Analyze Diet
The Journal of general virology2025; 106(12); 002181; doi: 10.1099/jgv.0.002181

Genetic characterization of equine arteritis virus associated with outbreaks in the UK, 2019.

Abstract: Equine arteritis virus (EAV) is the causative agent of equine viral arteritis, a notifiable respiratory and reproductive disease of equids that causes significant losses to the equine industry. This study presents a comprehensive analysis of two EAV outbreaks in the UK in 2019, combining virus isolation, sequencing and phylogenetic analysis to provide a holistic understanding of EAV dynamics in these outbreaks. Genetic characterization revealed that all outbreak strains were similar to viruses detected in the UK and Europe from 2004 to 2011, belonging to phylogroup D and clustering in two groups as expected based on epidemiological profiling. Bayesian phylogenetic analysis indicated the direction of transmission. The 2019 EAV strains showed maximum variability in glycoprotein (GP) 3, followed by GP2, non-structural protein 2, GP4 and GP5, with one strain displaying a unique truncation in GP4 at position 149, a feature not previously identified in arteriviruses. Polymorphisms in the CXCL16 gene have been implicated in differential susceptibility to the establishment of long-term carrier states of EAV in stallions. Genotypic analysis of the CXCL16 gene revealed that one horse possessed the homozygous genotype associated with resistance to persistent infection. In contrast, the remaining four horses exhibited the heterozygous genotype, which has been linked to an increased risk of developing a long-term carrier state and contributing to ongoing viral transmission. All infected horses exhibited the presence of neutralizing antibodies in their serum. This study underscores the importance of early detection of silent infections to reduce the spread and prevent clinical outbreaks.
Publication Date: 2025-12-03 PubMed ID: 41334982PubMed Central: PMC12674535DOI: 10.1099/jgv.0.002181Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

Genetic analysis of equine arteritis virus (EAV) from 2019 outbreaks in the UK revealed that the strains belonged to a known phylogenetic group linked to European viruses and showed genetic variations particularly in certain viral proteins. The study also examined host genetic factors influencing susceptibility to persistent infection, highlighting the need for early detection to control disease spread.

Background and Importance

  • Equine arteritis virus (EAV) causes equine viral arteritis, a disease affecting respiratory and reproductive systems in horses and related animals (equids).
  • The disease is notifiable, meaning outbreaks must be reported due to its economic impact on the equine industry caused by illness and loss of animals.
  • This study addresses two separate EAV outbreaks in the UK during 2019.

Research Methods

  • Virus Isolation: EAV was isolated from infected horses during the outbreaks to obtain live virus samples for study.
  • Sequencing: Genetic sequencing of the viral RNA was performed to determine the nucleotide and protein sequences of the virus strains involved.
  • Phylogenetic Analysis: The genetic sequences were compared both with each other and with known EAV strains from previous years (2004–2011) across the UK and Europe.
  • Bayesian Phylogenetic Analysis: A statistical method used to infer the evolutionary relationships and likely direction of virus transmission within and between outbreaks.
  • Host Genotype Characterization: Analysis of the CXCL16 gene polymorphisms in the horses was performed; this gene influences susceptibility to persistent viral infection in stallions.
  • Serological Testing: Detection of virus-neutralizing antibodies in horse serum to assess immune response and infection status.

Key Findings – Viral Genetics and Phylogeny

  • All 2019 outbreak viruses belonged to phylogroup D, consistent with strains previously detected in the UK and Europe between 2004 and 2011.
  • Phylogenetic trees clustered the outbreak viruses into two groups that matched epidemiological data, supporting transmission hypotheses.
  • Genetic variability was greatest in the viral glycoproteins, specifically GP3, then GP2, followed by non-structural protein 2, GP4, and GP5.
  • One viral strain exhibited a unique truncation (early stop) in glycoprotein GP4 at amino acid position 149, an unprecedented feature in arteriviruses, possibly affecting virus biology or immune evasion.
  • These findings reflect viral evolution and may have implications for virulence, transmission, and vaccine design.

Key Findings – Host Genetics and Immune Response

  • The CXCL16 gene polymorphisms analyzed showed that one of the horses carried a homozygous genotype linked to resistance against establishment of persistent (long-term carrier) infection.
  • Four other horses had heterozygous genotypes associated with increased risk of becoming long-term carriers.
  • Persistent carriers in stallions are important epidemiologically as they can shed virus over extended periods, perpetuating outbreaks.
  • All infected horses tested positive for neutralising antibodies, indicating exposure and immune activation.

Implications and Conclusions

  • The study emphasizes the importance of genetic monitoring of both virus and host to understand EAV epidemiology and risk factors.
  • Early detection of infected animals, including those with subclinical or silent infections, is crucial for controlling viral spread.
  • Knowledge of viral genetic diversity and host susceptibility genes can guide targeted interventions to prevent clinical outbreaks and limit economic impact.
  • The discovery of novel genetic features like the GP4 truncation may inform future research into viral pathogenicity and vaccine improvement.

Cite This Article

APA
Bhat S, Karunakaran S, Frossard JP, Choudhury B, Steinbach F. (2025). Genetic characterization of equine arteritis virus associated with outbreaks in the UK, 2019. J Gen Virol, 106(12), 002181. https://doi.org/10.1099/jgv.0.002181

Publication

ISSN: 1465-2099
NlmUniqueID: 0077340
Country: England
Language: English
Volume: 106
Issue: 12
PII: 002181

Researcher Affiliations

Bhat, Sushant
  • WOAH Reference Laboratory for EVA, Virology Department, Animal and Plant Health Agency, Weybridge, KT15 3NB, UK.
Karunakaran, Siva
  • WOAH Reference Laboratory for EVA, Virology Department, Animal and Plant Health Agency, Weybridge, KT15 3NB, UK.
Frossard, Jean-Pierre
  • WOAH Reference Laboratory for EVA, Virology Department, Animal and Plant Health Agency, Weybridge, KT15 3NB, UK.
Choudhury, Bhudipa
  • WOAH Reference Laboratory for EVA, Virology Department, Animal and Plant Health Agency, Weybridge, KT15 3NB, UK.
Steinbach, Falko
  • WOAH Reference Laboratory for EVA, Virology Department, Animal and Plant Health Agency, Weybridge, KT15 3NB, UK.

MeSH Terms

  • Horses
  • Animals
  • Equartevirus / genetics
  • Equartevirus / classification
  • Equartevirus / isolation & purification
  • Horse Diseases / virology
  • Horse Diseases / epidemiology
  • Disease Outbreaks / veterinary
  • Arterivirus Infections / veterinary
  • Arterivirus Infections / epidemiology
  • Arterivirus Infections / virology
  • United Kingdom / epidemiology
  • Phylogeny
  • Genotype
  • Antibodies, Viral / blood

Conflict of Interest Statement

The authors declare that there are no conflicts of interest.

References

This article includes 62 references
  1. OIE OIE terrestrial manual, Chapter 3.5.10. - Equine viral arteritis (infection with equine arteritis virus) 2018. [5-June-2023]. https://www.woah.org/fileadmin/Home/eng/Health_standards/tahm/3.05.10_EVA.pdf accessed.
  2. ICTV Family: Arteriviridae Chapter Version: ICTV Ninth Report; 2009 Taxonomy Release. [12-January-2024];2011 https://ictv.global/report_9th/RNApos/Nidovirales/Arteriviridae accessed.
  3. Snijder EJ, Kikkert M, Fang Y. Arterivirus molecular biology and pathogenesis.. J Gen Virol 2013;94:2141–2163.
    doi: 10.1099/vir.0.056341-0pubmed: 23939974google scholar: lookup
  4. Timoney PJ, McCollum WH, Roberts AW, Murphy TW. Demonstration of the carrier state in naturally acquired equine arteritis virus infection in the stallion.. Res Vet Sci 1986;41:279–280.
    doi: 10.1016/S0034-5288(18)30616-7pubmed: 3022363google scholar: lookup
  5. Timoney PJ, McCollum WH. Equine viral arteritis.. Vet Clin North Am Equine Pract 1993;9:295–309.
  6. Carossino M, Dini P, Kalbfleisch TS, Loynachan AT, Canisso IF. Equine arteritis virus long-term persistence is orchestrated by CD8+ T lymphocyte transcription factors, inhibitory receptors, and the CXCL16/CXCR6 axis.. PLoS Pathog 2019;15:e1007950.
  7. Balasuriya UBR, Hedges JF, Smalley VL, Navarrette A, McCollum WH. Genetic characterization of equine arteritis virus during persistent infection of stallions.. J Gen Virol 2004;85:379–390.
    doi: 10.1099/vir.0.19545-0pubmed: 14769895google scholar: lookup
  8. Miszczak F, Legrand L, Balasuriya UBR, Ferry-Abitbol B, Zhang J. Emergence of novel equine arteritis virus (EAV) variants during persistent infection in the stallion: origin of the 2007 French EAV outbreak was linked to an EAV strain present in the semen of a persistently infected carrier stallion.. Virology 2012;423:165–174.
    doi: 10.1016/j.virol.2011.11.028pubmed: 22209234google scholar: lookup
  9. Balasuriya UBR, Carossino M, Timoney PJ. Equine viral arteritis: a respiratory and reproductive disease of significant economic importance to the equine industry.. Equ Vet Ed 2018;30:497–512.
    doi: 10.1111/eve.12672google scholar: lookup
  10. HBLB International codes of practice 2023 – equine viral arteritis. 2023. [15-November-2023]. https://codes.hblb.org.uk/index.php/page/30 accessed.
  11. Bryans JT, Crowe ME, Doll ER, McCollum WH. Isolation of a filterable agent causing arteritis of horses and abortion by mares; its differentiation from the equine abortion (influenza) virus.. Cornell Vet 1957;47:3–41.
    pubmed: 13397177
  12. Laabassi F, Amelot G, Laugier C, Zientara S, Nasri AM. Prevalence of equine viral arteritis in Algeria.. Rev Sci Tech 2014;33:967–974.
    doi: 10.20506/rst.33.3.2334pubmed: 25812220google scholar: lookup
  13. Otzdorff C, Beckmann J, Goehring LS. Equine Arteritis Virus (EAV) outbreak in a show stallion population.. Viruses 2021;13:2142.
    doi: 10.3390/v13112142pmc: PMC8621670pubmed: 34834949google scholar: lookup
  14. Gaudaire D, Lazić S, Lupulović D, Petrovic T, Lazić G. Complete genome sequence of an equine arteritis virus strain isolated from a Lipizzaner stallion in 2015 in Serbia.. Microbiol Resour Announc 2019;8:e00250-19.
    doi: 10.1128/MRA.00250-19pmc: PMC6728632pubmed: 31488522google scholar: lookup
  15. Rivas J, Neira V, Mena J, Brito B, Garcia A. Identification of a divergent genotype of equine arteritis virus from South American donkeys.. Transbound Emerg Dis 2017;64:1655–1660.
    doi: 10.1111/tbed.12703pubmed: 28921885google scholar: lookup
  16. Cruz F, Fores P, Mughini-Gras L, Ireland J, Moreno MA. Seroprevalence and factors associated with seropositivity to equine arteritis virus in Spanish Purebred horses in Spain. Equine Vet J 2016;48:573–577.
    doi: 10.1111/evj.12500pubmed: 26278700google scholar: lookup
  17. Lazić S, Lupulović D, Gaudaire D, Petrovic T, Lazić G. Serological evidence of equine arteritis virus infection and phylogenetic analysis of viral isolates in semen of stallions from Serbia. BMC Vet Res 2017;13:316.
    doi: 10.1186/s12917-017-1226-xpmc: PMC5678800pubmed: 29115996google scholar: lookup
  18. Amat JP, Vergne T, Tapprest J, Ferry B, Hans A. Estimating the incidence of equine viral arteritis and the sensitivity of its surveillance in the French breeding stock. Vet Microbiol 2016;192:34–42.
    doi: 10.1016/j.vetmic.2016.06.010pubmed: 27527762google scholar: lookup
  19. Jiménez D, Romero-Zuñiga JJ, Dolz G. Serosurveillance of infectious agents in equines of the Central Valley of Costa Rica. Open Vet J 2014;4:107–112.
    doi: 10.5455/OVJ.2014.v4.i2.p107pmc: PMC4629603pubmed: 26623349google scholar: lookup
  20. Wood JL, Chirnside ED, Mumford JA, Higgins AJ. First recorded outbreak of equine viral arteritis in the United Kingdom. Vet Rec 1995;136:381–385.
    doi: 10.1136/vr.136.15.381pubmed: 7604517google scholar: lookup
  21. The equine viral arteritis order. [15-November-2023];1995 https://www.legislation.gov.uk/uksi/1995/1755/contents/made accessed.
  22. Newton JR, Wood JL, Castillo-Olivares FJ, Mumford JA. Serological surveillance of equine viral arteritis in the United Kingdom since the outbreak in 1993. Vet Rec 1999;145:511–516.
    doi: 10.1136/vr.145.18.511pubmed: 10576624google scholar: lookup
  23. Manser P, Westcott D. Equine viral arteritis in a stallion. Vet Rec 2005;156:28.
    pubmed: 15658568
  24. Crabtree JR, Newton JR. Equine viral arteritis (EVA): a potential trapdoor for the practicing veterinary surgeon in the United Kingdom. Equ Vet Ed 2020;32:378–385.
    doi: 10.1111/eve.12974google scholar: lookup
  25. Steinbach F, Westcott DG, McGowan SL, Grierson SS, Frossard JP. Re-emergence of a genetic outlier strain of equine arteritis virus: impact on phylogeny. Virus Res 2015;202:144–150.
  26. APHA Equine viral arteritis: epidemiology reports. 2019. [15-November-2023]. https://www.gov.uk/government/publications/epidemiology-report-eva-virus-2019 accessed.
  27. Lattimer J, Roberts H, Barnard M, Paterson A, Bell I. Investigating an outbreak of equine viral arteritis at two connected premises. Vet Rec 2020;187:e113.
    doi: 10.1136/vr.m4756pubmed: 33288633google scholar: lookup
  28. APHA Epidemiology report detailing the investigation of EVA virus disclosed on a premises in Shropshire. 2019. [20-November-2023]. https://www.gov.uk/government/publications/epidemiology-report-eva-virus-2019/epidemiology-report-detailing-the-investigation-of-eva-virus-disclosed-on-a-premises-in-shropshire-july-2019 accessed.
  29. Stadejek T, Bj Rklund H, Bascu Ana CR, Ciabatti IM, Scicluna MT. Genetic diversity of equine arteritis virus. J Gen Virol 1999;80 (Pt 3):691–699.
    doi: 10.1099/0022-1317-80-3-691pubmed: 10092009google scholar: lookup
  30. Balasuriya UBR, Leutenegger CM, Topol JB, McCollum WH, Timoney PJ. Detection of equine arteritis virus by real-time TaqMan reverse transcription-PCR assay. J Virol Methods 2002;101:21–28.
    doi: 10.1016/s0166-0934(01)00416-5pubmed: 11849680google scholar: lookup
  31. Toussaint JF, Sailleau C, Breard E, Zientara S, De Clercq K. Bluetongue virus detection by two real-time RT-qPCRs targeting two different genomic segments. J Virol Methods 2007;140:115–123.
  32. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 2018;35:1547–1549.
    doi: 10.1093/molbev/msy096pmc: PMC5967553pubmed: 29722887google scholar: lookup
  33. Pavlidis P, Noble WS. Matrix2png: a utility for visualizing matrix data. Bioinformatics 2003;19:295–296.
  34. Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol 2012;61:539–542.
    doi: 10.1093/sysbio/sys029pmc: PMC3329765pubmed: 22357727google scholar: lookup
  35. Letunic I, Bork P. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation. Nucleic Acids Res 2021;49:W293–W296.
    doi: 10.1093/nar/gkab301pmc: PMC8265157pubmed: 33885785google scholar: lookup
  36. Huelsenbeck JP, Ronquist F, Nielsen R, Bollback JP. Bayesian inference of phylogeny and its impact on evolutionary biology. Science 2001;294:2310–2314.
    doi: 10.1126/science.1065889pubmed: 11743192google scholar: lookup
  37. Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 2001;17:754–755.
  38. Reed LJ, Muench H. A simple method of estimating fifty per cent endpoints12. Am J Hyg 1938;27:493–497.
  39. NetNGlyc 1.0 N-linked glycosylation sites in human proteins. 2023. [13-November-2023]. https://services.healthtech.dtu.dk/services/NetNGlyc-1.0/ accessed.
  40. Crooks GE, Hon G, Chandonia JM, Brenner SE. WebLogo: a sequence logo generator. Genome Res 2004;14:1188–1190.
    doi: 10.1101/gr.849004pmc: PMC419797pubmed: 15173120google scholar: lookup
  41. Kosakovsky Pond SL, Frost SDW. Not so different after all: a comparison of methods for detecting amino acid sites under selection. Mol Biol Evol 2005;22:1208–1222.
    doi: 10.1093/molbev/msi105pubmed: 15703242google scholar: lookup
  42. Murrell B, Wertheim JO, Moola S, Weighill T, Scheffler K. Detecting individual sites subject to episodic diversifying selection. PLoS Genet 2012;8:e1002764.
  43. Murrell B, Moola S, Mabona A, Weighill T, Sheward D. FUBAR: a fast, unconstrained bayesian approximation for inferring selection. Mol Biol Evol 2013;30:1196–1205.
    doi: 10.1093/molbev/mst030pmc: PMC3670733pubmed: 23420840google scholar: lookup
  44. Sarkar S, Bailey E, Go YY, Cook RF, Kalbfleisch T. Allelic variation in CXCL16 determines CD3+ T lymphocyte susceptibility to equine arteritis virus infection and establishment of long-term carrier state in the stallion. PLoS Genet 2016;12:e1006467.
  45. Rola J, Larska M, Rola JG, Belák S, Autorino GL. Epizotiology and phylogeny of equine arteritis virus in hucul horses. Vet Microbiol 2011;148:402–407.
    doi: 10.1016/j.vetmic.2010.09.008pubmed: 20956062google scholar: lookup
  46. Balasuriya UBR, Dobbe JC, Heidner HW, Smalley VL, Navarrette A. Characterization of the neutralization determinants of equine arteritis virus using recombinant chimeric viruses and site-specific mutagenesis of an infectious cDNA clone. Virology 2004;321:235–246.
    doi: 10.1016/j.virol.2003.12.015pubmed: 15051384google scholar: lookup
  47. Balasuriya UBR, Patton JF, Rossitto PV, Timoney PJ, McCollum WH. Neutralization determinants of laboratory strains and field isolates of equine arteritis virus: identification of four neutralization sites in the amino-terminal ectodomain of the GL envelope glycoprotein. Virology 1997;232:114–128.
    doi: 10.1006/viro.1997.8551pubmed: 9185595google scholar: lookup
  48. Balasuriya UB, Timoney PJ, McCollum WH, MacLachlan NJ. Phylogenetic analysis of open reading frame 5 of field isolates of equine arteritis virus and identification of conserved and nonconserved regions in the GL envelope glycoprotein. Virology 1995;214:690–697.
    doi: 10.1006/viro.1995.0087pubmed: 8553578google scholar: lookup
  49. Metz GE, Ocampos GPM, Serena MS, Gambaro SE, Nosetto E. Extended phylogeny of the equine arteritis virus sequences including South American sequences. Intervirology 2011;54:30–36.
    doi: 10.1159/000318925pubmed: 20689314google scholar: lookup
  50. Hedges JF, Balasuriya UB, Topol JB, Lee DW, MacLachlan NJ. Genetic variation of ORFs 3 and 4 of equine arteritis virus. Adv Exp Med Biol 2001;494:69–72.
    doi: 10.1007/978-1-4615-1325-4_10pubmed: 11774546google scholar: lookup
  51. Lauck M, Alkhovsky SV, Bào Y, Bailey AL, Shevtsova ZV. Historical outbreaks of simian hemorrhagic fever in captive macaques were caused by distinct arteriviruses. J Virol 2015;89:8082–8087.
    doi: 10.1128/JVI.01046-15pmc: PMC4505640pubmed: 25972539google scholar: lookup
  52. Oğuzoğlu TÇ, Karapınar Z, Bilge-Dagalp S. Partial sequence of the orf1b gene fragment of equine arteritis viruses detected in turkey and phylogenic analysis. Revue de Medecine Veterinaire 2013.
  53. Mittelholzer C, Stadejek T, Johansson I, Baule C, Ciabatti I. Extended phylogeny of equine arteritis virus: division into new subgroups. J Vet Med B Infect Dis Vet Public Health 2006;53:55–58.
  54. Vanmechelen B, Vergote V, Laenen L, Koundouno FR, Bore JA. Expanding the arterivirus host spectrum: Olivier’s shrew virus 1, a novel arterivirus discovered in African giant shrews. Sci Rep 2018;8:11171.
    doi: 10.1038/s41598-018-29560-xpmc: PMC6057926pubmed: 30042503google scholar: lookup
  55. Snijder EJ, Meulenberg JJ. The molecular biology of arteriviruses. J Gen Virol 1998;79 (Pt 5):961–979.
    doi: 10.1099/0022-1317-79-5-961pubmed: 9603311google scholar: lookup
  56. Dortmans JCFM, Buter GJ, Dijkman R, Houben M, Duinhof TF. Molecular characterization of type 1 porcine reproductive and respiratory syndrome viruses (PRRSV) isolated in the Netherlands from 2014 to 2016. PLoS One 2019;14:e0218481.
  57. Kvisgaard LK, Hjulsager CK, Kristensen CS, Lauritsen KT, Larsen LE. Genetic and antigenic characterization of complete genomes of type 1 Porcine Reproductive and Respiratory Syndrome viruses (PRRSV) isolated in Denmark over a period of 10 years. Virus Res 2013;178:197–205.
  58. Hedges JF, Balasuriya UB, Timoney PJ, McCollum WH, MacLachlan NJ. Genetic divergence with emergence of novel phenotypic variants of equine arteritis virus during persistent infection of stallions. J Virol 1999;73:3672–3681.
  59. Vigerust DJ, Shepherd VL. Virus glycosylation: role in virulence and immune interactions. Trends Microbiol 2007;15:211–218.
    doi: 10.1016/j.tim.2007.03.003pmc: PMC7127133pubmed: 17398101google scholar: lookup
  60. Feng T, Zhang J, Chen Z, Pan W, Chen Z. Glycosylation of viral proteins: implication in virus–host interaction and virulence. Virulence 2022;13:670–683.
  61. Balasuriya UB, Patton JF, Rossitto PV, Timoney PJ, McCollum WH. Neutralization determinants of laboratory strains and field isolates of equine arteritis virus: identification of four neutralization sites in the amino-terminal ectodomain of the G(L) envelope glycoprotein. Virology 1997;232:114–128.
    doi: 10.1006/viro.1997.8551pubmed: 9185595google scholar: lookup
  62. Wagner HM, Balasuriya UBR, James MacLachlan N. The serologic response of horses to equine arteritis virus as determined by competitive enzyme-linked immunosorbent assays (c-ELISAs) to structural and non-structural viral proteins. Comp Immunol Microbiol Infect Dis 2003;26:251–260.
    doi: 10.1016/S0147-9571(02)00054-1pubmed: 12676125google scholar: lookup

Citations

This article has been cited 0 times.