Martinet-Edelist C, Deutsch V, Tuffereau C, Genty N
Virology. 1984 May;135(1):266-78. doi: 10.1016/0042-6822(84)90136-3.
Vesicular stomatitis virus (VSV) subviral particles (nucleocapsids and G-depleted particles) were used to infect various cells (chicken embryo, HeLa, and BHK21 cells). These particles bind to and penetrate into host cells; the association of G-depleted particles to cells was even better than that of normal virions. The parental genomes of subviral particles and virions were degraded at the same rate in the infected cells. Nevertheless, these subviral particles had a very low infectivity, synthesized very little viral macromolecules, and had very little, if any, effect on the various host cells used. Furthermore , subviral particles could be rescued in chicken embryo cells by uv-irradiated VSV virions, demonstrating that subviral particles actually penetrated into cells, and that their arrested cycle could be unblocked up to a certain point. On the other hand, subviral particles were not rescued in HeLa cells, suggesting a dependence on the host cell system.
水泡性口炎病毒(VSV)亚病毒颗粒(核衣壳和G缺失颗粒)被用于感染各种细胞(鸡胚细胞、HeLa细胞和BHK21细胞)。这些颗粒能结合并穿透宿主细胞;G缺失颗粒与细胞的结合甚至比正常病毒粒子更好。在感染的细胞中,亚病毒颗粒和亲本病毒粒子的基因组以相同的速率降解。然而,这些亚病毒颗粒的感染性非常低,合成的病毒大分子极少,并且对所使用的各种宿主细胞几乎没有影响。此外,紫外线照射的VSV病毒粒子可在鸡胚细胞中拯救亚病毒颗粒,这表明亚病毒颗粒实际上能穿透细胞,并且它们停滞的周期在一定程度上可以被解除阻断。另一方面,亚病毒颗粒在HeLa细胞中无法被拯救,这表明其对宿主细胞系统存在依赖性。