| Literature DB >> 28602802 |
Weiheng Su1, Xue Li2, Meili Chen3, Wenwen Dai4, Shiyang Sun4, Shuai Wang4, Xin Sheng2, Shixiang Sun2, Chen Gao2, Ali Hou1, Yan Zhou1, Bo Sun1, Feng Gao1, Jingfa Xiao2, Zhewen Zhang5, Chunlai Jiang6.
Abstract
Enterovirus 71 (EV71) and coxsackievirus A16 (CVA16) have been considered major pathogens of hand, foot and mouth disease (HFMD) throughout the world for decades. In recent years, coxsackievirus A6 (CVA6) and coxsackievirus A10 (CVA10) have raised attention as two other serious pathogens of HFMD. The present study focused on the synonymous codon usage of four viruses isolated from 2008 to 2015, with particular attention on P1 (encoding capsid proteins) and P2-P3 regions (both encoding non-structural proteins) in the genomic RNA. Relative synonymous codon usage, effective number of codons, neutrality and correspondence were analyzed. The results indicated that these viruses prefer A/T at the third position in codons rather than G/C. The most frequent codons of 4 essential and 2 semi-essential amino acids, as well as a key amino acid of metabolic junctions (Glu) used in the four viruses are also the most frequently used in humans. Effective number of codons (ENC) values indicated weak codon usage bias in all the viruses. Relatively, the force of mutation pressure in the P1 region was found to be stronger than that in the P2-P3 region, and this force in the P1 region of CVA6 and EV71 was stronger than that of CVA10 and A16. The neutrality analysis results implied that mutation pressure plays a minor role in shaping codon bias of these viruses. Correspondence analysis indicated that the codon usage of EV71 strains varied much more than that of other viruses. In conclusion, the present study provides novel and comparative insight into the evolution of HFMD pathogens at the codon level.Entities:
Keywords: Coxsackievirus A10; Coxsackievirus A16; Coxsackievirus A6; Enterovirus 71; Synonymous codon usage
Mesh:
Substances:
Year: 2017 PMID: 28602802 DOI: 10.1016/j.meegid.2017.06.004
Source DB: PubMed Journal: Infect Genet Evol ISSN: 1567-1348 Impact factor: 3.342