Emergence of crucial evidence catalyzing the origin tracing of SARS-CoV-2
Since the emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), its genetic and geographical origins remain unclear, resulting in suspicions about its natural origin. In one of our previous studies, we reported the presence of a furin cleavage site RRAR in the junction region be...
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description | Since the emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), its genetic and geographical origins remain unclear, resulting in suspicions about its natural origin. In one of our previous studies, we reported the presence of a furin cleavage site RRAR in the junction region between S1 and S2 subunits of the spike protein, which was discovered as the first crucial clue for the origin tracing of SARS-CoV-2. In the present study, we conducted an integrative analysis of new genome data from bat Sarbecovirus strains reported after the COVID-19 outbreak. The primary results included the identification of BANAL-20-52, Rp22DB159, and S18CXBatR24 as three close relatives of SARS-CoV-2 and the successful detection of seven out of nine key genomic features (designated as RC0-7 and ORF8) observed in wild types of SARS-CoV-2 in the three close relatives from Laos, Vietnam, and Yunnan province of China, respectively. The most significant contribution of the present study lies in the detection of RC1 in wild genotype in a bat Sarbecovirus population BANAL-20-52 belonging to. Encoding a segment of the NSP3 protein, RC1 was discovered as the second crucial clue for the origin tracing of SARS-CoV-2. Although RC0, encoding the junction furin cleavage site, remains undetected outside of the SARS-CoV-2 genome, Feuang of Laos is the sole place where eight of the nine wild-type features (RC1-7 and ORF8) have been detected. |
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In one of our previous studies, we reported the presence of a furin cleavage site RRAR in the junction region between S1 and S2 subunits of the spike protein, which was discovered as the first crucial clue for the origin tracing of SARS-CoV-2. In the present study, we conducted an integrative analysis of new genome data from bat Sarbecovirus strains reported after the COVID-19 outbreak. The primary results included the identification of BANAL-20-52, Rp22DB159, and S18CXBatR24 as three close relatives of SARS-CoV-2 and the successful detection of seven out of nine key genomic features (designated as RC0-7 and ORF8) observed in wild types of SARS-CoV-2 in the three close relatives from Laos, Vietnam, and Yunnan province of China, respectively. The most significant contribution of the present study lies in the detection of RC1 in wild genotype in a bat Sarbecovirus population BANAL-20-52 belonging to. Encoding a segment of the NSP3 protein, RC1 was discovered as the second crucial clue for the origin tracing of SARS-CoV-2. Although RC0, encoding the junction furin cleavage site, remains undetected outside of the SARS-CoV-2 genome, Feuang of Laos is the sole place where eight of the nine wild-type features (RC1-7 and ORF8) have been detected.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0309557</identifier><identifier>PMID: 39213297</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; China - epidemiology ; Chiroptera - virology ; Cleavage ; Coronaviruses ; COVID-19 ; COVID-19 - epidemiology ; COVID-19 - virology ; Disease transmission ; Furin ; Furin - genetics ; Furin - metabolism ; Genome, Viral ; Genomes ; Genomic analysis ; Genotypes ; Geographical distribution ; Humans ; Hypotheses ; Mutation ; NSP3 protein ; Peptides ; Phylogenetics ; Phylogeny ; Population studies ; Proteins ; Sarbecovirus ; SARS-CoV-2 - genetics ; SARS-CoV-2 - isolation & purification ; Severe acute respiratory syndrome coronavirus 2 ; Software ; Spike Glycoprotein, Coronavirus - genetics ; Spike protein ; Tracing ; Viral diseases ; Virus research</subject><ispartof>PloS one, 2024-08, Vol.19 (8), p.e0309557</ispartof><rights>Copyright: © 2024 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2024 Public Library of Science</rights><rights>2024 Chen 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>2024 Chen 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c516t-7433ce11ab2744f9c4a7ee204a3900dcbe6d5ced9b2dce9d4e512abf8984e2733</cites><orcidid>0000-0001-5502-7794 ; 0000-0002-8919-1338</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0309557&type=printable$$EPDF$$P50$$Gplos$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0309557$$EHTML$$P50$$Gplos$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,860,2095,2914,23846,27903,27904,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39213297$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Anjorin, AbdulAzeez Adeyemi</contributor><creatorcontrib>Chen, Shunmei</creatorcontrib><creatorcontrib>Ruan, Cihan</creatorcontrib><creatorcontrib>Guo, Yutong</creatorcontrib><creatorcontrib>Chang, Jia</creatorcontrib><creatorcontrib>Yan, Haohao</creatorcontrib><creatorcontrib>Chen, Liang</creatorcontrib><creatorcontrib>Duan, Yongzhong</creatorcontrib><creatorcontrib>Duan, Guangyou</creatorcontrib><creatorcontrib>Bei, Jinlong</creatorcontrib><creatorcontrib>Li, Xin</creatorcontrib><creatorcontrib>Gao, Shan</creatorcontrib><title>Emergence of crucial evidence catalyzing the origin tracing of SARS-CoV-2</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Since the emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), its genetic and geographical origins remain unclear, resulting in suspicions about its natural origin. In one of our previous studies, we reported the presence of a furin cleavage site RRAR in the junction region between S1 and S2 subunits of the spike protein, which was discovered as the first crucial clue for the origin tracing of SARS-CoV-2. In the present study, we conducted an integrative analysis of new genome data from bat Sarbecovirus strains reported after the COVID-19 outbreak. The primary results included the identification of BANAL-20-52, Rp22DB159, and S18CXBatR24 as three close relatives of SARS-CoV-2 and the successful detection of seven out of nine key genomic features (designated as RC0-7 and ORF8) observed in wild types of SARS-CoV-2 in the three close relatives from Laos, Vietnam, and Yunnan province of China, respectively. The most significant contribution of the present study lies in the detection of RC1 in wild genotype in a bat Sarbecovirus population BANAL-20-52 belonging to. Encoding a segment of the NSP3 protein, RC1 was discovered as the second crucial clue for the origin tracing of SARS-CoV-2. 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Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Shunmei</au><au>Ruan, Cihan</au><au>Guo, Yutong</au><au>Chang, Jia</au><au>Yan, Haohao</au><au>Chen, Liang</au><au>Duan, Yongzhong</au><au>Duan, Guangyou</au><au>Bei, Jinlong</au><au>Li, Xin</au><au>Gao, Shan</au><au>Anjorin, AbdulAzeez Adeyemi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emergence of crucial evidence catalyzing the origin tracing of SARS-CoV-2</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2024-08-30</date><risdate>2024</risdate><volume>19</volume><issue>8</issue><spage>e0309557</spage><pages>e0309557-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Since the emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), its genetic and geographical origins remain unclear, resulting in suspicions about its natural origin. In one of our previous studies, we reported the presence of a furin cleavage site RRAR in the junction region between S1 and S2 subunits of the spike protein, which was discovered as the first crucial clue for the origin tracing of SARS-CoV-2. In the present study, we conducted an integrative analysis of new genome data from bat Sarbecovirus strains reported after the COVID-19 outbreak. The primary results included the identification of BANAL-20-52, Rp22DB159, and S18CXBatR24 as three close relatives of SARS-CoV-2 and the successful detection of seven out of nine key genomic features (designated as RC0-7 and ORF8) observed in wild types of SARS-CoV-2 in the three close relatives from Laos, Vietnam, and Yunnan province of China, respectively. The most significant contribution of the present study lies in the detection of RC1 in wild genotype in a bat Sarbecovirus population BANAL-20-52 belonging to. Encoding a segment of the NSP3 protein, RC1 was discovered as the second crucial clue for the origin tracing of SARS-CoV-2. Although RC0, encoding the junction furin cleavage site, remains undetected outside of the SARS-CoV-2 genome, Feuang of Laos is the sole place where eight of the nine wild-type features (RC1-7 and ORF8) have been detected.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>39213297</pmid><doi>10.1371/journal.pone.0309557</doi><tpages>e0309557</tpages><orcidid>https://orcid.org/0000-0001-5502-7794</orcidid><orcidid>https://orcid.org/0000-0002-8919-1338</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals China - epidemiology Chiroptera - virology Cleavage Coronaviruses COVID-19 COVID-19 - epidemiology COVID-19 - virology Disease transmission Furin Furin - genetics Furin - metabolism Genome, Viral Genomes Genomic analysis Genotypes Geographical distribution Humans Hypotheses Mutation NSP3 protein Peptides Phylogenetics Phylogeny Population studies Proteins Sarbecovirus SARS-CoV-2 - genetics SARS-CoV-2 - isolation & purification Severe acute respiratory syndrome coronavirus 2 Software Spike Glycoprotein, Coronavirus - genetics Spike protein Tracing Viral diseases Virus research |
title | Emergence of crucial evidence catalyzing the origin tracing of SARS-CoV-2 |
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