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Inhibition of HECT E3 ligases as potential therapy for COVID-19
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987752/ https://www.ncbi.nlm.nih.gov/pubmed/33762578 http://dx.doi.org/10.1038/s41419-021-03513-1 |
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author | Novelli, Giuseppe Liu, Jing Biancolella, Michela Alonzi, Tonino Novelli, Antonio Patten, J. J. Cocciadiferro, Dario Agolini, Emanuele Colona, Vito Luigi Rizzacasa, Barbara Giannini, Rosalinda Bigio, Benedetta Goletti, Delia Capobianchi, Maria Rosaria Grelli, Sandro Mann, Justin McKee, Trevor D. Cheng, Ke Amanat, Fatima Krammer, Florian Guarracino, Andrea Pepe, Gerardo Tomino, Carlo Tandjaoui-Lambiotte, Yacine Uzunhan, Yurdagul Tubiana, Sarah Ghosn, Jade Notarangelo, Luigi D. Su, Helen C. Abel, Laurent Cobat, Aurélie Elhanan, Gai Grzymski, Joseph J. Latini, Andrea Sidhu, Sachdev S. Jain, Suresh Davey, Robert A. Casanova, Jean-Laurent Wei, Wenyi Pandolfi, Pier Paolo |
author_facet | Novelli, Giuseppe Liu, Jing Biancolella, Michela Alonzi, Tonino Novelli, Antonio Patten, J. J. Cocciadiferro, Dario Agolini, Emanuele Colona, Vito Luigi Rizzacasa, Barbara Giannini, Rosalinda Bigio, Benedetta Goletti, Delia Capobianchi, Maria Rosaria Grelli, Sandro Mann, Justin McKee, Trevor D. Cheng, Ke Amanat, Fatima Krammer, Florian Guarracino, Andrea Pepe, Gerardo Tomino, Carlo Tandjaoui-Lambiotte, Yacine Uzunhan, Yurdagul Tubiana, Sarah Ghosn, Jade Notarangelo, Luigi D. Su, Helen C. Abel, Laurent Cobat, Aurélie Elhanan, Gai Grzymski, Joseph J. Latini, Andrea Sidhu, Sachdev S. Jain, Suresh Davey, Robert A. Casanova, Jean-Laurent Wei, Wenyi Pandolfi, Pier Paolo |
author_sort | Novelli, Giuseppe |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7987752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79877522021-03-24 Inhibition of HECT E3 ligases as potential therapy for COVID-19 Novelli, Giuseppe Liu, Jing Biancolella, Michela Alonzi, Tonino Novelli, Antonio Patten, J. J. Cocciadiferro, Dario Agolini, Emanuele Colona, Vito Luigi Rizzacasa, Barbara Giannini, Rosalinda Bigio, Benedetta Goletti, Delia Capobianchi, Maria Rosaria Grelli, Sandro Mann, Justin McKee, Trevor D. Cheng, Ke Amanat, Fatima Krammer, Florian Guarracino, Andrea Pepe, Gerardo Tomino, Carlo Tandjaoui-Lambiotte, Yacine Uzunhan, Yurdagul Tubiana, Sarah Ghosn, Jade Notarangelo, Luigi D. Su, Helen C. Abel, Laurent Cobat, Aurélie Elhanan, Gai Grzymski, Joseph J. Latini, Andrea Sidhu, Sachdev S. Jain, Suresh Davey, Robert A. Casanova, Jean-Laurent Wei, Wenyi Pandolfi, Pier Paolo Cell Death Dis Article 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. Nature Publishing Group UK 2021-03-24 /pmc/articles/PMC7987752/ /pubmed/33762578 http://dx.doi.org/10.1038/s41419-021-03513-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Novelli, Giuseppe Liu, Jing Biancolella, Michela Alonzi, Tonino Novelli, Antonio Patten, J. J. Cocciadiferro, Dario Agolini, Emanuele Colona, Vito Luigi Rizzacasa, Barbara Giannini, Rosalinda Bigio, Benedetta Goletti, Delia Capobianchi, Maria Rosaria Grelli, Sandro Mann, Justin McKee, Trevor D. Cheng, Ke Amanat, Fatima Krammer, Florian Guarracino, Andrea Pepe, Gerardo Tomino, Carlo Tandjaoui-Lambiotte, Yacine Uzunhan, Yurdagul Tubiana, Sarah Ghosn, Jade Notarangelo, Luigi D. Su, Helen C. Abel, Laurent Cobat, Aurélie Elhanan, Gai Grzymski, Joseph J. Latini, Andrea Sidhu, Sachdev S. Jain, Suresh Davey, Robert A. Casanova, Jean-Laurent Wei, Wenyi Pandolfi, Pier Paolo Inhibition of HECT E3 ligases as potential therapy for COVID-19 |
title | Inhibition of HECT E3 ligases as potential therapy for COVID-19 |
title_full | Inhibition of HECT E3 ligases as potential therapy for COVID-19 |
title_fullStr | Inhibition of HECT E3 ligases as potential therapy for COVID-19 |
title_full_unstemmed | Inhibition of HECT E3 ligases as potential therapy for COVID-19 |
title_short | Inhibition of HECT E3 ligases as potential therapy for COVID-19 |
title_sort | inhibition of hect e3 ligases as potential therapy for covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987752/ https://www.ncbi.nlm.nih.gov/pubmed/33762578 http://dx.doi.org/10.1038/s41419-021-03513-1 |
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