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一种新型犬呼吸道冠状病毒的发现支持β冠状病毒1之间的基因重组。

Discovery of a novel canine respiratory coronavirus support genetic recombination among betacoronavirus1.

作者信息

Lu Shuai, Wang Yanqun, Chen Yingzhu, Wu Bingjie, Qin Kun, Zhao Jincun, Lou Yongliang, Tan Wenjie

机构信息

Institute of Medical Virology, Wenzhou Medical University, Wenzhou 325000, China; Key Laboratory of Medical Virology, Ministry of Health, National Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, China.

Key Laboratory of Medical Virology, Ministry of Health, National Institute for Viral Disease Control and Prevention, China CDC, Beijing 102206, China; State Key Laboratory of Respiratory Diseases, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.

出版信息

Virus Res. 2017 Jun 2;237:7-13. doi: 10.1016/j.virusres.2017.05.006. Epub 2017 May 13.

Abstract

Although canine respiratory coronavirus (CRCoV) is an important respiratory pathogen that is prevalent in many countries, only one complete genome sequence of CRCoV (South Korea strain K37) has been obtained to date. Genome-wide analyses and recombination have rarely been conducted, as small numbers of samples and limited genomic characterization have previously prevented further analyses. Herein, we report a unique CRCoV strain, denoted strain BJ232, derived from a CRCoV-positive dog with a mild respiratory infection. Phylogenetic analysis based on complete genome of all available coronaviruses consistently show that CRCoV BJ232 is most closely related to human coronavirus OC43 (HCoV-OC43) and BCoV, forming a separate clade that split off early from other Betacoronavirus 1. Based on the phylogenetic and SimPlot analysis we propose that CRCoV-K37 was derived from genetic recombination between CRCoV-BJ232 and BCoV. In detail, spike (S) gene of CRCoV-K37 clustered with CRCoV-BJ232. However orf1ab, membrane (M) and nucleocapsid (N) genes were more related to Bovine coronavirus (BCoV) than CRCoV-B232. Molecular epidemic analysis confirmed the prevalence of CRCoV-BJ232 lineage around the world for a long time. Recombinant events among Betacoronavirus 1 may have implications for CRCoV transmissibility. All these findings provide further information regarding the origin of CRCoV.

摘要

尽管犬呼吸道冠状病毒(CRCoV)是一种在许多国家流行的重要呼吸道病原体,但迄今为止仅获得了一个CRCoV的完整基因组序列(韩国毒株K37)。由于样本数量少和基因组特征有限,以前阻碍了进一步分析,因此很少进行全基因组分析和重组研究。在此,我们报告了一种独特的CRCoV毒株,命名为BJ232毒株,它源自一只患有轻度呼吸道感染的CRCoV阳性犬。基于所有可用冠状病毒完整基因组的系统发育分析一致表明,CRCoV BJ232与人类冠状病毒OC43(HCoV-OC43)和牛冠状病毒(BCoV)关系最为密切,形成了一个与其他贝塔冠状病毒1早期分离的单独进化枝。基于系统发育和SimPlot分析,我们提出CRCoV-K37源自CRCoV-BJ232和BCoV之间的基因重组。详细而言,CRCoV-K37的刺突(S)基因与CRCoV-BJ232聚类。然而,开放阅读框1ab(orf1ab)、膜(M)和核衣壳(N)基因与牛冠状病毒(BCoV)的关系比与CRCoV-B232的关系更密切。分子流行病学分析证实,CRCoV-BJ232谱系在全球长期流行。贝塔冠状病毒1之间的重组事件可能对CRCoV的传播性有影响。所有这些发现为CRCoV的起源提供了进一步的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8665/7114567/2c9d4726cbb3/gr1_lrg.jpg

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