Minicircle DNA vector vaccine platform for foot-and-mouth disease and methods thereof

Patent metadata

Field	Value
Publication number	US-10604548-B2
Application number	US-201815958218-A
Country	US
Kind code	B2
Filing date	Apr 20, 2018
Priority date	Dec 8, 2015
Publication date	Mar 31, 2020
Grant date	Mar 31, 2020

Abstract

This application is directed generally to minicircle DNA vectors for the vaccination of foot-and-mouth disease (FMD). The transgene expression cassette in the minicircle DNA vector includes: a eukaryotic translation initiation nucleotide sequence, a mutant nucleotide sequence that encodes a foot-and-mouth disease virus (FMDV) capsid polyprotein precursor that contains at least one mutation to eliminate a restriction enzyme recognition site, a nucleotide sequence that encodes a protease that cleaves the MEW capsid polyprotein precursor into plurality of FMDV capsid proteins and a translational regulatory element to regulate the expression of the protease. The minicircle DNA vectors can be transfected directly into the cell of a mammalian host. When transfected into the mammalian host cell, virus-like particles can be produced intrinsically to stimulate the mammalian host's immune system to develop adaptive immunity toward foot-and-mouth disease.

First claim

What is claimed:

1. A method of vaccinating a mammal against a foot-and-mouth disease virus (FMDV), the method comprising administering a vector comprising a mutant nucleotide sequence which when expressed in a host cell of the mammal induces production of FMDV virus-like particles (VLP) by the host cell,
wherein the mutant nucleotide sequence encodes a FMDV capsid polyprotein precursor comprising one or more silent mutations to a nucleotide sequence encoding a wild-type FMDV capsid polyprotein precursor that removes one or more restriction enzyme recognition sites, wherein all occurrences of said one or more restriction enzyme recognition sites are removed from the nucleotide sequence.

2. The method of claim 1 , wherein the mutant nucleotide sequence comprises at least one of one through twenty-two (1-22) silent mutations, one through fifteen (1-15) silent mutations, or one through ten (1-10) silent mutations that remove one or more restriction enzyme recognition sites.

3. The method of claim 2 , wherein said one of one through twenty-two (1-22) silent mutations, one through fifteen (1-15) silent mutations, or one through ten (1-10) silent mutations are selected from the group consisting of C99, C285, T345, G354, A369, C408, C468, G498, C528, A588, C597, C627, C957, G1170, T1518, C1578, T1593, C1665, C1836, C2010, A2190, and combinations thereof.

4. The method of claim 2 , wherein said one of one through twenty-two (1-22) silent mutations, one through fifteen (1-15) silent mutations, or one through ten (1-10) silent mutations are selected from the group consisting of C99T, C285T, T345A, G354A, A369G, C408T, C468A, G498A, C528T, A588T, C597T, C627T, C957A, G1170C, T1518C, C1578A, T1593A, C1665G, C1836G, C2010T, A2190T, and combinations thereof.

5. The method of claim 1 , further comprising administering an adjuvant with the vector.

6. A method for determining whether a mammal is vaccinated against or infected with foot-and-mouth disease virus (FMDV), the method comprising:
a. detecting a first antibody's presence in a sample from the mammal; and
b. detecting a second antibody's presence or absence in the sample,
wherein presence of the first antibody and absence of the second antibody indicates vaccination of the mammal with a vector comprising a mutant nucleotide sequence which when expressed in a host cell of the mammal induces production of FMDV virus-like particles (VLP) by the host cell,
wherein the mutant nucleotide sequence encodes a FMDV capsid polyprotein precursor comprising one or more silent mutations to a nucleotide sequence encoding a wild-type FJDV capsid polyprotein precursor that removes one or more restriction enzyme recognition sites, wherein all occurrences of said one or more restriction enzyme recognition sites are removed from the nucleotide sequence.

7. The method of claim 6 , wherein the mutant nucleotide sequence comprises at least one of one through twenty-two (1-22) silent mutations, one through fifteen (1-15) silent mutations, or one through ten (1-10) silent mutations that remove one or more restriction enzyme recognition sites.

8. The method of claim 7 , wherein said one of one through twenty-two (1-22) silent mutations, one through fifteen (1-15) silent mutations, or one through ten (1-10) silent mutations are selected from the group consisting of C99, C285, T345, G354, A369, C408, C468, G498, C528, A588, C597, C627, C957, G1170, T1518, C1578, T1593, C1665, C1836, C2010, A2190, and combinations thereof.

9. The method of claim 7 , wherein said one of one through twenty-two (1-22) silent mutations, one through fifteen (1-15) silent mutations, or one through ten (1-10) silent mutations are selected from the group consisting of C99T, C285T, T345A, G354A, A369G, C408T, C468A, G498A, C528T, A588T, C597T, C627T, C957A, G1170C, T1518C, C1578A, T1593A, C1665G, C1836G, C2010T, A2190T, and combinations thereof.

10. The method of claim 6 , wherein the mammal produced the first antibody responsive to vaccination with the vector.

11. The method of claim 6 , wherein the second antibody comprises a plurality of antibodies that do not include the first antibody.

12. The method of claim 11 , wherein the plurality of antibodies comprises at least one antibody against FMDV non-structural proteins.

13. The method of claim 11 , wherein the plurality of antibodies are associated with FMDV infection.

14. The method of claim 6 , wherein detecting the first antibody's presence utilizes an immunoassay.

15. The method of claim 14 , wherein the immunoassay comprises an enzyme linked immunosorbent assay (ELISA).

16. The method of claim 6 , wherein detecting the second antibody's presence or absence utilizes an immunoassay.

17. The method of claim 16 , wherein the immunoassay comprises an enzyme linked immunosorbent assay (ELISA).

Assignees

• The Government Of The Us Secretary Department Of Homeland Security
• The Government Of The Us Secretary Of Homeland Security

Inventors

• Puckette Michael
• Rasmussen Max
• Neilan John

Classifications

• C12N2770/32122

  New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title

• G01N2800/26

  Infectious diseases, e.g. generalised sepsis · CPC title

• G01N33/56983

  Viruses · CPC title

• C12N2770/32123

  Virus like particles [VLP] · CPC title

• C07K14/005 Primary

  from viruses · CPC title