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Clinical and diagnostic laboratory immunology2001; 8(3); 645-646; doi: 10.1128/CDLI.8.3.645-646.2001

Detection of antibodies to Babesia equi in horses by a latex agglutination test using recombinant EMA-1.

Abstract: A latex agglutination test (LAT) using recombinant equi merozoite antigen 1 (EMA-1) for the detection of antibodies to Babesia equi was developed. The LAT was able to differentiate very clearly between sera from B. equi-infected horses and sera from Babesia caballi-infected horses or from normal horses. The LAT results were identical to those of a previously developed enzyme-linked immunosorbent assay. These results indicate that LAT using recombinant EMA-1 might be very useful as a routine screening method for the diagnosis of B. equi infection.
Publication Date: 2001-05-01 PubMed ID: 11329474PubMed Central: PMC96117DOI: 10.1128/CDLI.8.3.645-646.2001Google Scholar: Lookup
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  • 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 article is about the development of a latex agglutination test (LAT) using a specific antigen, named equi merozoite antigen 1 (EMA-1), for the detection of antibodies to Babesia equi, a parasite that infects horses.

Introduction to the Research

  • The research focused on the development and testing of a latex agglutination test (LAT) to detect antibodies for Babesia equi, a protozoan parasite with a global distribution which infects the red blood cells of horses. This parasite causes a disease named equine piroplasmosis, which presents with fever, anemia, jaundice, and in severe cases, death.
  • The test uses a specific antigen known as equi merozoite antigen 1 (EMA-1). Antigens are substances (usually proteins) on the surface of cells, viruses, fungi, or bacteria. The immune system recognizes them as an enemy and produces antibodies which serve as a marker and defense mechanism.

Aims of the Research

  • The main goal of the research was to identify whether or not the developed LAT could clearly differentiate between sera (a component of blood) from B. equi-infected horses and sera from Babesia caballi-infected horses or non-infected (normal) horses.
  • Another important aspect of this study was to compare the results of the developed LAT to those of a previously developed biochemical test called the enzyme-linked immunosorbent assay (ELISA). ELISA is a common laboratory test that measures the concentration of an analyte (a subject of measurement) in a liquid by measuring the intensity of the color formed.

Research Findings

  • The results of the study showed that the developed LAT was accurate in differentiating between B. equi-infected horses and Babesia caballi-infected or non-infected horses, thus proving its efficacy in diagnosing B. equi infection.
  • Furthermore, when correlating the results of the LAT to the ELISA, the results were found to be identical. This suggests that the LAT designed using EMA-1 is reliable and serves as an effective alternative to the ELISA for the detection of Babesia equi.

Conclusion of the Research

  • The research concluded that the LAT using recombinant EMA-1 could be highly useful as a routine screening method for the diagnosis of B. equi infection.
  • The test not just proved to be effective, but may also be more convenient considering the simplicity and speed of LAT, which does not require specialized equipment and can provide results within a short period of time.

Cite This Article

APA
Xuan X, Igarashi I, Tanaka T, Fukumoto S, Nagasawa H, Fujisaki K, Mikami T. (2001). Detection of antibodies to Babesia equi in horses by a latex agglutination test using recombinant EMA-1. Clin Diagn Lab Immunol, 8(3), 645-646. https://doi.org/10.1128/CDLI.8.3.645-646.2001

Publication

ISSN: 1071-412X
NlmUniqueID: 9421292
Country: United States
Language: English
Volume: 8
Issue: 3
Pages: 645-646

Researcher Affiliations

Xuan, X
  • National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan. gen@obihiro.ac.jp
Igarashi, I
    Tanaka, T
      Fukumoto, S
        Nagasawa, H
          Fujisaki, K
            Mikami, T

              MeSH Terms

              • Animals
              • Antibodies, Protozoan / immunology
              • Antigens, Protozoan / genetics
              • Antigens, Protozoan / immunology
              • Babesia / immunology
              • Babesiosis / diagnosis
              • Babesiosis / immunology
              • Babesiosis / parasitology
              • Horses
              • Latex Fixation Tests
              • Membrane Proteins / genetics
              • Membrane Proteins / immunology
              • Protozoan Proteins / genetics
              • Protozoan Proteins / immunology
              • Recombinant Proteins / genetics
              • Recombinant Proteins / immunology

              References

              This article includes 10 references
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              Citations

              This article has been cited 3 times.
              1. Tirosh-Levy S, Gottlieb Y, Fry LM, Knowles DP, Steinman A. Twenty Years of Equine Piroplasmosis Research: Global Distribution, Molecular Diagnosis, and Phylogeny. Pathogens 2020 Nov 8;9(11).
                doi: 10.3390/pathogens9110926pubmed: 33171698google scholar: lookup
              2. Yong T, Huan-chun C, Shao-bo X, Ya-li Q, Qi-gai H, Yu-qi R. Development of a latex agglutination test using the major epitope domain of glycoprotein E of pseudorabies virus expressed in E. coli to differentiate between immune responses in pigs naturally infected or vaccinated with pseudorabies virus. Vet Res Commun 2005 Aug;29(6):487-97.
                doi: 10.1007/s11259-005-1865-4pubmed: 16215839google scholar: lookup
              3. 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.