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嗜热古菌病毒进入过程的初步观察

First insights into the entry process of hyperthermophilic archaeal viruses.

机构信息

Institut Pasteur, Unité Biologie Moléculaire du Gène chez les Extrêmophiles, Département de Microbiologie, Paris, France.

出版信息

J Virol. 2013 Dec;87(24):13379-85. doi: 10.1128/JVI.02742-13. Epub 2013 Oct 2.

Abstract

A decisive step in a virus infection cycle is the recognition of a specific receptor present on the host cell surface, subsequently leading to the delivery of the viral genome into the cell interior. Until now, the early stages of infection have not been thoroughly investigated for any virus infecting hyperthermophilic archaea. Here, we present the first study focusing on the primary interactions between the archaeal rod-shaped virus Sulfolobus islandicus rod-shaped virus 2 (SIRV2) (family Rudiviridae) and its hyperthermoacidophilic host, S. islandicus. We show that SIRV2 adsorption is very rapid, with the majority of virions being irreversibly bound to the host cell within 1 min. We utilized transmission electron microscopy and whole-cell electron cryotomography to demonstrate that SIRV2 virions specifically recognize the tips of pilus-like filaments, which are highly abundant on the host cell surface. Following the initial binding, the viral particles are found attached to the sides of the filaments, suggesting a movement along these appendages toward the cell surface. Finally, we also show that SIRV2 establishes superinfection exclusion, a phenomenon not previously described for archaeal viruses.

摘要

在病毒感染周期中,决定性的一步是识别宿主细胞表面存在的特定受体,随后将病毒基因组递送到细胞内部。到目前为止,还没有对任何感染高温嗜热古菌的病毒进行深入研究。在这里,我们首次研究了杆状古菌病毒 Sulfolobus islandicus 杆状病毒 2(SIRV2)(家族 Rudiviridae)与其高温嗜酸宿主 S. islandicus 之间的初步相互作用。我们表明,SIRV2 的吸附非常迅速,大多数病毒粒子在 1 分钟内不可逆地与宿主细胞结合。我们利用透射电子显微镜和全细胞电子晶体断层扫描技术证明,SIRV2 病毒粒子特异性地识别宿主细胞表面大量存在的类似于菌毛的细丝的尖端。在最初的结合之后,发现病毒颗粒附着在丝状结构的侧面,表明它们沿着这些附属物向细胞表面移动。最后,我们还表明,SIRV2 建立了超级感染排斥现象,这是以前在古菌病毒中没有描述过的现象。

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The wonderful world of archaeal viruses.古菌病毒的奇妙世界。
Annu Rev Microbiol. 2013;67:565-85. doi: 10.1146/annurev-micro-092412-155633.

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