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Kinetics of antibody response to Ehrlichia canis immunoreactive proteins

Jere W McBride1, Richard E Corstvet, Steven D Gaunt

  • 1Department of Pathology, Sealy Center for Vaccine Development, and Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, Texas 77555-0609, USA. jemcbride@utmb.edu

Infection and Immunity
|April 22, 2003
PubMed

Insights

This study tracked antibody responses in dogs infected with Ehrlichia canis, identifying key proteins like p28, gp140, and gp200 that elicit immune reactions. Early recognition of certain antigens suggests their importance in canine ehrlichiosis diagnosis and vaccines.

Area of Science:

  • Veterinary Immunology
  • Molecular Biology
  • Infectious Diseases

Background:

  • Ehrlichia canis causes canine ehrlichiosis, a significant tick-borne disease.
  • Key immunoreactive proteins, including p28, gp140, and gp200, are known targets in canine ehrlichiosis.
  • The kinetics of antibody response to these antigens are not well understood.

Purpose of the Study:

  • To investigate the antibody response kinetics to Ehrlichia canis antigens in experimentally infected dogs.
  • To identify immunodominant E. canis antigens recognized during acute and convalescent infection phases.
  • To evaluate the potential of recombinant proteins (p28, gp140, gp200) as diagnostic or vaccine candidates.

Main Methods:

  • Experimental infection of dogs with E. canis.
  • Monitoring of acute-phase serum antibody responses over six weeks.
  • Analysis of antibody response to whole-cell lysates and recombinant proteins (p28, gp140, gp200).
  • Identification of major immunoreactive antigens based on intensity and quantity.

Main Results:

  • A T-helper 1-type immune response, characterized by IgG2 antibodies, was observed in most dogs.
  • Early infection recognized 19-, 37-, 75-, and 140-kDa proteins as major antigens.
  • Later infection identified 28-, 47-, 95-kDa proteins and the 200-kDa glycoprotein.
  • All dogs developed antibodies against recombinant gp140, gp200, and p28 by the convalescent phase.

Conclusions:

  • The study elucidates the antibody response kinetics to E. canis antigens in dogs.
  • Identified major immunoreactive proteins are immunodominant, with some antigens showing early dominance.
  • Recombinant p28, gp140, and gp200 are promising candidates for immunodiagnostics and vaccines against canine ehrlichiosis.

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