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柯萨奇病毒与准种理论:肠道病毒的进化

Coxsackieviruses and quasispecies theory: evolution of enteroviruses.

作者信息

Domingo E, Martin V, Perales C, Escarmis C

机构信息

Centro de Biología Molecular "Severo Ochoa"(CSIC-UAM), Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

出版信息

Curr Top Microbiol Immunol. 2008;323:3-32. doi: 10.1007/978-3-540-75546-3_1.

Abstract

Enterovirus populations display quasispecies dynamics, characterized by high rates of mutation and recombination, followed by competition, selection, and random drift acting on heterogeneous mutant spectra. Direct experimental evidence indicates that high mutation rates and complex mutant spectra can serve for the adaptation of enteroviruses to complex environments. Studies with the RNA-dependent RNA polymerase of picornaviruses suggest that multiple enzyme sites may influence the template-copying fidelity (incorporation of incorrect vs correct nucleotide) during RNA replication. Mutation and recombination are an unavoidable consequence of the molecular mechanisms inherent to the process of viral genome replication and underlie the diversification of enterovirus genomes as they multiply in human and animal hosts. The diversity of disease manifestations associated with closely related enteroviruses is probably attributable to profound biological effects of some mutations that, because of their limited number, do not necessarily affect the phylogenetic position of the virus. The combination of highly dynamic mutant spectra with unpredictable alterations of biological behavior by minimal genetic change defies classical classification schemes. The result is the need to update the grouping of enteroviruses quite frequently into genetic and serological types and subtypes. The tolerance of enterovirus genomes to remain replication-competent despite multiple mutation and recombination events encourages the engineering of live-attenuated vaccines. Also, the application of quasispecies theory to an understanding of the limits of viral genomes to accept mutations, together with an increasingly deeper understanding of the mechanisms of mutagenesis by nucleoside analogs, has paved the way for the application of lethal mutagenesis as a new antiviral strategy.

摘要

肠道病毒群体呈现准种动态,其特征为高突变率和重组率,随后是作用于异质突变谱的竞争、选择和随机漂变。直接实验证据表明,高突变率和复杂的突变谱有助于肠道病毒适应复杂环境。对小RNA病毒的RNA依赖性RNA聚合酶的研究表明,多个酶位点可能会影响RNA复制过程中的模板复制保真度(掺入错误与正确核苷酸)。突变和重组是病毒基因组复制过程中固有分子机制不可避免的结果,也是肠道病毒基因组在人类和动物宿主中增殖时多样化的基础。与密切相关的肠道病毒相关的疾病表现多样性可能归因于某些突变的深远生物学效应,由于这些突变数量有限,不一定会影响病毒的系统发育位置。高度动态的突变谱与最小遗传变化导致的生物行为不可预测改变相结合,使得经典分类方案难以适用。结果是需要相当频繁地将肠道病毒更新为遗传和血清学类型及亚型。尽管发生多次突变和重组事件,肠道病毒基因组仍能保持复制能力,这一特性促进了减毒活疫苗的研发。此外,准种理论在理解病毒基因组接受突变的限度方面的应用,以及对核苷类似物诱变机制的日益深入了解,为将致死诱变作为一种新的抗病毒策略的应用铺平了道路。

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