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Development of a flow cytometric immunoassay for recombinant bovine somatotropin-induced antibodies in serum of dairy cows

机译:重组牛生长激素诱导奶牛血清中抗体的流式细胞仪免疫分析方法的建立

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Administration of recombinant bovine somatotropin (rbST) to enhance milk production in dairy cows is banned within the European Union. Therefore, methods for pinpointing rbST abuse are required. Due to the problematic detection of rbST itself in serum, methods are also focused on detecting changes in rbST-related biomarkers. In this study, a fast and easy-to-perform microsphere-based flow cytometric immunoassay (FCIA) for detection of rbST-induced antibodies in serum was developed. Until now, detection of rbST-induced antibodies was also problematic due to non-specific binding of serum proteins resulting in a high rate of false positive results. Therefore, five different sample preparation methods, i.e. dilution, octanoic acid precipitation, filtration, protein G purification, and a previously described generic FCIA sample preparation were critically compared to overcome non-specific binding to the microspheres. Only the generic FCIA sample pretreatment was effective in reducing non-specific binding. As a result, an absolute decision level for detecting rbST antibodies in serum of dairy cows was determined and its applicability was demonstrated. In accordance with biological expectations from literature, rbST antibodies were induced in three out of four rbST-treated dairy cows. These rbST-induced antibodies were successfully detected for up to 4weeks after the last rbST treatment, whereas no false positive results were obtained for 27 untreated dairy cows. This is the first method, able to overcome the interference of serum proteins and therefore, can be applied with high confidence for screening unknown herds of cattle for rbST antibodies, an important biomarker for pinpointing at rbST abuse in cattle.
机译:欧盟内部禁止使用重组牛生长激素(rbST)来提高奶牛的产奶量。因此,需要用于确定rbST滥用的方法。由于在血清中检测rbST本身存在问题,因此方法也集中于检测rbST相关生物标记的变化。在这项研究中,开发了一种快速,易于执行的基于微球的流式细胞术免疫分析(FCIA),用于检测血清中rbST诱导的抗体。到目前为止,由于血清蛋白的非特异性结合,导致rbST诱导的抗体的检测还存在问题,从而导致假阳性结果的发生率很高。因此,严格地比较了五种不同的样品制备方法,即稀释,辛酸沉淀,过滤,蛋白G纯化和先前描述的通用FCIA样品制备,以克服与微球的非特异性结合。仅通用FCIA样品预处理可有效减少非特异性结合。结果,确定了用于检测奶牛血清中的rbST抗体的绝对决定水平,并证明了其适用性。根据文献的生物学期望,在四只经rbST处理的奶牛中,有三只被诱导产生rbST抗体。在最后一次rbST处理后长达4周内成功检测到了这些rbST诱导的抗体,而对于27例未经处理的奶牛,未获得假阳性结果。这是第一种能够克服血清蛋白干扰的方法,因此可以高度可靠地用于筛查未知牛群中的rbST抗体,rbST抗体是确定牛rbST滥用的重要生物标记。

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