Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Viruses. 2018 Nov 1;10(11):600. doi: 10.3390/v10110600.
RNA viruses replicate with low fidelity due to the error-prone nature of the RNA-dependent RNA polymerase, which generates approximately one mutation per round of genome replication. Due to the large population sizes produced by RNA viruses during replication, this results in a cloud of closely related virus variants during host infection, of which small increases or decreases in replication fidelity have been shown to result in virus attenuation in vivo, but not typically in vitro. Since the discovery of the first RNA virus fidelity mutants during the mid-aughts, the field has exploded with the identification of over 50 virus fidelity mutants distributed amongst 7 RNA virus families. This review summarizes the current RNA virus fidelity mutant literature, with a focus upon the definition of a fidelity mutant as well as methods to confirm any mutational changes associated with the fidelity mutant. Due to the complexity of such a definition, in addition to reports of unstable virus fidelity phenotypes, the future translational utility of these mutants and applications for basic science are examined.
RNA 病毒由于 RNA 依赖的 RNA 聚合酶易错的性质,复制保真度较低,该聚合酶每一轮基因组复制会产生大约一个突变。由于 RNA 病毒在复制过程中会产生大量的种群,这会导致宿主感染过程中出现一群密切相关的病毒变体,其中复制保真度的微小增加或减少已被证明会导致病毒在体内衰减,但通常不会在体外衰减。自从本世纪初发现第一个 RNA 病毒保真度突变体以来,该领域已经发现了超过 50 种 RNA 病毒保真度突变体,分布在 7 种 RNA 病毒家族中。本综述总结了当前的 RNA 病毒保真度突变体文献,重点介绍了保真度突变体的定义以及确认与保真度突变体相关的任何突变变化的方法。由于这种定义的复杂性,以及不稳定的病毒保真度表型的报告,这些突变体的未来转化应用和基础科学的应用都受到了检验。