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瘟病毒的形态发生:来自长颈鹿-1株超微结构研究的新见解

Morphogenesis of pestiviruses: new insights from ultrastructural studies of strain Giraffe-1.

作者信息

Schmeiser Stefanie, Mast Jan, Thiel Heinz-Jürgen, König Matthias

机构信息

Institut für Virologie, FB Veterinärmedizin, Justus-Liebig-Universität Giessen, Giessen, Germany.

出版信息

J Virol. 2014 Mar;88(5):2717-24. doi: 10.1128/JVI.03237-13. Epub 2013 Dec 18.

Abstract

Knowledge on the morphogenesis of pestiviruses is limited due to low virus production in infected cells. In order to localize virion morphogenesis and replication sites of pestiviruses and to examine intracellular virion transport, a cell culture model was established to facilitate ultrastructural studies. Based on results of virus growth kinetic analysis and quantification of viral RNA, pestivirus strain Giraffe-1 turned out to be a suitable candidate for studies on virion generation and export from culture cells. Using conventional transmission electron microscopy and single-tilt electron tomography, we found virions located predominately in the lumen of the endoplasmic reticulum (ER) in infected cells and were able to depict the budding process of virions at ER membranes. Colocalization of the viral core protein and the envelope glycoprotein E2 with the ER marker protein disulfide isomerase (PDI) was demonstrated by immunogold labeling of cryosections. Moreover, pestivirions could be shown in transport vesicles and the Golgi complex and during exocytosis. Interestingly, viral capsid protein and double-stranded RNA (dsRNA) were detected in multivesicular bodies (MVBs), which implies that the endosomal compartment plays a role in pestiviral replication. Significant cellular membrane alterations such as those described for members of the Flavivirus and Hepacivirus genera were not found. Based on the gained morphological data, we present a consistent model of pestivirus morphogenesis.

摘要

由于瘟病毒在受感染细胞中的产量较低,关于瘟病毒形态发生的知识有限。为了定位瘟病毒的病毒粒子形态发生和复制位点,并研究细胞内病毒粒子的运输,建立了一种细胞培养模型以促进超微结构研究。根据病毒生长动力学分析结果和病毒RNA定量,瘟病毒长颈鹿-1株被证明是研究病毒粒子从培养细胞产生和输出的合适候选对象。使用传统透射电子显微镜和单倾电子断层扫描,我们发现病毒粒子主要位于受感染细胞内质网(ER)的腔内,并能够描绘病毒粒子在内质网膜上的出芽过程。通过对冷冻切片的免疫金标记证明了病毒核心蛋白和包膜糖蛋白E2与内质网标记蛋白二硫键异构酶(PDI)的共定位。此外,瘟病毒粒子可在运输小泡、高尔基体复合体以及胞吐过程中显示。有趣的是,在多囊泡体(MVBs)中检测到病毒衣壳蛋白和双链RNA(dsRNA),这意味着内体区室在瘟病毒复制中起作用。未发现如黄病毒属和丙型肝炎病毒属成员所描述的明显细胞膜改变。基于获得的形态学数据,我们提出了一个一致的瘟病毒形态发生模型。

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