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通过超级感染ME病毒对脊髓灰质炎病毒诱导的膜复合物进行修饰和利用。

Modification and exploitation of a poliovirus-induced membrane complex by superinfecting ME virus.

作者信息

Zeichhardt H, Habermehl K O, Diefenthal W

出版信息

J Gen Virol. 1981 Aug;55(Pt 2):265-74. doi: 10.1099/0022-1317-55-2-265.

Abstract

The replication of Mouse Elberfeld (ME) virus was accelerated when HEp-2 cells were mixedly infected with poliovirus in the presence of guanidine. The latent period of the replication of ME virus was shortened by 3 h when cells were preinfected for at least 2 h with poliovirus and inhibited by guanidine. Simultaneous infection with poliovirus and ME virus resulted in a shortening by 1 h of the latent period of ME virus replication. The accelerated replication of ME virus was shown to be due to modification and exploitation of a membrane complex induced by poliovirus in the presence of guanidine; on superinfection ME virus successively modified this poliovirus-induced complex of 470S ("light' complex) into a "heavy' complex of 700S specific for ME virus.

摘要

当在胍存在的情况下,HEp - 2细胞被脊髓灰质炎病毒混合感染时,小鼠埃尔伯费尔德(ME)病毒的复制加速。当细胞用脊髓灰质炎病毒预感染至少2小时并被胍抑制时,ME病毒复制的潜伏期缩短了3小时。脊髓灰质炎病毒和ME病毒同时感染导致ME病毒复制潜伏期缩短1小时。ME病毒复制的加速被证明是由于在胍存在的情况下脊髓灰质炎病毒诱导的膜复合物的修饰和利用;在重叠感染时,ME病毒将这种脊髓灰质炎病毒诱导的470S(“轻”复合物)复合物依次修饰成ME病毒特异性的700S“重”复合物。

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