Division of Vector-Borne Diseases, Centers for Disease Control and Prevention, Fort Collins, Colorado, United States of America.
PLoS Negl Trop Dis. 2012;6(5):e1639. doi: 10.1371/journal.pntd.0001639. Epub 2012 May 1.
Rift Valley fever virus is an arthropod-borne human and animal pathogen responsible for large outbreaks of acute and febrile illness throughout Africa and the Arabian Peninsula. Reverse genetics technology has been used to develop deletion mutants of the virus that lack the NSs and/or NSm virulence genes and have been shown to be stable, immunogenic and protective against Rift Valley fever virus infection in animals. We assessed the potential for these deletion mutant viruses to infect and be transmitted by Aedes mosquitoes, which are the principal vectors for maintenance of the virus in nature and emergence of virus initiating disease outbreaks, and by Culex mosquitoes which are important amplification vectors.
Aedes aegypti and Culex quinquefasciatus mosquitoes were fed bloodmeals containing the deletion mutant viruses. Two weeks post-exposure mosquitoes were assayed for infection, dissemination, and transmission. In Ae. aegypti, infection and transmission rates of the NSs deletion virus were similar to wild type virus while dissemination rates were significantly reduced. Infection and dissemination rates for the NSm deletion virus were lower compared to wild type. Virus lacking both NSs and NSm failed to infect Ae. aegypti. In Cx. quinquefasciatus, infection rates for viruses lacking NSm or both NSs and NSm were lower than for wild type virus.
CONCLUSIONS/SIGNIFICANCE: In both species, deletion of NSm or both NSs and NSm reduced the infection and transmission potential of the virus. Deletion of both NSs and NSm resulted in the highest level of attenuation of virus replication. Deletion of NSm alone was sufficient to nearly abolish infection in Aedes aegypti mosquitoes, indicating an important role for this protein. The double deleted viruses represent an ideal vaccine profile in terms of environmental containment due to lack of ability to efficiently infect and be transmitted by mosquitoes.
裂谷热病毒是一种节肢动物传播的人畜共患病病原体,可导致非洲和阿拉伯半岛的急性和发热疾病大规模爆发。反向遗传学技术已被用于开发缺失突变体病毒,这些病毒缺乏 NSs 和/或 NSm 毒力基因,并且已被证明在动物中稳定、具有免疫原性和对裂谷热病毒感染具有保护作用。我们评估了这些缺失突变病毒感染和通过埃及伊蚊(Aedes aegypti)和致倦库蚊(Culex quinquefasciatus)传播的潜力,埃及伊蚊是病毒在自然界中维持和引发病毒病爆发的主要传播媒介,而致倦库蚊则是重要的扩增传播媒介。
埃及伊蚊和致倦库蚊吸食含有缺失突变病毒的血餐。暴露后两周,检测蚊子的感染、传播和传播情况。在埃及伊蚊中,NSs 缺失病毒的感染和传播率与野生型病毒相似,而传播率显著降低。NSm 缺失病毒的感染和传播率较野生型低。同时缺失 NSs 和 NSm 的病毒无法感染埃及伊蚊。在致倦库蚊中,缺失 NSm 或 NSs 和 NSm 的病毒感染率均低于野生型病毒。
结论/意义:在这两种物种中,缺失 NSm 或 NSs 和 NSm 都会降低病毒的感染和传播潜力。同时缺失 NSs 和 NSm 导致病毒复制的衰减程度最高。单独缺失 NSm 就足以使埃及伊蚊几乎无法感染病毒,表明该蛋白的重要作用。由于缺乏有效感染和通过蚊子传播的能力,缺失 NSm 的双缺失病毒在环境控制方面代表了理想的疫苗特征。