Zhang Guo-Ging, Chen Xiao-Yun, Qian Ping, Chen Huan-Chun, Li Xiang-Min
State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, Hubei, PR China; The Animal Multiplication Farm of Hubei Province, The Hubei Animal Husbandry and Veterinary Bureau, No.69 Xiongchu Ave., Wuchang District, Wuhan 4300064, PR China.
China Institute of Veterinary Drug Control, No.8 south street of Zhongguancun, Haidian district, Beijing, PR China.
Res Vet Sci. 2016 Feb;104:181-7. doi: 10.1016/j.rvsc.2015.12.009. Epub 2015 Dec 17.
In this study, SeV was used as a vector to express capsid precursor polypeptide (P1) of Foot-and-mouth disease virus (FMDV) by using reverse genetics. The rescue recombinant SeV (rSeV-P1) can efficiently propagate and express P1 protein by Western blot and IFA analysis. To evaluate the immunogenicity of rSeV-P1, BALB/c mice were divided into several groups and immunized intramuscularly with various doses of rSeV-P1, rSeV-eGFP, PBS and commercial FMD vaccine, respectively, and then challenged with an intraperitoneal injection of 1 × 10(6) TCID50 of virulent serotype O FMDV O/ES/2001 strain 4 weeks after booster immunization. Mice vaccinated with rSeV-P1 acquired FMDV-specific ELISA antibodies, neutralizing antibodies as well as cellular immune response. Meantime, mice immunized with rSeV-P1 (dose-dependent) had the ability to inhibit the replication of FMDV in the sera after FMDV challenge. Our results indicated that the recombinant SeV-P1 virus could be utilized as an alternative strategy to develop a new generation of safety and efficacious vaccine against FMDV infection.