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TMEM41B Is a Pan-flavivirus Host Factor.
Hoffmann, H-Heinrich; Schneider, William M; Rozen-Gagnon, Kathryn; Miles, Linde A; Schuster, Felix; Razooky, Brandon; Jacobson, Eliana; Wu, Xianfang; Yi, Soon; Rudin, Charles M; MacDonald, Margaret R; McMullan, Laura K; Poirier, John T; Rice, Charles M.
  • Hoffmann HH; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Schneider WM; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Rozen-Gagnon K; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Miles LA; Human Oncology & Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Schuster F; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA; Institute of Virology, Medical Faculty "Carl Gustav Carus", Technische Universität Dresden, Dresden, Germany.
  • Razooky B; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Jacobson E; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Wu X; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Yi S; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • Rudin CM; Druckenmiller Center for Lung Cancer Research and Department of Medicine, Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • MacDonald MR; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.
  • McMullan LK; Virus Special Pathogens Branch, Division of High Consequence Pathogens and Pathology, Centers of Disease Control and Prevention, Atlanta, GA, USA.
  • Poirier JT; Laura and Isaac Perlmutter Cancer Center, New York University Langone Health, New York, NY, USA. Electronic address: john.poirier@nyulangone.org.
  • Rice CM; Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA. Electronic address: ricec@rockefeller.edu.
Cell ; 184(1): 133-148.e20, 2021 01 07.
Article in English | MEDLINE | ID: covidwho-987228
ABSTRACT
Flaviviruses pose a constant threat to human health. These RNA viruses are transmitted by the bite of infected mosquitoes and ticks and regularly cause outbreaks. To identify host factors required for flavivirus infection, we performed full-genome loss of function CRISPR-Cas9 screens. Based on these results, we focused our efforts on characterizing the roles that TMEM41B and VMP1 play in the virus replication cycle. Our mechanistic studies on TMEM41B revealed that all members of the Flaviviridae family that we tested require TMEM41B. We tested 12 additional virus families and found that SARS-CoV-2 of the Coronaviridae also required TMEM41B for infection. Remarkably, single nucleotide polymorphisms present at nearly 20% in East Asian populations reduce flavivirus infection. Based on our mechanistic studies, we propose that TMEM41B is recruited to flavivirus RNA replication complexes to facilitate membrane curvature, which creates a protected environment for viral genome replication.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Flavivirus Infections / Flavivirus / Membrane Proteins Limits: Animals / Humans Language: English Journal: Cell Year: 2021 Document Type: Article Affiliation country: J.cell.2020.12.005

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Flavivirus Infections / Flavivirus / Membrane Proteins Limits: Animals / Humans Language: English Journal: Cell Year: 2021 Document Type: Article Affiliation country: J.cell.2020.12.005