C-Terminal region of 48-kDa rhoptry protein for serological detection of Babesia caballi antibodies in horses.
Abstract: A recombinant C-terminal antigen derived from Babesia caballi 48-kDa rhoptry protein (rBc48/CT) was made for the development of a serologically diagnostic test. Antiserum raised against the rBc48/CT reacted specifically with the corresponding native protein by Western blotting and the indirect fluorescent antibody test (IFAT). Next, an indirect enzyme-linked immunosorbent assay (Bc48/CT-ELISA) and an immunochromatographic test based on the Bc48/CT (Bc48/CT-ICT) were constructed and employed for the detection of an antibody to B. caballi in a variety of equine sera. The results of Bc48/CT-ELISA and Bc48/CT-ICT were highly concordant with those of IFAT and ELISA, with full-length protein of Bc48 used as the reference tests. Our results demonstrate the success of Bc48/CT as antigen for the serological diagnosis of B. caballi infection in horses.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.
Publication Date: 2012-02-25 PubMed ID: 22387861DOI: 10.1016/j.parint.2012.02.006Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research revolves around the development of serological tests to diagnose Babesia caballi, a blood parasite in horses, using a C-terminal antigen created from a Babesia caballi-protein.
Creation of Recombinant Antigen
- The researchers created a recombinant C-terminal antigen derived from the 48-kDa rhoptry protein of Babesia caballi (rBc48/CT).
- The purpose of creating this antigen was to develop a serological diagnostic test. Serological tests aim to detect the presence of antibodies in the blood, which are generated by the immune system in response to an infection.
Antiserum Reactions
- The researchers also raised an antiserum against the rBc48/CT. They then studied how this antiserum reacted specifically with the corresponding native protein.
- This was accomplished using Western blotting, a method used to detect specific protein molecules from mixtures, and the indirect fluorescent antibody test (IFAT), a method used to detect specific antigens or antibodies in a sample.
Construction of Diagnostic Tests
- The researchers created two diagnostic tests based on the rBc48/CT— an indirect enzyme-linked immunosorbent assay (Bc48/CT-ELISA) and an immunochromatographic test (Bc48/CT-ICT).
- The aim of these tests was to detect an antibodies against Babesia caballi in a variety of equine sera.
Comparison with Reference Tests
- The researchers compared the results of the Bc48/CT-ELISA and Bc48/CT-ICT tests with those of IFAT and ELISA, which used the full-length protein of Bc48 as reference tests.
- The results of the Bc48/CT-ELISA and Bc48/CT-ICT tests were highly consistent with those of the reference tests.
Conclusion
- The study concluded that the the Bc48/CT antigen proved successful for the serological diagnosis of Babesia caballi infection in horses.
In simpler terms, the research shares the successful implementation of a derived antigen based test to diagnose a parasitic infection in horses. It highlights the consistent results with other reference tests and establishes the new findings as a credible and effective approach for serological diagnosis.
Cite This Article
APA
Terkawi MA, Alhasan H, Ueno A, Ratthanophart J, Luo Y, Cao S, Kamyingkird K, Aboulaila M, Youn-Kyoung G, Nishikawa Y, Yokoyama N, Xuan X, Igarashi I.
(2012).
C-Terminal region of 48-kDa rhoptry protein for serological detection of Babesia caballi antibodies in horses.
Parasitol Int, 61(3), 493-496.
https://doi.org/10.1016/j.parint.2012.02.006 Publication
Researcher Affiliations
- National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan.
MeSH Terms
- Animals
- Antibodies, Protozoan / blood
- Antibodies, Protozoan / immunology
- Antigens, Protozoan / immunology
- Babesia / growth & development
- Babesia / immunology
- Babesia / isolation & purification
- Blotting, Western
- Enzyme-Linked Immunosorbent Assay / methods
- Fluorescent Antibody Technique / methods
- Horses / immunology
- Horses / parasitology
- Immune Sera / immunology
- Protozoan Proteins / immunology
- Recombinant Proteins / immunology
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