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用于快速检测多种动物中SARS-CoV-2暴露情况的数字免疫测定法。

Digital Immunoassay for Rapid Detection of SARS-CoV-2 exposure in a Broad Spectrum of Animals.

作者信息

Li Siyan, Wang Weijing, Liu Weinan, Chen Chi, Shepherd Skye, Yuan Fangfeng, Reinhart Jennifer M, Diel Diego G, Cunningham Brian T, Fang Ying

机构信息

Department of Pathobiology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

出版信息

IEEE Sens J. 2025 Jul 15;25(14):26599-26607. doi: 10.1109/jsen.2025.3575008. Epub 2025 Jun 4.

Abstract

The ability of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) to infect a wide-range of species raises significant concerns regarding both human-to-animal and animal-to-human transmission. There is an increasing demand for highly sensitive, rapid, and simple diagnostic assays capable of detecting viral infection across various species. In this study, we developed a biosensor assay based on a blocking ELISA (bELISA) immunoassay format. The assay employs a photonic crystal (PC) biosensor, gold-nanoparticle (AuNP) tags, SARS-CoV-2 nucleocapsid (N) protein, and specific anti-N monoclonal antibody (mAb) to detect antibody responses in animals exposed to SARS-CoV-2. Based on an evaluation of 162 cat serum samples with known antibody status, an optimal percentage of inhibition (PI) cut-off value of 0.5877 resulted in a diagnostic sensitivity of 97.80% and a diagnostic specificity of 98.67%. The assay demonstrated high repeatability with low variation coefficients across different conditions, ensuring consistent performance. Additionally, the assay successfully detected anti-N antibody responses in ferrets and deer as early as 14 days post-infection (DPI), and in cats infected with both Omicron (B.1.1.529) and B.1 D614G (B.1) variants as early as 7 DPI. These results highlight the assay's ability to detect infections early and reliably across species and its capability to identify multiple variants of SARS-CoV-2. This test platform provides an important tool for rapid field surveillance of SARS-CoV-2 infection across multiple species.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染多种物种的能力引发了对人传动物和动物传人传播的重大担忧。对能够检测跨物种病毒感染的高灵敏度、快速且简单的诊断检测方法的需求日益增加。在本研究中,我们基于阻断酶联免疫吸附测定(bELISA)免疫测定形式开发了一种生物传感器检测方法。该检测方法采用光子晶体(PC)生物传感器、金纳米颗粒(AuNP)标签、SARS-CoV-2核衣壳(N)蛋白和特异性抗N单克隆抗体(mAb)来检测暴露于SARS-CoV-2的动物中的抗体反应。基于对162份已知抗体状态的猫血清样本的评估,0.5877的最佳抑制百分比(PI)临界值导致诊断灵敏度为97.80%,诊断特异性为98.67%。该检测方法在不同条件下表现出高重复性和低变异系数,确保了一致的性能。此外,该检测方法最早在感染后14天(DPI)成功检测到雪貂和鹿中的抗N抗体反应,在感染奥密克戎(B.1.1.529)和B.1 D614G(B.1)变体的猫中最早在7 DPI检测到。这些结果突出了该检测方法跨物种早期可靠检测感染的能力及其识别SARS-CoV-2多种变体的能力。该测试平台为跨多个物种的SARS-CoV-2感染的快速现场监测提供了重要工具。

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