登革热
登革热病毒
体内
信使核糖核酸
病毒学
体外
核糖核酸
生物
免疫学
基因
生物化学
生物技术
作者
Mausumi Basu,Chiara Zurla,Tabassum Tasnim Auroni,Daryll Vanover,Lorena C. S. Chaves,Heena Sadhwani,Heather Pathak,Rahul Basu,Jared Beyersdorf,Oluwatomi Olufunke Amuda,Amany Elsharkawy,Varun Mosur,Robert A. Arthur,Henry Claussen,Loren E. Sasser,James A. Wroe,Hannah E. Peck,Mukesh Kumar,Margo A. Brinton,Philip J. Santangelo
出处
期刊:Nature microbiology
日期:2024-06-05
卷期号:9 (8): 2160-2172
被引量:2
标识
DOI:10.1038/s41564-024-01726-6
摘要
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. Potent CRISPR guides targeting conserved dengue virus regions can treat dengue-2 and -3 infection in vivo in mice when co-delivered with Cas13 by lipid nanoparticles.
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