Controlled release vaccines and methods of treating
Methods and compositions for the treatment of Brucella induced diseases and disorders are disclosed herein. In preferred embodiments, the invention relates to vaccines. In additional embodiments, the invention relates to formulations capable of releasing said vaccines at a controlled rate of release in vivo. In further embodiments, the invention relates to modified strains of the bacteria Brucella melitensis and Brucella abortus . In still further embodiments, the invention relates to compositions that do not induce clinical symptoms or splenomegaly in a subject receiving said compositions.
1. A vaccine composition comprising:
a Brucella strain comprising one or more attenuating gene knockouts selected from at least one of ΔvjbR, ΔmucR, ΔmanB/A, ΔvirB1, ΔvirB2, ΔvirB3, ΔvirB4, ΔvirB5, ΔvirB6, ΔvirB7, ΔvirB8, ΔvirB9, ΔvirB10, or ΔvirB11;
a diagnostic gene knockout, wherein the diagnostic gene knockout is a differentiation of infected animals from vaccinated animals (DIVA) marker comprising ΔvirB12, Δbcsp31, Δasp24, or any combination thereof; and
an encapsulating agent comprising vitelline protein B capable of releasing the Brucella strain at a predetermined rate, wherein the vaccine is free of side-effects.
2. The vaccine composition of claim 1 , wherein the Brucella is selected from the group consisting of Brucella melitensis and Brucella abortus.
3. The vaccine composition of claim 1 , wherein said DIVA marker is selected from ΔvirB12 or Δbcsp31.
4. The vaccine composition of claim 1 , wherein the attenuating gene knockout comprises ΔvjbR, ΔmucR, ΔvirB2, or ΔmanB/A.
5. The vaccine composition of claim 1 , wherein the Brucella strain comprises ΔmucR/DIVA, ΔvjbR/DIVA, ΔvirB2/DIVA, ΔmanB/A/DIVA, or any combinations thereof.
6. The vaccine composition of claim 1 , wherein the strain comprises ΔvjbR/ΔmucR/DIVA mutant, ΔvirB2/ ΔmanB/A/DIVA mutant, ΔvirB2/ΔvjbR/DIVA mutant, ΔvirB2/ΔmucR/DIVA mutant, ΔvjbR /ΔmanB/A/DIVA mutant, and ΔmucR/ΔmanB/A/DIVA mutant.
7. The vaccine composition of claim 1 , further comprising one or more antibiotic markers.
8. The vaccine composition of claim 1 , wherein the vaccine is used for a prophylaxis, an amelioration of symptoms, a treatment, or any combinations thereof against brucellosis in a human or an animal subject.
9. The vaccine composition of claim 1 , wherein the vaccine is administered by an oral, an intranasal, a parenteral, an intradermal, an intramuscular, an intraperitoneal, an intravenous, a subcutaneous, an epidural, a mucosal, a rectal, a vaginal, a sublingual, or a buccal route.