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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.
  • Novelli G; Department of Biomedicine and Prevention, Tor Vergata University of Rome, 00133, Rome, Italy. novelli@med.uniroma2.it.
  • Liu J; IRCCS Neuromed, Pozzilli, (IS), Italy. novelli@med.uniroma2.it.
  • Biancolella M; Department of Pharmacology, School of Medicine, University of Nevada, Reno, NV, 89557, USA. novelli@med.uniroma2.it.
  • Alonzi T; Department of Pathology, Beth Israel Deaconess Cancer Center, Harvard Medical School, Boston, MA, 02215, USA.
  • Novelli A; Department of Biology, Tor Vergata University, 00133, Rome, Italy.
  • Patten JJ; Translational Research Unit, Department of Epidemiology and Preclinical Research, National Institute for Infectious Diseases Lazzaro Spallanzani - IRCCS, 00149, Rome, Italy.
  • Cocciadiferro D; Laboratory of Medical Genetics, IRCCS Bambino Gesù Children's Hospital, 00165, Rome, Italy.
  • Agolini E; National Emerging Infectious Diseases Laboratories, Boston University, Boston, MA, USA.
  • Colona VL; Laboratory of Medical Genetics, IRCCS Bambino Gesù Children's Hospital, 00165, Rome, Italy.
  • Rizzacasa B; Laboratory of Medical Genetics, IRCCS Bambino Gesù Children's Hospital, 00165, Rome, Italy.
  • Giannini R; Department of Biomedicine and Prevention, Tor Vergata University of Rome, 00133, Rome, Italy.
  • Bigio B; Department of Biomedicine and Prevention, Tor Vergata University of Rome, 00133, Rome, Italy.
  • Goletti D; Department of Biomedicine and Prevention, Tor Vergata University of Rome, 00133, Rome, Italy.
  • Capobianchi MR; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, 10065, USA.
  • Grelli S; Translational Research Unit, Department of Epidemiology and Preclinical Research, National Institute for Infectious Diseases Lazzaro Spallanzani - IRCCS, 00149, Rome, Italy.
  • Mann J; Laboratory of Virology, Department of Epidemiology and Preclinical Research, National Institute for Infectious Diseases Lazzaro Spallanzani - IRCCS, 00149, Rome, Italy.
  • McKee TD; Department of Experimental Medicine, Tor Vergata University of Rome, 00133, Rome, Italy.
  • Cheng K; HistoWiz Inc, Brooklyn, NY, 11226, USA.
  • Amanat F; HistoWiz Inc, Brooklyn, NY, 11226, USA.
  • Krammer F; HistoWiz Inc, Brooklyn, NY, 11226, USA.
  • Guarracino A; Department of Microbiology, Icahn school of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Pepe G; Department of Microbiology, Icahn school of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Tomino C; Department of Biology, Tor Vergata University, 00133, Rome, Italy.
  • Tandjaoui-Lambiotte Y; Department of Biology, Tor Vergata University, 00133, Rome, Italy.
  • Uzunhan Y; San Raffaele University of Rome, 00166, Rome, Italy.
  • Tubiana S; Intensive Care Unit, Avicenne Hospital, APHP, Bobigny, France.
  • Ghosn J; INSERM U1272 Hypoxia & Lung, Bobigny, France.
  • Notarangelo LD; Infection, Antimicrobials, Modelling, Evolution (IAME), INSERM, UMRS1137, University of Paris, Paris, France.
  • Su HC; AP-HP, Bichat Claude Bernard Hospital, Infectious and Tropical Disease Department, Paris, France.
  • Grzymski JJ; Laboratory of Clinical Immunology, NIAID, NIH, Bethesda, MD, USA.
  • Latini A; Laboratory of Clinical Immunology, NIAID, NIH, Bethesda, MD, USA.
  • Sidhu SS; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, 10065, USA.
  • Jain S; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM, Necker Hospital for Sick Children, Paris, France.
  • Davey RA; University of Paris, Imagine Institute, Paris, France.
  • Casanova JL; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, 10065, USA.
  • Wei W; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM, Necker Hospital for Sick Children, Paris, France.
  • Pandolfi PP; University of Paris, Imagine Institute, Paris, France.
Cell Death Dis ; 12(4): 310, 2021 03 24.
Article in English | MEDLINE | ID: covidwho-1149708
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ubiquitin-Protein Ligases / COVID-19 / COVID-19 Drug Treatment Type of study: Prognostic study Topics: Variants Limits: Adult / Aged / Animals / Female / Humans / Male / Middle aged Language: English Journal: Cell Death Dis Year: 2021 Document Type: Article Affiliation country: S41419-021-03513-1

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ubiquitin-Protein Ligases / COVID-19 / COVID-19 Drug Treatment Type of study: Prognostic study Topics: Variants Limits: Adult / Aged / Animals / Female / Humans / Male / Middle aged Language: English Journal: Cell Death Dis Year: 2021 Document Type: Article Affiliation country: S41419-021-03513-1