J Proteome Res. 2020 Apr 3;19(4):1351-1360. doi: 10.1021/acs.jproteome.0c00129. Epub 2020 Mar 24.
As the infection of 2019-nCoV coronavirus is quickly developing into a global pneumonia epidemic, the careful analysis of its transmission and cellular mechanisms is sorely needed. In this Communication, we first analyzed two recent studies that concluded that snakes are the intermediate hosts of 2019-nCoV and that the 2019-nCoV spike protein insertions share a unique similarity to HIV-1. However, the reimplementation of the analyses, built on larger scale data sets using state-of-the-art bioinformatics methods and databases, presents clear evidence that rebuts these conclusions. Next, using metagenomic samples from , we assembled a draft genome of the 2019-nCoV-like coronavirus, which shows 73% coverage and 91% sequence identity to the 2019-nCoV genome. In particular, the alignments of the spike surface glycoprotein receptor binding domain revealed four times more variations in the bat coronavirus RaTG13 than in the coronavirus compared with 2019-nCoV, suggesting the pangolin as a missing link in the transmission of 2019-nCoV from bats to human.
由于 2019 年新型冠状病毒(2019-nCoV)的感染迅速发展成为全球肺炎疫情,非常需要仔细分析其传播和细胞机制。在本通讯中,我们首先分析了两项最近的研究,这两项研究得出的结论是蛇类是 2019-nCoV 的中间宿主,并且 2019-nCoV 刺突蛋白插入具有与 HIV-1 独特的相似性。然而,使用更大规模的数据集和最先进的生物信息学方法和数据库重新实施分析,提供了明确的证据反驳了这些结论。接下来,我们使用来自 的宏基因组样本,组装了 2019-nCoV 样冠状病毒的基因组草图,其覆盖率为 73%,与 2019-nCoV 基因组的序列同一性为 91%。特别是,在刺突表面糖蛋白受体结合域的比对中,与 2019-nCoV 相比,蝙蝠冠状病毒 RaTG13 中有四倍的变异,表明穿山甲是 2019-nCoV 从蝙蝠传播到人类的缺失环节。