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Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea

Bats have been widely known as natural reservoir hosts of zoonotic diseases, such as severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) caused by coronaviruses (CoVs). In the present study, we investigated the whole genomic sequence of a SARS-like bat CoV (16BO133)...

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Autores principales: Kim, Yongkwan, Son, Kidong, Kim, Young-Sik, Lee, Sook-Young, Jheong, Weonhwa, Oem, Jae-Ku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089380/
https://www.ncbi.nlm.nih.gov/pubmed/31076983
http://dx.doi.org/10.1007/s11262-019-01668-w
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author Kim, Yongkwan
Son, Kidong
Kim, Young-Sik
Lee, Sook-Young
Jheong, Weonhwa
Oem, Jae-Ku
author_facet Kim, Yongkwan
Son, Kidong
Kim, Young-Sik
Lee, Sook-Young
Jheong, Weonhwa
Oem, Jae-Ku
author_sort Kim, Yongkwan
collection PubMed
description Bats have been widely known as natural reservoir hosts of zoonotic diseases, such as severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) caused by coronaviruses (CoVs). In the present study, we investigated the whole genomic sequence of a SARS-like bat CoV (16BO133) and found it to be 29,075 nt in length with a 40.9% G+C content. Phylogenetic analysis using amino acid sequences of the ORF 1ab and the spike gene showed that the bat coronavirus strain 16BO133 was grouped with the Beta-CoV lineage B and was closely related to the JTMC15 strain isolated from Rhinolophus ferrumequinum in China. However, 16BO133 was distinctly located in the phylogenetic topology of the human SARS CoV strain (Tor2). Interestingly, 16BO133 showed complete elimination of ORF8 regions induced by a frame shift of the stop codon in ORF7b. The lowest amino acid identity of 16BO133 was identified at the spike region among various ORFs. The spike region of 16BO133 showed 84.7% and 75.2% amino acid identity with Rf1 (SARS-like bat CoV) and Tor2 (human SARS CoV), respectively. In addition, the S gene of 16BO133 was found to contain the amino acid substitution of two critical residues (N479S and T487 V) associated with human infection. In conclusion, we firstly carried out whole genome characterization of the SARS-like bat coronavirus discovered in the Republic of Korea; however, it presumably has no human infectivity. However, continuous surveillance and genomic characterization of coronaviruses from bats are necessary due to potential risks of human infection induced by genetic mutation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11262-019-01668-w) contains supplementary material, which is available to authorized users.
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spelling pubmed-70893802020-03-23 Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea Kim, Yongkwan Son, Kidong Kim, Young-Sik Lee, Sook-Young Jheong, Weonhwa Oem, Jae-Ku Virus Genes Short Report Bats have been widely known as natural reservoir hosts of zoonotic diseases, such as severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) caused by coronaviruses (CoVs). In the present study, we investigated the whole genomic sequence of a SARS-like bat CoV (16BO133) and found it to be 29,075 nt in length with a 40.9% G+C content. Phylogenetic analysis using amino acid sequences of the ORF 1ab and the spike gene showed that the bat coronavirus strain 16BO133 was grouped with the Beta-CoV lineage B and was closely related to the JTMC15 strain isolated from Rhinolophus ferrumequinum in China. However, 16BO133 was distinctly located in the phylogenetic topology of the human SARS CoV strain (Tor2). Interestingly, 16BO133 showed complete elimination of ORF8 regions induced by a frame shift of the stop codon in ORF7b. The lowest amino acid identity of 16BO133 was identified at the spike region among various ORFs. The spike region of 16BO133 showed 84.7% and 75.2% amino acid identity with Rf1 (SARS-like bat CoV) and Tor2 (human SARS CoV), respectively. In addition, the S gene of 16BO133 was found to contain the amino acid substitution of two critical residues (N479S and T487 V) associated with human infection. In conclusion, we firstly carried out whole genome characterization of the SARS-like bat coronavirus discovered in the Republic of Korea; however, it presumably has no human infectivity. However, continuous surveillance and genomic characterization of coronaviruses from bats are necessary due to potential risks of human infection induced by genetic mutation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11262-019-01668-w) contains supplementary material, which is available to authorized users. Springer US 2019-05-10 2019 /pmc/articles/PMC7089380/ /pubmed/31076983 http://dx.doi.org/10.1007/s11262-019-01668-w Text en © Springer Science+Business Media, LLC, part of Springer Nature 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Short Report
Kim, Yongkwan
Son, Kidong
Kim, Young-Sik
Lee, Sook-Young
Jheong, Weonhwa
Oem, Jae-Ku
Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea
title Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea
title_full Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea
title_fullStr Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea
title_full_unstemmed Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea
title_short Complete genome analysis of a SARS-like bat coronavirus identified in the Republic of Korea
title_sort complete genome analysis of a sars-like bat coronavirus identified in the republic of korea
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089380/
https://www.ncbi.nlm.nih.gov/pubmed/31076983
http://dx.doi.org/10.1007/s11262-019-01668-w
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