Neu Ursula, Stehle Thilo, Atwood Walter J
Interfakultäres Institut für Biochemie, Universität Tübingen, Germany.
Virology. 2009 Feb 20;384(2):389-99. doi: 10.1016/j.virol.2008.12.021. Epub 2009 Jan 21.
This review summarizes the field's major findings related to the characterization of polyomavirus structures and to the characterization of virus receptors and mechanisms of host cell invasion. The four members of the family that have received the most attention in this regard are the mouse polyomavirus (mPyV), the monkey polyomavirus SV40, and the two human polyomaviruses, JCV and BKV. The structures of both the mPyV and SV40 alone and in complex with receptor fragments have been solved to high resolution. The majority of polyomaviruses recognize terminal sialic acid in either an alpha2,3 linkage or an alpha2,6 linkage to the underlying galactose. Studies on virus structure, receptor utilization and mechanisms of entry have led to new insights into how these viruses interact in an active way with cells to ensure the nuclear delivery and expression of their genomes. Critical work on virus entry has led to the discovery of a pH neutral endocytic compartment that accepts cargo from caveolae and to novel roles for endoplasmic reticulum (ER) associated factors in virus uncoating and penetration of ER membranes. This review will summarize the major findings and compare and contrast the mechanisms used by these viruses to infect cells.
本综述总结了该领域与多瘤病毒结构特征、病毒受体特征以及宿主细胞入侵机制相关的主要研究成果。在这方面受到最多关注的该病毒科的四个成员是小鼠多瘤病毒(mPyV)、猴多瘤病毒SV40以及两种人类多瘤病毒JCV和BKV。mPyV和SV40单独的结构以及与受体片段复合物的结构均已得到高分辨率解析。大多数多瘤病毒识别与潜在半乳糖以α2,3连接或α2,6连接的末端唾液酸。对病毒结构、受体利用和进入机制的研究为这些病毒如何与细胞进行主动相互作用以确保其基因组的核内递送和表达带来了新的见解。关于病毒进入的关键研究导致发现了一个pH中性的内吞区室,它从小窝接受货物,并发现了内质网(ER)相关因子在病毒脱壳和内质网膜穿透中的新作用。本综述将总结主要研究成果,并比较和对比这些病毒用于感染细胞的机制。