| Literature DB >> 33686287 |
Leentje Persoons1, Els Vanstreels1, Sander Jansen1, Jim Baggen2, Dominique Van Looveren1,3, Bram Boeckx4,5, Vincent Geudens6, Julie De Man1, Dirk Jochmans1, Joost Wauters7, Els Wauters6, Bart M Vanaudenaerde6, Diether Lambrechts4,5, Johan Neyts1, Kai Dallmeier1, Hendrik Jan Thibaut1,3, Maarten Jacquemyn1, Piet Maes8, Dirk Daelemans9.
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.Entities:
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Year: 2021 PMID: 33686287 DOI: 10.1038/s41588-021-00805-2
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330