Monoclonal Antibody against Babesia equi : Characterization and Potential Application of Antigen for Serodiagnosis

Author:

Avarzed Abgaandorjiin1,Igarashi Ikuo1,De Waal Daniel T.2,Kawai Satoru3,Oomori Yukio4,Inoue Noboru1,Maki Yoshiyuki1,Omata Yoshitaka5,Saito Atsushi5,Nagasawa Hideyuki1,Toyoda Yutaka1,Suzuki Naoyoshi1

Affiliation:

1. The Research Center for Protozoan Molecular Immunology1 and

2. Parasitology Division, Onderstepoort Veterinary Institute, Onderstepoort 0110, South Africa2

3. Department of Medical Zoology, Dokkyo University School of Medicine, Mibu, Tochigi 321-02,3 and

4. Department of Anatomy, Asahikawa Medical College, Asahikawa, Hokkaido 070,4 Japan, and

5. Department of Veterinary Physiology,5 Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555,

Abstract

ABSTRACT Monoclonal antibody (MAb) BEG3 was produced against Babesia equi parasites to define a species-specific antigen for diagnostic use. The MAb reacted with single, paired, and Maltese cross forms of B. equi , and no reaction was observed with this MAb on acetone-fixed Babesia caballi , Babesia ovata , or Babesia microti parasites in the indirect immunofluorescent antibody test. Confocal laser and immunoelectron microscopic studies showed that the antigen which was recognized by this MAb was located on the surface of B. equi parasites. This MAb recognized a 19-kDa protein of B. equi antigen and did not react with B. caballi antigen or normal horse erythrocytes in immunoblot analysis. This MAb also significantly inhibited the in vitro growth of the B. equi parasite. Preliminary studies using partially purified antigen, which was separated by high-pressure liquid chromatography and recognized by the MAb, suggested that it is a suitable antigen for enzyme-linked immunosorbent assay detection of anti- B. equi antibodies in naturally infected horse sera.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference28 articles.

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2. Prevalence of equine piroplasmosis in Central Mongolia;Avarzed A.;Onderstepoort J. Vet. Res.,1997

3. Improved in vitro cultivation of Babesia caballi;Avarzed A.;J. Vet. Med. Sci.,1997

4. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

5. Equine piroplasmosis: an update on diagnosis, treatment and prevention;Brüning A.;Br. Vet. J.,1996

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