Cellular host factors for SARS-CoV-2 infection

被引:126
|
作者
Baggen, Jim [1 ]
Vanstreels, Els [1 ]
Jansen, Sander [1 ]
Daelemans, Dirk [1 ]
机构
[1] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Virol & Chemotherapy, Rega Inst, Leuven, Belgium
关键词
EBOLA-VIRUS; ENTRY; COMPLEX; REPLICATION; PATHWAY; PROTEIN; ACTIVATION; INHIBITION; RECEPTORS; RETROMER;
D O I
10.1038/s41564-021-00958-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The coronavirus disease 2019 (COVID-19) pandemic has claimed millions of lives and caused a global economic crisis. No effective antiviral drugs are currently available to treat infections of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The medical need imposed by the pandemic has spurred unprecedented research efforts to study coronavirus biology. Every virus depends on cellular host factors and pathways for successful replication. These proviral host factors represent attractive targets for antiviral therapy as they are genetically more stable than viral targets and may be shared among related viruses. The application of various 'omics' technologies has led to the rapid discovery of proviral host factors that are required for the completion of the SARS-CoV-2 life cycle. In this Review, we summarize insights into the proviral host factors that are required for SARS-CoV-2 infection that were mainly obtained using functional genetic and interactome screens. We discuss cellular processes that are important for the SARS-CoV-2 life cycle, as well as parallels with non-coronaviruses. Finally, we highlight host factors that could be targeted by clinically approved molecules and molecules in clinical trials as potential antiviral therapies for COVID-19. Proviral host factors for SARS-CoV-2 infection, cellular processes that are important in SARS-CoV-2 replication and host factors that could be targeted by antiviral therapies for COVID-19 are reviewed.
引用
收藏
页码:1219 / 1232
页数:14
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