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Peer-reviewed veterinary case report

Investigating the use of protein saver cards for storage and subsequent detection of bovine anti-Brucella abortus smooth lipopolysaccharide antibodies and gamma interferon.

Journal:
Clinical and vaccine immunology : CVI
Year:
2013
Authors:
Duncombe, Lucy et al.
Affiliation:
Animal Health and Veterinary Laboratories Agency · United Kingdom

Plain-English summary

This study looked at a new way to collect and store blood samples from cows to help diagnose bovine brucellosis, a disease caused by the Brucella abortus bacteria. Researchers tested Protein Saver cards, which can hold blood serum and plasma samples, to see if they could reliably detect antibodies and a specific immune response in cows. They found that the results from samples stored on these cards were very similar to those from fresh samples, meaning they could be used interchangeably for testing. However, while the antibody levels in serum samples remained stable for up to 10 days at room temperature, the levels of a specific immune marker in plasma samples decreased over that same period. Overall, the Protein Saver cards showed promise for storing blood samples, but careful attention is needed for plasma samples over time.

Abstract

Brucella abortus, a smooth strain of the genus Brucella, is the causative agent of bovine brucellosis. To support the ongoing development of diagnostic tests for bovine brucellosis, the use of Protein Saver cards (Whatman) for bovine blood serum and plasma sample collection has been evaluated. These cards offer significant logistical and safety alternatives to transporting and storing liquid samples and may aid in diagnostic programs and validation studies. To evaluate the utility of these cards, 204 bovine blood serum samples from Brucella-infected and noninfected animals were stored on and eluted from the Protein Saver cards. Anti-Brucella smooth lipopolysaccharide (sLPS) antibody titers for the serum eluates were compared to those of the unprocessed original serum samples by indirect enzyme-linked immunosorbent assay (ELISA). The results showed a highly significant correlation between titers from the serum eluates and the unprocessed sera. Therefore, under these circumstances, serum eluates and unprocessed serum samples may be used interchangeably. Blood plasma from 113 mitogen-stimulated whole-blood samples was added to and eluted from the Protein Saver cards. The gamma interferon (IFN-γ) titers in the plasma eluates were compared to those of the unprocessed plasma samples obtained by IFN-γ ELISA. The results showed a significant correlation between the plasma eluates and the unprocessed plasma samples. To derive a signal in the plasma eluate, it was necessary to develop a novel and highly sensitive ELISA for the detection of IFN-γ. The serum samples stored on cards at room temperature over a 10-day period showed little variation in antibody titers. However, the plasma eluates showed a progressive loss of IFN-γ recovery over 10 days when stored at room temperature.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/23986318/