Li Yuetao, Zhao Yongkun, Wang Cuiling, Zheng Xuexing, Wang Hualei, Gai Weiwei, Jin Hongli, Yan Feihu, Qiu Boning, Gao Yuwei, Li Nan, Yang Songtao, Xia Xianzhu
College of Animal Science and Veterinary Medicine, Henan Institute of Science and Technology, Xinxiang 453003, China.
Institute of Military Veterinary Medicine, Academy of Military Medical Science, Changchun 130122, China.
J Vet Sci. 2018 Mar 31;19(2):200-206. doi: 10.4142/jvs.2018.19.2.200.
Rift Valley fever (RVF) is an acute, febrile zoonotic disease that is caused by the RVF virus (RVFV). RVF is mainly prevalent on the Arabian Peninsula, the African continent, and several islands in the Indian Ocean near southeast Africa. RVFV has been classified by the World Organisation for Animal Health (OIE) as a category A pathogen. To avoid biological safety concerns associated with use of the pathogen in RVFV neutralization assays, the present study investigated and established an RVFV pseudovirus-based neutralization assay. This study used the human immunodeficiency virus (HIV) lentiviral packaging system and RVFV structural proteins to successfully construct RVFV pseudoviruses. Electron microscopy observation and western blotting indicated that the size, structure, and shape of the packaged pseudoviruses were notably similar to those of HIV lentiviral vectors. Infection inhibition assay results showed that an antibody against RVFV inhibited the infective ability of the RVFV pseudoviruses, and an antibody neutralization assay for RVFV detection was then established. This study has successfully established a neutralization assay based on RVFV pseudoviruses and demonstrated that this method can be used to effectively evaluate antibody neutralization.
裂谷热(RVF)是一种由裂谷热病毒(RVFV)引起的急性发热性人畜共患病。RVF主要流行于阿拉伯半岛、非洲大陆以及非洲东南部附近印度洋的几个岛屿。RVFV已被世界动物卫生组织(OIE)列为A类病原体。为避免在RVFV中和试验中使用病原体带来的生物安全问题,本研究调查并建立了基于RVFV假病毒的中和试验。本研究利用人类免疫缺陷病毒(HIV)慢病毒包装系统和RVFV结构蛋白成功构建了RVFV假病毒。电子显微镜观察和蛋白质印迹表明,包装的假病毒的大小、结构和形状与HIV慢病毒载体显著相似。感染抑制试验结果显示,抗RVFV抗体抑制了RVFV假病毒的感染能力,随后建立了用于RVFV检测的抗体中和试验。本研究成功建立了基于RVFV假病毒的中和试验,并证明该方法可用于有效评估抗体中和作用。