Pichinde virus reverse genetics systems and methods of use
Provided herein are genetically engineered Pichinde viruses that include three ambisense genomic segments. The first genomic segment includes a coding region encoding a Z protein and a coding region encoding a L RdRp protein. The second genomic segment includes a coding region encoding a nucleoprotein (NP) and the third genomic segment includes a coding region encoding a glycoprotein. Each of the second and third genomic segments optionally include an additional coding region that may encode an antigen or a detectable marker. Also provided herein is a reverse genetics system for making a genetically engineered Pichinde virus, and a collection of vectors that can be used to produce a genetically engineered Pichinde virus. Further provided are methods for using a reverse genetics system, and methods for producing an immune response in a subject.
1. A genetically engineered Pichinde virus comprising:
three separate ambisense genomic segments,
wherein the first genomic segment comprises a coding region encoding a Z protein and a coding region encoding a L RNA-dependent RNA polymerase protein,
wherein the second genomic segment comprises a coding region encoding a nucleoprotein (NP) and a first restriction enzyme site, and
wherein the third genomic segment comprises a coding region encoding a glycoprotein and a second restriction enzyme site.
2. The virus of claim 1 wherein the second genomic segment comprises a multiple cloning site, and wherein the first restriction enzyme site is part of the multiple cloning site.
3. The virus of claim 1 wherein the third genomic segment comprises a multiple cloning site, and wherein the second restriction enzyme site is part of the multiple cloning site.
4. The virus of claim 1 wherein the second genomic segment further comprises a coding region encoding a first protein inserted at the first restriction site.
5. The virus of claim 1 wherein the third genomic segment further comprises a coding region encoding a second protein inserted at the first restriction site.
6. The virus of claim 1 wherein the second genomic segment further comprises a coding region encoding a first protein inserted at the first restriction site, and the third genomic segment further comprises a coding region encoding a second protein inserted at the first restriction site.
7. The virus of claim 6 wherein the first protein and the second protein are selected from an antigen and a detectable marker.
8. The virus of claim 7 wherein the antigen is a protein expressed by a viral pathogen, a prokaryotic pathogen, or a eukaryotic pathogen.
9. The virus of claim 6 wherein the first protein and the second protein are different.
10. The virus of claim 6 wherein the first protein and the second protein are the same.
11. The virus of claim 1 wherein the nucleoprotein comprises at least one mutation that reduces exoribonuclease activity of the nucleoprotein, wherein the mutation is a mutation of at least one RNase catalytic residue.
12. The virus of claim 11 wherein the at least one mutation is selected from the group consisting of an aspartic acid at amino acid 380 of SEQ ID NO:3, a glutamic acid at amino acid 382 of SEQ ID NO:3, an aspartic acid at amino acid 525 of SEQ ID NO:3, a histidine at amino acid 520 of SEQ ID NO:3, an aspartic acid at amino acid 457 of SEQ ID NO:3, or a combination thereof, wherein the aspartic acid, glutamic acid, or histidine is substituted with any other amino acid.
13. The virus of claim 1 wherein the glycoprotein comprises at least one mutation that alters the activity of the glycoprotein, wherein when the glycoprotein comprises SEQ ID NO:4 the mutation is selected from an asparagine at amino acid 20, an asparagine at amino acid 404, or a combination thereof, and wherein the asparagine is substituted with any other amino acid.
14. The genetically engineered Pichinde virus of claim 1 wherein the NP comprises an amino acid sequence having at least 80% identity to SEQ ID NO:3 and wherein any substitution is a conservative substitution.
15. The genetically engineered Pichinde virus of claim 1 wherein the NP comprises an amino acid sequence having at least 95% identity to SEQ ID NO:3.
16. An infectious virus particle comprising the three genomic segments of claim 1 .
17. A composition comprising the infectious virus particle of claim 16 , wherein the infectious virus particle is isolated.
18. A method for producing an immune response in a subject, comprising
administering to a subject the infectious virus particle of claim 16 , wherein the second genomic segment further comprises a coding region encoding a first antigen inserted at the first restriction site, or the third genomic segment further comprises a coding region encoding a second antigen inserted at the first restriction site.
19. The method of claim 18 wherein the subject is a vertebrate.
20. The method of claim 19 wherein the vertebrate is a mammal.
21. The method of claim 20 wherein the mammalian is a human.
22. The method of claim 18 wherein the vertebrate is avian.
23. The method of claim 18 wherein the immune response comprises a humoral immune response.
24. The method of claim 18 wherein the immune response comprises a cell-mediated immune response.
25. The method of claim 18 wherein the first antigen or the second antigen is a protein expressed by a viral pathogen, a prokaryotic pathogen, or a eukaryotic pathogen, and wherein the subject is at risk of exposure to the viral pathogen, the prokaryotic pathogen, or the eukaryotic pathogen.
26. The method of claim 18 wherein the administering comprises administering at least two populations of infectious virus particles, wherein each population of infectious virus particle encodes a different antigen.
27. The method of claim 18 , wherein the second genomic segment encodes the first antigen and the third genomic segment encodes the second antigen.
28. A collection of vectors comprising:
a first vector encoding a first genomic segment comprising a coding region encoding a Z protein and a coding region encoding a L RdRp protein, wherein the coding region encoding the Z protein is antigenomic,
a second vector encoding a second genomic segment comprising a coding region encoding a nucleoprotein (NP) and a first restriction enzyme site, wherein the coding region encoding the NP is antigenomic, and
a third vector encoding a third genomic segment comprises a coding region encoding a glycoprotein and a second restriction enzyme site, wherein the coding region encoding the glycoprotein is antigenomic.
29. The collection of claim 28 wherein the vectors are plasmids.
30. The collection of claim 28 wherein the plasmids further comprise a T7 promoter.
31. The collection of claim 28 wherein the second genomic segment comprises a multiple cloning site, and wherein the first restriction enzyme site is part of the multiple cloning site.
32. The collection of claim 28 wherein the third genomic segment comprises a multiple cloning site, and wherein the second restriction enzyme site is part of the multiple cloning site.
33. The collection of claim 28 wherein the second genomic segment further comprises a coding region encoding a first protein inserted at the first restriction site.
34. The collection of claim 28 wherein the third genomic segment further comprises a coding region encoding a second protein inserted at the first restriction site.
35. The collection of claim 28 wherein the second genomic segment further comprises a coding region encoding a first protein inserted at the first restriction site, and the third genomic segment further comprises a coding region encoding a second protein inserted at the first restriction site.
36. The collection of claim 35 wherein the first protein and the second protein are selected from an antigen and a detectable marker.
37. The collection of claim 36 wherein the antigen is a protein expressed by a viral pathogen, a prokaryotic pathogen, or a eukaryotic pathogen.
38. The collection of claim 35 wherein the first protein and the second protein are different.
39. The collection of claim 35 wherein the first protein and the second protein are the same.
40. The collection of vectors of claim 28 wherein the NP comprises an amino acid sequence having at least 80% identity to SEQ ID NO:3, and wherein any substitution is a conservative substitution.
41. The collection of vectors of claim 28 wherein the NP comprises an amino acid sequence having at least 95% identity to SEQ ID NO:3.
42. A method for making a genetically engineered Pichinde virus comprising:
introducing into a cell the collection of vectors of claim 28 ; and
incubating the cells in a medium wherein the first, second, and third genomic segments are expressed and packaged.
43. The method of claim 42 further comprising isolating an infectious virus particle from the medium.
44. The method of claim 42 wherein the cells express a T7 polymerase.
45. The isolated infectious virus particle of claim 42 .
46. A composition comprising the isolated infectious virus particle of claim 45 .
47. A method for using a reverse genetics system, comprising:
introducing into a cell the three vectors of genomic segments of claim 42 ;
incubating the cell wherein the three genomic segments are transcribed and the coding regions of each genomic segment are expressed.
48. The method of claim 47 further comprising isolating infectious virus particles produced by the cell, wherein each infectious virus particle comprises the three genomic segments.
49. The method of claim 47 wherein the introducing comprises transfecting a cell with the three genomic segments.
50. The method of claim 47 wherein the introducing comprises contacting the cell with an infectious virus particle comprising the three genomic segments.
51. The method of claim 47 wherein the cell is ex vivo.
52. The method of claim 47 wherein the cell is a vertebrate cell.
53. The method of claim 52 wherein the vertebrate cell is a mammalian cell.
54. The method of claim 53 wherein the mammalian cell is a human cell.
55. The method of claim 52 wherein the vertebrate cell is an avian cell.
56. The method of claim 55 wherein the avian cell is a chicken embryonic fibroblast.
57. A reverse genetics system for making a genetically engineered Pichinde virus comprising three vectors,
wherein a first vector encodes a first genomic segment comprising a coding region encoding a Z protein and a coding region encoding a L RdRp protein, wherein the coding region encoding the Z protein is antigenomic,
wherein the second vector encodes a second genomic segment comprising a coding region encoding a nucleoprotein (NP) and a first restriction enzyme site, wherein the coding region encoding the NP is antigenomic,
wherein the third vector encodes a third genomic segment comprises a coding region encoding a glycoprotein and a second restriction enzyme site, wherein the coding region encoding the glycoprotein is antigenomic.
58. The reverse genetics system of claim 57 wherein each plasmid comprises a T7 promoter.
59. The reverse genetics system of claim 57 wherein the NP comprises an amino acid sequence having at least 80% identity to SEQ ID NO:3, and wherein any substitution is a conservative substitution.
60. The reverse genetics system of claim 57 wherein the NP comprises an amino acid sequence having at least 95% identity to SEQ ID NO:3.