Department of Cell and Developmental Biology, School of Biological Sciences, University of California, San Diego, La Jolla, California, USA.
CSIRO Health and Biosecurity, Australian Centre for Disease Preparedness, Geelong, Australia.
CRISPR J. 2023 Dec;6(6):543-556. doi: 10.1089/crispr.2023.0056.
Escalating vector disease burdens pose significant global health risks, as such innovative tools for targeting mosquitoes are critical. CRISPR-Cas technologies have played a crucial role in developing powerful tools for genome manipulation in various eukaryotic organisms. Although considerable efforts have focused on utilizing class II type II CRISPR-Cas9 systems for DNA targeting, these modalities are unable to target RNA molecules, limiting their utility against RNA viruses. Recently, the Cas13 family has emerged as an efficient tool for RNA targeting; however, the application of this technique in mosquitoes, particularly , has yet to be fully realized. In this study, we engineered an antiviral strategy termed REAPER (vRNA Expression Activates Poisonous Effector Ribonuclease) that leverages the programmable RNA-targeting capabilities of CRISPR-Cas13 and its potent collateral activity. REAPER remains concealed within the mosquito until an infectious blood meal is uptaken. Upon target viral RNA infection, REAPER activates, triggering programmed destruction of its target arbovirus such as chikungunya. Consequently, Cas13-mediated RNA targeting significantly reduces viral replication and viral prevalence of infection, and its promiscuous collateral activity can even kill infected mosquitoes within a few days. This innovative REAPER technology adds to an arsenal of effective molecular genetic tools to combat mosquito virus transmission.
不断升级的病媒传播疾病给全球健康带来了重大风险,因此针对蚊子的创新工具至关重要。CRISPR-Cas 技术在开发针对各种真核生物基因组操作的强大工具方面发挥了关键作用。尽管人们已经投入了相当大的努力来利用 II 类 CRISPR-Cas9 系统进行 DNA 靶向,但这些方法无法靶向 RNA 分子,限制了它们在对抗 RNA 病毒方面的应用。最近,Cas13 家族已成为一种有效的 RNA 靶向工具;然而,该技术在蚊子中的应用尚未得到充分实现。在这项研究中,我们设计了一种名为 REAPER(vRNA Expression Activates Poisonous Effector Ribonuclease)的抗病毒策略,利用了 CRISPR-Cas13 的可编程 RNA 靶向能力及其强大的附带活性。REAPER 在蚊子体内处于潜伏状态,直到摄入了感染性的血液餐。一旦目标病毒 RNA 感染,REAPER 就会被激活,引发对其目标虫媒病毒(如基孔肯雅热病毒)的程序性破坏。因此,Cas13 介导的 RNA 靶向显著降低了病毒复制和感染的病毒流行率,其杂乱无章的附带活性甚至可以在几天内杀死感染的蚊子。这项创新的 REAPER 技术增加了一系列有效的分子遗传工具,以对抗蚊子传播的病毒。