Abstract

Porcine epidemic diarrhea virus (PEDV), which classified in the genus Alphacoronavirus, family Coronaviridae, is one of the most important pathogens that cause heavy economic losses in pig industry. Although intensive mutation and recombination analysis of PEDV strains were provided, systematic genome analysis were needed to elucidate the evolution mechanism and codon usage adaptation profiles of the pathogen. Here, a comprehensive investigation was carried out to reveal the systematic evolutionary processes of synonymous codon usage and host-adapted evolution phenotype of PEDV genome. We found a low codon usage bias (CUB) in PEDV genome and that nucleotide compositions, natural selection, mutation pressure and geographical diversity shapes the codon usage patterns of PEDV, with natural selection dominated the overall codon usage bias in PEDV than the others. By using the relative codon deoptimization index (RCDI) and similarity index (SiD) analysis, we observed that genotype II PEDV strains showed the highest level of adaptation phenotype to Sus scrofa than another divergent clade. To the best of our knowledge, this is the first comprehensive report elaborating the codon usage and host adaptation of PEDV. The findings offer an insight into our understanding of factors involved in PEDV evolution, adaptation and fitness toward their hosts.

Highlights

  • Porcine epidemic diarrhea virus (PEDV) is a pathogen causing vomiting, diarrhea, dehydration and high lethality in piglets

  • In order to determine the relationship of PEDV strains selected in this study, we first carried out phylogenetic analysis of the complete coding sequence of PEDV by using neighbor-Joining (NJ) and maximum-likelihood (ML) algorithms method

  • Nucleotide content of 56 complete coding sequences was calculated to evaluate the potential impact of compositional constraints on codon usage pattern of PEDV

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Summary

Introduction

Porcine epidemic diarrhea virus (PEDV) is a pathogen causing vomiting, diarrhea, dehydration and high lethality in piglets. This pathogen was first identified in Belgium in 1978 (Pensaert and de Bouck, 1978), and since it has been identified in other countries of the world, including China, Japan, South Korea and Thailand in Asia. The only accessory protein ORF3 has ion channel activity (Wang et al, 2012), and was found beneficial to virus proliferation (Wang et al, 2012; Ye et al, 2015; Si et al, 2020). Phylogenetic analysis showed that PEDV could be divided into two genotypes (G1 and G2) and five subgenotypes (G1a, G1b, G2a, G2b, and G2c) based on complete sequence of S gene (Fan et al, 2017; Hsueh et al, 2020; Wang H. et al, 2020; Wang X.W. et al, 2020)

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