Analyze Diet
Parasitology international2012; 61(3); 493-496; doi: 10.1016/j.parint.2012.02.006

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.
Publication Date: 2012-02-25 PubMed ID: 22387861DOI: 10.1016/j.parint.2012.02.006Google 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
  • Research Support
  • Non-U.S. Gov't

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 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

ISSN: 1873-0329
NlmUniqueID: 9708549
Country: Netherlands
Language: English
Volume: 61
Issue: 3
Pages: 493-496

Researcher Affiliations

Terkawi, Mohamad Alaa
  • National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan.
Alhasan, Hend
    Ueno, Akio
      Ratthanophart, Jadsada
        Luo, Yuzi
          Cao, Shinuo
            Kamyingkird, Ketsarin
              Aboulaila, Mahmoud
                Youn-Kyoung, Goo
                  Nishikawa, Yoshifumi
                    Yokoyama, Naoaki
                      Xuan, Xuenan
                        Igarashi, Ikuo

                          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

                          Citations

                          This article has been cited 0 times.