TY - JOUR
T1 - A DNA vaccine candidate provides protection against Rift Valley Fever virus in sheep under natural field conditions
AU - Mhamadi, Moufid
AU - Babuadze, George
AU - Badji, Aminata
AU - Nepveu-Traversy, Marie Edith
AU - Ndiaye, El Hadji
AU - Gaye, Alioune
AU - Ndiaye, Mignane
AU - Mhamadi, Moundhir
AU - Mendy, Frank William
AU - Touré, Cheikh Talibouya
AU - Dieng, Idrissa
AU - Dia, Moussa
AU - Bob, Ndeye Sakha
AU - de La Vega, Marc-Antoine
AU - Faye, Ousmane
AU - Sall, Amadou Alpha
AU - Diallo, Mawlouth
AU - Kobinger, Gary
AU - Faye, Oumar
AU - Fausther-Bovendo, Hugues
N1 - Publisher Copyright:
Copyright © 2025 Mhamadi, Babuadze, Badji, Nepveu-Traversy, Ndiaye, Gaye, Ndiaye, Mhamadi, Mendy, Touré, Dieng, Dia, Bob, de La Vega, Faye, Sall, Diallo, Kobinger, Faye and Fausther-Bovendo.
PY - 2025
Y1 - 2025
N2 - Rift Valley Fever virus (RVFV) is a mosquito-borne zoonotic pathogen, that causes significant morbidity and mortality in livestock, including high abortion rates in pregnant animals and elevated case fatality in neonates, representing a major threat to both animal and human health. Vaccination is the most effective countermeasure to reduce RVFV’s impact. In this study, we designed a veterinary DNA vaccine encoding a consensus RVFV glycoprotein precursor (GPC), optimized for expression in sheep. The construct was evaluated for immunogenicity in mice and sheep and for protective efficacy in sheep raised under natural field conditions in Senegal, West Africa. The vaccine induced robust humoral responses characterized by high neutralizing antibody titers in both mice and sheep. Under natural exposure, vaccinated sheep showed reduced infection rates (3.2%) compared with controls (14.3%), and neutralizing antibody responses persisted for more than one year. Importantly, the vaccine was well tolerated, including in pregnant animals, with no adverse outcomes such as abortions or fetal abnormalities. These findings demonstrate that a DNA-based RVFV vaccine can elicit durable immunity and provide protection in livestock under real-world conditions. This study highlights the potential of DNA vaccines as a safe, effective, and affordable alternative to existing veterinary vaccines and supports their further development as a key strategy to reduce RVFV transmission and improve animal and human health outcomes in endemic regions.
AB - Rift Valley Fever virus (RVFV) is a mosquito-borne zoonotic pathogen, that causes significant morbidity and mortality in livestock, including high abortion rates in pregnant animals and elevated case fatality in neonates, representing a major threat to both animal and human health. Vaccination is the most effective countermeasure to reduce RVFV’s impact. In this study, we designed a veterinary DNA vaccine encoding a consensus RVFV glycoprotein precursor (GPC), optimized for expression in sheep. The construct was evaluated for immunogenicity in mice and sheep and for protective efficacy in sheep raised under natural field conditions in Senegal, West Africa. The vaccine induced robust humoral responses characterized by high neutralizing antibody titers in both mice and sheep. Under natural exposure, vaccinated sheep showed reduced infection rates (3.2%) compared with controls (14.3%), and neutralizing antibody responses persisted for more than one year. Importantly, the vaccine was well tolerated, including in pregnant animals, with no adverse outcomes such as abortions or fetal abnormalities. These findings demonstrate that a DNA-based RVFV vaccine can elicit durable immunity and provide protection in livestock under real-world conditions. This study highlights the potential of DNA vaccines as a safe, effective, and affordable alternative to existing veterinary vaccines and supports their further development as a key strategy to reduce RVFV transmission and improve animal and human health outcomes in endemic regions.
KW - DNA vaccine
KW - electroporation (EP)
KW - field study
KW - glycoprotein precursor
KW - neutralizing antibodies (NAbs)
KW - RVFV
KW - sheep
KW - veterinary vaccine
UR - https://www.scopus.com/pages/publications/105015539555
UR - https://www.scopus.com/inward/citedby.url?scp=105015539555&partnerID=8YFLogxK
U2 - 10.3389/fcimb.2025.1628877
DO - 10.3389/fcimb.2025.1628877
M3 - Article
C2 - 40934014
AN - SCOPUS:105015539555
SN - 2235-2988
VL - 15
JO - Frontiers in Cellular and Infection Microbiology
JF - Frontiers in Cellular and Infection Microbiology
M1 - 1628877
ER -