Analyze Diet
Equine veterinary journal2021; 54(2); 299-305; doi: 10.1111/evj.13443

Horses vaccinated with live attenuated intranasal strangles vaccine seroconvert to SEQ2190 and SeM.

Abstract: The dual antigen iELISA uses two Streptococcus equi subsp equi surface protein antigens composed of N-terminal portions of SEQ2190 (Antigen A) and SeM (Antigen C). It is currently used to identify animals exposed to S. equi which have developed an immune response to the target antigens. Objective: To determine the usefulness of the dual antigen iELISA in a population of horses vaccinated with Pinnacle IN. We hypothesised that horses vaccinated for strangles with a live attenuated, non-encapsulated SeM-2 strain of S. equi, would seroconvert when tested 5 weeks later by the dual antigen iELISA. Methods: Prospective case-control study. Methods: Three separate serum samples were obtained from 26 client-owned horses vaccinated annually with Pinnacle IN and 26 university-owned (non-vaccinates): at annual strangles vaccination (S1), 5-week post-vaccination (S2) from vaccinates, and a third (S3) (at 10 weeks) from vaccinates who received a booster. Seropositivity was defined as an OD450 nm value ≥0.5 for one or both antigens. Mixed-effects ordered logistic regression analysis was used to identify factors associated with a suspect seropositive and seropositive value on the combined Antigen A and Antigen C iELISA. Post hoc pairwise comparisons of linear predictive margins were used to assess the differences in OD450 at a specific time between Antigens A and C. Results: Nineteen of 25 (76%) vaccinates were seropositive at S2 compared to 1 of 26 (4%) non-vaccinates. When adjusted for sample number, vaccinates were more likely to be seropositive or suspect than non-vaccinates (OR 14; P = .02, 95% CI 1.62-122.03). The OD450 value was significantly larger for Antigen C than Antigen A for vaccinates (P < .001; 95% CI 0.13-0.26) when normalised by age, sex and breed. Conclusions: Guttural pouch sampling for S. equi in seroconverted horses was unavailable. Conclusions: With a high rate of seroconversion to both antigens, the use of the dual antigen iELISA is not recommended in populations vaccinated with Pinnacle IN.
Publication Date: 2021-03-18 PubMed ID: 33630353DOI: 10.1111/evj.13443Google 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.

The research article explores how horses that are vaccinated with a live attenuated intranasal strangles vaccine (Pinnacle IN) react to a dual antigen iELISA, a test used to identify animals that have been exposed to bacteria Streptococcus equi and developed an immune response.

About the iELISA Test

  • The iELISA test uses two antigens, SEQ2190 (Antigen A) and SeM (Antigen C), which are made from surface proteins of the Streptococcus equi bacteria.
  • The test is intended to identify whether the examined animal has been exposed to the bacterium and has formed an immune response against it.

Objective and Methodology of the Study

  • The researchers aimed to determine how effective the iELISA test is when applied to a group of horses vaccinated with Pinnacle IN.
  • They hypothesized that the horses vaccinated with this particular strain would show a positive immune response (seroconvert) when tested 5 weeks after the vaccination.
  • The study monitored 26 client-owned horses that were given annual Pinnacle IN vaccinations (vaccinates) and 26 university-owned horses that were not vaccinated (non-vaccinates).
  • Three serum samples were collected from the vaccinated horses: at the time of the annual vaccination, 5 weeks after the vaccination, and 10 weeks after the vaccination following a booster shot.
  • An OD450 nm value of more than or equal to 0.5 for one or both antigens was considered a positive immune response (seropositivity).
  • The researchers used statistical analysis to find factors related to a suspected or positive immune response.

Results of the Study

  • Of the vaccinated horses, 76% were seropositive 5 weeks after the vaccination while only 4% of the non-vaccinated horses were seropositive.
  • Even after adjusting for sample number, the vaccinated horses were more likely to be seropositive or suspect than the non-vaccinated horses.
  • Antigen C resulted in a significantly higher OD450 value than Antigen A among the vaccinated horses, after normalizing for age, sex, and breed.

Conclusions

  • The researchers were unable to sample the guttural pouch to check for the presence of S. equi in seroconverted horses.

Cite This Article

APA
Boyle AG, Mitchell C, Stefanovski D, Waller AS. (2021). Horses vaccinated with live attenuated intranasal strangles vaccine seroconvert to SEQ2190 and SeM. Equine Vet J, 54(2), 299-305. https://doi.org/10.1111/evj.13443

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 54
Issue: 2
Pages: 299-305

Researcher Affiliations

Boyle, Ashley G
  • Department of Clinical Studies New Bolton Center, University of Pennsylvania, Kennett Square, PA, USA.
Mitchell, Catriona
  • Department of Microbiology, Animal Health Trust, Kentford, Newmarket, Suffolk, UK.
Stefanovski, Darko
  • Department of Clinical Studies New Bolton Center, University of Pennsylvania, Kennett Square, PA, USA.
Waller, Andrew S
  • Department of Microbiology, Animal Health Trust, Kentford, Newmarket, Suffolk, UK.
  • Intervacc AB, Hägersten, Sweden.

MeSH Terms

  • Animals
  • Case-Control Studies
  • Horse Diseases / prevention & control
  • Horses
  • Streptococcal Infections / prevention & control
  • Streptococcal Infections / veterinary
  • Streptococcus equi
  • Vaccines

Grant Funding

  • University of Pennsylvania
  • Clinical Studies New Bolton Center

References

This article includes 20 references
  1. Boyle AG, Timoney JF, Newton JR, Hines MT, Waller AS, Buchanan BR. Streptococcus equi infections in horses: guidelines for treatment, control, and prevention of strangles-revised consensus statement.. J Vet Intern Med 2018;32(2):633-47.
  2. Davidson A, Traub-Dargatz JL, Magnuson R, Hill A, Irwin V, Newton R. Lack of correlation between antibody titers to fibrinogen-binding protein of Streptococcus equi and persistent carriers of strangles.. J Vet Diagn Invest 2008;20(4):457-62.
  3. Robinson C, Steward KF, Potts N, Barker C, Hammond TA, Pierce K. Combining two serological assays optimises sensitivity and specificity for the identification of Streptococcus equi subsp. equi exposure.. Vet J 2013;197(2):188-91.
  4. Waller AS. New perspectives for the diagnosis, control, treatment, and prevention of strangles in horses.. Vet Clin North Am Equine Pract 2014;30(3):591-607.
  5. Sweeney CR, Timoney JF, Newton JR, Hines MT. Streptococcus equi infections in horses: guidelines for treatment, control, and prevention of strangles.. J Vet Intern Med 2005;19(1):123-34.
  6. Sheoran AS, Sponseller BT, Holmes MA, Timoney JF. Serum and mucosal antibody isotype responses to M-like protein (SeM) of Streptococcus equi in convalescent and vaccinated horses.. Vet Immunol Immunopathol 1997;59(3-4):239-51.
  7. Velineni S, DeNegri R, Artiushin SC, Timoney JF. Comparison of specificities of serum antibody responses of horses to clinical infections caused by Streptococcus equi or zooepidemicus.. Vet Microbiol 2015;180(3-4):253-9.
  8. Traub-Dargatz J, Garber L, Marshall K, Kopral C, Wiedenheft K, Digianantonio R, Pelzel McCluskey A. Comparing Strangles Control Strategies With Other Infection-Control Strategies on United States Equine Operations [abstract].. Proceedings of the Havemeyer Foundation Workshop, Getting to Grips with Strangles and other Streptococcal Diseases 2017; 32.
  9. Tscheschlok L, Venner M, Steward K, Böse R, Riihimäki M, Pringle J. Decreased clinical severity of strangles in weanlings associated with restricted seroconversion to optimized Streptococcus equi ssp equi Assays.. J Vet Intern Med 2018;32(1):459-64.
  10. Pringle J, Storm E, Waller A, Riihimäki M. Influence of penicillin treatment of horses with strangles on seropositivity to Streptococcus equi ssp. equi-specific antibodies.. J Vet Intern Med 2020;34(1):294-9.
  11. Harris SR, Robinson C, Steward KF, Webb KS, Paillot R, Parkhill J. Genome specialization and decay of the strangles pathogen, Streptococcus equi, is driven by persistent infection.. Genome Res 2015;25:1360-71.
  12. El-Hage CM, Bannai H, Wiethoelter AK, Firestone SM, Heislers CM, Allen JL. Serological responses of Australian horses using a commercial duplex indirect ELISA following vaccination against strangles.. Aust Vet J 2019;97(7):220-4.
  13. Robinson C, Frykberg L, Flock M, Guss B, Waller AS, Flock JI. Strangvac: a recombinant fusion protein vaccine that protects against strangles, caused by Streptococcus equi.. Vaccine 2018;36(11):1484-90.
  14. Robinson C, Waller AS, Frykberg L, Flock M, Zachrisson O, Guss B. Intramuscular vaccination with Strangvac is safe and induces protection against equine strangles caused by Streptococcus equi [published online ahead of print, 2020 Jun 2].. Vaccine 2020;S0264-410X(20)30691-5.
  15. Khatibzadeh SM, Gold CB, Keggan AE, Perkins GA, Glaser AL, Dubovi EJ. West Nile virus-specific immunoglobulin isotype responses in vaccinated and infected horses.. Am J Vet Res 2015;76(1):92-100.
  16. Wagner B, Goodman LB, Babasyan S, Freer H, Torsteinsdóttir S, Svansson V. Antibody and cellular immune responses of naïve mares to repeated vaccination with an inactivated equine herpesvirus vaccine.. Vaccine 2015;33(42):5588-97.
  17. . Vaccinations for Adult Horses.. .
  18. . Pinnacle I.N. Intranasal Streptococcus equi vaccine.. .
  19. Riihimäki M, Aspán A, Ljung H, Pringle J. Long term dynamics of a Streptococcus equi ssp equi outbreak, assessed by qPCR and culture and seM sequencing in silent carriers of strangles.. Vet Microbiol 2018;223:107-12.
  20. Durham AE, Kemp-Symonds J. Failure of serological testing for antigens A and C of Streptococcus equi subspecies equi to identify guttural pouch carriers.. Equine Vet J 2021;53:38-43.
    doi: 10.1111/evj.13276google scholar: lookup

Citations

This article has been cited 4 times.
  1. Jaramillo-Morales C, James K, Barnum S, Vaala W, Chappell DE, Schneider C, Craig B, Bain F, Barnett DC, Gaughan E, Pusterla N. Voluntary Biosurveillance of Streptococcus equi Subsp. equi in Nasal Secretions of 9409 Equids with Upper Airway Infection in the USA. Vet Sci 2023 Jan 20;10(2).
    doi: 10.3390/vetsci10020078pubmed: 36851382google scholar: lookup
  2. Martin KH, Redding LE, Boyle AG. Factors Influencing Veterinarian Opinion on Reporting of Equine Strangles in the United States. J Equine Vet Sci 2022 Jul;114:103947.
    doi: 10.1016/j.jevs.2022.103947pubmed: 35417769google scholar: lookup
  3. Frosth S, Morris ERA, Wilson H, Frykberg L, Jacobsson K, Parkhill J, Flock JI, Wood T, Guss B, Aanensen DM, Boyle AG, Riihimäki M, Cohen ND, Waller AS. Conservation of vaccine antigen sequences encoded by sequenced strains of Streptococcus equi subsp. equi. Equine Vet J 2023 Jan;55(1):92-101.
    doi: 10.1111/evj.13552pubmed: 35000217google scholar: lookup
  4. Wan J, Weldon E, Ganser G, Morris ERA, Hughes EV, Bordin AI, Heine PA, Hust M, Cohen ND, Gill JJ, Liu M. Immunogenic Streptococcus equi cell surface proteins identified by ORFeome phage display. mSphere 2025 Dec 23;10(12):e0062625.
    doi: 10.1128/msphere.00626-25pubmed: 41288106google scholar: lookup