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本文引用的文献

1
Toll-like receptor 3 (TLR3) plays a major role in the formation of rabies virus Negri Bodies.Toll样受体3(TLR3)在狂犬病病毒内基小体的形成中起主要作用。
PLoS Pathog. 2009 Feb;5(2):e1000315. doi: 10.1371/journal.ppat.1000315. Epub 2009 Feb 27.
2
LABORATORY: A NEW METHOD FOR STAINING NEGRI BODIES OF RABIES.实验室:一种用于狂犬病内基氏小体染色的新方法。
Am J Public Health (N Y). 1927 Oct;17(10):1080-1. doi: 10.2105/ajph.17.10.1080.
3
Aggresomes and pericentriolar sites of virus assembly: cellular defense or viral design?病毒装配的聚集体和中心粒周围位点:细胞防御还是病毒设计?
Annu Rev Microbiol. 2007;61:149-67. doi: 10.1146/annurev.micro.57.030502.090836.
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Viral hijacking of cellular ubiquitination pathways as an anti-innate immunity strategy.病毒劫持细胞泛素化途径作为一种抗先天免疫策略。
Viral Immunol. 2006 Summer;19(3):349-62. doi: 10.1089/vim.2006.19.349.
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Visualization of intracellular transport of vesicular stomatitis virus nucleocapsids in living cells.活细胞中水泡性口炎病毒核衣壳的细胞内运输可视化
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Aggresomes and autophagy generate sites for virus replication.聚集体和自噬为病毒复制产生位点。
Science. 2006 May 12;312(5775):875-8. doi: 10.1126/science.1126766.
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Dynamics of viral RNA synthesis during measles virus infection.麻疹病毒感染期间病毒RNA合成的动力学
J Virol. 2005 Jun;79(11):6900-8. doi: 10.1128/JVI.79.11.6900-6908.2005.
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Virus factories: associations of cell organelles for viral replication and morphogenesis.病毒工厂:用于病毒复制和形态发生的细胞器关联
Biol Cell. 2005 Feb;97(2):147-72. doi: 10.1042/BC20040058.
9
Tracking fluorescence-labeled rabies virus: enhanced green fluorescent protein-tagged phosphoprotein P supports virus gene expression and formation of infectious particles.追踪荧光标记的狂犬病病毒:增强型绿色荧光蛋白标记的磷蛋白P支持病毒基因表达和感染性颗粒的形成。
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10
Formation of aggresome-like structures in herpes simplex virus type 2-infected cells and a potential role in virus assembly.2型单纯疱疹病毒感染细胞中聚集体样结构的形成及其在病毒组装中的潜在作用。
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狂犬病病毒感染细胞中内基小体(NBs)的功能特性:内基小体是病毒转录和复制位点的证据。

Functional characterization of Negri bodies (NBs) in rabies virus-infected cells: Evidence that NBs are sites of viral transcription and replication.

作者信息

Lahaye Xavier, Vidy Aurore, Pomier Carole, Obiang Linda, Harper Francis, Gaudin Yves, Blondel Danielle

机构信息

CNRS, UMR, INRA, IFR, Gif sur Yvette, France.

出版信息

J Virol. 2009 Aug;83(16):7948-58. doi: 10.1128/JVI.00554-09. Epub 2009 Jun 3.

DOI:10.1128/JVI.00554-09
PMID:19494013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2715764/
Abstract

Rabies virus infection induces the formation of cytoplasmic inclusion bodies that resemble Negri bodies found in the cytoplasm of some infected nerve cells. We have studied the morphogenesis and the role of these Negri body-like structures (NBLs) during viral infection. The results indicate that these spherical structures (one or two per cell in the initial stage of infection), composed of the viral N and P proteins, grow during the virus cycle before appearing as smaller structures at late stages of infection. We have shown that the microtubule network is not necessary for the formation of these inclusion bodies but is involved in their dynamics. In contrast, the actin network does not play any detectable role in these processes. These inclusion bodies contain Hsp70 and ubiquitinylated proteins, but they are not misfolded protein aggregates. NBLs, in fact, appear to be functional structures involved in the viral life cycle. Specifically, using in situ fluorescent hybridization techniques, we show that all viral RNAs (genome, antigenome, and every mRNA) are located inside the inclusion bodies. Significantly, short-term RNA labeling in the presence of BrUTP strongly suggests that the NBLs are the sites where viral transcription and replication take place.

摘要

狂犬病病毒感染会诱导细胞质内包含体的形成,这些包含体类似于在一些受感染神经细胞的细胞质中发现的内基小体。我们研究了这些类内基小体结构(NBLs)在病毒感染过程中的形态发生及其作用。结果表明,这些由病毒N蛋白和P蛋白组成的球形结构(在感染初期每个细胞中有一个或两个),在病毒复制周期中生长,在感染后期呈现为较小的结构。我们已经表明,微管网络对于这些包含体的形成不是必需的,但参与了它们的动态变化。相比之下,肌动蛋白网络在这些过程中没有发挥任何可检测到的作用。这些包含体含有热休克蛋白70(Hsp70)和泛素化蛋白,但它们不是错误折叠的蛋白聚集体。事实上,NBLs似乎是参与病毒生命周期的功能性结构。具体而言,使用原位荧光杂交技术,我们表明所有病毒RNA(基因组、反基因组和每个mRNA)都位于包含体内。值得注意的是,在5-溴尿嘧啶三磷酸(BrUTP)存在下的短期RNA标记强烈表明,NBLs是病毒转录和复制发生的位点。