Basu Mausumi, Zurla Chiara, Auroni Tabassum T, Vanover Daryll, Chaves Lorena C S, Sadhwani Heena, Pathak Heather, Basu Rahul, Beyersdorf Jared P, Amuda Oluwatomi O, Elsharkawy Amany, Mosur Varun, Arthur Robert A, Claussen Henry, Sasser Loren E, Wroe Jay A, Peck Hannah E, Kumar Mukesh, Brinton Margo A, Santangelo Philip J
Department of Biology, Georgia State University, Atlanta, GA, USA.
Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, USA.
Nat Microbiol. 2024 Aug;9(8):2160-2172. doi: 10.1038/s41564-024-01726-6. Epub 2024 Jun 5.
Dengue is a major global health threat, and there are no approved antiviral agents. Prior research using Cas13 only demonstrated dengue mitigation in vitro. Here we demonstrate that systemic delivery of mRNA-encoded Cas13a and guide RNAs formulated in lipid nanoparticles can be used to treat dengue virus (DENV) 2 and 3 in mice. First, we identified guides against DENV 2 and 3 that demonstrated in vitro efficacy. Next, we confirmed that Cas13 enzymatic activity is necessary for DENV 2 or DENV 3 mitigation in vitro. Last, we show that a single dose of lipid-nanoparticle-formulated mRNA-encoded Cas13a and guide RNA, administered 1 day post-infection, promotes survival of all infected animals and serum viral titre decreases on days 2 and 3 post-infection after lethal challenge in mice. Off-target analysis in mice using RNA sequencing showed no collateral cleavage. Overall, these data demonstrate the potential of mRNA-encoded Cas13 as a pan-DENV drug.
登革热是全球主要的健康威胁,目前尚无获批的抗病毒药物。先前使用Cas13的研究仅在体外证明了对登革热的缓解作用。在此,我们证明,通过脂质纳米颗粒系统性递送mRNA编码的Cas13a和引导RNA可用于治疗小鼠体内的登革热病毒(DENV)2型和3型感染。首先,我们鉴定出了对DENV 2型和3型具有体外疗效的引导RNA。其次,我们证实了Cas13酶活性对于体外缓解DENV 2型或DENV 3型感染是必需的。最后,我们表明,在感染后1天给予单剂量脂质纳米颗粒配制的mRNA编码的Cas13a和引导RNA,可提高所有感染动物的存活率,并且在对小鼠进行致死性攻击后,感染后第2天和第3天血清病毒滴度降低。使用RNA测序对小鼠进行的脱靶分析显示没有附带切割。总体而言,这些数据证明了mRNA编码的Cas13作为一种泛DENV药物的潜力。