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Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of the recent pandemic COVID-19, is reported to have originated from bats, with its intermediate host unknown to date. Here, we screened 26 animal counterparts of the human ACE2 (hACE2), the receptor for SARS-CoV-2 and...

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Autores principales: Wu, Lili, Chen, Qian, Liu, Kefang, Wang, Jia, Han, Pengcheng, Zhang, Yanfang, Hu, Yu, Meng, Yumin, Pan, Xiaoqian, Qiao, Chengpeng, Tian, Siyu, Du, Pei, Song, Hao, Shi, Weifeng, Qi, Jianxun, Wang, Hong-Wei, Yan, Jinghua, Gao, George Fu, Wang, Qihui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526519/
https://www.ncbi.nlm.nih.gov/pubmed/33020722
http://dx.doi.org/10.1038/s41421-020-00210-9
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author Wu, Lili
Chen, Qian
Liu, Kefang
Wang, Jia
Han, Pengcheng
Zhang, Yanfang
Hu, Yu
Meng, Yumin
Pan, Xiaoqian
Qiao, Chengpeng
Tian, Siyu
Du, Pei
Song, Hao
Shi, Weifeng
Qi, Jianxun
Wang, Hong-Wei
Yan, Jinghua
Gao, George Fu
Wang, Qihui
author_facet Wu, Lili
Chen, Qian
Liu, Kefang
Wang, Jia
Han, Pengcheng
Zhang, Yanfang
Hu, Yu
Meng, Yumin
Pan, Xiaoqian
Qiao, Chengpeng
Tian, Siyu
Du, Pei
Song, Hao
Shi, Weifeng
Qi, Jianxun
Wang, Hong-Wei
Yan, Jinghua
Gao, George Fu
Wang, Qihui
author_sort Wu, Lili
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of the recent pandemic COVID-19, is reported to have originated from bats, with its intermediate host unknown to date. Here, we screened 26 animal counterparts of the human ACE2 (hACE2), the receptor for SARS-CoV-2 and SARS-CoV, and found that the ACE2s from various species, including pets, domestic animals and multiple wild animals, could bind to SARS-CoV-2 receptor binding domain (RBD) and facilitate the transduction of SARS-CoV-2 pseudovirus. Comparing to SARS-CoV-2, SARS-CoV seems to have a slightly wider range in choosing its receptor. We further resolved the cryo-electron microscopy (cryo-EM) structure of the cat ACE2 (cACE2) in complex with the SARS-CoV-2 RBD at a resolution of 3 Å, revealing similar binding mode as hACE2 to the SARS-CoV-2 RBD. These results shed light on pursuing the intermediate host of SARS-CoV-2 and highlight the necessity of monitoring susceptible hosts to prevent further outbreaks.
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spelling pubmed-75265192020-10-01 Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2 Wu, Lili Chen, Qian Liu, Kefang Wang, Jia Han, Pengcheng Zhang, Yanfang Hu, Yu Meng, Yumin Pan, Xiaoqian Qiao, Chengpeng Tian, Siyu Du, Pei Song, Hao Shi, Weifeng Qi, Jianxun Wang, Hong-Wei Yan, Jinghua Gao, George Fu Wang, Qihui Cell Discov Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of the recent pandemic COVID-19, is reported to have originated from bats, with its intermediate host unknown to date. Here, we screened 26 animal counterparts of the human ACE2 (hACE2), the receptor for SARS-CoV-2 and SARS-CoV, and found that the ACE2s from various species, including pets, domestic animals and multiple wild animals, could bind to SARS-CoV-2 receptor binding domain (RBD) and facilitate the transduction of SARS-CoV-2 pseudovirus. Comparing to SARS-CoV-2, SARS-CoV seems to have a slightly wider range in choosing its receptor. We further resolved the cryo-electron microscopy (cryo-EM) structure of the cat ACE2 (cACE2) in complex with the SARS-CoV-2 RBD at a resolution of 3 Å, revealing similar binding mode as hACE2 to the SARS-CoV-2 RBD. These results shed light on pursuing the intermediate host of SARS-CoV-2 and highlight the necessity of monitoring susceptible hosts to prevent further outbreaks. Springer Singapore 2020-09-29 /pmc/articles/PMC7526519/ /pubmed/33020722 http://dx.doi.org/10.1038/s41421-020-00210-9 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wu, Lili
Chen, Qian
Liu, Kefang
Wang, Jia
Han, Pengcheng
Zhang, Yanfang
Hu, Yu
Meng, Yumin
Pan, Xiaoqian
Qiao, Chengpeng
Tian, Siyu
Du, Pei
Song, Hao
Shi, Weifeng
Qi, Jianxun
Wang, Hong-Wei
Yan, Jinghua
Gao, George Fu
Wang, Qihui
Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2
title Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2
title_full Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2
title_fullStr Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2
title_full_unstemmed Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2
title_short Broad host range of SARS-CoV-2 and the molecular basis for SARS-CoV-2 binding to cat ACE2
title_sort broad host range of sars-cov-2 and the molecular basis for sars-cov-2 binding to cat ace2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526519/
https://www.ncbi.nlm.nih.gov/pubmed/33020722
http://dx.doi.org/10.1038/s41421-020-00210-9
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