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Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats

Bats have been identified as a natural reservoir of a variety of coronaviruses (CoVs). Several of them have caused diseases in humans and domestic animals by interspecies transmission. Considering the diversity of bat coronaviruses, bat species and populations, we expect to discover more bat CoVs th...

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Autores principales: Wang, Ning, Luo, Chuming, Liu, Haizhou, Yang, Xinglou, Hu, Ben, Zhang, Wei, Li, Bei, Zhu, Yan, Zhu, Guangjian, Shen, Xurui, Peng, Cheng, Shi, Zhengli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521148/
https://www.ncbi.nlm.nih.gov/pubmed/31022925
http://dx.doi.org/10.3390/v11040379
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author Wang, Ning
Luo, Chuming
Liu, Haizhou
Yang, Xinglou
Hu, Ben
Zhang, Wei
Li, Bei
Zhu, Yan
Zhu, Guangjian
Shen, Xurui
Peng, Cheng
Shi, Zhengli
author_facet Wang, Ning
Luo, Chuming
Liu, Haizhou
Yang, Xinglou
Hu, Ben
Zhang, Wei
Li, Bei
Zhu, Yan
Zhu, Guangjian
Shen, Xurui
Peng, Cheng
Shi, Zhengli
author_sort Wang, Ning
collection PubMed
description Bats have been identified as a natural reservoir of a variety of coronaviruses (CoVs). Several of them have caused diseases in humans and domestic animals by interspecies transmission. Considering the diversity of bat coronaviruses, bat species and populations, we expect to discover more bat CoVs through virus surveillance. In this study, we described a new member of alphaCoV (BtCoV/Rh/YN2012) in bats with unique genome features. Unique accessory genes, ORF4a and ORF4b were found between the spike gene and the envelope gene, while ORF8 gene was found downstream of the nucleocapsid gene. All the putative genes were further confirmed by reverse-transcription analyses. One unique gene at the 3’ end of the BtCoV/Rh/YN2012 genome, ORF9, exhibits ~30% amino acid identity to ORF7a of the SARS-related coronavirus. Functional analysis showed ORF4a protein can activate IFN-β production, whereas ORF3a can regulate NF-κB production. We also screened the spike-mediated virus entry using the spike-pseudotyped retroviruses system, although failed to find any fully permissive cells. Our results expand the knowledge on the genetic diversity of bat coronaviruses. Continuous screening of bat viruses will help us further understand the important role played by bats in coronavirus evolution and transmission.
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spelling pubmed-65211482019-06-03 Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats Wang, Ning Luo, Chuming Liu, Haizhou Yang, Xinglou Hu, Ben Zhang, Wei Li, Bei Zhu, Yan Zhu, Guangjian Shen, Xurui Peng, Cheng Shi, Zhengli Viruses Article Bats have been identified as a natural reservoir of a variety of coronaviruses (CoVs). Several of them have caused diseases in humans and domestic animals by interspecies transmission. Considering the diversity of bat coronaviruses, bat species and populations, we expect to discover more bat CoVs through virus surveillance. In this study, we described a new member of alphaCoV (BtCoV/Rh/YN2012) in bats with unique genome features. Unique accessory genes, ORF4a and ORF4b were found between the spike gene and the envelope gene, while ORF8 gene was found downstream of the nucleocapsid gene. All the putative genes were further confirmed by reverse-transcription analyses. One unique gene at the 3’ end of the BtCoV/Rh/YN2012 genome, ORF9, exhibits ~30% amino acid identity to ORF7a of the SARS-related coronavirus. Functional analysis showed ORF4a protein can activate IFN-β production, whereas ORF3a can regulate NF-κB production. We also screened the spike-mediated virus entry using the spike-pseudotyped retroviruses system, although failed to find any fully permissive cells. Our results expand the knowledge on the genetic diversity of bat coronaviruses. Continuous screening of bat viruses will help us further understand the important role played by bats in coronavirus evolution and transmission. MDPI 2019-04-24 /pmc/articles/PMC6521148/ /pubmed/31022925 http://dx.doi.org/10.3390/v11040379 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Ning
Luo, Chuming
Liu, Haizhou
Yang, Xinglou
Hu, Ben
Zhang, Wei
Li, Bei
Zhu, Yan
Zhu, Guangjian
Shen, Xurui
Peng, Cheng
Shi, Zhengli
Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats
title Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats
title_full Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats
title_fullStr Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats
title_full_unstemmed Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats
title_short Characterization of a New Member of Alphacoronavirus with Unique Genomic Features in Rhinolophus Bats
title_sort characterization of a new member of alphacoronavirus with unique genomic features in rhinolophus bats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521148/
https://www.ncbi.nlm.nih.gov/pubmed/31022925
http://dx.doi.org/10.3390/v11040379
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