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从单个细菌人工染色体中拯救严重急性呼吸综合征冠状病毒2型。

Rescue of SARS-CoV-2 from a single bacterial artificial chromosome.

作者信息

Ye Chengjin, Chiem Kevin, Park Jun-Gyu, Oladunni Fatai, Platt Roy Neal, Anderson Tim, Almazan Fernando, de la Torre Juan Carlos, Martinez-Sobrido Luis

出版信息

bioRxiv. 2020 Jul 22:2020.07.22.216358. doi: 10.1101/2020.07.22.216358.

DOI:10.1101/2020.07.22.216358
PMID:32743573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7386490/
Abstract

An infectious coronavirus disease 2019 (COVID-19) emerged in the city of Wuhan (China) in December 2019, causing a pandemic that has dramatically impacted public health and socioeconomic activities worldwide. A previously unknown coronavirus, Severe Acute Respiratory Syndrome CoV-2 (SARS-CoV-2), has been identified as the causative agent of COVID-19. To date, there are no United States (US) Food and Drug Administration (FDA)-approved vaccines or therapeutics available for the prevention or treatment of SARS-CoV-2 infection and/or associated COVID-19 disease, which has triggered a large influx of scientific efforts to develop countermeasures to control SARS-CoV-2 spread. To contribute to these efforts, we have developed an infectious cDNA clone of the SARS-CoV-2 USA-WA1/2020 strain based on the use of a bacterial artificial chromosome (BAC). Recombinant (r)SARS-CoV-2 was readily rescued by transfection of the BAC into Vero E6 cells. Importantly, the BAC-derived rSARS-CoV-2 exhibited growth properties and plaque sizes in cultured cells comparable to those of the SARS-CoV-2 natural isolate. Likewise, rSARS-CoV-2 showed similar levels of replication to that of the natural isolate in nasal turbinates and lungs of infected golden Syrian hamsters. This is, to our knowledge, the first BAC based reverse genetics system for the generation of infectious rSARS-CoV-2 that displays similar features to that of a natural viral isolate. This SARS-CoV-2 BAC-based reverse genetics will facilitate studies addressing several important questions in the biology of SARS-CoV-2, as well as the identification of antivirals and development of vaccines for the treatment of SARS-CoV-2 infection and associated COVID-19 disease.

摘要

2019年12月,一种具有传染性的冠状病毒病2019(COVID-19)在中国武汉市出现,引发了一场大流行,对全球公共卫生和社会经济活动产生了巨大影响。一种此前未知的冠状病毒,即严重急性呼吸综合征冠状病毒2(SARS-CoV-2),已被确定为COVID-19的病原体。迄今为止,美国食品药品监督管理局(FDA)尚未批准用于预防或治疗SARS-CoV-2感染和/或相关COVID-19疾病的疫苗或治疗方法,这引发了大量科研力量致力于开发控制SARS-CoV-2传播的对策。为助力这些努力,我们基于细菌人工染色体(BAC)构建了SARS-CoV-2美国-WA1/2020毒株的感染性cDNA克隆。将该BAC转染至Vero E6细胞后,可轻易拯救出重组(r)SARS-CoV-2。重要的是,BAC衍生的rSARS-CoV-2在培养细胞中的生长特性和噬斑大小与SARS-CoV-2天然分离株相当。同样,rSARS-CoV-2在感染的金黄叙利亚仓鼠的鼻甲和肺中的复制水平与天然分离株相似。据我们所知,这是首个基于BAC的用于产生具有与天然病毒分离株相似特征的感染性rSARS-CoV-2的反向遗传学系统。这种基于SARS-CoV-2 BAC的反向遗传学将有助于研究解决SARS-CoV-2生物学中的几个重要问题,以及鉴定用于治疗SARS-CoV-2感染和相关COVID-19疾病的抗病毒药物和开发疫苗。