Analyze Diet
Equine veterinary journal2010; 42(8); 713-720; doi: 10.1111/j.2042-3306.2010.00109.x

Description of the first recorded major occurrence of equine viral arteritis in France.

Abstract: The vast majority of equine arteritis virus (EAV) infections are inapparent or relatively mild, but may occasionally cause outbreaks of equine viral arteritis. The event observed in France during the summer of 2007 was the most important seen in the country, with mortality and disruption of economic activity. Objective: To describe the different stages seen during the outbreak and to show how molecular tools were used for both the detection and management of the crisis. Methods: EAV detection was performed by real-time reverse transcription-polymerase chain reaction (RT-PCR) in blood, nasal swabs, semen or organ samples. Characterisation of EAV strains was performed by sequencing the ORF5 fragment. Results: The outbreak affected 18 premises in 5 counties in western France, which represented the index, 8 primary and 9 secondary premises. Artificial insemination in draught horses was responsible for the virus spread. Eight mortality cases were observed, including one fetus, 5 young foals and 2 mature horses. Forty-three individuals had positive results by real-time RT-PCR. The range of measured cycle threshold (Ct) values varied from 19.8 to 40.4 depending on the biological samples. Phylogenetic analysis revealed that the 33 isolated strains all clustered within the EU-2 subgroup. Conclusions: The mortality rate attests to the virulence of the strain involved in this outbreak. Real-time RT-PCR was used for the first time in order to follow-up an epidemic disease in horses. Conclusions: The early detection of 3 signals with high Ct values attest the importance of taking low signals into account in field conditions.
Publication Date: 2010-09-14 PubMed ID: 21039801DOI: 10.1111/j.2042-3306.2010.00109.xGoogle 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
  • Research Support
  • Non-U.S. Gov't

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.

This research paper describes the first significant outbreak of Equine Viral Arteritis (EVA) in France in 2007 and the use of molecular tools for its detection and management.

About Equine Viral Arteritis (EVA) and the Outbreak

Equine Viral Arteritis (EVA) is a disease generally prevalent in horses, and most instances of EVA infections are undetectable or mild. However, occasionally, the virus can cause severe outbreaks, as was the case in France in 2007. This particular outbreak was significant, causing not only mortality but also economic disruption. Over five counties in western France were impacted, with EVA detected in 18 distinct premises, including the original source (index) and 18 subsequent sites.

  • The virus spread primarily through artificial insemination in draught horses.
  • Eight fatalities were recorded, involving young foals, mature horses, and a fetus.
  • 43 individuals tested positive through real-time Reverse Transcription-Polymerase Chain Reaction (RT-PCR).

Detection and Characterisation of EAV Strains

The research team used real-time RT-PCR to detect the presence of the EAV in various samples – blood, nasal swabs, semen, or organ samples.

  • The cycle threshold (Ct) values, or the number of cycles needed in PCR to amplify the viral RNA to a detectable level, ranged from 19.8 to 40.4, depending on the samples.
  • This was the first time that real-time RT-PCR was used to monitor an epidemic in horses, showcasing its effectiveness.
  • The isolated strains were then characterised by sequencing the ORF5 fragment, providing insight into the specific type of EAV responsible for the outbreak.

Analysis of the EAV Strains

The analysis of the isolated strains showed that all 33 strains belonged to the EU-2 subgroup, indicating a common source. The high mortality rate associated with the outbreak signifies the virulence of this specific strain.

  • Early detection of 3 signals with high Ct values illustrated the need to consider low signals in field conditions to prevent or manage future outbreaks effectively.

Conclusion

This research underscores the importance of molecular tools like RT-PCR for the early detection and management of viral outbreaks such as EVA. Also, continuous monitoring and analysis of such outbreaks can provide a better understanding of various viral strains, their virulence, spread mechanisms, and more, ultimately contributing to effective disease management strategies.

Cite This Article

APA
Pronost S, Pitel PH, Miszczak F, Legrand L, Marcillaud-Pitel C, Hamon M, Tapprest J, Balasuriya UB, Freymuth F, Fortier G. (2010). Description of the first recorded major occurrence of equine viral arteritis in France. Equine Vet J, 42(8), 713-720. https://doi.org/10.1111/j.2042-3306.2010.00109.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 42
Issue: 8
Pages: 713-720

Researcher Affiliations

Pronost, S
  • Animal Health Department, Frank Duncombe Laboratory, Caen, France. s.pronost@cg14.fr
Pitel, P H
    Miszczak, F
      Legrand, L
        Marcillaud-Pitel, C
          Hamon, M
            Tapprest, J
              Balasuriya, U B R
                Freymuth, F
                  Fortier, G

                    MeSH Terms

                    • Animals
                    • Arterivirus Infections / epidemiology
                    • Arterivirus Infections / veterinary
                    • Disease Outbreaks / veterinary
                    • Equartevirus / genetics
                    • France / epidemiology
                    • Horse Diseases / epidemiology
                    • Horses
                    • Phylogeny

                    Citations

                    This article has been cited 10 times.
                    1. Carnet F, Perrin-Cocon L, Paillot R, Lotteau V, Pronost S, Vidalain PO. An inventory of adjuvants used for vaccination in horses: the past, the present and the future. Vet Res 2023 Mar 2;54(1):18.
                      doi: 10.1186/s13567-023-01151-3pubmed: 36864517google scholar: lookup
                    2. Moyo NA, Westcott D, Simmonds R, Steinbach F. Equine Arteritis Virus in Monocytic Cells Suppresses Differentiation and Function of Dendritic Cells. Viruses 2023 Jan 16;15(1).
                      doi: 10.3390/v15010255pubmed: 36680295google scholar: lookup
                    3. Knox A, Beddoe T. Isothermal Nucleic Acid Amplification Technologies for the Detection of Equine Viral Pathogens. Animals (Basel) 2021 Jul 20;11(7).
                      doi: 10.3390/ani11072150pubmed: 34359278google scholar: lookup
                    4. Tapprest J, Foucher N, Linster M, Laloy E, Cordonnier N, Amat JP, Hendrikx P. Resumeq: A Novel Way of Monitoring Equine Diseases Through the Centralization of Necropsy Data. Front Vet Sci 2019;6:135.
                      doi: 10.3389/fvets.2019.00135pubmed: 31134214google scholar: lookup
                    5. Amat JP, Hendrikx P, Tapprest J, Leblond A, Dufour B. Comparative evaluation of three surveillance systems for infectious equine diseases in France and implications for future synergies. Epidemiol Infect 2015 Oct;143(14):3122-33.
                      doi: 10.1017/S0950268815000217pubmed: 25712325google scholar: lookup
                    6. Steinbach F, Westcott DG, McGowan SL, Grierson SS, Frossard JP, Choudhury B. Re-emergence of a genetic outlier strain of equine arteritis virus: Impact on phylogeny. Virus Res 2015 Apr 16;202:144-50.
                    7. Hans A, Gaudaire D, Manuguerra JC, Leon A, Gessain A, Laugier C, Berthet N, Zientara S. Combination of an unbiased amplification method and a resequencing microarray for detecting and genotyping equine arteritis virus. J Clin Microbiol 2015 Jan;53(1):287-91.
                      doi: 10.1128/JCM.01935-14pubmed: 25339390google scholar: lookup
                    8. Balasuriya UB, Zhang J, Go YY, MacLachlan NJ. Experiences with infectious cDNA clones of equine arteritis virus: lessons learned and insights gained. Virology 2014 Aug;462-463:388-403.
                      doi: 10.1016/j.virol.2014.04.029pubmed: 24913633google scholar: lookup
                    9. Balasuriya UB, Go YY, MacLachlan NJ. Equine arteritis virus. Vet Microbiol 2013 Nov 29;167(1-2):93-122.
                      doi: 10.1016/j.vetmic.2013.06.015pubmed: 23891306google scholar: lookup
                    10. Miszczak F, Shuck KM, Lu Z, Go YY, Zhang J, Sells S, Vabret A, Pronost S, Fortier G, Timoney PJ, Balasuriya UB. Evaluation of two magnetic-bead-based viral nucleic acid purification kits and three real-time reverse transcription-PCR reagent systems in two TaqMan assays for equine arteritis virus detection in semen. J Clin Microbiol 2011 Oct;49(10):3694-6.
                      doi: 10.1128/JCM.01187-11pubmed: 21832018google scholar: lookup