Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
Gladstone Institutes, San Francisco, CA 94158, USA; Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA; Quantitative Biosciences Institute COVID-19 Research Group (QCRG), University of California, San Francisco, San Francisco, CA 94158, USA; Biomedical Sciences Graduate Program, University of California, San Francisco, San Francisco, CA 94143, USA.
Cell. 2021 Jan 7;184(1):106-119.e14. doi: 10.1016/j.cell.2020.12.004. Epub 2020 Dec 9.
The Coronaviridae are a family of viruses that cause disease in humans ranging from mild respiratory infection to potentially lethal acute respiratory distress syndrome. Finding host factors common to multiple coronaviruses could facilitate the development of therapies to combat current and future coronavirus pandemics. Here, we conducted genome-wide CRISPR screens in cells infected by SARS-CoV-2 as well as two seasonally circulating common cold coronaviruses, OC43 and 229E. This approach correctly identified the distinct viral entry factors ACE2 (for SARS-CoV-2), aminopeptidase N (for 229E), and glycosaminoglycans (for OC43). Additionally, we identified phosphatidylinositol phosphate biosynthesis and cholesterol homeostasis as critical host pathways supporting infection by all three coronaviruses. By contrast, the lysosomal protein TMEM106B appeared unique to SARS-CoV-2 infection. Pharmacological inhibition of phosphatidylinositol kinases and cholesterol homeostasis reduced replication of all three coronaviruses. These findings offer important insights for the understanding of the coronavirus life cycle and the development of host-directed therapies.
冠状病毒科是一类病毒,可引起人类从轻度呼吸道感染到潜在致命性急性呼吸窘迫综合征等疾病。寻找对多种冠状病毒都通用的宿主因素,可以促进针对当前和未来冠状病毒大流行的治疗方法的开发。在这里,我们在感染 SARS-CoV-2 以及两种季节性流行的普通感冒冠状病毒 OC43 和 229E 的细胞中进行了全基因组 CRISPR 筛选。这种方法正确地鉴定了不同的病毒进入因子 ACE2(用于 SARS-CoV-2)、氨肽酶 N(用于 229E)和糖胺聚糖(用于 OC43)。此外,我们还确定了磷脂酰肌醇磷酸生物合成和胆固醇稳态是所有三种冠状病毒感染所必需的关键宿主途径。相比之下,溶酶体蛋白 TMEM106B 似乎是 SARS-CoV-2 感染所特有的。磷脂酰肌醇激酶和胆固醇稳态的药理学抑制降低了所有三种冠状病毒的复制。这些发现为理解冠状病毒生命周期和开发宿主定向治疗提供了重要的见解。