Genetic characterization of equine arteritis virus during persistent infection of stallions

Udeni B R Balasuriya1, Jodi F Hedges1, Victoria L Smalley1

  • 1Bernard and Gloria Salick Equine Viral Disease Laboratory, Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.

Insights

Equine arteritis virus (EAV) persists in stallions. Viral genome sequencing revealed significant variation in structural genes, but conserved replicase genes, suggesting immune evasion isn't key to persistent EAV infection.

Area of Science:

  • Virology
  • Equine Infectious Diseases
  • Molecular Biology

Background:

  • Equine arteritis virus (EAV) establishes persistent infections in the reproductive tracts of carrier stallions.
  • Understanding the genetic basis of EAV persistence is crucial for managing the disease.

Purpose of the Study:

  • To determine the complete genome sequences of EAV strains isolated from a carrier stallion over a five-year period.
  • To analyze the genetic variation within EAV during persistent infection and assess its potential role in immune evasion.

Main Methods:

  • Whole-genome sequencing of EAV isolates CW96 and CW01 from a carrier stallion.
  • Comparative sequence analysis of EAV genomes, focusing on replicase and structural genes.
  • Neutralization assays using polyclonal equine antisera.
  • Northern blot analysis of viral RNA from persistently infected stallions.

Main Results:

  • EAV isolates CW96 and CW01 showed only 85.6-85.7% nucleotide identity to a reference EAV strain, with variations in leader and ORF1a sequences.
  • Significant genetic variation was observed in structural protein genes (ORF3 and ORF5), leading to novel viral variants.
  • Replicase genes (ORF1a, ORF1b) and ORF7 were highly conserved.
  • All EAV variants were neutralized by polyclonal antisera, and no large genomic deletions or defective interfering particles were detected.

Conclusions:

  • Genetic variation in EAV structural genes occurs during persistent infection but does not appear to facilitate immune evasion.
  • Conserved replicase genes suggest they are critical for viral replication and maintenance.
  • Defective interfering particles are unlikely to play a role in the persistence or clearance of EAV in carrier stallions.