Viral adaption of staphylococcal phage: A genome-based analysis of the selective preference based on codon usage Bias

被引:12
作者
Ge, Zhiyi [1 ]
Li, Xuerui [1 ]
Cao, Xiaoan [1 ]
Wang, Rui [4 ]
Hu, Wen [2 ]
Gen, Ling [1 ]
Han, Shengyi [1 ,3 ]
Shang, Youjun [1 ]
Liu, Yongsheng [1 ]
Zhou, Jian-hua [1 ]
机构
[1] Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Lanzhou 730046, Gansu, Peoples R China
[2] Gansu Police Vocat Coll, Lanzhou 730046, Gansu, Peoples R China
[3] Gansu Agr Univ, Coll Vet Med, Lanzhou 730070, Gansu, Peoples R China
[4] Univ Southern Calif, Viterbi Sch Engn, Los Angeles, CA 90089 USA
基金
国家重点研发计划;
关键词
Staphylococcal phage; Synonymous codon usage; Host limitation; Phagic phenotype; Genome evolution; TRANSFER-RNA ABUNDANCE; SYNONYMOUS CODON; ESCHERICHIA-COLI; ADAPTATION; GENES; INFECTIONS; AUREUS; EFFICIENCY; EVOLUTION; VIRULENT;
D O I
10.1016/j.ygeno.2020.08.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Given the high therapeutic value of the staphylococcal phage, the genome co-evolution of the phage and the host has gained great attention. Though the genome-wide AT richness in staphylococcal phages has been well-studied with nucleotide usage bias, here we proved that host factor, lifestyle and taxonomy are also important factors in understanding the phage nucleotide usages bias using information entropy formula. Such correlation is especially prominent when it comes to the synonymous codon usages of staphylococcal phages, despite the overall scattered codon usage pattern represented by principal component analysis. This strong relationship is explained by nucleotide skew which testified that the usage biases of nucleotide at different codon positions are acting on synonymous codons. Therefore, our study reveals a hidden relationship of genome evolution with host limitation and phagic phenotype, providing new insight into phage genome evolution at genetic level.
引用
收藏
页码:4657 / 4665
页数:9
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