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水泡性口炎病毒感染细胞中缺陷干扰颗粒的延迟形成:自身干扰期间病毒蛋白和RNA合成的动力学研究

Delayed formation of defective interfering particles in vesicular stomatitis virus-infected cells: kinetic studies of viral protein and RNA synthesis during autointerference.

作者信息

Von Laer D M, Mack D, Kruppa J

机构信息

Department of Molecular Biology, University of Hamburg, Federal Republic of Germany.

出版信息

J Virol. 1988 Apr;62(4):1323-9. doi: 10.1128/JVI.62.4.1323-1329.1988.

Abstract

The time course of defective interfering (DI) particle and B particle release from vesicular stomatitis virus-infected BHK-21 cells was studied at different multiplicities of defective and infective particles. Particle release was progressively delayed in cells infected with an increasing DI-to-B particle ratio. The delayed particle release during interference was found to be connected with a reduced but prolonged synthesis of viral proteins, a slower accumulation of viral proteins, and a delayed shutoff of cellular protein synthesis. The relative synthesis of M and G proteins was reduced during interference, whereas the relative synthesis of N and NS proteins was increased. On the level of genomic RNA replication, we found that DI RNA was replicated more slowly during interference than the standard genomic RNA was during acute infection. The ratio of DI particles to B particles which were released increased throughout the infectious cycle. At a given time in the infectious cycle, this ratio was independent of the multiplicity of infecting DI and B particles. On the basis of the kinetic studies, we argue that cells infected with higher amounts of DI particles compared with B particles synthesize a higher DI-to-B particle ratio and release these progeny particles later than cells infected with a low DI-to-B particle ratio.

摘要

在不同的缺陷型和感染性颗粒复数感染情况下,研究了水疱性口炎病毒感染的BHK - 21细胞中缺陷干扰(DI)颗粒和B颗粒释放的时间进程。随着感染细胞中DI与B颗粒比例的增加,颗粒释放逐渐延迟。发现在干扰期间延迟的颗粒释放与病毒蛋白合成减少但持续时间延长、病毒蛋白积累较慢以及细胞蛋白合成的延迟关闭有关。在干扰期间,M和G蛋白的相对合成减少,而N和NS蛋白的相对合成增加。在基因组RNA复制水平上,我们发现干扰期间DI RNA的复制比急性感染期间标准基因组RNA的复制更慢。在整个感染周期中,释放的DI颗粒与B颗粒的比例增加。在感染周期的给定时间,该比例与感染的DI和B颗粒的复数无关。基于动力学研究,我们认为与B颗粒相比,感染大量DI颗粒的细胞合成的DI与B颗粒比例更高,并且比感染低DI与B颗粒比例的细胞更晚释放这些子代颗粒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/783b/253144/a1919129b1ce/jvirol00083-0242-a.jpg

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