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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
Abstract:
The causative agent of heartwater, Ehrlichia ruminantium, is a tick-transmitted pathogen that infects bovine endothelial cells. Due to the obligate intracellular nature of this organism obtaining pure material in sufficient quantities for challenge studies is difficult. A murine model is frequently used to study potential vaccine candidates but giving reproducible challenges in this model for heartwater has always been problematic. We have therefore performed a series of experiments to optimize the parameters governing the reproducibility of challenge material. Two cryoprotectants were compared for the preparation of challenge material, buffered lactose peptone (BLP) and sucrose-potassium-glutamate (SPG). In addition two sources of virulent E. ruminantium were used, infected bovine endothelial cultures and infected mouse spleen homogenates. We also examined practical parameters affecting the reproducibility of challenge experiments: the time it takes to deliver the challenge material, the length of time a mouse remains immune to E. ruminantium challenge, and the effect of a given challenge dose. Finally, we performed a pilot study to determine whether mice could be used to titrate challenge material to be used for experiments in sheep. We found that: (a) E. ruminantium-infected mouse spleen homogenate provides more reproducible challenges than tissue culture material; (b) SPG is a better cryoprotectant than BLP; (c) challenge material should be used within 20min of thawing; (d) it is not essential to use syngeneic material for murine challenge experiments; (e) Balb/c mice are more sensitive to E. ruminantium challenge than C57BL/6J mice; (f) mice immunized by infection and treatment for use as positive immune controls should be challenged within 3 months of immunization; and (g) mice should be challenged with a dose not exceeding 10 LD(50)s.
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.