Safety and immunogenicity of recombinant Rift Valley fever MP-12 vaccine candidates in sheep.
Academic Article
Overview
Research
Identity
Additional Document Info
Other
View All
Overview
abstract
The safety and immunogenicity of two authentic recombinant (ar) Rift Valley fever (RVF) viruses, one with a deletion in the NSs region of the S RNA segment (arMP-12NSs16/198) and the other with a large deletion of the NSm gene in the pre Gn region of the M RNA segment (arMP-12NSm21/384) of the RVF MP-12 vaccine virus were tested in crossbred ewes at 30-50 days of gestation. First, we evaluated the neutralizing antibody response, measured by plaque reduction neutralization (PRNT(80)), and clinical response of the two viruses in groups of four ewes each. The virus dose was 110(5)plaque forming units (PFU). Control groups of four ewes each were also inoculated with a similar dose of RVF MP-12 or the parent recombinant virus (arMP-12). Neutralizing antibody was first detected in 3 of 4 animals inoculated with arMP-12NSm21/384 on Day 5 post inoculation and all four animals had PRNT(80) titers of 1:20 on Day 6. Neutralizing antibody was first detected in 2 of 4 ewes inoculated with arMP-12NSs16/198 on Day 7 and all had PRNT(80) titers of 1:20 on Day 10. We found the mean PRNT(80) response to arMP-12NSs16/198 to be 16- to 25-fold lower than that of ewes inoculated with arMP-12NSm21/384, arMP-12 or RVF MP-12. No abortions occurred though a single fetal death in each of the arMP-12 and RVF MP-12 groups was found at necropsy. The poor PRNT(80) response to arMP-12NSs16/198 caused us to discontinue further testing of this candidate and focus on arMP-12NSm21/384. A dose escalation study of arMP-12NSm21/384 showed that 110(3)plaque forming units (PFU) stimulate a PRNT(80) response comparable to doses of up to 110(5)PFU of this virus. With further study, the arMP-12NSm21/384 virus may prove to be a safe and efficacious candidate for a livestock vaccine. The large deletion in the NSm gene may also provide a negative marker that will allow serologic differentiation of naturally infected animals from vaccinated animals.
Morrill, J. C., Laughlin, R. C., Lokugamage, N., Pugh, R., Sbrana, E., Weise, W. J., ... Peters, C. J.
citation count
50
complete list of authors
Morrill, John C||Laughlin, Richard C||Lokugamage, Nandadeva||Pugh, Roberta||Sbrana, Elena||Weise, William J||Adams, L Garry||Makino, Shinji||Peters, CJ