Initial Phase of Replication of Plus-Stranded RNA Viruses

V. Zhdanov
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引用次数: 3

Abstract

The author presents theoretical mean-field analysis of the initial phase of the kinetics of intracellular replication of plus-stranded RNA viruses, which are abundant and include, e.g., the hepatitis C virus (HCV). The treatment is based on the conventional concept that the replication process of such viruses takes place at the membrane complexes formed with participation of viral proteins, e.g., NS5A in the HCV case. The key novel prediction supported by Monte Carlo calculations is that this scheme may be insufficient in order to describe the very initial phase of the process, because the initial intracellular viral RNA and protein populations may in this case go extinct rather than overcome the kinetic barrier for transition to the full-scale infection of a host cell. Practically, this means that in such situations, the conventional replication scenario should be complemented by another pathway, e.g., by replication outside the membrane without viral proteins, which operates in the very beginning.
正链RNA病毒复制的初始阶段
作者提出了理论平均场分析的动力学的初始阶段的正链RNA病毒的细胞内复制,这是丰富的,包括,例如,丙型肝炎病毒(HCV)。治疗是基于传统的概念,即这类病毒的复制过程发生在病毒蛋白参与形成的膜复合体上,例如在HCV病例中,NS5A。蒙特卡罗计算支持的关键新预测是,该方案可能不足以描述该过程的最初阶段,因为在这种情况下,初始细胞内病毒RNA和蛋白质种群可能会灭绝,而不是克服过渡到宿主细胞全面感染的动力学屏障。实际上,这意味着在这种情况下,传统的复制场景应该由另一种途径补充,例如,在膜外复制,不需要病毒蛋白,这在一开始就起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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