Suppr超能文献

从挪威大鼠中发现一种新型冠状病毒——中国大鼠冠状病毒HKU24,这支持了β冠状病毒1的鼠源起源,并对β冠状病毒A谱系的祖先具有启示意义。

Discovery of a novel coronavirus, China Rattus coronavirus HKU24, from Norway rats supports the murine origin of Betacoronavirus 1 and has implications for the ancestor of Betacoronavirus lineage A.

作者信息

Lau Susanna K P, Woo Patrick C Y, Li Kenneth S M, Tsang Alan K L, Fan Rachel Y Y, Luk Hayes K H, Cai Jian-Piao, Chan Kwok-Hung, Zheng Bo-Jian, Wang Ming, Yuen Kwok-Yung

机构信息

State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China Research Centre of Infection and Immunology, The University of Hong Kong, Hong Kong, China Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China Department of Microbiology, The University of Hong Kong, Hong Kong, China.

Department of Microbiology, The University of Hong Kong, Hong Kong, China.

出版信息

J Virol. 2015 Mar;89(6):3076-92. doi: 10.1128/JVI.02420-14. Epub 2014 Dec 31.

Abstract

UNLABELLED

We discovered a novel Betacoronavirus lineage A coronavirus, China Rattus coronavirus (ChRCoV) HKU24, from Norway rats in China. ChRCoV HKU24 occupied a deep branch at the root of members of Betacoronavirus 1, being distinct from murine coronavirus and human coronavirus HKU1. Its unique putative cleavage sites between nonstructural proteins 1 and 2 and in the spike (S) protein and low sequence identities to other lineage A betacoronaviruses (βCoVs) in conserved replicase domains support ChRCoV HKU24 as a separate species. ChRCoV HKU24 possessed genome features that resemble those of both Betacoronavirus 1 and murine coronavirus, being closer to Betacoronavirus 1 in most predicted proteins but closer to murine coronavirus by G+C content, the presence of a single nonstructural protein (NS4), and an absent transcription regulatory sequence for the envelope (E) protein. Its N-terminal domain (NTD) demonstrated higher sequence identity to the bovine coronavirus (BCoV) NTD than to the mouse hepatitis virus (MHV) NTD, with 3 of 4 critical sugar-binding residues in BCoV and 2 of 14 contact residues at the MHV NTD/murine CEACAM1a interface being conserved. Molecular clock analysis dated the time of the most recent common ancestor of ChRCoV HKU24, Betacoronavirus 1, and rabbit coronavirus HKU14 to about the year 1400. Cross-reactivities between other lineage A and B βCoVs and ChRCoV HKU24 nucleocapsid but not spike polypeptide were demonstrated. Using the spike polypeptide-based Western blot assay, we showed that only Norway rats and two oriental house rats from Guangzhou, China, were infected by ChRCoV HKU24. Other rats, including Norway rats from Hong Kong, possessed antibodies only against N protein and not against the spike polypeptide, suggesting infection by βCoVs different from ChRCoV HKU24. ChRCoV HKU24 may represent the murine origin of Betacoronavirus 1, and rodents are likely an important reservoir for ancestors of lineage A βCoVs.

IMPORTANCE

While bats and birds are hosts for ancestors of most coronaviruses (CoVs), lineage A βCoVs have never been found in these animals and the origin of Betacoronavirus lineage A remains obscure. We discovered a novel lineage A βCoV, China Rattus coronavirus HKU24 (ChRCoV HKU24), from Norway rats in China with a high seroprevalence. The unique genome features and phylogenetic analysis supported the suggestion that ChRCoV HKU24 represents a novel CoV species, occupying a deep branch at the root of members of Betacoronavirus 1 and being distinct from murine coronavirus. Nevertheless, ChRCoV HKU24 possessed genome characteristics that resemble those of both Betacoronavirus 1 and murine coronavirus. Our data suggest that ChRCoV HKU24 represents the murine origin of Betacoronavirus 1, with interspecies transmission from rodents to other mammals having occurred centuries ago, before the emergence of human coronavirus (HCoV) OC43 in the late 1800s. Rodents are likely an important reservoir for ancestors of lineage A βCoVs.

摘要

未加标签

我们从中国的挪威大鼠中发现了一种新型的乙型冠状病毒A属冠状病毒,即中国大鼠冠状病毒(ChRCoV)HKU24。ChRCoV HKU24在乙型冠状病毒1成员的根部占据一个深分支,与鼠冠状病毒和人冠状病毒HKU1不同。其非结构蛋白1和2之间以及刺突(S)蛋白中独特的假定切割位点,以及在保守复制酶结构域中与其他A属乙型冠状病毒(βCoV)的低序列同一性,支持ChRCoV HKU24作为一个独立的物种。ChRCoV HKU24具有类似于乙型冠状病毒1和鼠冠状病毒的基因组特征,在大多数预测蛋白中更接近乙型冠状病毒1,但在G+C含量、单个非结构蛋白(NS4)的存在以及包膜(E)蛋白的转录调控序列缺失方面更接近鼠冠状病毒。其N端结构域(NTD)与牛冠状病毒(BCoV)的NTD相比,与小鼠肝炎病毒(MHV)的NTD具有更高的序列同一性,BCoV中4个关键糖结合残基中的3个以及MHV NTD/鼠CEACAM1a界面处14个接触残基中的2个是保守的。分子钟分析确定ChRCoV HKU24、乙型冠状病毒1和兔冠状病毒HKU14的最近共同祖先的时间约为公元1400年。已证明其他A属和B属βCoV与ChRCoV HKU24核衣壳之间存在交叉反应,但与刺突多肽不存在交叉反应。使用基于刺突多肽的蛋白质印迹分析,我们表明只有来自中国广州的挪威大鼠和两只东方家鼠被ChRCoV HKU24感染。其他大鼠,包括来自香港的挪威大鼠,仅拥有针对N蛋白的抗体,而不拥有针对刺突多肽的抗体,这表明它们受到了与ChRCoV HKU24不同的βCoV的感染。ChRCoV HKU24可能代表乙型冠状病毒1的鼠源,并且啮齿动物可能是A属βCoV祖先的重要储存宿主。

重要性

虽然蝙蝠和鸟类是大多数冠状病毒(CoV)祖先的宿主,但从未在这些动物中发现A属βCoV,并且乙型冠状病毒A属的起源仍然不明。我们从中国血清阳性率高的挪威大鼠中发现了一种新型A属βCoV,即中国大鼠冠状病毒HKU

相似文献

3
Identification of the Receptor-Binding Domain of the Spike Glycoprotein of Human Betacoronavirus HKU1.
J Virol. 2015 Sep;89(17):8816-27. doi: 10.1128/JVI.03737-14. Epub 2015 Jun 17.
6
Detection of alpha- and betacoronaviruses in rodents from Yunnan, China.
Virol J. 2017 May 26;14(1):98. doi: 10.1186/s12985-017-0766-9.
10
Detection of a virus related to betacoronaviruses in Italian greater horseshoe bats.
Epidemiol Infect. 2011 Feb;139(2):216-9. doi: 10.1017/S0950268810001147. Epub 2010 May 18.

引用本文的文献

2
Paramyxo- and coronavirus diversity and host associations in non-volant small mammals: evidence of viral sharing.
Virus Evol. 2025 May 22;11(1):veaf041. doi: 10.1093/ve/veaf041. eCollection 2025.
3
Infectious potential and circulation of SARS-CoV-2 in wild rats.
PLoS One. 2025 May 12;20(5):e0316882. doi: 10.1371/journal.pone.0316882. eCollection 2025.
4
Determinants of susceptibility to SARS-CoV-2 infection in murine ACE2.
J Virol. 2025 Jun 17;99(6):e0054325. doi: 10.1128/jvi.00543-25. Epub 2025 May 12.
5
Surveillance for SARS-CoV-2 in Norway Rats () from Southern Ontario.
Transbound Emerg Dis. 2023 May 26;2023:7631611. doi: 10.1155/2023/7631611. eCollection 2023.
7
Utilizing HCoV-OC43 to better understand the neurological impact of COVID-19.
Brain Behav Immun Health. 2024 Nov 9;42:100905. doi: 10.1016/j.bbih.2024.100905. eCollection 2024 Dec.
8
Identification of the critical residues of TMPRSS2 for entry and host range of human coronavirus HKU1.
J Virol. 2024 Dec 17;98(12):e0158724. doi: 10.1128/jvi.01587-24. Epub 2024 Nov 11.
10
Structural basis for mouse receptor recognition by bat SARS2-like coronaviruses.
Proc Natl Acad Sci U S A. 2024 Aug 6;121(32):e2322600121. doi: 10.1073/pnas.2322600121. Epub 2024 Jul 31.

本文引用的文献

1
Receptor usage and cell entry of bat coronavirus HKU4 provide insight into bat-to-human transmission of MERS coronavirus.
Proc Natl Acad Sci U S A. 2014 Aug 26;111(34):12516-21. doi: 10.1073/pnas.1405889111. Epub 2014 Aug 11.
3
Evidence for camel-to-human transmission of MERS coronavirus.
N Engl J Med. 2014 Jun 26;370(26):2499-505. doi: 10.1056/NEJMoa1401505. Epub 2014 Jun 4.
4
Novel betacoronavirus in dromedaries of the Middle East, 2013.
Emerg Infect Dis. 2014 Apr;20(4):560-72. doi: 10.3201/eid2004.131769.
5
Middle East respiratory syndrome coronavirus in dromedary camels: an outbreak investigation.
Lancet Infect Dis. 2014 Feb;14(2):140-5. doi: 10.1016/S1473-3099(13)70690-X. Epub 2013 Dec 17.
6
Ecology, evolution and classification of bat coronaviruses in the aftermath of SARS.
Antiviral Res. 2014 Jan;101:45-56. doi: 10.1016/j.antiviral.2013.10.013. Epub 2013 Oct 31.
7
Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor.
Nature. 2013 Nov 28;503(7477):535-8. doi: 10.1038/nature12711. Epub 2013 Oct 30.
8
Middle East respiratory syndrome coronavirus neutralising serum antibodies in dromedary camels: a comparative serological study.
Lancet Infect Dis. 2013 Oct;13(10):859-66. doi: 10.1016/S1473-3099(13)70164-6. Epub 2013 Aug 9.
10
Crystal structure of bovine coronavirus spike protein lectin domain.
J Biol Chem. 2012 Dec 7;287(50):41931-8. doi: 10.1074/jbc.M112.418210. Epub 2012 Oct 22.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验