Compositions and methods of enhancing immune responses
Provided herein are Salmonella enteritidis 13A strains and compositions comprising these strains. Also provided are methods of enhancing an immune response against Influenza A and methods of reducing morbidity associated with an Influenza A infection. Methods of enhancing an immune response to a vaccine vector by expressing a polypeptide of CD 154 capable of binding CD40 are also disclosed. Methods of developing a bacterial vaccine vector are disclosed. Methods of generating scarless site-specific mutations in a bacterium are also disclosed.
1. A vaccine vector comprising a polynucleotide sequence encoding an antigenic polypeptide and a CD154 polynucleotide sequence encoding a CD154 polypeptide capable of binding CD40, wherein the CD154 polypeptide has fewer than about 50 amino acids and comprises amino acids 140-149 of SEQ ID NO:26 or a homolog thereof, wherein the antigenic polypeptide is an Influenza polypeptide and wherein the polynucleotide sequence encoding the antigenic polypeptide and the CD154 polynucleotide sequence are expressed on the surface of the vaccine vector.
2. The vaccine vector of claim 1 , wherein the polynucleotide sequence encoding the antigenic Influenza polypeptide is an Influenza M2e polynucleotide encoding an Influenza M2e polypeptide.
3. The vaccine vector of claim 2 , wherein the Influenza M2e polypeptide is selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:20, an immunogenic fragment of SEQ ID NO:1, an immunogenic fragment of SEQ ID NO:2, an immunogenic fragment of SEQ ID NO:3 and an immunogenic fragment of SEQ ID NO:4.
4. The vaccine vector of claim 1 , wherein the antigenic polypeptide and the CD154 polypeptide are encoded by the same polynucleotide sequence.
5. The vaccine vector of claim 1 , wherein the polynucleotide sequence encoding the antigenic Influenza polypeptide and the CD154 polynucleotide sequence are inserted within a sequence encoding an external portion of a transmembrane protein.
6. The vaccine vector of claim 1 , wherein the vaccine vector is a bacterium.
7. The vaccine vector of claim 6 , wherein the bacterium is a Salmonella strain of any of (a) Salmonella enteritidis having ATCC deposit number PTA-7871, (b) a Salmonella strain capable of colonizing a subject, (c) a Salmonella strain comprising a mutation in an aromatization pathway, (d) a Salmonella strain comprising a mutation within aroA, (e) a Salmonella strain comprising a mutation in a stress response pathway and (f) a Salmonella strain comprising a mutation in htrA.
8. A method of enhancing an immune response against Influenza in a subject comprising administering to the subject a vaccine vector in an amount effective to enhance the immune response of the subject to Influenza in response to vaccination, the vaccine vector comprising a CD154 polynucleotide sequence encoding a CD154 polypeptide capable of binding CD40 and a polynucleotide sequence encoding an Influenza polypeptide, wherein the CD154 polypeptide has fewer than about 50 amino acids and comprises amino acids 140-149 of SEQ ID NO:26 or a homolog thereof and wherein the CD154 polypeptide is expressed on the surface of the vaccine vector.
9. The method of claim 8 , wherein the antigenic Influenza polypeptide and the CD154 polypeptide are encoded by the same polynucleotide sequence.
10. The method of claim 8 , wherein the polynucleotide sequence encoding the antigenic Influenza polypeptide and the CD154 polynucleotide sequence are inserted within a sequence encoding an external portion of a transmembrane protein.
11. The method of claim 8 , wherein the vaccine vector is a bacterium.
12. The method of claim 11 , wherein the bacterium is a Salmonella strain of any of (a) Salmonella enteritidis having ATCC deposit number PTA-7871, (b) a Salmonella strain capable of colonizing a subject, (c) a Salmonella strain comprising a mutation in an aromatization pathway, (d) a Salmonella strain comprising a mutation within aroA, (e) Salmonella strain comprising a mutation in a stress response pathway and (f) a Salmonella strain comprising a mutation in htrA.
13. The method of claim 8 , wherein the polynucleotide sequence encoding the Influenza polypeptide encodes an Influenza A M2e polypeptide in an amount effective to enhance the immune response of the subject to Influenza A.
14. The method of claim 13 , wherein the Influenza M2e polypeptide is selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ NO:3, SEQ ID NO:4, SEQ II) NO:5, SEQ ID NO:20, an immunogenic fragment of SEQ ID NO:1, an immunogenic fragment of SEQ ID NO:2, an immunogenic fragment of SEQ ID NO:3 and an immunogenic fragment of SEQ ID NO:4.
15. A method of enhancing the immune response against Influenza A in a subject comprising administering to the subject a bacterium comprising at least one Influenza A M2e polynucleotide sequence encoding an Influenza A M2e polypeptide in an amount effective to enhance the immune response of the subject to Influenza A and a CD154 polynucleotide sequence encoding a CD154 polypeptide capable of binding CD40, wherein the CD154 polypeptide has fewer than about 50 amino acids and comprises amino acids 140-149 of SEQ ID NO:26 or a homolog thereof and wherein the CD154 polypeptide is expressed on the surface of the bacterium.
16. The method of claim 15 , wherein the bacterium is a Salmonella strain of any of (a) Salmonella enteritidis having ATCC deposit number PTA-7871, (b) a Salmonella strain capable of colonizing a subject, (c) a Salmonella strain comprising a mutation in an aromatization pathway, (d) a Salmonella strain comprising a mutation within aroA, (e) a Salmonella strain comprising a mutation in a stress response pathway and, (e) a Salmonella strain comprising a mutation in htrA.
17. The method of claim 15 , wherein the Influenza A M2e polypeptide and the CD154 polypeptide are encoded by the same polynucleotide sequence.
18. The method of claim 15 , wherein the polynucleotide sequence encoding the Influenza A M2e polypeptide and the CD154 polynucleotide sequence are inserted within a sequence encoding an external portion of a transmembrane protein.
19. The method of claim 15 , wherein the Influenza M2e polypeptide is selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEC) ID NO:4, SEQ ID NO:5, SEQ ID NO:20, an immunogenic fragment of SEQ ID NO: 1, an immunogenic fragment of SEQ ID NO:2, an immunogenic fragment of SEQ ID NO:3 and an immunogenic fragment of SEQ ID NO:4.
20. A method of reducing influenza A-related morbidity in a subject comprising administering to the subject a bacterium comprising at least one Influenza A M2e polynucleotide sequence encoding an Influenza A M2e polypeptide in an amount effective to reduce Influenza A related morbidity and a CD154 polynucleotide sequence encoding a CD154 polypeptide capable of binding CD40, wherein the CD154 polypeptide has fewer than about 50 amino acids and comprises amino acids 140-149 of SEQ ID NO:26 or a homolog thereof and wherein the CD154 polypeptide is expressed on the surface of the bacterium.
21. The method of claim 20 , wherein the bacterium is a Salmonella strain of any of (a) Salmonella enteritidis having ATCC deposit number PTA-7871, (b) a Salmonella strain capable of colonizing a subject, (c) a Salmonella strain comprising as mutation in an aromatization pathway, (d) a Salmonella strain comprising a mutation within aroA, (e) a Salmonella strain comprising a mutation in a stress response pathway and (1) a Salmonella strain comprising a mutation in htrA.
22. The method of claim 20 , wherein the Influenza A M2e polypeptide and the CD154 polypeptide are encoded by the same polynucleotide sequence.
23. The method of claim 20 , wherein the polynucleotide sequence encoding the Influenza A M2e polypeptide and the CD154 polynucleotide sequence are inserted within a sequence encoding an external portion of a transmembrane protein.
24. The method of claim 20 , wherein the Influenza M2e polypeptide is selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:20, an immunogenic fragment of SEQ ID NO:1, an immunogenic fragment of SEQ ID NO:2, an immunogenic fragment of SEQ ID NO:3 and an immunogenic fragment of SEQ ID NO:4.
25. A method for developing a bacterial vaccine vector comprising:
a) selecting a bacterium capable of colonizing a subject;
b) attenuating the bacterium to generate an attenuated bacterium;
c) incorporating a CD154 polynucleotide sequence encoding a CD154 polypeptide capable of binding CD40 into the attenuated bacterium to generate a vaccine vector, wherein the CD154 polypeptide has fewer than 50 amino acids and comprises amino acids 140-149 of CD154 SEQ ID NO:26 or a homolog thereof, and
d) incorporating a second polynucleotide sequence encoding an antigenic polypeptide into the chromosome of the vaccine vector, wherein the CD154 polypeptide and the antigenic polypeptide are expressed on the surface of the vaccine vector.
26. The method of claim 25 , wherein the CD154 polypeptide and the antigenic polypeptide are encoded by the same polynucleotide sequence.
27. The method of claim 25 , wherein the second polynucleotide sequence encoding the antigenic polypeptide and the CD154 polynucleotide sequence are inserted within a sequence encoding an external portion of a transmembrane protein.