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Genetic Screens Identify Host Factors for SARS-CoV-2 and Common Cold Coronaviruses.
Wang, Ruofan; Simoneau, Camille R; Kulsuptrakul, Jessie; Bouhaddou, Mehdi; Travisano, Katherine A; Hayashi, Jennifer M; Carlson-Stevermer, Jared; Zengel, James R; Richards, Christopher M; Fozouni, Parinaz; Oki, Jennifer; Rodriguez, Lauren; Joehnk, Bastian; Walcott, Keith; Holden, Kevin; Sil, Anita; Carette, Jan E; Krogan, Nevan J; Ott, Melanie; Puschnik, Andreas S.
  • Wang R; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
  • Simoneau CR; Gladstone Institutes, San Francisco, CA 94158, USA; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA; Biomedical Scie
  • Kulsuptrakul J; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
  • Bouhaddou M; Gladstone Institutes, San Francisco, CA 94158, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA; Quantitative Biosciences Institute (QBI), University of California, San Francisco, San Francisco, CA 94158, US
  • Travisano KA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
  • Hayashi JM; Gladstone Institutes, San Francisco, CA 94158, USA; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA.
  • Carlson-Stevermer J; Synthego Corporation, Menlo Park, CA 94025, USA.
  • Zengel JR; Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.
  • Richards CM; Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.
  • Fozouni P; Gladstone Institutes, San Francisco, CA 94158, USA; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA; Biomedical Scie
  • Oki J; Synthego Corporation, Menlo Park, CA 94025, USA.
  • Rodriguez L; UCSF CoLabs, Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Joehnk B; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Walcott K; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Holden K; Synthego Corporation, Menlo Park, CA 94025, USA.
  • Sil A; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Carette JE; Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.
  • Krogan NJ; Gladstone Institutes, San Francisco, CA 94158, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA; Quantitative Biosciences Institute (QBI), University of California, San Francisco, San Francisco, CA 94158, US
  • Ott M; Gladstone Institutes, San Francisco, CA 94158, USA; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA. Electronic addr
  • Puschnik AS; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA. Electronic address: andreas.puschnik@czbiohub.org.
Cell ; 184(1): 106-119.e14, 2021 01 07.
Article in English | MEDLINE | ID: covidwho-1064913
ABSTRACT
The Coronaviridae are a family of viruses that cause disease in humans ranging from mild respiratory infection to potentially lethal acute respiratory distress syndrome. Finding host factors common to multiple coronaviruses could facilitate the development of therapies to combat current and future coronavirus pandemics. Here, we conducted genome-wide CRISPR screens in cells infected by SARS-CoV-2 as well as two seasonally circulating common cold coronaviruses, OC43 and 229E. This approach correctly identified the distinct viral entry factors ACE2 (for SARS-CoV-2), aminopeptidase N (for 229E), and glycosaminoglycans (for OC43). Additionally, we identified phosphatidylinositol phosphate biosynthesis and cholesterol homeostasis as critical host pathways supporting infection by all three coronaviruses. By contrast, the lysosomal protein TMEM106B appeared unique to SARS-CoV-2 infection. Pharmacological inhibition of phosphatidylinositol kinases and cholesterol homeostasis reduced replication of all three coronaviruses. These findings offer important insights for the understanding of the coronavirus life cycle and the development of host-directed therapies.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus Infections / Coronavirus / Host-Pathogen Interactions / Genome-Wide Association Study / SARS-CoV-2 / COVID-19 Limits: Animals / Humans Language: English Journal: Cell Year: 2021 Document Type: Article Affiliation country: J.cell.2020.12.004

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus Infections / Coronavirus / Host-Pathogen Interactions / Genome-Wide Association Study / SARS-CoV-2 / COVID-19 Limits: Animals / Humans Language: English Journal: Cell Year: 2021 Document Type: Article Affiliation country: J.cell.2020.12.004