Genetically engineered foot and mouth disease virus and related proteins, polynucleotides, compositions, methods and systems
Genetically engineered Foot and Mouth Disease Virus (FMDV) and related engineered proteins and polynucleotides, nanolipoprotein particles, compositions, methods and systems are described. The genetically engineered FMDV is modified by the strategic insertion of a protein tag into select regions of the FMDV genome which encode viral proteins that are exposed on the surface of the FMDV viral capsid. The inserted protein tag is displayed as a decoration or attachment on the viral capsid surface.
1. A vaccine comprising
(i) one or more genetically modified Foot and Mouth Disease Virus (FMDV) having a viral capsid comprising
a protein tag up to 100 amino acids inserted in an engineered FMDV VP1 protein and presented on an external surface of the viral capsid,
and/or
(ii) one or more FMD functionalized nanolipoprotein particle comprising a scaffold protein and a functionalized membrane forming lipid presenting
a tag substrate attached to the protein tag presented on the external surface of the viral capsid of the one or more genetically modified FMDV,
together with
(iii) a pharmaceutically acceptable vehicle,
wherein the protein tag is inserted in the engineered FDMV VP1 protein at an insertion position selected from
any one of position −1 to position +6 relative to an FMDV 2A N-terminus of the engineered FDMV VP1 protein,
and
any one of position −1 to position −7 relative to an FMD VP1 C-terminus of the engineered FDMV VP1 protein.
2. The vaccine of claim 1 , wherein the protein tag is from 1 to 20 amino acids in length.
3. The vaccine of claim 1 , wherein the protein tag comprises a peptide tag selected from the group consisting of AviTag, Calmodulin-tag, polyglutamate tag, E-tag, FLAG-tag, HA-tag, His-tag, Myc-tag, NE-tag, S-tag, SBP-tag, Softag 1, Softag 3, Strep-tag, TC tag, V5 tag, VSV-tag, Xpress tag, Isopeptag, SpyTag, and SnoopTag.
4. The vaccine of claim 1 , wherein the protein tag is a polyhistidine tag.
5. The vaccine of claim 4 , wherein the sequence of the polyhistidine tag is HHHHHHKQ (SEQ ID NO:16) or HHHHHHIIAPAK (SEQ ID NO:17).
6. The vaccine of claim 1 , wherein the insertion position is selected from any one of position −1 to position −4 relative to the FMD VP1 C-terminus.
7. The vaccine of claim 1 , wherein the insertion position is −1 relative to the FMD VP1 C-terminus.
8. The vaccine of claim 1 , wherein the genetically modified FMDV is encoded by a polynucleotide having sequence SEQ ID NO: 3.
9. The vaccine of claim 1 , wherein the tag substrate is a molecule chelating a bivalent metal ion and the protein tag is a polyhistidine molecule.
10. The vaccine of claim 1 , wherein the tag substrate is a negatively charged moiety and the protein tag is a poly-arginine molecule.
11. The vaccine of claim 1 , wherein the tag substrate is avidin or a derivative thereof and the protein tag is selected from the group consisting of Avi-Tag, SBP-tag and Strep-tag.
12. The vaccine of claim 1 , wherein the functionalized membrane forming lipid is a biological molecule.
13. The vaccine of claim 1 , wherein the FMDV functionalized nanolipoprotein particle further comprises a membrane forming lipid.
14. The vaccine of claim 1 , wherein the scaffold protein is an apolipoprotein.
15. The vaccine of claim 1 , wherein the FMDV functionalized nanolipoprotein particle further comprises one or more adjuvants attached to a tag substrate presented on the functionalized nanolipoprotein surface.
16. The vaccine of claim 15 , wherein the one or more adjuvants are selected from the group consisting of f-Met-Leu-Phe, muramyl dipeptide, saponins, toxins, oligonucleotide CpG motifs, immunostimulatory carbohydrates, immunostimulatory polysaccharides, cytokines, chemokines and derivatives thereof.
17. The vaccine of claim 1 , wherein the FMDV functionalized nanolipoprotein particle further comprises one or more adjuvants selected from the group consisting of hydrophobic adjuvants, amphipathic adjuvants, hydrophilic adjuvants synthetically appended with a hydrophobic moiety.
18. The vaccine of claim 1 , wherein the FMDV functionalized nanolipoprotein particle further comprises at least one amphipathic adjuvant selected from the group consisting of mono-phosphorylated Lipid A, lipopolysaccharides, squalene, sorbitol oleate esters, alpha-galactosyl ceramide, lipotichoic acid and saponins.
19. The vaccine of claim 18 , wherein the at least one amphipathic adjuvant are multiple amphipathic adjuvants.
20. The vaccine of claim 1 , wherein the vaccine further comprises one or more additional immunomodulatory components.
21. The vaccine of claim 20 , wherein the immunomodulatory component is an adjuvant or a cytokine.
22. The vaccine of claim 1 , wherein the FMDV is in a chemically inactivated form.
23. A method to treat or prevent FMD in a cloven-hoofed animal, the method comprising administering to the cloven-hoofed animal an effective amount of the vaccine of claim 1 .
24. The method of claim 23 , wherein the vaccine comprises a chemically-inactivated genetically engineered marker FMDV in an effective amount to delay onset or severity of FMD in the cloven-hoofed animal.
25. The method of claim 23 , wherein the vaccine comprises a chemically-inactivated genetically engineered marker FMDV in an effective amount to protect the cloven-hoofed animal against FMD.
26. The method of claim 23 , wherein the effective amount comprises from about 10 2 to about 10 8 pfu of the one or more genetically modified FMDV alone or in combination with one or more FMD functionalized nanolipoprotein particle.
27. The method of claim 23 , wherein the effective amount comprises from about 10 3 to about 10 7 pfu of the one or more genetically modified FMDV alone or in combination with one or more FMD functionalized nanolipoprotein particle.