基因组规模识别SARS-CoV-2和泛冠状病毒宿主因子网络
William M Schneider1, Joseph M Luna1, H-Heinrich Hoffmann1
1Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY 10065, USA.
Cell
|December 31, 2020
概括
研究人员确定了严重急性呼吸综合征冠状病毒2 (SARS-CoV-2) 和其他人类冠状病毒感染的关键细胞因子. 这一发现有助于开发新的COVID-19和未来的病毒性流行病治疗方法.
科学领域:
- 病毒学
- 分子生物学
- 遗传学
背景情况:
- 由SARS-CoV-2引起的COVID-19大流行突显了了解冠状病毒与宿主相互作用的迫切需要.
- 由SARS-CoV-2和其他人类冠状病毒利用的细胞因子尚未完全理解.
研究的目的:
- 识别对SARS-CoV-2和季节性人类冠状病毒生命周期至关重要的宿主因素和途径.
- 揭示目前和未来的冠状病毒爆发的潜在治疗目标.
主要方法:
- 用全基因组的CRISPR淘汰查来评估感染期间的宿主依赖性.
- 使用SARS-CoV-2和三种常见的人类冠状病毒 (HCoV-OC43,HCoV-NL63,HCoV-229E) 进行了查.
主要成果:
- 确定了具有泛冠状病毒和病毒特异性的宿主因素和途径.
- 关键的依赖性包括糖氨基糖生物合成,SREBP信号,BMP信号和GPI生物合成.
- 发现跨膜蛋白41B (TMEM41B) 对所有测试的冠状病毒的感染是绝对必要的.
结论:
- 这项研究提供了人类冠状病毒宿主因素的全面资源.
- 鉴定出来的因素,特别是TMEM41B,是抗病毒疗法的有希望的目标.
- 了解这些宿主-病原体相互作用对于疫情准备至关重要.
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