Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
J Virol. 2018 May 14;92(11). doi: 10.1128/JVI.00027-18. Print 2018 Jun 1.
Zoonotic viruses circulate as swarms in animal reservoirs and can emerge into human populations, causing epidemics that adversely affect public health. Portable, safe, and effective vaccine platforms are needed in the context of these outbreak and emergence situations. In this work, we report the generation and characterization of an alphavirus replicon vaccine platform based on a non-select agent, attenuated Venezuelan equine encephalitis (VEE) virus vaccine, strain 3526 (VRP 3526). Using both noroviruses and coronaviruses as model systems, we demonstrate the utility of the VRP 3526 platform in the generation of recombinant proteins, production of virus-like particles, and efficacy as a vaccine against emergent viruses. Importantly, packaging under biosafety level 2 (BSL2) conditions distinguishes VRP 3526 from previously reported alphavirus platforms and makes this approach accessible to the majority of laboratories around the world. In addition, improved outcomes in the vulnerable aged models as well as against heterologous challenge suggest improved efficacy compared to that of previously attenuated VRP approaches. Taking these results together, the VRP 3526 platform represents a safe and highly portable system that can be rapidly deployed under BSL2 conditions for generation of candidate vaccines against emerging microbial pathogens. While VEE virus replicon particles provide a robust, established platform for antigen expression and vaccination, its utility has been limited by the requirement for high-containment-level facilities for production and packaging. In this work, we utilize an attenuated vaccine strain capable of use at lower biocontainment level but retaining the capacity of the wild-type replicon particle. Importantly, the new replicon platform provides equal protection for aged mice and following heterologous challenge, which distinguishes it from other attenuated replicon platforms. Together, the new system represents a highly portable, safe system for use in the context of disease emergence.
人畜共患病病毒在动物宿主中呈群集形式传播,可能会传入人类群体,引发对公共健康产生不利影响的流行病。在这些爆发和出现的情况下,需要便携式、安全和有效的疫苗平台。在这项工作中,我们报告了一种基于非选择性制剂、减毒委内瑞拉马脑炎(VEE)病毒疫苗株 3526(VRP 3526)的甲病毒复制子疫苗平台的生成和表征。我们使用诺如病毒和冠状病毒作为模型系统,证明了 VRP 3526 平台在生成重组蛋白、生产病毒样颗粒和作为针对新兴病毒的疫苗的功效方面的实用性。重要的是,在生物安全 2 级(BSL2)条件下进行包装使 VRP 3526 有别于之前报道的甲病毒平台,使这种方法可以被全球大多数实验室所接受。此外,在脆弱的老年模型中的改善结果以及对异源挑战的改善表明,与之前的减毒 VRP 方法相比,该方法的疗效有所提高。综合这些结果,VRP 3526 平台代表了一种安全且高度便携的系统,可以在 BSL2 条件下快速部署,用于生成针对新兴微生物病原体的候选疫苗。虽然 VEE 病毒复制子颗粒为抗原表达和疫苗接种提供了一个强大的、已建立的平台,但由于其生产和包装需要高生物安全水平设施,其应用受到限制。在这项工作中,我们利用一种能够在较低生物安全水平下使用但保留野生型复制子颗粒能力的减毒疫苗株。重要的是,新的复制子平台为老年小鼠和异源挑战后提供了同等的保护,这使其有别于其他减毒复制子平台。总的来说,该新系统代表了一种在疾病出现情况下高度便携、安全的系统。