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基于主要免疫原 VP6 的鼠轮状病毒 EDIM 的高敏感 ELISA 血清学检测方法。

Highly sensitive ELISA for the serological detection of murine rotavirus EDIM based on its major immunogen VP6.

机构信息

Institute for Bioanalytical Chemistry, Faculty of Chemistry and Mineralogy, Universität Leipzig, Leipzig, Germany; GVG Diagnostics GmbH, Leipzig, Germany.

Institute of Virology, Faculty of Veterinary Medicine, Universität Leipzig, Leipzig, Germany.

出版信息

J Virol Methods. 2018 Dec;262:72-78. doi: 10.1016/j.jviromet.2018.07.016. Epub 2018 Aug 23.

Abstract

Precise health monitoring of laboratory animals is a critical factor for surveillance and accuracy of animal experiments. Rotavirus epizootic diarrhea of infant mice (EDIM) leads to infections in mice that can influence animal studies, e.g., by altering the intestinal physiology. Thus, the aim of this study was establishing a highly sensitive and specific ELISA for the serological detection of EDIM infections in rodents. First, virus proteins were separated by SDS-PAGE and immunogenic proteins were visualized by immunoblotting and identified after in-gel digestion by tandem mass spectrometry. Subsequently, the major immunogen VP6 (virus protein 6) was expressed in Escherichia coli in high yields, purified by affinity chromatography, and used to establish an indirect ELISA. The diagnostic sensitivity and specificity were both above 99 % and the selectivity better than 98.7 % for animals infected by other pathogens listed by the Federation of Laboratory Animal Science Associations. Importantly, the Strep-rVP6-His-ELISA was more sensitive than a commercial virus-based ELISA and is a time- and cost-efficient complement to EDIM-specific immune-fluorescence assays. In conclusion, the assay can improve health monitoring by reducing the risk of missed EDIM infections in animal housing facilities, thereby improving animal welfare, reliability of animal studies, and protection of precious mice breeds.

摘要

精确的实验动物健康监测是动物实验监测和准确性的关键因素。轮状病毒幼鼠爆发性腹泻(EDIM)会导致感染,从而影响动物研究,例如改变肠道生理机能。因此,本研究旨在建立一种高灵敏度和特异性的 ELISA 方法,用于检测啮齿动物的 EDIM 感染。首先,通过 SDS-PAGE 分离病毒蛋白,通过免疫印迹法观察免疫原性蛋白,并在胶内消化后通过串联质谱法进行鉴定。随后,在大肠杆菌中高效表达主要免疫原 VP6(病毒蛋白 6),通过亲和层析进行纯化,并用于建立间接 ELISA。该诊断方法的敏感性和特异性均高于 99%,对其他病原体的选择性优于 98.7%,这些病原体已被实验室动物科学协会联合会列出。重要的是,Strep-rVP6-His-ELISA 比商品化的基于病毒的 ELISA 更敏感,是 EDIM 特异性免疫荧光检测的一种高效、省时的补充方法。总之,该方法可通过降低动物饲养设施中 EDIM 感染漏检的风险来改善健康监测,从而提高动物福利、动物研究的可靠性和珍贵鼠种的保护。

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