Mhamadi Moufid, Babuadze George Giorgi, Badji Aminata, Nepveu-Traversy Marie-Edith, Ndiaye El Hadji, Gaye Alioune, Ndiaye Mignane, Mhamadi Moundhir, Mendy Frank William, Touré Cheikh Talibouya, Dieng Idrissa, Dia Moussa, Bob Ndeye Sakha, de La Vega Marc-Antoine, Faye Ousmane, Sall Amadou Alpha, Diallo Mawlouth, Kobinger Gary, Faye Oumar, Fausther-Bovendo Hugues
Virology Department, The Pasteur Institute of Dakar, Dakar, Senegal.
Vaccine Research Center, Department of Preclinical Trials, The Institut Pasteur of Dakar, Dakar, Senegal.
Front Cell Infect Microbiol. 2025 Aug 26;15:1628877. doi: 10.3389/fcimb.2025.1628877. eCollection 2025.
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.
裂谷热病毒(RVFV)是一种由蚊子传播的人畜共患病原体,可导致家畜出现严重发病和死亡,包括怀孕动物的高流产率和新生儿的高病死率,对动物和人类健康均构成重大威胁。疫苗接种是减少RVFV影响的最有效对策。在本研究中,我们设计了一种兽医DNA疫苗,其编码一种经优化可在绵羊中表达的裂谷热病毒糖蛋白前体(GPC)共识序列。该构建体在小鼠和绵羊中进行了免疫原性评估,并在西非塞内加尔的自然野外条件下饲养的绵羊中进行了保护效力评估。该疫苗在小鼠和绵羊中均诱导了以高中和抗体滴度为特征的强烈体液免疫反应。在自然暴露情况下,与对照组(14.3%)相比,接种疫苗的绵羊感染率降低(3.2%),且中和抗体反应持续了一年多。重要的是,该疫苗耐受性良好,包括在怀孕动物中,未出现流产或胎儿异常等不良后果。这些发现表明,基于DNA的裂谷热病毒疫苗可引发持久免疫力,并在实际条件下为家畜提供保护。本研究突出了DNA疫苗作为现有兽医疫苗的一种安全、有效且经济实惠的替代品的潜力,并支持将其进一步开发作为减少裂谷热病毒传播以及改善流行地区动物和人类健康状况的关键策略。