Institute of Human Infection and Immunity, Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-0610, USA.
Virology. 2013 Mar 15;437(2):81-8. doi: 10.1016/j.virol.2012.11.013. Epub 2013 Jan 22.
Venezuelan equine encephalitis virus (VEEV) is an arbovirus that causes periodic outbreaks that impact equine and human populations in the Americas. One of the VEEV subtypes located in Mexico and Central America (IE) has recently been recognized as an important cause of equine disease and death, and human exposure also appears to be widespread. Here, we describe the use of an Internal Ribosome Entry Site (IRES) from encephalomyocarditis virus to stably attenuate VEEV, creating a vaccine candidate independent of unstable point mutations. Mice infected with this virus produced antibodies and were protected against lethal VEEV challenge. This IRES-based vaccine was unable to establish productive infection in mosquito cell cultures or in intrathoracically injected Aedes taeniorhynchus, demonstrating that it cannot be transmitted from a vaccinee. These attenuation, efficacy and safety results justify further development for humans or equids of this new VEEV vaccine candidate.
委内瑞拉马脑炎病毒(VEEV)是一种虫媒病毒,会定期爆发,影响美洲的马和人群。在墨西哥和中美洲(IE)发现的一种 VEEV 亚型最近被认为是马疾病和死亡的重要原因,人类接触也似乎很普遍。在这里,我们描述了使用脑炎心肌炎病毒的内部核糖体进入位点(IRES)来稳定减毒 VEEV,从而创造了一种不依赖不稳定点突变的疫苗候选物。感染这种病毒的小鼠产生了抗体,并能抵抗致死性 VEEV 攻击。这种基于 IRES 的疫苗不能在蚊子细胞培养物或经胸注射的致倦库蚊中建立有效的感染,表明它不能从疫苗接种者传播。这些减毒、疗效和安全性结果证明,这种新的 VEEV 疫苗候选物在人类或马属动物中进一步开发是合理的。