The detection of a specific antibody response can provide indirect support for infection/disease. Submitting acute and convalescent (paired) serum samples are often critical for meaningful interpretation of titers. For most diseases paired serum samples should, on average, be collected 2-4 weeks apart. The presence of maternal antibody in animals less than six months of age and a history of vaccination can complicate interpretation.
False negative results can occur when testing early in infection.
Contaminated or hemolyzed sera can significantly affect results leading to false positive or false negative results.
Samples with moderate to severe levels of hemolysis will be rejected.
Samples collected prior to colostrum intake are critical for diagnosis of in utero infections.
Sample Processing:
Collect blood in a red top tube. Label the samples (animal ID and corresponding sample number from the submission form). Label acute or convalescent, if applicable.
Allow the sample to clot at room temperature.
Note: Processing too quickly and delaying separation of the serum from the clot can increase the amounts of cellular products and degree of hemolysis, potentially affecting test results.
Centrifuge the sample at 1000-1300 x g for 10 minutes.
Remove the serum into a clean tube (no additives). Avoid transfer of any cellular elements.
Maintain the sample at 4˚C. For best results, submit the sample to be received by the laboratory within 72 hours of collection.
Package the sample for shipping. Include a submission form with the samples. Record any pertinent sample or case history information to help with the interpretation of results.
Transport sample on ice pack. Avoid freeze-thaw cycles.
>1 ml of sera is ideal to ensure adequate sample for all testing requested and allows for repeat or follow-up testing if needed.