清脆的
病毒学
冠状病毒
大流行
生物
病毒
2019年冠状病毒病(COVID-19)
爆发
甲型流感病毒
病毒复制
计算生物学
作者
Timothy R. Abbott,Girija Dhamdhere,Yanxia Liu,Xueqiu Lin,Laine E. Goudy,Leiping Zeng,Augustine Chemparathy,Stephen Chmura,Nicholas S. Heaton,Robert J. Debs,Tara Pande,Drew Endy,Marie La Russa,David B. Lewis,Lei S. Qi
标识
DOI:10.1101/2020.03.13.991307
摘要
ABSTRACT The outbreak of the coronavirus disease 2019 (COVID-19), caused by the Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2), has infected more than 100,000 people worldwide with over 3,000 deaths since December 2019. There is no cure for COVID-19 and the vaccine development is estimated to require 12-18 months. Here we demonstrate a CRISPR-Cas13-based strategy, PAC-MAN ( P rophylactic A ntiviral C RISPR in huMAN cells), for viral inhibition that can effectively degrade SARS-CoV-2 sequences and live influenza A virus (IAV) genome in human lung epithelial cells. We designed and screened a group of CRISPR RNAs (crRNAs) targeting conserved viral regions and identified functional crRNAs for cleaving SARS-CoV-2. The approach is effective in reducing respiratory cell viral replication for H1N1 IAV. Our bioinformatic analysis showed a group of only six crRNAs can target more than 90% of all coronaviruses. The PAC-MAN approach is potentially a rapidly implementable pan-coronavirus strategy to deal with emerging pandemic strains.
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