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麻疹病毒核糖核酸与蛋白质合成:6-氮尿苷和环己酰亚胺对病毒复制的影响

Measles virus ribonucleic acid and protein synthesis: effects of 6-azauridine and cycloheximide on viral replication.

作者信息

Portner A, Bussell R H

出版信息

J Virol. 1973 Jan;11(1):46-53. doi: 10.1128/JVI.11.1.46-53.1973.

Abstract

Cycloheximide and 6-azauridine were employed to study the time course of measles virus protein and nucleic acid syntheses in AV3 cells. Synthesis of ribonucleic acid (RNA) essential for infectivity was first detected at 6 hr and increased concurrently with the formation of essential protein. Maximum levels of virus-specific RNA and protein were present by 18 hr, a time when only 5% of progeny virus was detected. Essential RNA and protein syntheses preceded the formation of infectious virus by at least 10 to 12 hr. The time course of RNA and protein syntheses essential for the formation of complement-fixing (CF) antigen and salt-dependent agglutinin (SDA) was also determined. RNA synthesis essential for the formation of SDA was first detected at 2 hr and was present maximally by 6 hr, whereas SDA-protein increased concurrently with the protein essential for infectivity. This suggested that the last protein essential for infectivity may be SDA. RNA synthesis essential for the formation of CF antigen was first detected at 4 hr, while CF-protein increased at 5 hr and preceded SDA-protein and protein essential for infectivity by approximately 3 hr. Reversal of inhibition of protein synthesis by cycloheximide indicated that early protein synthesis (1 to 3 hr) was required for the formation of infectious virus. The data suggest that the relatively long eclipse period observed with measles virus is related to a long maturation period rather than to late formation of early proteins, viral RNA, or structural proteins.

摘要

采用放线菌酮和6-氮尿苷研究了麻疹病毒在AV3细胞中蛋白质和核酸合成的时间进程。感染性必需的核糖核酸(RNA)合成在6小时首次检测到,并与必需蛋白质的形成同时增加。到18小时时出现病毒特异性RNA和蛋白质的最高水平,此时仅检测到5%的子代病毒。必需RNA和蛋白质合成比感染性病毒的形成至少提前10至12小时。还确定了补体结合(CF)抗原和盐依赖性凝集素(SDA)形成所必需的RNA和蛋白质合成的时间进程。SDA形成所必需的RNA合成在2小时首次检测到,并在6小时达到最大值,而SDA蛋白与感染性必需蛋白同时增加。这表明感染性必需的最后一种蛋白可能是SDA。CF抗原形成所必需的RNA合成在4小时首次检测到,而CF蛋白在5小时增加,比SDA蛋白和感染性必需蛋白提前约3小时。放线菌酮对蛋白质合成抑制作用的逆转表明,感染性病毒的形成需要早期蛋白质合成(1至3小时)。数据表明,麻疹病毒观察到的相对较长的隐蔽期与较长的成熟期有关,而不是与早期蛋白质、病毒RNA或结构蛋白的晚期形成有关。

相似文献

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Latency of human measles virus in hamster cells.人麻疹病毒在仓鼠细胞中的潜伏期。
J Virol. 1972 Nov;10(5):995-1001. doi: 10.1128/JVI.10.5.995-1001.1972.

本文引用的文献

1
MEASLES VIRUS.麻疹病毒
Arch Gesamte Virusforsch. 1965;16:57-80. doi: 10.1007/BF01253793.
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DELAY IN THE MULTIPLICATION OF INFLUENZA VIRUS.流感病毒增殖的延迟
Virology. 1965 Feb;25:289-302. doi: 10.1016/0042-6822(65)90207-2.
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Use of actinomycin D to unmask RNA synthesis induced by Newcastle disease virus.
Biochem Biophys Res Commun. 1962 Sep 25;9:156-61. doi: 10.1016/0006-291x(62)90106-7.

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