Sindbis Virus Replicase-based DNA Vaccine Construct Encoding FMDV-specific Multivalent Epitope Gene: Studies on its Immune Responses in Guinea Pigs

被引:5
作者
Dar, P. A. [2 ]
Ganesh, K. [2 ]
Nagarajan, G. [3 ]
Sarika, S. [1 ]
Reddy, G. R. [1 ]
Suryanarayana, V. V. S. [1 ]
机构
[1] Indian Vet Res Inst, Mol Virol Lab, Bengaluru 560024, Karnataka, India
[2] Indian Vet Res Inst, FMD Res Ctr, Bengaluru 560024, Karnataka, India
[3] Natl Res Ctr Camel, Bikaner, Rajasthan, India
关键词
MOUTH-DISEASE VIRUS; CYTOTOXIC T-LYMPHOCYTES; DOUBLE-STRANDED-RNA; ENHANCED IMMUNOGENICITY; STRUCTURAL GENES; EXPRESSION; IMMUNIZATION; VECTORS; PROTEIN; SWINE;
D O I
10.1111/j.1365-3083.2012.02733.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Foot-and-mouth disease (FMD) is still a perennial global menace affecting livestock health and production. It is imperative to figure out new ways to curb this disease. In this study, a sindbis virus replicase-based DNA vaccine, pSinCMV-Vac-MEG990, encoding a multivalent epitope gene (representing tandemly linked VP1 C-terminal halves of three foot-and-mouth disease virus (FMDV) serotypes) was constructed. In vitro transfection studies in BHK-21 cells revealed that the construct was able to express FMDV-specific antigen but does not overproduce the antigen. Immunization of guinea pigs with the construct at dose rate of 10, 5, 2 and 1 mu g per animal through intramuscular route showed significant neutralizing antibody induction at all doses against all serotype tested as compared to non-immunized controls. On viral challenge of guinea pigs 4 week post-immunization with 1000 GPID50 of FMDV serotype A, it was observed that the immunization not only delayed the appearance and reduced the severity of FMD lesions significantly (P < 0.05) but also provided complete protection in several guinea pigs. In fact, two of six and one of six guinea pigs were completely protected in 10 and 5 mu g immunized groups, respectively. These results suggest that the development of the replicase-based DNA vaccine may provide a promising approach as an alternative vaccine strategy for controlling FMD.
引用
收藏
页码:345 / 353
页数:9
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