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Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor
Severe respiratory disease coronavirus-2 (SARS-CoV-2) has been the most devastating disease COVID-19 in the century. One of the unsolved scientific questions of SARS-CoV-2 is the animal origin of this virus. Bats and pangolins are recognized as the most probable reservoir hosts that harbour highly s...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344244/ https://www.ncbi.nlm.nih.gov/pubmed/34263709 http://dx.doi.org/10.1080/22221751.2021.1956373 |
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author | Guo, Hua Hu, Ben Si, Hao-Rui Zhu, Yan Zhang, Wei Li, Bei Li, Ang Geng, Rong Lin, Hao-Feng Yang, Xing-Lou Zhou, Peng Shi, Zheng-Li |
author_facet | Guo, Hua Hu, Ben Si, Hao-Rui Zhu, Yan Zhang, Wei Li, Bei Li, Ang Geng, Rong Lin, Hao-Feng Yang, Xing-Lou Zhou, Peng Shi, Zheng-Li |
author_sort | Guo, Hua |
collection | PubMed |
description | Severe respiratory disease coronavirus-2 (SARS-CoV-2) has been the most devastating disease COVID-19 in the century. One of the unsolved scientific questions of SARS-CoV-2 is the animal origin of this virus. Bats and pangolins are recognized as the most probable reservoir hosts that harbour highly similar SARS-CoV-2 related viruses (SARSr-CoV-2). This study identified a novel lineage of SARSr-CoVs, including RaTG15 and seven other viruses, from bats at the same location where we found RaTG13 in 2015. Although RaTG15 and the related viruses share 97.2% amino acid sequence identities with SARS-CoV-2 in the conserved ORF1b region, it only shows less than 77.6% nucleotide identity to all known SARSr-CoVs at the genome level, thus forming a distinct lineage in the Sarbecovirus phylogenetic tree. We found that the RaTG15 receptor-binding domain (RBD) can bind to ACE2 from Rhinolophus affinis, Malayan pangolin, and use it as an entry receptor, except for ACE2 from humans. However, it contains a short deletion and has different key residues responsible for ACE2 binding. In addition, we showed that none of the known viruses in bat SARSr-CoV-2 lineage discovered uses human ACE2 as efficiently as the pangolin-derived SARSr-CoV-2 or some viruses in the SARSr-CoV-1 lineage. Therefore, further systematic and longitudinal studies in bats are needed to prevent future spillover events caused by SARSr-CoVs or to understand the origin of SARS-CoV-2 better. |
format | Online Article Text |
id | pubmed-8344244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-83442442021-08-09 Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor Guo, Hua Hu, Ben Si, Hao-Rui Zhu, Yan Zhang, Wei Li, Bei Li, Ang Geng, Rong Lin, Hao-Feng Yang, Xing-Lou Zhou, Peng Shi, Zheng-Li Emerg Microbes Infect Research Article Severe respiratory disease coronavirus-2 (SARS-CoV-2) has been the most devastating disease COVID-19 in the century. One of the unsolved scientific questions of SARS-CoV-2 is the animal origin of this virus. Bats and pangolins are recognized as the most probable reservoir hosts that harbour highly similar SARS-CoV-2 related viruses (SARSr-CoV-2). This study identified a novel lineage of SARSr-CoVs, including RaTG15 and seven other viruses, from bats at the same location where we found RaTG13 in 2015. Although RaTG15 and the related viruses share 97.2% amino acid sequence identities with SARS-CoV-2 in the conserved ORF1b region, it only shows less than 77.6% nucleotide identity to all known SARSr-CoVs at the genome level, thus forming a distinct lineage in the Sarbecovirus phylogenetic tree. We found that the RaTG15 receptor-binding domain (RBD) can bind to ACE2 from Rhinolophus affinis, Malayan pangolin, and use it as an entry receptor, except for ACE2 from humans. However, it contains a short deletion and has different key residues responsible for ACE2 binding. In addition, we showed that none of the known viruses in bat SARSr-CoV-2 lineage discovered uses human ACE2 as efficiently as the pangolin-derived SARSr-CoV-2 or some viruses in the SARSr-CoV-1 lineage. Therefore, further systematic and longitudinal studies in bats are needed to prevent future spillover events caused by SARSr-CoVs or to understand the origin of SARS-CoV-2 better. Taylor & Francis 2021-08-04 /pmc/articles/PMC8344244/ /pubmed/34263709 http://dx.doi.org/10.1080/22221751.2021.1956373 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Guo, Hua Hu, Ben Si, Hao-Rui Zhu, Yan Zhang, Wei Li, Bei Li, Ang Geng, Rong Lin, Hao-Feng Yang, Xing-Lou Zhou, Peng Shi, Zheng-Li Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor |
title | Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor |
title_full | Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor |
title_fullStr | Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor |
title_full_unstemmed | Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor |
title_short | Identification of a novel lineage bat SARS-related coronaviruses that use bat ACE2 receptor |
title_sort | identification of a novel lineage bat sars-related coronaviruses that use bat ace2 receptor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344244/ https://www.ncbi.nlm.nih.gov/pubmed/34263709 http://dx.doi.org/10.1080/22221751.2021.1956373 |
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