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Procedurally similar competitive immunoassay systems for the serodiagnosis of Babesia equi, Babesia caballi, Trypanosoma equiperdum, and Burkholderia mallei infection in horses.

Abstract: Procedurally similar competitive enzyme-linked immunoassay (cELISA) methods were developed for the serodiagnosis of Babesia equi and Babesia caballi (piroplasmosis), Trypanosoma equiperdum (dourine), and Burkholderia mallei (glanders) infections in horses. Apparent test specificities for the B. equi, B. caballi, T. equiperdum, and B. mallei cELISAs were 99.2%, 99.5%, 98.9%, and 98.9%, respectively. Concordances and kappa values between the complement fixation (CF) and the cELISA procedures for the serodiagnosis of B. equi, B. caballi, T. equiperdum, and B. mallei infections in experimentally exposed horses were 76% and 0.55, 89% and 0.78, 97% and 0.95, and 70% and 0.44, respectively. The cELISA method may be a technically more reproducible, objective, and convenient approach for piroplasmosis, dourine, and glanders serodiagnosis in qualifying animals for international movement and disease eradication programs than the CF systems currently in use. Use of the cELISA method also obviated the problems associated with testing hemolyzed or anticomplementary sera.
Publication Date: 2000-02-26 PubMed ID: 10690775DOI: 10.1177/104063870001200108Google Scholar: Lookup
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  • Journal Article

Summary

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The research developed and assessed procedurally similar competitive enzyme-linked immunoassay (cELISA) methods for diagnosis of Babesia equi, Babesia caballi, Trypanosoma equiperdum, and Burkholderia mallei infections in horses. The findings suggest that the cELISA method is technically more reproducible, objective, and convenient for diagnosis in qualifying animals for international movement and disease eradication programs than currently used methods.

Development of the cELISA Methods

  • The researchers developed similar competitive enzyme-linked immunoassay (cELISA) methods for the diagnosis of four different infections: Babesia equi, Babesia caballi, Trypanosoma equiperdum, and Burkholderia mallei, in horses. These infections are known respectively as piroplasmosis, dourine, and glanders.
  • cELISA methods use a competitive process where a labeled reagent competes with unlabeled antigen in a sample for binding specific antibody sites. This is a common method used in clinical diagnostics for the detection of certain compounds (antigens) in a specimen.

Testing and Analysis

  • The test specificities for these cELISA methods were found to be consistently high, with Babesia equi at 99.2%, Babesia caballi at 99.5%, Trypanosoma equiperdum at 98.9%, and Burkholderia mallei at 98.9%.
  • These results suggest that these cELISA methods are highly accurate and reliable, with a very low likelihood of producing false positive results.

Comparison with Existing Methods

  • The researchers also compared the cELISA methods with the existing complement fixation (CF) methods.
  • They found that the concordances between the CF and the cELISA methods for the serodiagnosis of the four infections were relatively high, indicating a strong agreement between the two methods.
  • However, the researchers note that the cELISA methods may be a more technically reproducible, objective, and convenient approach than the CF methods currently in use.

Implications of the Research

  • The use of the cELISA method also solved the issues related to testing hemolyzed or anticomplementary sera, which are types of blood samples that can influence the results of a test.
  • This suggests that the cELISA method can be used in various settings such as in checking animals for diseases during international transportation or in disease eradication programs.

Cite This Article

APA
Katz J, Dewald R, Nicholson J. (2000). Procedurally similar competitive immunoassay systems for the serodiagnosis of Babesia equi, Babesia caballi, Trypanosoma equiperdum, and Burkholderia mallei infection in horses. J Vet Diagn Invest, 12(1), 46-50. https://doi.org/10.1177/104063870001200108

Publication

ISSN: 1040-6387
NlmUniqueID: 9011490
Country: United States
Language: English
Volume: 12
Issue: 1
Pages: 46-50

Researcher Affiliations

Katz, J
  • Diagnostic Bacteriology Laboratory, National Veterinary Services Laboratories, US Department of Agriculture, Animal and Health Inspection Services, Ames, IA 50010, USA.
Dewald, R
    Nicholson, J

      MeSH Terms

      • Animals
      • Antigens, Protozoan / analysis
      • Babesia / immunology
      • Babesiosis / diagnosis
      • Babesiosis / immunology
      • Burkholderia / immunology
      • Burkholderia Infections / diagnosis
      • Burkholderia Infections / immunology
      • Burkholderia Infections / veterinary
      • Dourine / diagnosis
      • Dourine / immunology
      • Enzyme-Linked Immunosorbent Assay / methods
      • Enzyme-Linked Immunosorbent Assay / veterinary
      • Glanders / diagnosis
      • Glanders / immunology
      • Horse Diseases / diagnosis
      • Horse Diseases / parasitology
      • Horses
      • Sensitivity and Specificity
      • Serologic Tests / methods
      • Trypanosoma / immunology
      • Trypanosomiasis / diagnosis
      • Trypanosomiasis / immunology
      • Trypanosomiasis / veterinary

      Citations

      This article has been cited 7 times.
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