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