1. First insights into the protective effects of a recombinant swinepox virus expressing truncated MRP of Streptococcus suis type 2 in mice.
- Author
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Huang D, Zhu H, Lin H, Xu J, and Lu C
- Subjects
- Animals, Antibodies, Bacterial biosynthesis, Antibodies, Bacterial blood, Antigens, Bacterial genetics, Bacterial Proteins genetics, Cell Line, Female, Gene Expression Regulation, Bacterial, Genetic Vectors, Mice, Polymerase Chain Reaction veterinary, Random Allocation, Reassortant Viruses genetics, Reassortant Viruses immunology, Serial Passage, Streptococcal Infections prevention & control, Streptococcus suis genetics, Suipoxvirus immunology, Swine, Vaccination veterinary, Vaccines, Synthetic genetics, Vaccines, Synthetic immunology, Antigens, Bacterial immunology, Bacterial Proteins immunology, Bacterial Vaccines genetics, Bacterial Vaccines immunology, Streptococcal Infections veterinary, Streptococcus suis immunology, Suipoxvirus genetics, Swine Diseases prevention & control
- Abstract
To explore the potential of the swinepox virus (SPV) as vector for Streptococcus suis vaccines, a vector system was developed for the construction of a recombinant SPV carrying bacterial genes. Using this system, a recombinant virus expressing truncated muramidase-released protein (MRP) of S. suis type 2 (SS2), designated rSPV-MRP, was produced and identified by PCR, western blotting and immunofluorescence assays. The rSPV-MRP was found to be only slightly attenuated in PK-15 cells, when compared with the wild-type virus. After immunization intramuscularly with rSPV-MRP, SS2 inactive vaccine (positive control), wild-type SPV (negative control) and PBS (blank control) respectively, all CD1 mice were challenged with a lethal dose or a sublethal dose of SS2 highly virulent strain ZY05719. While SS2 inactive vaccine protected all mice, immunization with rSPV-MRP resulted in 60% survival and protected mice against a lethal dose of the highly virulent SS2 strain, compared with the negative control (P < 0.05). Our data indicate that animals immunized with rSPV-MRP had a significantly reduced bacterial burden in all organs examined, compared to negative controls and blank controls (P <0.05). Antibody titers of the rSPV-MRP-vaccinated group were significantly higher (P <0.001), when compared to negative controls and blank controls. Antibody titers were also significantly higher in the vaccinated group at all time points post-vaccination (P <0.001), compared with the positive controls. These initial results demonstrated that the rSPV-MRP provided mice with protection from systemic SS2 infection. If SPV recombinants have the potential as S. suis vaccines for the use in pigs has to be evaluated in further studies.
- Published
- 2012