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Bovine leptospirosis: serological findings in aborting cows
The Veterinary Record
|February 20, 1982
Summary
Microscopic agglutination (MA) testing for leptospirosis in aborted fetuses shows limited diagnostic value. Many cows with leptospiral abortions have low antibody titres or no detectable antibodies, impacting accurate diagnosis.
Area of Science:
- Veterinary Medicine
- Immunology
- Bacteriology
Background:
- Leptospirosis is a significant cause of abortion in cattle.
- Accurate diagnosis of leptospiral abortion is crucial for herd management and disease control.
- Microscopic agglutination (MA) testing is a common method for detecting antibodies against Leptospira.
Purpose of the Study:
- To evaluate the diagnostic utility of antibody titres determined by the microscopic agglutination (MA) test in cows experiencing abortions.
- To compare the effectiveness of MA testing with complement fixation and plate agglutination tests for diagnosing leptospiral abortion.
Main Methods:
- Antibody titres were determined using the microscopic agglutination (MA) test.
- The study involved 149 cows that aborted leptospire-infected fetuses and 156 cows that aborted fetuses not apparently infected with leptospires.
- Complement fixation and plate agglutination tests were also assessed.
Main Results:
- Differences in MA titre distribution were observed between cows with infected and non-infected fetuses, but these differences had limited diagnostic value.
- 81.2% of cows with titres ≥ 1:1000 had infected fetuses, but these represented only 46.3% of all cows with leptospiral abortions.
- 22.8% of cows that aborted infected fetuses had no detectable antibodies.
- MA test was more valuable than complement fixation and plate agglutination tests.
Conclusions:
- The microscopic agglutination (MA) test has limited value in diagnosing leptospiral abortion in cattle due to variations in antibody titres.
- A significant percentage of cows with leptospiral abortions exhibit low or undetectable antibody titres, complicating diagnosis.
- MA testing is superior to complement fixation and plate agglutination tests for this diagnostic purpose.