Peric T, Comin A, Corazzin M, Montillo M, Prandi A
Dipartimento di Scienze Agroalimentari, Ambientali e Animali, DI4A, Università degli Studi di Udine, Via delle Scienze 206, 33100 Udine, Italy.
Laboratorij za vede o okolju in življenju, Univerza v Novi Gorici, Vipavska 13, 5000 Nova Gorica, Slovenia.
Heliyon. 2020 Oct 16;6(10):e05230. doi: 10.1016/j.heliyon.2020.e05230. eCollection 2020 Oct.
Radioimmunoassay (RIA) methods have always represented a technique of choice for the determination of steroids in biological samples. The Amplified Luminescent Proximity Homogenous Assay-Linked Immunosorbent Assay (AlphaLISA) is now emerging as the new-generation immunoassay technology that does not require washing/separation steps. The aim of this study was to adapt the Perkin-Elmer's AlphaLISA kit for wool cortisol and compare it with a RIA wool cortisol assay. Wool from lambs, 35 at birth (A0) and 54 at two months old (A2), was collected and each extract was evaluated for wool cortisol concentrations (HCC) both by RIA and AlphaLISA immunoassay. The two methods showed good precision, sensitivity and specificity for determining HCC. Both methods were able to detect significant differences between the high and the low HCC assessed in lambs at A0 and A2 ( < 0.01). The HCC assessed with RIA were significantly higher than those assessed with AlphaLISA ( < 0.01). Moreover, the correlation between HCC measured using the AlphaLISA and RIA methods was strong ( = 0.878). The regression analyses show a constant and not proportional error. This could be due to the diversity in the dosage steps and to the diversity of the molecules used in the two methods. Results support the validity of using AlphaLISA as an alternative method to RIA for the quantification of cortisol in sheep wool and considering the performances showed it has a great potential to be further applied as an excellent tool to evaluate HCC in samples derived from animal species.
放射免疫分析(RIA)方法一直是测定生物样品中类固醇的首选技术。放大发光邻近均相分析-酶联免疫吸附测定(AlphaLISA)目前正作为一种无需洗涤/分离步骤的新一代免疫分析技术崭露头角。本研究的目的是使珀金埃尔默公司的AlphaLISA试剂盒适用于羊毛皮质醇检测,并将其与RIA羊毛皮质醇检测方法进行比较。收集了出生时35只(A0)和两个月大时54只(A2)羔羊的羊毛,对每份提取物分别采用RIA和AlphaLISA免疫分析法评估羊毛皮质醇浓度(HCC)。两种方法在测定HCC时均显示出良好的精密度、灵敏度和特异性。两种方法都能够检测出A0和A2羔羊中高HCC和低HCC之间的显著差异(<0.01)。用RIA评估的HCC显著高于用AlphaLISA评估的HCC(<0.01)。此外,使用AlphaLISA和RIA方法测得的HCC之间的相关性很强(=0.878)。回归分析显示误差恒定但不成比例。这可能是由于两种方法在剂量步骤上的差异以及所使用分子的差异。结果支持将AlphaLISA作为RIA的替代方法用于定量绵羊羊毛中的皮质醇,并且考虑到其性能表现,它有很大潜力进一步作为评估动物物种来源样品中HCC的优秀工具加以应用。