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口蹄疫病毒而非牛肠道病毒,通过非结构蛋白3Cpro靶向宿主细胞细胞骨架。

Foot-and-mouth disease virus, but not bovine enterovirus, targets the host cell cytoskeleton via the nonstructural protein 3Cpro.

作者信息

Armer Hannah, Moffat Katy, Wileman Thomas, Belsham Graham J, Jackson Terry, Duprex W Paul, Ryan Martin, Monaghan Paul

机构信息

Institute for Animal Health, Woking, Surrey, United Kingdom.

出版信息

J Virol. 2008 Nov;82(21):10556-66. doi: 10.1128/JVI.00907-08. Epub 2008 Aug 27.

Abstract

Foot-and-mouth disease virus (FMDV), a member of the Picornaviridae, is a pathogen of cloven-hoofed animals and causes a disease of major economic importance. Picornavirus-infected cells show changes in cell morphology and rearrangement of cytoplasmic membranes, which are a consequence of virus replication. We show here, by confocal immunofluorescence and electron microscopy, that the changes in morphology of FMDV-infected cells involve changes in the distribution of microtubule and intermediate filament components during infection. Despite the continued presence of centrosomes in infected cells, there is a loss of tethering of microtubules to the microtubule organizing center (MTOC) region. Loss of labeling for gamma-tubulin, but not pericentrin, from the MTOC suggests a targeting of gamma-tubulin (or associated proteins) rather than a total breakdown in MTOC structure. The identity of the FMDV protein(s) responsible was determined by the expression of individual viral nonstructural proteins and their precursors in uninfected cells. We report that the only viral nonstructural protein able to reproduce the loss of gamma-tubulin from the MTOC and the loss of integrity of the microtubule system is FMDV 3C(pro). In contrast, infection of cells with another picornavirus, bovine enterovirus, did not affect gamma-tubulin distribution, and the microtubule network remained relatively unaffected.

摘要

口蹄疫病毒(FMDV)是小RNA病毒科的成员,是偶蹄动物的病原体,可引发具有重大经济影响的疾病。感染小RNA病毒的细胞会出现细胞形态变化和细胞质膜重排,这是病毒复制的结果。我们通过共聚焦免疫荧光和电子显微镜观察发现,FMDV感染细胞的形态变化涉及感染过程中微管和中间丝成分分布的改变。尽管受感染细胞中中心体持续存在,但微管与微管组织中心(MTOC)区域的连接却丧失了。MTOC区域中γ-微管蛋白(而非中心粒外周蛋白)标记的缺失表明,γ-微管蛋白(或相关蛋白)是靶向作用的对象,而非MTOC结构完全瓦解。通过在未感染细胞中表达单个病毒非结构蛋白及其前体,确定了相关FMDV蛋白的身份。我们报告称,唯一能够重现MTOC中γ-微管蛋白缺失和微管系统完整性丧失的病毒非结构蛋白是FMDV 3C蛋白酶。相比之下,用另一种小RNA病毒牛肠道病毒感染细胞不会影响γ-微管蛋白的分布,微管网络也相对未受影响。

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