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Preparation of Ehrlichia ruminantium challenge material for quantifiable and reproducible challenge in mice and sheep

Kelly A Brayton1, Nicola E Collins, Francina van Strijp

  • 1Molecular Biology Section, Onderstepoort Veterinary Institute, Onderstepoort 0110, South Africa. kbrayton@vetmed.wsu.edu

Veterinary Parasitology
|February 13, 2003
PubMed

Insights

Optimizing challenge material for Ehrlichia ruminantium (heartwater) studies in mice is crucial. Mouse spleen homogenates with SPG cryoprotectant offer reproducible challenges, guiding vaccine development.

Area of Science:

  • Veterinary Microbiology
  • Immunology
  • Pathogen Research

Background:

  • Heartwater, caused by Ehrlichia ruminantium, is a tick-borne disease affecting cattle.
  • The obligate intracellular nature of E. ruminantium complicates obtaining sufficient challenge material.
  • Reproducible challenge models are essential for evaluating vaccine candidates, particularly in murine systems.

Purpose of the Study:

  • To optimize parameters for reproducible Ehrlichia ruminantium challenge material in murine models.
  • To compare cryoprotectants and sources of virulent E. ruminantium.
  • To investigate practical factors influencing challenge experiment reproducibility.

Main Methods:

  • Comparison of two cryoprotectants: buffered lactose peptone (BLP) and sucrose-potassium-glutamate (SPG).
  • Evaluation of two virulent E. ruminantium sources: infected bovine endothelial cultures and infected mouse spleen homogenates.
  • Assessment of challenge material delivery time, duration of immunity, and challenge dose effects.

Main Results:

  • Infected mouse spleen homogenates yielded more reproducible challenges than tissue culture material.
  • SPG proved superior to BLP as a cryoprotectant.
  • Challenge material efficacy decreased after 20 minutes post-thawing.
  • Syngeneic material was not essential for murine challenges.
  • Balb/c mice exhibited higher sensitivity to E. ruminantium challenge than C57BL/6J mice.
  • Optimal challenge dose should not exceed 10 LD(50)s.

Conclusions:

  • Standardized protocols using mouse spleen homogenates and SPG cryoprotection enhance reproducibility in E. ruminantium challenge studies.
  • Understanding these parameters is vital for accurate vaccine efficacy assessment in murine models.
  • Further research can refine the use of mice for titrating challenge material for sheep experiments.

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