Journals / Turkish Journal of Veterinary and Animal Sciences / 2013 / Cilt: 37 - Sayı: 4

Immunokinetics of Theileria equi specific antibodies: a comparison in serial and single dilution ELISA antibody end titres

Pages
429–433
Publication Date
2013-04-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Sample analysis revealed overall seroprevalence of 91.01% in the horse population.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Theileria equi, a haemoprotozoan of equids, is responsible for endemic infection/latency in tropical/subtropical parts of the world.
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Key Findings & Data:Sequential serum samples were collected up to 90 days postinfection (PI) from 4 donkeys experimentally infected with T. equi.
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Conclusion & Impact:Sample analysis revealed overall seroprevalence of 91.01% in the horse population.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Babesia equi · ELISA · equine piroplasmosis

Abstract

Theileria equi, a haemoprotozoan of equids, is responsible for endemic infection/latency in tropical/subtropical parts of the world. The present study investigated the immunokinetics of T. equi infection in experimental animals and the diagnostic applicability of single dilution ELISA vis-à-vis conventional serial dilution ELISA. Sequential serum samples were collected up to 90 days postinfection (PI) from 4 donkeys experimentally infected with T. equi. Immunokinetics of T. equi antibodies end titre were determined by serial and single dilution ELISA. A significant rise in initial ELISA antibody end titre (1:800 in serial dilution ELISA and from 1:600 to 1:650 in single dilution ELISA) was observed from day 9 PI in all 4 donkeys, which plateaued between days 66 and 73 PI (end antibody titre varied between 1:6400 to 1:25,600 and 1:6050 to 1:22,100). The efficacy of these ELISAs was also determined by testing 256 field serum samples at 1:200 dilution, collected from apparently healthy animals. Sample analysis revealed overall seroprevalence of 91.01% in the horse population. The frequency distribution of antibody titre of these field samples by single dilution ELISA exhibited that most of the positive horses had high levels of specific antibodies. This study has emphasised the usefulness of single dilution ELISA as a diagnostic assay in determining the end antibody titre by testing it at a single dilution of 1:200.

Özet

Theileria equi, a haemoprotozoan of equids, is responsible for endemic infection/latency in tropical/subtropical parts of the world. The present study investigated the immunokinetics of T. equi infection in experimental animals and the diagnostic applicability of single dilution ELISA vis-à-vis conventional serial dilution ELISA. Sequential serum samples were collected up to 90 days postinfection (PI) from 4 donkeys experimentally infected with T. equi. Immunokinetics of T. equi antibodies end titre were determined by serial and single dilution ELISA. A significant rise in initial ELISA antibody end titre (1:800 in serial dilution ELISA and from 1:600 to 1:650 in single dilution ELISA) was observed from day 9 PI in all 4 donkeys, which plateaued between days 66 and 73 PI (end antibody titre varied between 1:6400 to 1:25,600 and 1:6050 to 1:22,100). The efficacy of these ELISAs was also determined by testing 256 field serum samples at 1:200 dilution, collected from apparently healthy animals. Sample analysis revealed overall seroprevalence of 91.01% in the horse population. The frequency distribution of antibody titre of these field samples by single dilution ELISA exhibited that most of the positive horses had high levels of specific antibodies. This study has emphasised the usefulness of single dilution ELISA as a diagnostic assay in determining the end antibody titre by testing it at a single dilution of 1:200.

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Cite This Article

KUMAR, Y., MALHOTRA, D. V., NICHANI, A. K., KUMAR, A., DHAR, S., KUMAR, S. (2013). Immunokinetics of Theileria equi specific antibodies: a comparison in serial and single dilution ELISA antibody end titres. Turkish Journal of Veterinary and Animal Sciences, Cilt: 37 - Sayı: 4, 429–433. https://ajindex.com/articles/121741

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References (11)

  1. Kumar, S., Kumar, R.: Diagnosis of Babesia equi infection: an update on the methods available. Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources, 2007; 2: 1– USDA: Equine piroplasmosis domestic pathways assessment 2011: pathways assessment for the spread of the causative agents of equine piroplasmosis from the movement of a horse from quarantined premises within the contiguous United States. USDA: Fort Collins, CO, USA. 2011.
  2. Kumar, S., Sugimoto, C., Igarashi, I.: Equine babesiosis in Asia. In: Asian Parasitology, Vol. 4 – Toxoplasmosis and Babesiosis in Asia. AAA Committee – The Federation of Asian Parasitologists, Department of Infection and Host Defense, Chiba University Graduate School of Medicine, Inohana, Chiba, Japan. 2005, 187–195.
  3. Malhotra, D.V., Gautam, O.P., Banerjee, D.P.: Prevalence of latent cases of Babesia equi infection in some parts of NorthWest India as measured by capillary tube agglutination test. Equine Vet. J., 1978; 10: 24–26.
  4. Kumar, S., Malhotra, D.V, Dhar, S.: Serodiagnosis of Babesia equi infection – a comparison of Dot-ELISA, complement fixation test and capillary tube agglutination test. Vet. Parasitol., 1997; 69: 171–176.
  5. Kumar, S., Kumar, Y., Malhotra, D.V., Dhar, S., Nichani, A.K.: Standardisation and comparison of serial dilution and single dilution enzyme linked immunosorbent assay (ELISA) using different antigenic preparations of the Babesia (Theileria) equi parasite. Vet. Res., 2003; 34: 71–83.
  6. Mahoney, D.F., Saal, J.R.: Bovine babesiosis: Thick blood films for the detection of parasitaemia. Aust. Vet. J., 1961; 37: 44–47.
  7. Friedhoff, K., Bose, R.: Recent developments in diagnostics of some tick-borne diseases. In: Uilenberg, G., Permin, A., Hansen, J.W. Eds. Use of Applicable Biotechnological Methods for Diagnosing Haemoparasites. Proceedings of the Expert Consultation, Merida, Mexico, 4–6 October 1993.
  8. FAO, Rome, Italy. 1994, 46–57.
  9. Madden, P.A., Holbrook, A.A.: Equine piroplasmosis: indirect fluorescent antibody test for Babesia caballi. Am. J. Vet. Res., 1968; 29: 117–123.
  10. Knowles, D.P. Jr, Kappmeyer, L.S., Stiller, D., Hennager, S.G., Perryman, L.E.: Antibody to a recombinant merozoite protein epitope identified horses infected with Babesia equi. J. Clin. Microbiol., 1992; 30: 3122–3126.
  11. Ikadai, H., Xuan, X., Igarashi, I., Tanaka, S., Kanemaru, T., Nagasawa, H., Fujisaki, K., Suzuki, N., Mikami, T.: Cloning and expression of a 48-kilodalton Babesia caballi merozoite rhoptry protein and