotides at positions 178 to 234 were the signal peptide sequence, the nucleotides at positions 235 to 498 were the StxB coding sequence, and the nucleotides at positions 511 to 648 were the Tri sequence. The amino acid sequence of the StxBTri protein was shown in SEQ ID No. 14, in which from the N terminus, the nucleotides at positions 1 to 19 were the DsbA signal peptide sequence, the nucleotides at positions 20 to 107 were the StxB amino acid sequence, the nucleotides at positions 108 to 111 were a flexible linker, and the nucleotides at positions 112 to 157 were the Tri sequence.
LTBTri expression vector construction: In the LTBTri expression cassette, the expression of LTBTri was initiated by the tac promoter. The expression cassette was named tacLTBTri, and had a nucleotide sequence shown in SEQ ID No. 15, wherein the nucleotides at positions 103 to 131 were the tac promoter sequence, and the nucleotides at positions 178 to 729 were the coding sequence of LTBTri (LTBTri protein sequentially included DsbA signal peptide, LTB, Tri, and His tag from N terminal to C terminal). Specifically from the 5′ end, the nucleotides at positions 178 to 234 were the signal peptide sequence, the nucleotides at positions 235 to 543 were the LTB coding sequence, and the nucleotides at positions 556 to 693 were the Tri sequence. The amino acid sequence of the LTBTri protein was shown in SEQ ID No. 16, in which from the N terminus, the nucleotides at positions 1 to 19 were the DsbA signal peptide sequence, the nucleotides at positions 20 to 122 were the LTB amino acid sequence, the nucleotides at positions 123 to 126 were a flexible linker, and the nucleotides at positions 127 to 172 were the Tri sequence.
SubBTri expression vector construction: In the SubBTri expression cassette, the expression of SubBTri was initiated by the tac promoter. The expression cassette was named tacSubBTri, and had a nucleotide sequence shown in SEQ ID No. 17, wherein the nucleotides at positions 103 to 131 were the tac promoter sequence, and the nucleotides at positions 178 to 840 were the coding sequence of SubBTri (SubBTri protein sequentially included DsbA signal peptide, SubB, Tri, and His tag from N terminal to C terminal). Specifically from the 5′ end, the nucleotides at positions 178 to 234 were the signal peptide sequence, the nucleotides at positions 235 to 654 were the SubB coding sequence, and the nucleotides at positions 667 to 804 were the Tri sequence. The amino acid sequence of the SubBTri protein was shown in SEQ ID No. 18, in which from the N terminus, the nucleotides at positions 1 to 19 were the DsbA signal peptide sequence, the nucleotides at positions 20 to 159 were the SubB amino acid sequence, the nucleotides at positions 160 to 163 were a flexible linker, and the nucleotides at positions 164 to 209 were the Tri sequence.
The DNA molecules shown in SEQ ID No. 11, SEQ ID No. 13, SEQ ID No. 15, and SEQ ID No. 17 were respectively digested with XbaI and XhoI to obtain gene fragments. pET28a(+) was digested with XbaI and XhoI to obtain large fragments of the vector. The gene fragments and the large fragments of the vector were ligated to obtain recombinant vectors respectively containing the DNA molecules shown in SEQ ID No. 11, SEQ ID No. 13, SEQ ID No. 15, and SEQ ID No. 17, and the recombinant vectors were named pET28-tacB5Tri (B5 was CTB, StxB, LTB, and SubB, respectively).
2) Construction and Expression of B5Tri Expression Strains
The pET28-tacB5Tri vector was transformed into BL21 competence, coated with LB solid medium containing kanamycin at a final concentration of 50 μg/mL, and subjected to a positive clone to obtain BL21/pET28-tacB5Tri. The BL21/pET28-tacB5Tri was selected and inoculated in LB medium containing kanamycin at a final concentration of 50 μg/mL for culture at 37° C. and 220 rpm for 10 h, and then transferred to 5 mL of LB medium containing kanamycin at a final concentration of 50 μg/mL for culture at 37° C. and 220 rpm until an OD600 reached about 0.6, followed by adding IPTG with a final concentration of 1 mM, reducing a temperature to 30° C., and inducing for 10 h.
1 mL of each bacterial solution induced at 30° C. for 10 h was taken and centrifuged to collect bacterial cells. The bacterial cells were suspended with 1× reduction buffer (50 mM pH 6.8 Tris-HCl, 1.6% SDS, 0.02% bromophenol blue, 8% glycerol, 20 mM DTT), and underwent a boiling water bath for 10 min and a 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). After the electrophoresis, the proteins were transferred to poly (vinylidene fluoride) (PVDF) membrane at a constant voltage of 20 V for 1 h with Bio-Lab semi-dry transfer apparatus. The protein expression bands were detected using mouse-derived HRP-Anti-His tag monoclonal antibodies.
The BL21/pET28-tacB5Tri was inoculated in LB medium containing kanamycin at a final concentration of 50 μg/mL for culture at 37° C. and 220 rpm for 10 h, and then transferred to 5 L of LB medium for culture at 37° C. and 220 rpm until an OD600 reached about 0.6, followed by adding IPTG with a final concentration of 1 mM, reducing a temperature to 30° C., and inducing for 10 h.
Sample treatment: bacterial cells obtained above after an induction at 30° C. for 10 h were taken and added with 400 mL of a loading buffer (20 mM pH 7.5 Tris-HCl, 0.2 M NaCl, 10 mM imidazole), ultrasonically broken (ultrasound worked for 3 s and paused for 5 s, with cumulative ultrasonic time of 30 min), and centrifuged at 12000 g to collect a supernatant.
Sample purification: a column bed was first washed with 0.5 M NaOH aqueous solution for at least 3 bed volumes, and then deionized water was used to adjust pH to neutral. Subsequently, 0.5 M NiSO4 aqueous solution was used to equilibrate at least 3 bed volumes, and then B1 solution (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 500 mM imidazole) was used to equilibrate at least one bed volume, and finally Al solution (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 10 mM imidazole) was used to equilibrate at least 3 bed volumes, each of the above was performed at a flow rate of 4 mL/min. A sample was loaded from an A pipeline, washed with Al solution (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 10 mM imidazole) to remove unbound proteins until the ultraviolet absorption (280 nm) was close to 0 mAU, and finally eluted with 100% B1 (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 500 mM imidazole). 30 mL of eluate was collected to obtain a purified sample, and then the purified sample passed through a molecular sieve (superdex 200) with a mobile phase of 1×PBS, pH 7.4.
Four fusion proteins (CTBTri, StxBTri, LTBTri, SubBTri) were analyzed by Coomassie brilliant blue staining after passing through molecular sieves (
3.1.1 Construction of Neisseria meningitidis glycosyltransferase PglL expression vector: the amino acid sequence of the Neisseria meningitidis glycosyltransferase PglL (GeneBank: JN200826.1) was shown in SEQ ID No. 19, and its coding sequence included the nucleotides at positions 180 to 1994 of SEQ ID No. 20. The nucleotides at positions 1 to 6 of SEQ ID No. 20 were the XbaI recognition site, and the nucleotides at positions 105 to 2240 of SEQ ID No. 20 were the sequence of the PglL expression cassette. In the PglL expression cassette, the expression of PglL was initiated by the tac promoter, and the expression cassette was named tacpglL. Specifically in SEQ ID No. 20, the nucleotides at positions 105 to 133 were the tac promoter sequence, the nucleotides at positions 180 to 1994 were the coding sequence of Neisseria meningitidis glycosyltransferase PglL, the nucleotides at positions 2475 to 2480 were the SacI recognition sequence, and the nucleotides at positions 2486 to 2491 were the XhoI recognition site.
The DNA molecule shown in SEQ ID No. 20 was digested with XbaI and XhoI to obtain gene fragments. pET28a(+) was digested with XbaI and XhoI to obtain large fragments of the vector. The gene fragments and the large fragments of the vector were ligated to obtain a recombinant vector containing the DNA molecule shown in SEQ ID No. 20, and the recombinant vector was named pET28-tacpglL.
3.1.2 Fusion of B5Tri sequence and O-glycosylation site (B5Tri4573): PilE was the pilin of Neisseria meningitidis. In Neisseria meningitidis, PilE can be 0-glycosylated under the catalysis of glycosyltransferase PglL. The glycosylation site was the serine at position 63 of the PilE. In order to obtain the glycosylation sequence, 29 amino acids S45-K73, from the serine (S45) at position 45 of the N terminal of the PilE to the lysine (K73) at position 73, were intercepted and fused to the C terminus of B5Tri; at the same time, in order to avoid steric hindrance effect between B5 and Tri peptide fragment, the B5 and Tri peptide fragment were connected by 4 flexible amino acids.
The amino acid sequence of CTBTri4573 was shown in SEQ ID No. 21, and the gene sequence was shown in positions 178 to 816 of SEQ ID No. 22. In SEQ ID No. 22, the nucleotides at positions 1 to 6 were the XbaI recognition site, the nucleotides at positions 103 to 131 were the tac promoter sequence, the nucleotides at positions 178 to 792 were the coding sequence of CTBTri4573, the nucleotides at positions 793 to 798 were the XhoI recognition sequence, and the nucleotides at positions 799 to 816 were the His tag.
The amino acid sequence of StxBTri4573 was shown in SEQ ID No. 23, and the gene sequence was shown in positions 178 to 771 of SEQ ID No. 24. In SEQ ID No. 24, the nucleotides at positions 1 to 6 were the XbaI recognition site, the nucleotides at positions 103 to 131 were the tac promoter sequence, the nucleotides at positions 178 to 747 were the coding sequence of StxBTri4573, the nucleotides at positions 748 to 753 were the XhoI recognition sequence, and the nucleotides at positions 754 to 771 were the His tag.
The amino acid sequence of LTBTri4573 was shown in SEQ ID No. 25, and the gene sequence was shown in positions 178 to 816 of SEQ ID No. 26. In SEQ ID No. 26, the nucleotides at positions 1 to 6 were the XbaI recognition site, the nucleotides at positions 103 to 131 were the tac promoter sequence, the nucleotides at positions 178 to 792 were the coding sequence of LTBTri4573, the nucleotides at positions 793 to 798 were the XhoI recognition sequence, and the nucleotides at positions 799 to 816 were the His tag.
The amino acid sequence of SubBTri4573 was shown in SEQ ID No. 27, and the gene sequence was shown in positions 178 to 927 of SEQ ID No. 28. In SEQ ID No. 28, the nucleotides at positions 1 to 6 were the XbaI recognition site, the nucleotides at positions 103 to 131 were the tac promoter sequence, the nucleotides at positions 178 to 903 were the coding sequence of SubBTri4573, the nucleotides at positions 904 to 909 were the XhoI recognition sequence, and the nucleotides at positions 910 to 927 were the His tag.
The DNA molecules shown in SEQ ID No. 22, SEQ ID No. 24, SEQ ID No. 26, and SEQ ID No. 28 were respectively digested with XbaI and XhoI to obtain gene fragments. pET28a(+) was digested with XbaI and XhoI to obtain large fragments of the vector. The gene fragments and the large fragments of the vector were ligated to obtain recombinant vectors, and the recombinant vectors were named pET28-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively).
The specific method for constructing B5Tri4573 glycosylation expression vector was as follows:
Primers SacI-UP (SEQ ID NO. 32) and XhoI-Down (SEQ ID NO. 33) were respectively used to amplify pET28-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively) to obtain the corresponding amplification products, and the amplification products were digested with SacI and XhoI to obtain DNA fragments. pET28-tacpglL was digested with SacI and XhoI to obtain large fragments of the vector. The gene fragments were connected to the large fragments of the vector to obtain recombinant plasmids, named pET28-tacpglL-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively), in which the expression cassette (i.e., tacB5Tri4573) composed of the coding gene of B5Tri4573 was located downstream of the pglL expression cassette (tacpglL). The recombinant plasmids were sent for sequencing, and the results were all correct.
The attenuated Shigella 301DWP where O-antigen ligase was knocked out was inoculated into LB liquid medium. Since the bacterium lacked O-antigen ligase, free O-antigen can be produced. After overnight culture at 30° C., 1 ml of culture solution was transferred to 100 mL of low-salt LB liquid medium for culture at 30° C. until an OD600 reached 0.6. Subsequently, bacterial cells were collected by centrifugation, washed four times with a 10 vol % sterile aqueous glycerol solution, and finally resuspended with 400 uL of the 10 vol % sterile aqueous glycerol solution to obtain 301DWP competent cells for transformation by electroporation, which were sub-packed for use.
The plasmids pET28-tacpglL-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively) were transformed by electroporation into the 301DWP competent cells obtained in 3.2 above, coated with LB solid medium containing kanamycin at a final concentration of 50 μg/mL, and subjected to a positive clone to obtain 301DWP/pET28-tacpglL-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively).
301DWP/pET28-tacpglL-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively) were selected for monoclone, and inoculated in LB medium containing kanamycin at a final concentration of 50 μg/mL for culture at 37° C. until an OD600 reached approximately 0.6, followed by adding IPTG having a final concentration of 1 mM, reducing a temperature to 30° C., and inducing for 10 h.
Next day, 1 mL of each bacterial solution induced at 30° C. for 10 h above was taken and centrifuged to collect bacterial cells. The bacterial cells were suspended with 1× reduction buffer (50 mM pH 6.8 Tris-HCl, 1.6% SDS, 0.02% bromophenol blue, 8% glycerol, 20 mM DTT), and underwent a boiling water bath for 10 min and a 12% SDS-PAGE. After the electrophoresis, the proteins were transferred to PVDF membrane at a constant voltage of 20 V for 1 h with Bio-Lab semi-dry transfer apparatus, detected by using mouse-derived HRP-Anti-His tag monoclonal antibodies, the results were shown in
The 301DWP/pET28-tacpglL-tacB5Tri4573 (B5 was CTB, StxB, LTB, and SubB, respectively) were inoculated in LB medium containing kanamycin at a final concentration of 50 μg/mL for culture at 37° C. and 220 rpm for 10 h, and then transferred to 5 L of LB medium for culture at 37° C. and 220 rpm until an OD600 reached about 0.6, followed by adding IPTG with a final concentration of 1 mM, reducing a temperature to 30° C., and inducing for 10 h.
Sample treatment: bacterial cells obtained above after an induction at 30° C. for 10 h were taken and added with 400 mL of a loading buffer (20 mM pH 7.5 Tris-HCl, 0.2 M NaCl, 10 mM imidazole), ultrasonically broken (ultrasound worked for 3 s and paused for 5 s, with cumulative ultrasonic time of 30 min), and centrifuged at 12000 g to collect a supernatant.
Sample purification: a column bed was first washed with 0.5 M NaOH aqueous solution for at least 3 bed volumes, and then deionized water was used to adjust pH to neutral. Subsequently, 0.5 M NiSO4 aqueous solution was used to equilibrate at least 3 bed volumes, and then B1 solution (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 500 mM imidazole) was used to equilibrate at least one bed volume, and finally Al solution (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 10 mM imidazole) was used to equilibrate at least 3 bed volumes, each of the above was performed at a flow rate of 4 mL/min. A sample was loaded from an A pipeline, washed with Al solution (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 10 mM imidazole) to remove unbound proteins until the ultraviolet absorption (280 nm) was close to 0 mAU, and finally eluted with 100% B1 (20 mM pH 7.5 Tris-HCl, 0.5 M NaCl, 500 mM imidazole). 30 mL of eluate was collected to obtain a purified sample, and then the purified sample passed through a molecular sieve (superdex 200) with a mobile phase of 1×PBS, pH 7.4.
Four glycoproteins (CTBTri4573-OPS, StxBTri4573-OPS, LTBTri4573-OPS, SubBTri4573-OPS) were subjected to a Coomassie brilliant blue staining analysis after passing through a molecular sieve. The results were shown in
In the present embodiment, the immunological effect of B5Tri4573-OPS was evaluated. B5Tri4573-OPS referred to the glycosylated protein prepared in Embodiment 3 (B5 was CTB, StxB, LTB, and SubB, respectively). Forty 6-week-old female Balb/c mice were taken and randomly divided into 6 groups (PBS group, OPS group (polysaccharide alone), CTBTri4573-OPS group, StxBTri4573-OPS group, LTBTri573-OPS group, and SubBTri4573-OPS group). Each group of mice were injected subcutaneously with 2.5 μg of polysaccharide based on a polysaccharide content; immunized on the 1st, 15th, and 29th day, the tail bloods thereof were collected on the 10th day after the last immunization, and antibody titers of anti-Shigella flexneri type 2a O-antigen polysaccharide in the serum of each group of mice were measured by indirect enzyme-linked immunosorbent assay (ELISA). The enzyme-linked plate was coated with the extracted LPS of anti-Shigella flexneri type 2a 301 strain, with 10 μg of LPS per well, and other operating steps referred to the “Short Protocols in Molecular Biology”. The results were shown in
Forty 6-week-old female Balb/c mice were taken and randomly divided into 4 groups (PBS group (Control), OPS group, CTB4573-OPS, and CTBTri4573-OPS group). Among them, CTB4573-OPS was a glycoprotein prepared with CTB (without Tri sequence) as a substrate protein, and its preparation method referred to Pan C et al., mBio. 2016 Apr. 26; 7(2):e00443-16. Each group of mice were injected subcutaneously with 2.5 μg of polysaccharide based on a polysaccharide content; immunized on the 1st, 15th, and 29th day, the tail bloods thereof were collected on the 10th day after the last immunization, and antibody titers of anti-Shigella flexneri type 2a O-antigen polysaccharide in the serum of each group of mice were measured by indirect ELISA. The enzyme-linked plate was coated with the extracted LPS of anti-Shigella flexneri type 2a 301 strain, with 10 μg of LPS per well, and other operating steps referred to the “Short Protocols in Molecular Biology”.
The results were shown in
Furthermore, the immunological effects of nanoscale CTBTri4573-OPS with and without an aluminum adjuvant (Adj) were compared. The immunization protocol was the same as that described above, and a dose of the aluminum adjuvant was 10% of the total volume. It was found that the titer of IgG in the nanoscale CTBTri4573-OPS without adjuvant was significantly higher than that with adjuvant group (
Regarding whether the antibody in the serum after immunization had bactericidal activity, an in vitro bactericidal experiment was further carried out. The Shigella 301 wild strains were cultured in LB liquid medium at 37° C. in a shaker at 220 rpm until an OD600 reached 2.0, followed by diluting with normal saline to obtain a 100-200 CFU/10 μL dilution. 10 μL of the diluted bacterial solution and 10 μL of immunized mouse serum undergoing a doubling dilution (maintaining in a 56° C. water bath for 30 min in advance to inactivate complement components) were mixed and incubated at 37° C. for 1 h. After the incubation, 20 μL of complement was added to each tube for well mixing and incubation at 37° C. for 1 h. All the resultants were coated on an LB plate, and incubated overnight at 37° C. The total plate count was recorded next day, and the sterilization rate was calculated.
The results were shown in
To further confirm the above effects, two weeks after the last immunization, the mice were injected intraperitoneally with Shigella flexneri 301 wild strains at a dose of 5 times the half lethal dose (4.35×107 CFU), namely, 200 μl, followed by observing the death of the mice. The results were shown in
Although the specific embodiments of the present invention have been described in details, those skilled in the art will understand that various modifications and variations can be made to the details according to all the disclosure published, and these changes are within the protection scope of the present invention. The whole of the present invention is defined by the appended claims and any equivalents thereof.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201910352203.X | Apr 2019 | CN | national |
The present application is a U.S. National Phase of International Application Number PCT/CN2020/079266 filed Mar. 13, 2020, and claims priority to Chinese Application Number 201910352203.X filed Apr. 29, 2019.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/079266 | 3/13/2020 | WO |
