Literature detail

Protein Structure and Sequence Reanalysis of 2019-nCoV Genome Refutes Snakes as Its Intermediate Host and the Unique Similarity between Its Spike Protein Insertions and HIV-1.

Chengxin Zhang Wei Zheng Xiaoqiang Huang Eric W Bell Xiaogen Zhou Yang Zhang
PMID 32200634 2020 J Proteome Res eng ppublish
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Article

Publication summary

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 <i>Manis javanica</i>, 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 <i>Manis</i> coronavirus compared with 2019-nCoV, suggesting the pangolin as a missing link in the transmission of 2019-nCoV from bats to human.

2019-nCoV Malayan pangolins metagenome assembly spike protein Host-Pathogen Interactions Models, Molecular Amino Acid Sequence Animals Betacoronavirus Coronavirus Infections COVID-19 Eutheria Genome, Viral HIV-1 Humans Metagenome Pandemics Pneumonia, Viral

Structured evidence records

Evidence records

3 total
1 records
Extraction confidence 0.80
Key finding

Comparative genomic analyses suggest transmission of a 2019-nCoV-like coronavirus between bats and Malayan pangolins.

Virus
Location
Not specified
Supporting text

The alignments of the spike surface glycoprotein receptor binding domain revealed four times more variations in the bat coronavirus RaTG13 than in the Manis coronavirus compared with 2019-nCoV, suggesting the pangolin as a missing link in the transmission of 2019-nCoV from bats to human.

Method
metagenomic assembly; sequence alignment
Study design
phylogenetic analysis
Transmission direction
animal-to-animal
1 records
Extraction confidence 0.90
Key finding

Metagenomic and sequence alignment analyses showed that a pangolin coronavirus genome is 91% identical to SARS-CoV-2 and its spike receptor-binding domain is more similar than that of bat coronavirus RaTG13, supporting pangolins as a potential intermediate host.

Virus
Location
Not specified
Supporting text

Using metagenomic samples from Manis javanica, we assembled a draft genome of the 2019-nCoV-like coronavirus, which shows 73% coverage and 91% sequence identity to the 2019-nCoV genome. Alignments of the spike surface glycoprotein receptor binding domain revealed more variations in the bat coronavirus RaTG13 than in the Manis coronavirus compared with 2019-nCoV, suggesting the pangolin as a missing link in transmission.

Genes or proteins
spike surface glycoprotein receptor binding domain
Analysis methods
metagenomic assembly; sequence alignment
1 records
Extraction confidence 0.70
Key finding

Sequence comparisons of the spike receptor binding domain showed the pangolin coronavirus has higher similarity to SARS-CoV-2 than bat coronavirus RaTG13, implying closer receptor-binding compatibility.

Virus
Location
Not specified
Supporting text

The alignments of the spike surface glycoprotein receptor binding domain revealed four times more variations in the bat coronavirus RaTG13 than in the Manis coronavirus compared with 2019-nCoV, suggesting the pangolin as a missing link in the transmission of 2019-nCoV from bats to human.

Method
sequence alignment; protein structure analysis
Receptors
spike surface glycoprotein receptor binding domain