Egress of archaeal viruses

IF 2.6 2区 生物学 Q3 CELL BIOLOGY
Diana P. Baquero, Junfeng Liu, David Prangishvili
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引用次数: 5

Abstract

Viruses of Archaea, arguably the most mysterious part of the virosphere due to their unique morphotypes and genome contents, exploit diverse mechanisms for releasing virus progeny from the host cell. These include virus release as a result of the enzymatic degradation of the cell wall or budding through it, common for viruses of Bacteria and Eukarya, as well as a unique mechanism of virus egress through small polygonal perforations on the cell surface. The process of the formation of these perforations includes the development of pyramidal structures on the membrane of the infected cell, which gradually grow by the expansion of their faces and eventually open like flower petals. This mechanism of virion release is operating exclusively in cells of hyperthermophilic hosts from the phylum Crenarchaeota, which are encased solely by a layer of surface proteins, S-layer. The review focuses on recent developments in understanding structural and biochemical details of all three types of egress mechanisms of archaeal viruses.

Take Aways

  • Many archaeal viruses exit the host via polygonal perforations on the cell membrane.
  • The molecular mechanism of exit via specific apertures is unique for archaeal viruses.
  • Some enveloped archaeal viruses exploit the budding mechanism for egress.

Abstract Image

古细菌病毒的出口
由于其独特的形态和基因组内容,古细菌病毒可以说是病毒圈中最神秘的部分,它们利用多种机制从宿主细胞释放病毒后代。这包括病毒通过细胞壁的酶降解或出芽而释放,这在细菌和真核生物的病毒中很常见,以及病毒通过细胞表面的小多边形穿孔排出的独特机制。这些穿孔的形成过程包括感染细胞膜上锥体结构的发育,这些锥体结构随着表面的扩张而逐渐生长,最终像花瓣一样张开。这种病毒粒子释放机制仅在嗜热的绿藻门宿主细胞中起作用,这些细胞仅被一层表面蛋白s层包裹。本文综述了在了解所有三种古细菌病毒出口机制的结构和生化细节方面的最新进展。许多古细菌病毒通过细胞膜上的多角形穿孔离开宿主。古细菌病毒通过特定孔口的分子机制是独特的。一些被包膜的古细菌病毒利用出芽机制出口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular Microbiology
Cellular Microbiology 生物-微生物学
CiteScore
9.70
自引率
0.00%
发文量
26
审稿时长
3 months
期刊介绍: Cellular Microbiology aims to publish outstanding contributions to the understanding of interactions between microbes, prokaryotes and eukaryotes, and their host in the context of pathogenic or mutualistic relationships, including co-infections and microbiota. We welcome studies on single cells, animals and plants, and encourage the use of model hosts and organoid cultures. Submission on cell and molecular biological aspects of microbes, such as their intracellular organization or the establishment and maintenance of their architecture in relation to virulence and pathogenicity are also encouraged. Contributions must provide mechanistic insights supported by quantitative data obtained through imaging, cellular, biochemical, structural or genetic approaches.
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