Genome-wide CRISPR screening identifies TMEM106B as a proviral host factor for SARS-CoV-2

被引:155
作者
Baggen, Jim [1 ]
Persoons, Leentje [1 ]
Vanstreels, Els [1 ]
Jansen, Sander [1 ]
Van Looveren, Dominique [1 ,2 ]
Boeckx, Bram [3 ,4 ]
Geudens, Vincent [5 ]
De Man, Julie [1 ]
Jochmans, Dirk [1 ]
Wauters, Joost [6 ]
Wauters, Els [5 ]
Vanaudenaerde, Bart M. [5 ]
Lambrechts, Diether [3 ,4 ]
Neyts, Johan [1 ]
Dallmeier, Kai [1 ]
Thibaut, Hendrik Jan [1 ,2 ]
Jacquemyn, Maarten [1 ]
Maes, Piet [7 ]
Daelemans, Dirk [1 ]
机构
[1] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Virol & Chemotherapy, Rega Inst, Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Virol & Chemotherapy, Translat Platform Virol & Chemotherapy,Rega Inst, Leuven, Belgium
[3] Katholieke Univ Leuven, Dept Human Genet, Lab Translat Genet, Leuven, Belgium
[4] VIB, Ctr Canc Biol, Leuven, Belgium
[5] Katholieke Univ Leuven, Dept Chron Dis & Metab, Lab Resp Dis & Thorac Surg BREATHE, Leuven, Belgium
[6] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Clin Infect & Inflammatory Disorders, Leuven, Belgium
[7] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Clin & Epidemiol Virol, Rega Inst, Leuven, Belgium
关键词
COVID-19;
D O I
10.1038/s41588-021-00805-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. Genome-wide CRISPR screens for proviral host factors of SARS-CoV-2 and HCoV-229E human coronaviruses show that the lysosomal protein TMEM106B is required for SARS-CoV-2 infection.
引用
收藏
页码:435 / +
页数:28
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