Technical note: Validation of an in-house bovine serum enzyme immunoassay for progesterone measurement

• Published in: Journal of dairy science 2021-02, Vol.104 (2), p.2455-2462
• Main Authors: Nadalin, A., Denis-Robichaud, J., Madureira, A.M.L., Burnett, T.A., Bauer, J., Vasconcelos, J.L.M., Pohler, K.G., Crespilho, A.M., Cerri, R.L.A.
• Format: Article
• Language: English
• Subjects: Animals; bovine; Cattle - blood; ELISA; Female; Immunoenzyme Techniques - methods; Immunoenzyme Techniques - veterinary; progesterone; Progesterone - blood; serum; validation
• ISSN: 0022-0302; 1525-3198
• DOI: 10.3168/jds.2020-18824

Measuring circulating progesterone (P4) of dairy cows is a key component of many research studies dealing with basic and applied reproduction physiology. The gold standard in dairy cows for the measurement of P4 in serum is radioimmunoassay (RIA), but it generates radioactive waste and requires licensed facilities. The purpose of this study was to develop and validate an in-house competitive enzyme immunoassay (EIA) to measure the P4 concentration in serum of dairy cattle. The secondary objective was to validate a commercial EIA. In the present study, a competitive EIA was developed using commercially available antibodies and conjugates. Ninety-six well microtiter plates were coated with the secondary antibody and incubated overnight. Following a washing step, the wells were blocked using the primary antibody. Serum samples were prepared by first extracting P4 using petroleum ether, then diluted in working conjugate solution. Samples were pipetted into the coated and blocked plates, then the matching HRP conjugate label (P4-3-HRP, East Coast Bio, North Berwick, ME) was added. The plates were incubated for 2 h, then washed. The substrate solution was added, and the plate was incubated up to 1 h at room temperature in the dark until a blue color had developed. A stop solution was added, and the optical density measured on a microplate reader was set at 450 nm. The binding proportion was calculated by a visible spectrum absorbance reader, and the amount of P4 was calculated using a log-logit regression line. The commercial EIA was executed as suggested by the manufacturer. The validation of the in-house EIA was done by calculating the inter- and intraassay coefficients of variation (CV) and evaluating the parallelism of diluted samples. The results from the in-house and commercial EIA were also compared with the ones from the RIA graphically (scatterplots and Bland-Altman plots) and statistically, using the Spearman correlation coefficient (r) and the Cohen's kappa statistics using a threshold of 1.0 ng/mL (κ). For the in-house EIA, the intraassay CV were all