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Deletion in the C-terminal region of the envelope glycoprotein in some of the Indian SARS-CoV-2 genome

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VIRUS RESEARCH
卷 291, 期 -, 页码 -

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DOI: 10.1016/j.virusres.2020.198222

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COVID-19; SARS-CoV-2; Viral assembly; Genome analysis; E protein

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An analysis of 2086 whole genome sequences from India revealed extensive amino acid deletions in the C-terminal region of the envelope glycoprotein in 34 Indian SARS-CoV-2 genomes, possibly due to adaptation to new geographical areas and hosts. Further studies are needed to understand the functional consequences of these deletions on the viral pathogenesis and host adaptation. Clinical information was only available for 9 out of 34 cases, all of which were asymptomatic.
The envelope glycoprotein (E) is the smallest structural component of SARS-CoVs; plays an essential role in the viral replication starting from envelope formation to assembly. The in silico analysis of 2086 whole genome sequences from India performed in this study provides the first observation on the extensive deletion of amino acid residues in the C-terminal region of the envelope glycoprotein in 34 Indian SARS-CoV-2 genomes. These amino acid deletions map to the homopentameric interface and PDZ binding motif (PBM) present in the C -terminal region of E protein as well as immediately after the reverse primer binding region as per Charite ' protocol in 26 of these genomes, hence, their detection through RT-qPCR may not be hampered and therefore E gene based RT-qPCR would still detect these isolates. Eight genomes from the State of Odisha had deletion even in the primer binding site. It is possible that the deletions in the C-terminal region of E protein of these genomes are a result of adapting to a newer geographical area and host. The information on the clinical status was available only for 9 out of 34 cases and these were asymptomatic. However, further studies are indispensable to understand the functional consequences of amino acid deletion in the C terminal region of SARS-CoV-2 envelope protein in the viral pathogenesis and host adaptation.

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