SARS-CoV-2 spike protein displays sequence similarities with paramyxovirus surface proteins; a bioinformatics study
Recent emergence of SARS-CoV-2 and associated COVID-19 pandemic have posed a great challenge for the scientific community. In this study, we performed bioinformatic analyses on SARS-CoV-2 protein sequences, trying to unravel potential molecular similarities between this newly emerged pathogen with n...
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description | Recent emergence of SARS-CoV-2 and associated COVID-19 pandemic have posed a great challenge for the scientific community. In this study, we performed bioinformatic analyses on SARS-CoV-2 protein sequences, trying to unravel potential molecular similarities between this newly emerged pathogen with non-coronavirus ssRNA viruses. Comparing the proteins of SARS-CoV-2 with non-coronavirus positive and negative strand ssRNA viruses revealed multiple sequence similarities between SARS-CoV-2 and non-coronaviruses, including similarities between RNA-dependent RNA-polymerases and helicases (two highly-conserved proteins). We also observed similarities between SARS-CoV-2 surface (i.e. spike) protein with paramyxovirus fusion proteins. This similarity was restricted to a segment of spike protein S2 subunit which is involved in cell fusion. We next analyzed spike proteins from SARS-CoV-2 “variants of concern” (VOCs) and “variants of interests” (VOIs) and found that some of these variants show considerably higher spike-fusion similarity with paramyxoviruses. The ‘spike-fusion’ similarity was also observed for some pathogenic coronaviruses other than SARS-CoV-2. Epitope analysis using experimentally verified data deposited in Immune Epitope Database (IEDB) revealed that several B cell epitopes as well as T cell and MHC binding epitopes map within the spike-fusion similarity region. These data indicate that there might be a degree of convergent evolution between SARS-CoV-2 and paramyxovirus surface proteins which could be of pathogenic and immunological importance. |
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In this study, we performed bioinformatic analyses on SARS-CoV-2 protein sequences, trying to unravel potential molecular similarities between this newly emerged pathogen with non-coronavirus ssRNA viruses. Comparing the proteins of SARS-CoV-2 with non-coronavirus positive and negative strand ssRNA viruses revealed multiple sequence similarities between SARS-CoV-2 and non-coronaviruses, including similarities between RNA-dependent RNA-polymerases and helicases (two highly-conserved proteins). We also observed similarities between SARS-CoV-2 surface (i.e. spike) protein with paramyxovirus fusion proteins. This similarity was restricted to a segment of spike protein S2 subunit which is involved in cell fusion. We next analyzed spike proteins from SARS-CoV-2 “variants of concern” (VOCs) and “variants of interests” (VOIs) and found that some of these variants show considerably higher spike-fusion similarity with paramyxoviruses. The ‘spike-fusion’ similarity was also observed for some pathogenic coronaviruses other than SARS-CoV-2. Epitope analysis using experimentally verified data deposited in Immune Epitope Database (IEDB) revealed that several B cell epitopes as well as T cell and MHC binding epitopes map within the spike-fusion similarity region. These data indicate that there might be a degree of convergent evolution between SARS-CoV-2 and paramyxovirus surface proteins which could be of pathogenic and immunological importance.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0260360</identifier><identifier>PMID: 34855795</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Amino acid sequence ; Bioinformatics ; Biology and life sciences ; Cell fusion ; Computer and Information Sciences ; Coronaviridae ; Coronaviruses ; COVID-19 ; Epitopes ; Fusion protein ; Health aspects ; Immunology ; Lymphocytes ; Lymphocytes T ; Major histocompatibility complex ; Medicine and health sciences ; Nucleotide sequence ; Pandemics ; Phylogenetics ; Proteins ; Research and Analysis Methods ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Similarity ; Spike protein ; T cells ; Viral diseases ; Viruses</subject><ispartof>PloS one, 2021-12, Vol.16 (12), p.e0260360-e0260360</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Ahmadi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Ahmadi et al 2021 Ahmadi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c669t-c32594507df9e0e9ba6ec63ffbec476cb884d10fd0499ac695016334cd3c06103</citedby><cites>FETCH-LOGICAL-c669t-c32594507df9e0e9ba6ec63ffbec476cb884d10fd0499ac695016334cd3c06103</cites><orcidid>0000-0003-4304-0048</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639087/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639087/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793</link.rule.ids></links><search><contributor>Ito, Etsuro</contributor><creatorcontrib>Ahmadi, Ehsan</creatorcontrib><creatorcontrib>Zabihi, Mohammad Reza</creatorcontrib><creatorcontrib>Hosseinzadeh, Ramin</creatorcontrib><creatorcontrib>Mohamed Khosroshahi, Leila</creatorcontrib><creatorcontrib>Noorbakhsh, Farshid</creatorcontrib><title>SARS-CoV-2 spike protein displays sequence similarities with paramyxovirus surface proteins; a bioinformatics study</title><title>PloS one</title><description>Recent emergence of SARS-CoV-2 and associated COVID-19 pandemic have posed a great challenge for the scientific community. In this study, we performed bioinformatic analyses on SARS-CoV-2 protein sequences, trying to unravel potential molecular similarities between this newly emerged pathogen with non-coronavirus ssRNA viruses. Comparing the proteins of SARS-CoV-2 with non-coronavirus positive and negative strand ssRNA viruses revealed multiple sequence similarities between SARS-CoV-2 and non-coronaviruses, including similarities between RNA-dependent RNA-polymerases and helicases (two highly-conserved proteins). We also observed similarities between SARS-CoV-2 surface (i.e. spike) protein with paramyxovirus fusion proteins. This similarity was restricted to a segment of spike protein S2 subunit which is involved in cell fusion. We next analyzed spike proteins from SARS-CoV-2 “variants of concern” (VOCs) and “variants of interests” (VOIs) and found that some of these variants show considerably higher spike-fusion similarity with paramyxoviruses. The ‘spike-fusion’ similarity was also observed for some pathogenic coronaviruses other than SARS-CoV-2. Epitope analysis using experimentally verified data deposited in Immune Epitope Database (IEDB) revealed that several B cell epitopes as well as T cell and MHC binding epitopes map within the spike-fusion similarity region. These data indicate that there might be a degree of convergent evolution between SARS-CoV-2 and paramyxovirus surface proteins which could be of pathogenic and immunological importance.</description><subject>Amino acid sequence</subject><subject>Bioinformatics</subject><subject>Biology and life sciences</subject><subject>Cell fusion</subject><subject>Computer and Information Sciences</subject><subject>Coronaviridae</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Epitopes</subject><subject>Fusion protein</subject><subject>Health aspects</subject><subject>Immunology</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Major histocompatibility complex</subject><subject>Medicine and health sciences</subject><subject>Nucleotide sequence</subject><subject>Pandemics</subject><subject>Phylogenetics</subject><subject>Proteins</subject><subject>Research and Analysis Methods</subject><subject>Severe acute respiratory 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spike protein displays sequence similarities with paramyxovirus surface proteins; a bioinformatics study</title><author>Ahmadi, Ehsan ; Zabihi, Mohammad Reza ; Hosseinzadeh, Ramin ; Mohamed Khosroshahi, Leila ; Noorbakhsh, Farshid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c669t-c32594507df9e0e9ba6ec63ffbec476cb884d10fd0499ac695016334cd3c06103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amino acid sequence</topic><topic>Bioinformatics</topic><topic>Biology and life sciences</topic><topic>Cell fusion</topic><topic>Computer and Information Sciences</topic><topic>Coronaviridae</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Epitopes</topic><topic>Fusion protein</topic><topic>Health aspects</topic><topic>Immunology</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Major histocompatibility complex</topic><topic>Medicine and health sciences</topic><topic>Nucleotide sequence</topic><topic>Pandemics</topic><topic>Phylogenetics</topic><topic>Proteins</topic><topic>Research and Analysis Methods</topic><topic>Severe acute respiratory syndrome</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Similarity</topic><topic>Spike protein</topic><topic>T cells</topic><topic>Viral diseases</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmadi, Ehsan</creatorcontrib><creatorcontrib>Zabihi, Mohammad Reza</creatorcontrib><creatorcontrib>Hosseinzadeh, Ramin</creatorcontrib><creatorcontrib>Mohamed Khosroshahi, Leila</creatorcontrib><creatorcontrib>Noorbakhsh, Farshid</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior 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of SARS-CoV-2 and associated COVID-19 pandemic have posed a great challenge for the scientific community. In this study, we performed bioinformatic analyses on SARS-CoV-2 protein sequences, trying to unravel potential molecular similarities between this newly emerged pathogen with non-coronavirus ssRNA viruses. Comparing the proteins of SARS-CoV-2 with non-coronavirus positive and negative strand ssRNA viruses revealed multiple sequence similarities between SARS-CoV-2 and non-coronaviruses, including similarities between RNA-dependent RNA-polymerases and helicases (two highly-conserved proteins). We also observed similarities between SARS-CoV-2 surface (i.e. spike) protein with paramyxovirus fusion proteins. This similarity was restricted to a segment of spike protein S2 subunit which is involved in cell fusion. We next analyzed spike proteins from SARS-CoV-2 “variants of concern” (VOCs) and “variants of interests” (VOIs) and found that some of these variants show considerably higher spike-fusion similarity with paramyxoviruses. The ‘spike-fusion’ similarity was also observed for some pathogenic coronaviruses other than SARS-CoV-2. Epitope analysis using experimentally verified data deposited in Immune Epitope Database (IEDB) revealed that several B cell epitopes as well as T cell and MHC binding epitopes map within the spike-fusion similarity region. These data indicate that there might be a degree of convergent evolution between SARS-CoV-2 and paramyxovirus surface proteins which could be of pathogenic and immunological importance.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34855795</pmid><doi>10.1371/journal.pone.0260360</doi><tpages>e0260360</tpages><orcidid>https://orcid.org/0000-0003-4304-0048</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acid sequence Bioinformatics Biology and life sciences Cell fusion Computer and Information Sciences Coronaviridae Coronaviruses COVID-19 Epitopes Fusion protein Health aspects Immunology Lymphocytes Lymphocytes T Major histocompatibility complex Medicine and health sciences Nucleotide sequence Pandemics Phylogenetics Proteins Research and Analysis Methods Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Similarity Spike protein T cells Viral diseases Viruses |
title | SARS-CoV-2 spike protein displays sequence similarities with paramyxovirus surface proteins; a bioinformatics study |
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