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Mouse model for central nervous system Neospora caninum infections
D S Lindsay1, S D Lenz, R A Cole
1Department of Pathobiology, College of Veterinary Medicine, Auburn University, Alabama 36849-5519, USA.
The Journal of Parasitology
|April 1, 1995
Summary
A new mouse model for Neospora caninum infection was developed without methylprednisolone acetate (MPA) treatment. Inbred BALB/c mice infected with the NC-1 strain showed central nervous system neosporosis, unlike other groups.
Area of Science:
- Veterinary Parasitology
- Immunology
- Infectious Diseases
Background:
- Neospora caninum causes significant disease in dogs and livestock.
- Current rodent models of neosporosis require immunosuppression with methylprednisolone acetate (MPA).
Purpose of the Study:
- To develop a novel inbred BALB/c mouse model for Neospora caninum infection without MPA treatment.
- To evaluate the susceptibility of BALB/c and HSD:ICR mice to different N. caninum strains.
Main Methods:
- Subcutaneous inoculation of inbred BALB/c mice and HSD:ICR mice with N. caninum tachyzoites (NC-1 and NC-3 strains).
- Monitoring of clinical signs, mortality, and brain lesions in inoculated mice.
- Comparison of infection outcomes between mouse strains and N. caninum strains.
Main Results:
- BALB/c mice inoculated with the NC-1 strain exhibited mortality and developed central nervous system neosporosis without MPA treatment.
- BALB/c mice inoculated with the NC-3 strain or HSD:ICR mice with either strain did not develop clinical neosporosis or die.
- Significantly more BALB/c mice infected with the NC-1 strain showed brain lesions compared to other inoculated groups.
Conclusions:
- The inbred BALB/c mouse model is susceptible to N. caninum (NC-1 strain) induced central nervous system neosporosis without immunosuppression.
- This model offers a valuable tool for studying neosporosis pathogenesis and evaluating therapeutic strategies.
- Strain and parasite isolate selection are critical factors in establishing experimental neosporosis models.