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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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
Researcher Affiliations
- Diagnostic Bacteriology Laboratory, National Veterinary Services Laboratories, US Department of Agriculture, Animal and Health Inspection Services, Ames, IA 50010, USA.
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.- Ichikawa Y, Iinuma Y, Okagawa T, Shimbo R, Enkhtuul B, Khurtsbaatar O, Kinoshita Y, Niwa H, Aoshima K, Kobayashi A, Batbaatar V, Ohashi K, Kimura T. Comparison of immunogenicity of 17 Burkholderia mallei antigens and whole cell lysate using indirect ELISA. J Vet Med Sci 2025 Apr 1;87(4):394-401.
- Grause JF, Elschner MC, Ledesma NA, Murphy G. Development and validation of a chemiluminescent western blot assay for glanders (Burkholderia mallei) serodetection. J Vet Diagn Invest 2024 Mar;36(2):283-286.
- Pal V, Kumar S, Malik P, Rai GP. Evaluation of recombinant proteins of Burkholderia mallei for serodiagnosis of glanders. Clin Vaccine Immunol 2012 Aug;19(8):1193-8.
- Elschner MC, Scholz HC, Melzer F, Saqib M, Marten P, Rassbach A, Dietzsch M, Schmoock G, de Assis Santana VL, de Souza MM, Wernery R, Wernery U, Neubauer H. Use of a Western blot technique for the serodiagnosis of glanders. BMC Vet Res 2011 Jan 19;7:4.
- Sprague LD, Zachariah R, Neubauer H, Wernery R, Joseph M, Scholz HC, Wernery U. Prevalence-dependent use of serological tests for diagnosing glanders in horses. BMC Vet Res 2009 Sep 1;5:32.
- Cunha CW, Kappmeyer LS, McGuire TC, Dellagostin OA, Knowles DP. Conformational dependence and conservation of an immunodominant epitope within the babesia equi erythrocyte-stage surface protein equi merozoite antigen 1. Clin Diagn Lab Immunol 2002 Nov;9(6):1301-6.
- Hirata H, Ikadai H, Yokoyama N, Xuan X, Fujisaki K, Suzuki N, Mikami T, Igarashi I. Cloning of a truncated Babesia equi gene encoding an 82-kilodalton protein and its potential use in an enzyme-linked immunosorbent assay. J Clin Microbiol 2002 Apr;40(4):1470-4.
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