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Identification of TMEM106B as proviral host factor for SARS-CoV-2
Jim Baggen; Leentje Persoons; Sander Jansen; Els Vanstreels; Maarten Jacquemyn; Dirk Jochmans; Johan Neyts; Kai Dallmeier; Piet Maes; Dirk Daelemans.
Afiliación
  • Jim Baggen; KU Leuven Rega institute
  • Leentje Persoons; KU Leuven Rega institute
  • Sander Jansen; KU Leuven Rega institute
  • Els Vanstreels; KU Leuven Rega institute
  • Maarten Jacquemyn; KU Leuven Rega institute
  • Dirk Jochmans; KU Leuven Rega institute
  • Johan Neyts; KU Leuven Rega institute
  • Kai Dallmeier; KU Leuven Rega institute
  • Piet Maes; KU Leuven, Rega institute
  • Dirk Daelemans; KU Leuven Rega institute
Preprint en Inglés | bioRxiv | ID: ppbiorxiv-316281
ABSTRACT
The ongoing COVID-19 pandemic is responsible for worldwide economic damage and nearly one million deaths. Potent drugs for the treatment of severe SARS-CoV-2 infections are not yet available. To identify host factors that support coronavirus infection, we performed genome-wide functional genetic screens with SARS-CoV-2 and the common cold virus HCoV-229E in non-transgenic human cells. These screens identified PI3K type 3 as a potential drug target against multiple coronaviruses. We discovered that the lysosomal protein TMEM106B is an important host factor for SARS-CoV-2 infection. Furthermore, we show that TMEM106B is required for replication in multiple human cell lines derived from liver and lung and is expressed in relevant cell types in the human airways. Our results identify new coronavirus host factors that may potentially serve as drug targets against SARS-CoV-2 or to quickly combat future zoonotic coronavirus outbreaks.
Licencia
cc_by_nc_nd
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Idioma: Inglés Año: 2020 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Idioma: Inglés Año: 2020 Tipo del documento: Preprint
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