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猴肾细胞培养中赛米利疱疹病毒复制的形态学观察

Morphological observations on the replication of herpesvirus saimiri in monkey kidney cell cultures.

作者信息

Morgan D G, Achong B G, Epstein M A

出版信息

J Gen Virol. 1976 Sep;32(3):461-70. doi: 10.1099/0022-1317-32-3-461.

Abstract

Owl and African green monkey kidney cell cultures have been infected with 1 p.f.u./cell of herpesvirus saimiri and sample cultures have been taken for examination by electron microscopy at 3 to 6 hourly intervals over a period of 7 days; the experiments were repeated several times. The peculiarly slow replication cycle of Herpesvirus saimiri has enabled distinct cytoplasmic and nuclear phases in virus maturation to be clearly distinguished; the overall fine structural features were similar in both cell types. Immature particles were first detected in the nucleus and cytoplasm 63 h after infection. Thereafter, abundant cytoplasmic immature particles matured by budding through cytoplasmic membranes until about 100 h, whereas nuclear immature particles budded through the inner nuclear membrane or intranuclear invaginations of it later, from about 100 h until cytolysis was complete at 160 h. Morphological differences were also observed between particles budding at cytoplasmic membranes and the nuclear envelope. At the former site the membrane overlying the bud showed an electron opaque thickening which imparted to the mature particle an asymmetrical appearance. Such thickenings of the envelope were not observed in mature particles of nuclear origin. Unusual tubular and laminated nuclear structures were seen towards the end of the replicative cycle corresponding with the phase of nuclear virus maturation by budding; the morphology of the latter structures is described.

摘要

将猫头鹰和非洲绿猴肾细胞培养物用每细胞1个空斑形成单位的赛米利疱疹病毒进行感染,并在7天的时间内每隔3至6小时采集样本培养物用于电子显微镜检查;这些实验重复了几次。赛米利疱疹病毒特别缓慢的复制周期使得病毒成熟过程中不同的细胞质和细胞核阶段能够被清晰区分;两种细胞类型的整体精细结构特征相似。感染后63小时首次在细胞核和细胞质中检测到未成熟颗粒。此后,大量的细胞质未成熟颗粒通过芽生穿过细胞质膜成熟,直至约100小时,而细胞核未成熟颗粒稍后从约100小时开始通过内核膜或其核内凹陷芽生,直至160小时细胞溶解完成。在细胞质膜和核膜处芽生的颗粒之间也观察到形态学差异。在前一个部位,覆盖芽的膜显示出电子不透明增厚,这使得成熟颗粒呈现不对称外观。在核源性成熟颗粒中未观察到包膜的这种增厚。在复制周期结束时,对应于通过芽生进行核病毒成熟的阶段,观察到异常的管状和层状核结构;描述了后者的形态。

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