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幽灵猎手——一种基于蛋白质免疫印迹法的平板检测方法,用于解决布鲁氏菌病血清学检测结果假阳性问题

Ghostbuster-A Western Blot-Based Panel Method to Resolve False-Positive Brucellosis Serology Test Results.

作者信息

Bányász Borbála, Antal József, Dénes Béla

机构信息

Institute of Isotopes Co., Ltd., 1121 Budapest, Hungary.

Omixon Biocomputing Ltd., 1117 Budapest, Hungary.

出版信息

Microorganisms. 2025 Mar 3;13(3):574. doi: 10.3390/microorganisms13030574.

Abstract

False-positive serologic results (FPSRs) of brucellosis occur from time to time in various livestock with all the consequences (quarantine, compulsory slaughter, etc.) that follow true-positive laboratory results. A method based on the Polyacrylamide Gel Electrophoresis/Western Blot of a protein panel for resolving the FPSRs in the diagnosis of brucellosis was developed. Within the context of limited positive serum sample availability in Europe, the method successfully discriminates -positive sera from samples containing antibodies raised against infections caused by other Gram-negative bacteria causing FPSRs. An average CV% of 1.36 was determined for both repeatability and reproducibility for the whole separation mw range, and the test achieved 1.00 Diagnostic Sensitivity and 1.00 Diagnostic Specificity. The method with pre-prepared WB panels provides a rapid (less than 3 h), easily standardizable, and validatable alternative to existing confirmation methods. The whole WB process of the proteins and the subsequent densitometry can be accomplished with commercially available equipment, ready-to-use reagents, and open-source software, providing cost-effectiveness. The results of this study could attract broader attention, since molecular species in the 35.0-75.0 kDa range can serve as antigens in serology and the same fraction can be considered in the development of synthetic vaccines.

摘要

布鲁氏菌病的假阳性血清学结果(FPSRs)在各种家畜中时有发生,随之而来的是与真阳性实验室结果相同的所有后果(检疫、强制屠宰等)。开发了一种基于蛋白质组聚丙烯酰胺凝胶电泳/蛋白质免疫印迹法的方法,用于解决布鲁氏菌病诊断中的FPSRs问题。在欧洲阳性血清样本有限的情况下,该方法成功地将阳性血清与含有针对其他导致FPSRs的革兰氏阴性菌感染产生的抗体的样本区分开来。对于整个分离分子量范围,重复性和再现性的平均变异系数(CV%)均为1.36,该检测的诊断敏感性为1.00,诊断特异性为1.00。带有预制蛋白质免疫印迹板的方法为现有确证方法提供了一种快速(少于3小时)、易于标准化和可验证的替代方法。蛋白质的整个蛋白质免疫印迹过程以及随后的光密度测定可以使用商用设备、即用型试剂和开源软件完成,具有成本效益。这项研究的结果可能会引起更广泛的关注,因为35.0 - 75.0 kDa范围内的分子物种可作为血清学中的抗原,并且在合成疫苗的开发中可以考虑相同的组分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c51d/11944415/f0f1126f0272/microorganisms-13-00574-g001.jpg

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