Suppr超能文献

[一株小鼠诺如病毒的分离、鉴定及基因分析]

[Isolation, identification and genetic analysis of a murine norovirus strain].

作者信息

Yuan Wen, Zhang Yu, Wang Jing, Liu Xiang-Mei, Zhao Wei-Bo, Huang Ren

出版信息

Bing Du Xue Bao. 2014 Jul;30(4):359-68.

Abstract

Murine norovirus (MNV) was first discovered in mice in 2003. MNV is a member of the genus Norovirus in the family Caliciviridae. It is one of the most important and prevalent pathogens of laboratory mice, and almost all mouse strains are susceptible to MNV infection. In this study, a MNV strain was isolated from the cecal contents of infected mice and identified by the cytopathic effect (CPE) assay, virus plaque assay, 50% tissue culture infectious dose (TCID50) assay, electron microscopy, indirect immunofluorescence assay (IFA) and nucleotide sequencing. On infection, the RAW264.7 cell line showed obvious cytopathic effects within 24 to 48 hours post-inoculation, as infected cells became rounded, bright and shrunken, with ultimate disintegration of the cell sheet. After the isolation of the MNV virus, the virus was plaque-purified in RAW264.7 cells. The TCID50 of the virus was 10(5.25/0.1 mL. Electron microscopic observations of the purified virus showed the presence of spherical and non-enveloped viral particles that were 30 to 35 nm in diameter. According to the identification results, the isolate was named as MNV Guangzhou/K162/09/CHN. Thereafter, five overlapping gene fragments that covered the entire open reading frame (ORF) were amplified by RT-PCR, and the 3'-untranslated region (UTR) and 5'-UTR were amplified using the 3'-rapid amplification of cDNA ends (RACE) and the 5'-RACE method, respectively. Each of the gene fragments were cloned and sequenced, and whole genome sequences of the strain were obtained by assembling the cDNA fragment sequences. The results showed that the length of the complete genome was 7 380 nucleotides (GenBank accession number: HQ317203). The comparison of nucleotide and deduced amino acid sequences of the isolate was performed against other MNV strains in the GenBank database. A phylogenetic tree based on VP1 nucleotide sequences was constructed using MEGA5.0 software. The homology of nucleotides between the MNV Guangzhou/K162/09/CHN strain and other MNV isolates ranged from 87.4% to 89.7%. Phylogenetic analysis showed that there was a close genetic relationship between the Guangzhou/K162/09/CHN strain and MNV strains isolated from Japan (S7-P2 and S7-PP3 isolates), Korea (K4 isolate), and Germany (Berlin/04/06/DE and Berlin/05/06/DE isolates). This is the first report of the isolation and identification of MNV in China, and the first report of the genetic analysis of its complete genome.

摘要

鼠诺如病毒(MNV)于2003年首次在小鼠中被发现。MNV是杯状病毒科诺如病毒属的成员。它是实验小鼠最重要且最普遍的病原体之一,几乎所有小鼠品系都易感染MNV。在本研究中,从感染小鼠的盲肠内容物中分离出一株MNV,并通过细胞病变效应(CPE)测定、病毒蚀斑测定、50%组织培养感染剂量(TCID50)测定、电子显微镜检查、间接免疫荧光测定(IFA)和核苷酸测序进行鉴定。感染时,RAW264.7细胞系在接种后24至48小时内出现明显的细胞病变效应,感染的细胞变得圆缩、明亮且皱缩,最终细胞单层解体。分离出MNV病毒后,该病毒在RAW264.7细胞中进行蚀斑纯化。该病毒的TCID50为10(5.25)/0.1 mL。对纯化病毒的电子显微镜观察显示存在直径为30至35 nm的球形无包膜病毒颗粒。根据鉴定结果,该分离株被命名为MNV广州/K162/09/CHN。此后,通过RT-PCR扩增覆盖整个开放阅读框(ORF)的五个重叠基因片段,并分别使用3'-cDNA末端快速扩增(RACE)和5'-RACE方法扩增3'-非翻译区(UTR)和5'-UTR。每个基因片段都进行了克隆和测序,并通过组装cDNA片段序列获得了该菌株的全基因组序列。结果显示,完整基因组长度为7380个核苷酸(GenBank登录号:HQ317203)。将该分离株的核苷酸和推导氨基酸序列与GenBank数据库中的其他MNV菌株进行比较。使用MEGA5.0软件构建基于VP1核苷酸序列的系统发育树。MNV广州/K162/09/CHN菌株与其他MNV分离株之间的核苷酸同源性范围为87.4%至89.7%。系统发育分析表明,广州/K162/09/CHN菌株与从日本分离的MNV菌株(S7-P2和S7-PP3分离株)、韩国(K4分离株)和德国(柏林/04/06/DE和柏林/05/06/DE分离株)之间存在密切的遗传关系。这是中国首次关于MNV分离和鉴定的报告,也是其全基因组遗传分析的首次报告。

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