Detection of Babesia caballi infection by enzyme-linked immunosorbent assay using recombinant 48-kDa merozoite rhoptry protein

Int J Parasitol. 2000 Apr 24;30(5):633-5. doi: 10.1016/s0020-7519(00)00008-4.

Abstract

The 48-kDa Babesia caballi merozoite rhoptry protein was expressed using a pGEX4T expression vector in Escherichia coli as glutathione S-transferase fusion protein (GST-BC48), and the expressed GST-BC48 was used in an ELISA to detect specific antibodies in serum samples. No cross-reaction was observed with sera from horses experimentally infected with Babesia equi. GST-BC48 ELISA was a highly sensitive and specific test when compared with the CFT. A total of 209 horse sera obtained from Central Mongolia were examined with the GST-BC48 ELISA and 46.4% (97/209) were found to be seropositive for B. caballi, suggesting that the GST-BC48 ELISA can be successfully used for both quarantine and epidemiological studies.

MeSH terms

  • Animals
  • Antigens, Protozoan / immunology*
  • Babesia / isolation & purification*
  • Babesiosis / diagnosis*
  • Cross Reactions
  • Enzyme-Linked Immunosorbent Assay / veterinary*
  • Horse Diseases / parasitology*
  • Horses
  • Molecular Weight
  • Protozoan Proteins / immunology*
  • Recombinant Proteins / immunology

Substances

  • Antigens, Protozoan
  • Protozoan Proteins
  • Recombinant Proteins
  • rhoptry-associated protein-1, Babesia