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Genome-wide CRISPR screening identifies TMEM106B as a proviral host factor for SARS-CoV-2.
Baggen, Jim; Persoons, Leentje; Vanstreels, Els; Jansen, Sander; Van Looveren, Dominique; Boeckx, Bram; Geudens, Vincent; De Man, Julie; Jochmans, Dirk; Wauters, Joost; Wauters, Els; Vanaudenaerde, Bart M; Lambrechts, Diether; Neyts, Johan; Dallmeier, Kai; Thibaut, Hendrik Jan; Jacquemyn, Maarten; Maes, Piet; Daelemans, Dirk.
  • Baggen J; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium. jim.baggen@kuleuven.be.
  • Persoons L; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Vanstreels E; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Jansen S; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Van Looveren D; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Boeckx B; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Translational Platform Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Geudens V; KU Leuven Department of Human Genetics, Laboratory for Translational Genetics, Leuven, Belgium.
  • De Man J; VIB Center for Cancer Biology, VIB, Leuven, Belgium.
  • Jochmans D; KU Leuven Department of Chronic Diseases and Metabolism, Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Leuven, Belgium.
  • Wauters J; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Wauters E; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Vanaudenaerde BM; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Clinical Infectious and Inflammatory Disorders, Leuven, Belgium.
  • Lambrechts D; KU Leuven Department of Chronic Diseases and Metabolism, Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Leuven, Belgium.
  • Neyts J; KU Leuven Department of Chronic Diseases and Metabolism, Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Leuven, Belgium.
  • Dallmeier K; KU Leuven Department of Human Genetics, Laboratory for Translational Genetics, Leuven, Belgium.
  • Thibaut HJ; VIB Center for Cancer Biology, VIB, Leuven, Belgium.
  • Jacquemyn M; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Maes P; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
  • Daelemans D; KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute, Leuven, Belgium.
Nat Genet ; 53(4): 435-444, 2021 04.
Article in English | MEDLINE | ID: covidwho-1123140
ABSTRACT
The ongoing COVID-19 pandemic has caused a global economic and health crisis. To identify host factors essential for coronavirus infection, we performed genome-wide functional genetic screens with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and human coronavirus 229E. These screens uncovered virus-specific as well as shared host factors, including TMEM41B and PI3K type 3. We discovered that SARS-CoV-2 requires the lysosomal protein TMEM106B to infect human cell lines and primary lung cells. TMEM106B overexpression enhanced SARS-CoV-2 infection as well as pseudovirus infection, suggesting a role in viral entry. Furthermore, single-cell RNA-sequencing of airway cells from patients with COVID-19 demonstrated that TMEM106B expression correlates with SARS-CoV-2 infection. The present study uncovered a collection of coronavirus host factors that may be exploited to develop drugs against SARS-CoV-2 infection or future zoonotic coronavirus outbreaks.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Genome, Human / Genome-Wide Association Study / CRISPR-Cas Systems / COVID-19 / Membrane Proteins / Nerve Tissue Proteins Type of study: Observational study Limits: Humans Language: English Journal: Nat Genet Journal subject: Genetics, Medical Year: 2021 Document Type: Article Affiliation country: S41588-021-00805-2

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Genome, Human / Genome-Wide Association Study / CRISPR-Cas Systems / COVID-19 / Membrane Proteins / Nerve Tissue Proteins Type of study: Observational study Limits: Humans Language: English Journal: Nat Genet Journal subject: Genetics, Medical Year: 2021 Document Type: Article Affiliation country: S41588-021-00805-2