State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Life Sciences, Yunnan University, No. 2 North Cuihu Road, Kunming, Yunnan 650091, China.
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Life Sciences, Yunnan University, No. 2 North Cuihu Road, Kunming, Yunnan 650091, China.
Curr Biol. 2020 Apr 6;30(7):1346-1351.e2. doi: 10.1016/j.cub.2020.03.022. Epub 2020 Mar 19.
An outbreak of coronavirus disease 2019 (COVID-19) caused by the 2019 novel coronavirus (SARS-CoV-2) began in the city of Wuhan in China and has widely spread worldwide. Currently, it is vital to explore potential intermediate hosts of SARS-CoV-2 to control COVID-19 spread. Therefore, we reinvestigated published data from pangolin lung samples from which SARS-CoV-like CoVs were detected by Liu et al. [1]. We found genomic and evolutionary evidence of the occurrence of a SARS-CoV-2-like CoV (named Pangolin-CoV) in dead Malayan pangolins. Pangolin-CoV is 91.02% and 90.55% identical to SARS-CoV-2 and BatCoV RaTG13, respectively, at the whole-genome level. Aside from RaTG13, Pangolin-CoV is the most closely related CoV to SARS-CoV-2. The S1 protein of Pangolin-CoV is much more closely related to SARS-CoV-2 than to RaTG13. Five key amino acid residues involved in the interaction with human ACE2 are completely consistent between Pangolin-CoV and SARS-CoV-2, but four amino acid mutations are present in RaTG13. Both Pangolin-CoV and RaTG13 lost the putative furin recognition sequence motif at S1/S2 cleavage site that can be observed in the SARS-CoV-2. Conclusively, this study suggests that pangolin species are a natural reservoir of SARS-CoV-2-like CoVs.
新型冠状病毒病(COVID-19)是由 2019 年新型冠状病毒(SARS-CoV-2)引起的疫情,最初在中国武汉市爆发,并已在全球范围内广泛传播。目前,探索 SARS-CoV-2 的潜在中间宿主对于控制 COVID-19 的传播至关重要。因此,我们重新研究了 Liu 等人发表的穿山甲肺部样本数据[1],该研究中检测到了 SARS-CoV 样 CoV。我们在死亡的马来亚穿山甲中发现了 SARS-CoV-2 样 CoV(命名为穿山甲-CoV)存在的基因组和进化证据。在全基因组水平上,穿山甲-CoV 与 SARS-CoV-2 和 BatCoV RaTG13 的相似度分别为 91.02%和 90.55%。除了 RaTG13 之外,穿山甲-CoV 是与 SARS-CoV-2 最接近的 CoV。穿山甲-CoV 的 S1 蛋白与 SARS-CoV-2 的关系比与 RaTG13 的关系更为密切。与人类 ACE2 相互作用的五个关键氨基酸残基在穿山甲-CoV 和 SARS-CoV-2 之间完全一致,但在 RaTG13 中存在四个氨基酸突变。穿山甲-CoV 和 RaTG13 都失去了 SARS-CoV-2 中可观察到的 S1/S2 切割位点上的假定弗林蛋白酶识别序列基序。综上所述,本研究表明穿山甲是 SARS-CoV-2 样 CoV 的天然宿主。