Abstract

Transmissible gastroenteritis virus (TGEV) is a coronavirus associated with diarrhea and high mortality in piglets. To gain insight into the evolution and adaptation of TGEV, a comprehensive analysis of phylogeny and codon usage bias was performed. The phylogenetic analyses of maximum likelihood and Bayesian inference displayed two distinct genotypes: genotypes I and II, and genotype I was classified into subtypes Ia and Ib. The compositional properties revealed that the coding sequence contained a higher number of A/U nucleotides than G/C nucleotides, and that the synonymous codon third position was A/U-enriched. The principal component analysis based on the values of relative synonymous codon usage (RSCU) showed the genotype-specific codon usage patterns. The effective number of codons (ENC) indicated moderate codon usage bias in the TGEV genome. Dinucleotide analysis showed that CpA and UpG were over-represented and CpG was under-represented in the coding sequence of the TGEV genome. The analyses of Parity Rule 2 plot, ENC-plot, and neutrality plot displayed that natural selection was the dominant evolutionary driving force in shaping codon usage preference in genotypes Ia and II. In addition, natural selection played a major role, while mutation pressure had a minor role in driving the codon usage bias in genotype Ib. The codon adaptation index (CAI), relative codon deoptimization index (RCDI), and similarity index (SiD) analyses suggested that genotype I might be more adaptive to pigs than genotype II. Current findings contribute to understanding the evolution and adaptation of TGEV.

Highlights

  • Transmissible gastroenteritis virus (TGEV) is a porcine enteropathogenic coronavirus, which causes watery diarrhea, severe villous atrophy, and high mortality in piglets

  • A total of 32 complete genomes of TGEV strains were downloaded from National Center for Biotechnology Information (NCBI) in July 2020 (Table S1)

  • TGEV AHHF strain and TGEV/USA/Illinois139/2006 strain were identified as potential recombinants (Figure S1)

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Summary

Introduction

Transmissible gastroenteritis virus (TGEV) is a porcine enteropathogenic coronavirus, which causes watery diarrhea, severe villous atrophy, and high mortality in piglets. In adult pigs and piglets greater than 3 weeks of age, the response to TGEV is milder, causing loss of appetite and diarrhea for 1 to 2 days [2]. ORF1a and ORF1b together encode viral replicase [13] and ORF3a is related to the TGEV virulence [2]. The evolution of codon usage bias is very complex. The relationships of codon usage between viruses and their hosts affect gene expression [23], viral protein translation [24], viral virulence [25], and evasion from host’s immune system [26]. A holistic analysis of codon usage bias is essential to understanding of viral evolution, host adaptability, and genome characteristics. The information obtained in the study can provide an insight into the TGEV evolution, and can be used to rationally design the attenuated TGEV strain that may have vaccine potential

Distinct Genotypes
Genotype-Specific Codon Usage Pattern
Dinucleotides Influence the Codon Usage Pattern of TGEV
Sequence Data
Recombination Detection and Phylogenetic Analysis
Compositional Properties and Principal Parameters Analysis
Relative Synonymous Codon Usage
Principal Component Analysis
Relative Dinucleotide Abundance Analysis
Effective Number of Codons Analysis
ENC-Plot Analysis
Parity Rule 2 Analysis
4.10. Neutrality Analysis
4.11. Codon Adaptation Index Analysis
4.12. Relative Codon Deoptimization Index Analysis
4.13. Similarity Index Analysis
4.14. Statistical Analysis
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