Slow Fitness Recovery in a Codon-Modified Viral Genome

被引:42
作者
Bull, J. J. [1 ,2 ,3 ]
Molineux, I. J. [1 ,4 ]
Wilke, C. O. [1 ,2 ,3 ]
机构
[1] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[2] Univ Texas Austin, Ctr Computat Biol & Bioinformat, Austin, TX 78712 USA
[3] Univ Texas Austin, Sect Integrat Biol, Austin, TX 78712 USA
[4] Univ Texas Austin, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
codon modification; vaccine design; fitness suppression; genome engineering; RNA SECONDARY-STRUCTURE; EVOLUTION; DNA; DEOPTIMIZATION; ATTENUATION; STABILITY; SEQUENCE; REGION;
D O I
10.1093/molbev/mss119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extensive synonymous codon modification of viral genomes appears to be an effective way of attenuating strains for use as live vaccines. An assumption of this method is that codon changes have individually small effects, such that codon-attenuated viruses will be slow to evolve back to high fitness (and thus to high virulence). The major capsid gene of the bacterial virus T7 was modified to have varying levels of suboptimal synonymous codons in different constructs, and fitnesses declined linearly with the number of changes. Adaptation of the most extreme design, with 182 codon changes, resulted in a slow fitness recovery by standards of previous experimental evolution with this virus, although fitness effects of substitutions were higher than expected from the average effect of an engineered codon modification. Molecular evolution during recovery was modest, and changes evolved both within the modified gene and outside it. Some changes within the modified gene evolved in parallel across replicates, but with no obvious explanation. Overall, the study supports the premise that codon-modified viruses recover fitness slowly, although the evolution is substantially more rapid than expected from the design principle.
引用
收藏
页码:2997 / 3004
页数:8
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