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Development and Validation of a Quantitative PCR Method for Equid Herpesvirus-2 Diagnostics in Respiratory Fluids
Published on: March 17, 2016
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.
Abstract:
Equine arteritis virus (EAV) causes a persistent infection of the reproductive tract of carrier stallions. The authors determined the complete genome sequences of viruses (CW96 and CW01) that were present 5 years apart in the semen of a carrier stallion (CW). The CW96 and CW01 viruses respectively had only 85.6 % and 85.7 % nucleotide identity to the published sequence of EAV (EAV030). The CW96 and CW01 viruses had two 1 nt insertions and a single 1 nt deletion in the leader sequence, and a 3 nt coding insertion in ORF1a; thus their genomes included 12 708 nt as compared to the 12 704 nt in EAV030. Variation between viruses present in the semen of stallion CW and EAV030 was especially marked in the replicase gene (ORF1a and 1b), and the greatest variation occurred in the portion of ORF1a encoding the nsp2 protein. The ORFs 3 and 5, which respectively encode the GP3 and GP5 envelope proteins, showed greatest variation amongst ORFs encoding structural EAV proteins. Comparative sequence analyses of CW96 and CW01 indicated that ORFs 1a, 1b and 7 were highly conserved during persistent infection, whereas there was substantial variation in ORFs 3 and 5. Although the variation that occurs in ORF5 results in the emergence of novel phenotypic viral variants as determined by neutralization assay, all variants were neutralized by high-titre polyclonal equine antisera, suggesting that immune evasion is unlikely to be responsible for the establishment of persistent EAV infection of carrier stallions. Northern blot analyses of RNA extracted from cell culture propagated viruses isolated from 10 different persistently infected stallions failed to demonstrate any large genomic deletions, suggesting that defective interfering particles are also unlikely to be important in either the maintenance or clearance of persistent EAV infection of the reproductive tract of carrier stallions.

