| Literature DB >> 33762578 |
Giuseppe Novelli1,2,3, Jing Liu4, Michela Biancolella5, Tonino Alonzi6, Antonio Novelli7, J J Patten8, Dario Cocciadiferro7, Emanuele Agolini7, Vito Luigi Colona9, Barbara Rizzacasa9, Rosalinda Giannini9, Benedetta Bigio10, Delia Goletti6, Maria Rosaria Capobianchi11, Sandro Grelli12, Justin Mann13, Trevor D McKee13, Ke Cheng13, Fatima Amanat14, Florian Krammer14, Andrea Guarracino5, Gerardo Pepe5, Carlo Tomino15, Yacine Tandjaoui-Lambiotte16,17, Yurdagul Uzunhan18, Sarah Tubiana19,20, Jade Ghosn21,22, Luigi D Notarangelo23, Helen C Su23, Laurent Abel10,24,25, Aurélie Cobat10,24,25, Gai Elhanan26,27, Joseph J Grzymski26,27, Andrea Latini9, Sachdev S Sidhu28, Suresh Jain29, Robert A Davey30, Jean-Laurent Casanova10,24,25,31, Wenyi Wei4, Pier Paolo Pandolfi32,33,34.
Abstract
SARS-CoV-2 is responsible for the ongoing world-wide pandemic which has already taken more than two million lives. Effective treatments are urgently needed. The enzymatic activity of the HECT-E3 ligase family members has been implicated in the cell egression phase of deadly RNA viruses such as Ebola through direct interaction of its VP40 Protein. Here we report that HECT-E3 ligase family members such as NEDD4 and WWP1 interact with and ubiquitylate the SARS-CoV-2 Spike protein. Furthermore, we find that HECT family members are overexpressed in primary samples derived from COVID-19 infected patients and COVID-19 mouse models. Importantly, rare germline activating variants in the NEDD4 and WWP1 genes are associated with severe COVID-19 cases. Critically, I3C, a natural NEDD4 and WWP1 inhibitor from Brassicaceae, displays potent antiviral effects and inhibits viral egression. In conclusion, we identify the HECT family members of E3 ligases as likely novel biomarkers for COVID-19, as well as new potential targets of therapeutic strategy easily testable in clinical trials in view of the established well-tolerated nature of the Brassicaceae natural compounds.Entities:
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Year: 2021 PMID: 33762578 PMCID: PMC7987752 DOI: 10.1038/s41419-021-03513-1
Source DB: PubMed Journal: Cell Death Dis Impact factor: 8.469