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口蹄疫病毒的进化:探索病毒灭绝的途径。

Foot-and-mouth disease virus evolution: exploring pathways towards virus extinction.

作者信息

Domingo E, Pariente N, Airaksinen A, Gonzaĺez-Lopez C, Sierra S, Herrera M, Grande-Pérez A, Lowenstein P R, Manrubia S C, Lázaro E, Escarmís 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. 2005;288:149-73. doi: 10.1007/3-540-27109-0_7.

Abstract

Foot-and-mouth disease virus (FMDV) is genetically and phenotypically variable. As a typical RNA virus, FMDV follows a quasispecies dynamics, with the many biological implications of such a dynamics. Mutant spectra provide a reservoir of FMDV variants, and minority subpopulations may become dominant in response to environmental demands or as a result of statistical fluctuations in population size. Accumulation of mutations in the FMDV genome occurs upon subjecting viral populations to repeated bottleneck events and upon viral replication in the presence of mutagenic base or nucleoside analogs. During serial bottleneck passages, FMDV survive during extended rounds of replication maintaining low average relative fitness, despite linear accumulation of mutations in the consensus genomic sequence. The critical event is the occurrence of a low frequency of compensatory mutations. In contrast, upon replication in the presence of mutagens, the complexity of mutant spectra increases, apparently no compensatory mutations can express their fitness-enhancing potential, and the virus can cross an error threshold for maintenance of genetic information, resulting in virus extinction. Low relative fitness and low viral load favor FMDV extinction in cell culture. The comparison of the molecular basis of resistance to extinction upon bottleneck passage and extinction by enhanced mutagenesis is providing new insights in the understanding of quasispecies dynamics. Such a comparison is contributing to the development of new antiviral strategies based on the transition of viral replication into error catastrophe.

摘要

口蹄疫病毒(FMDV)在基因和表型上具有变异性。作为一种典型的RNA病毒,FMDV遵循准种动态变化,这种动态变化具有许多生物学意义。突变谱为FMDV变体提供了一个库,少数亚群可能会因环境需求或种群大小的统计波动而成为优势群体。FMDV基因组中的突变积累发生在病毒群体经历反复瓶颈事件时,以及在存在诱变碱基或核苷类似物的情况下病毒复制时。在连续瓶颈传代过程中,尽管在共有基因组序列中突变呈线性积累,但FMDV在延长的复制轮次中存活下来,保持较低的平均相对适应性。关键事件是发生低频补偿性突变。相比之下,在诱变剂存在下复制时,突变谱的复杂性增加,显然没有补偿性突变能够发挥其适应性增强潜力,并且病毒可能越过维持遗传信息的错误阈值,导致病毒灭绝。低相对适应性和低病毒载量有利于FMDV在细胞培养中灭绝。对瓶颈传代时抗灭绝的分子基础与增强诱变导致灭绝的分子基础进行比较,为理解准种动态变化提供了新的见解。这种比较有助于基于病毒复制向错误灾难转变开发新的抗病毒策略。

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