Dâmaso C R, Moussatché N
Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Brazil.
Arch Virol. 1992;123(3-4):295-308. doi: 10.1007/BF01317265.
Human Hep-2 cells were submitted to hypertonic shock (210 mM NaCl) to block host protein synthesis before infection with vaccinia virus. With the start of infection, the medium isotonicity (116 mM NaCl) was restored, and the effect of viral infection on the recovery of host polyribosomes and protein synthesis was studied. Although host translation blockage was released together with infection, vaccinia virus did not affect immediately host protein synthesis. During the first hour of recovery, infected cells could perfectly rebuild the polyribosome profile and recuperate the rate of protein synthesis. Also, during recovery, formation of the initiation complex for protein synthesis was not affected by viral infection. In this period, viral mRNA and proteins were detected by slot blot and SDS-polyacrylamide gel electrophoresis. The inhibitory effect of vaccinia virus on host translation was observed after the second hour of infection. These findings suggest that vaccinia virus-mediated shutoff occurs in a later period during infection, in parallel with viral mRNA accumulation in the polyribosomes and after the on-set of viral DNA replication.
在用人痘病毒感染之前,将人肝癌细胞系Hep-2细胞置于高渗休克环境(210 mM NaCl)中,以阻断宿主蛋白合成。随着感染开始,恢复培养基等渗状态(116 mM NaCl),并研究病毒感染对宿主多核糖体恢复和蛋白合成的影响。尽管宿主翻译阻断随着感染一起解除,但痘苗病毒并未立即影响宿主蛋白合成。在恢复的第一个小时内,受感染细胞能够完美重建多核糖体图谱并恢复蛋白合成速率。此外,在恢复过程中,蛋白合成起始复合物的形成不受病毒感染的影响。在此期间,通过狭缝印迹法和SDS-聚丙烯酰胺凝胶电泳检测到病毒mRNA和蛋白。在感染后第二个小时观察到痘苗病毒对宿主翻译的抑制作用。这些发现表明,痘苗病毒介导的翻译关闭发生在感染后期,与病毒mRNA在多核糖体中的积累以及病毒DNA复制开始后同时发生。