Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, L8S 4K1, Canada.
Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, Ontario, L8S 4K1, Canada.
J Gen Virol. 2020 Dec;101(12):1251-1260. doi: 10.1099/jgv.0.001491. Epub 2020 Sep 9.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) recently emerged to cause widespread infections in humans. SARS-CoV-2 infections have been reported in the Kingdom of Saudi Arabia, where Middle East respiratory syndrome coronavirus (MERS-CoV) causes seasonal outbreaks with a case fatality rate of ~37 %. Here we show that there exists a theoretical possibility of future recombination events between SARS-CoV-2 and MERS-CoV RNA. Through computational analyses, we have identified homologous genomic regions within the ORF1ab and S genes that could facilitate recombination, and have analysed co-expression patterns of the cellular receptors for SARS-CoV-2 and MERS-CoV, ACE2 and DPP4, respectively, to identify human anatomical sites that could facilitate co-infection. Furthermore, we have investigated the likely susceptibility of various animal species to MERS-CoV and SARS-CoV-2 infection by comparing known virus spike protein-receptor interacting residues. In conclusion, we suggest that a recombination between SARS-CoV-2 and MERS-CoV RNA is possible and urge public health laboratories in high-risk areas to develop diagnostic capability for the detection of recombined coronaviruses in patient samples.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)最近出现并在人类中广泛传播。在沙特阿拉伯王国已经报告了 SARS-CoV-2 感染病例,中东呼吸综合征冠状病毒(MERS-CoV)每年都会季节性爆发,病死率约为 37%。在这里,我们表明 SARS-CoV-2 和 MERS-CoV RNA 之间存在未来发生重组事件的理论可能性。通过计算分析,我们已经确定了 ORF1ab 和 S 基因中可能促进重组的同源基因组区域,并分别分析了 SARS-CoV-2 和 MERS-CoV 的细胞受体 ACE2 和 DPP4 的共表达模式,以确定可能促进共感染的人体解剖部位。此外,我们通过比较已知的病毒刺突蛋白-受体相互作用残基,研究了各种动物物种对 MERS-CoV 和 SARS-CoV-2 感染的可能易感性。总之,我们建议 SARS-CoV-2 和 MERS-CoV RNA 之间可能发生重组,并敦促高风险地区的公共卫生实验室开发用于检测患者样本中重组冠状病毒的诊断能力。