A recombinant rabies virus (ERAGS) for use in a bait vaccine for swine.
10.7774/cevr.2016.5.2.169
- Author:
Dong Kun YANG
1
;
Ha Hyun KIM
;
Sung Suk CHOI
;
Seong Heon LEE
;
In Soo CHO
Author Information
1. Viral Disease Division, Animal and Plant Quarantine Agency, MAFRA, Gimcheon, Korea. yangdk@korea.kr
- Publication Type:Original Article
- Keywords:
Rabies;
Vaccines;
Swine
- MeSH:
Administration, Oral;
Brain;
Encephalitis;
Nucleocapsid;
Rabies virus*;
Rabies*;
Reverse Genetics;
Sus scrofa;
Swine*;
Vaccines
- From:Clinical and Experimental Vaccine Research
2016;5(2):169-174
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Rabies viruses (RABV) circulating worldwide in various carnivores occasionally cause fatal encephalitis in swine. In this study, the safety and immunogenicity of a recombinant rabies virus, the ERAGS strain constructed with a reverse genetics system, was evaluated in domestic pigs. MATERIALS AND METHODS: Growing pigs were administered 1 mL (108.0 FAID50/mL) of the ERAGS strain via intramuscular (IM) or oral routes and were observed for 4 weeks' post-inoculation. Three sows were also inoculated with 1 mL of the ERAGS strain via the IM route. The safety and immunogenicity in swine were evaluated using daily observation and a virus-neutralizing assay (VNA). Fluorescent antibody tests (FAT) for the RABV antigen and reverse transcriptase-polymerase chain reaction (RT-PCR) assays for the detection of the nucleocapsid (N) gene of RABV were conducted with brain tissues from the sows after necropsy. RESULTS: The growing pigs and sows administered the ERAGS strain did not exhibit any clinical sign of rabies during the test period test and did develop VNA titers. The growing pigs inoculated with the ERAGS strain via the IM route showed higher VNA titers than did those receiving oral administration. FAT and RT-PCR assays were unable to detect RABV in several tissues, including brain samples from the sows. CONCLUSION: Our results suggest that the ERAGS strain was safe in growing pigs and sows and induced moderate VNA titers in pigs.
