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与风疹病毒形态发生相关的复制复合体

Replication complexes associated with the morphogenesis of rubella virus.

作者信息

Lee J Y, Marshall J A, Bowden D S

机构信息

Macfarlane Burnet Centre for Medical Research, Fairfield Hospital, Victoria, Australia.

出版信息

Arch Virol. 1992;122(1-2):95-106. doi: 10.1007/BF01321120.

Abstract

Thin section electron microscopy was used to investigate cellular changes associated with the replication of rubella virus (RV) in Vero cells and to compare these changes to those of the related alphavirus, Semliki Forest virus (SFV). Conspicuous membrane-bound cytoplasmic vacuoles analogous to the alphavirus replication complexes were observed in RV infected cells but not in mock infected cells. The vacuoles were characterised by membrane-bound vesicles measuring about 60 nm which often displayed an irregular dense core and/or a network of fibres. These vesicles were morphologically distinct from RV particles and were generally located at regular intervals on the inner side of the surrounding membrane of the RV replication complex. Degenerating cellular material was often found in the membrane-bound vacuole of a replication complex. The replication complexes were intimately associated with the rough endoplasmic reticulum (RER), which was localised 45-75 nm from the surrounding membrane of the replication complex. Parallel studies of replication complexes in SFV infected cells did not reveal such an intimate association with the RER. RV replication complexes appeared as early as 8 h post infection (p.i.), before detection of RV particles by electron microscopy, and their peak production at 24 h p.i. coincided with the time of maximum virus titre.

摘要

采用超薄切片电子显微镜技术研究风疹病毒(RV)在Vero细胞中复制相关的细胞变化,并将这些变化与相关甲病毒——Semliki森林病毒(SFV)的细胞变化进行比较。在RV感染的细胞中观察到类似于甲病毒复制复合物的明显的膜结合细胞质空泡,而在 mock 感染的细胞中未观察到。这些空泡的特征是膜结合的囊泡,直径约60nm,通常显示出不规则的致密核心和/或纤维网络。这些囊泡在形态上与RV颗粒不同,通常以规则的间隔位于RV复制复合物周围膜的内侧。在复制复合物的膜结合空泡中经常发现退化的细胞物质。复制复合物与粗面内质网(RER)密切相关,粗面内质网位于距复制复合物周围膜45 - 75nm处。对SFV感染细胞中复制复合物的平行研究未发现与RER有如此密切的关联。RV复制复合物早在感染后8小时(p.i.)出现,在通过电子显微镜检测到RV颗粒之前,其在感染后24小时的产量峰值与病毒滴度最高的时间一致。

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