An immunoassay based on bioluminescent sensors for rapid detection of African swine fever virus antibodies.

IF 6.1 2区 医学 Q1 MICROBIOLOGY Journal of Clinical Microbiology Pub Date : 2024-10-16 Epub Date: 2024-09-05 DOI:10.1128/jcm.00463-24
Zhonghui Zhang, Jinming Wang, Qingli Niu, Guiquan Guan, Hong Yin, Jifei Yang
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Abstract

Serological assays for antibody detection have contributed significantly to the diagnosis and control of infectious diseases. African swine fever is the most devastating infectious disease of domestic pigs and wild boars, severely threatening the global pig industry in recent years. Here, we developed a rapid, simple, and sensitive immunoassay based on the split-luciferase system to detect IgG antibodies against African swine fever virus (ASFV). In this assay, the p30 protein of ASFV was genetically coupled to the LgBiT and SmBiT subunits of nanoluciferase, which were used as fusion probes for specific antibodies. Target engagement of the probes results in the reconstitution of a functional nanoluciferase, which further catalyzes bioluminescent reactions. Different orientations of the LgBiT and SmBiT-p30 fusion sensors were designed and investigated, and N-LgBiT/p30 and N-SmBiT/p30 were identified as a promising sensor pair for reforming active nanoluciferase in the presence of specific antibodies. After optimization, this split-luciferase complementation assay showed high sensitivity and specificity for the detection of ASFV antibodies. The analytical sensitivity of the assay was 16 times greater than that of the blocking enzyme-linked immunosorbent assay (ELISA) by the detection of serial dilutions of serum, and no cross-reaction was observed with other swine pathogens. As demonstrated in clinical samples, its performance is highly consistent with that of a commercial ELISA kit, with a concordance rate of 98.19%. This assay is simple and easy to perform, providing a more flexible and efficient approach for the measurement of ASFV antibodies in clinical applications.

Importance: The study is about a homogeneous split-luciferase assay for antibody detection. Split nanoluciferase biosensors for the detection of ASFV antibodies were designed. This sensor platform enables the sensitive and specific detection of antibodies. The split-luciferase assay is simple, rapid, and easy to use.

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基于生物发光传感器的免疫测定法,用于快速检测非洲猪瘟病毒抗体。
用于检测抗体的血清学检测方法为诊断和控制传染病做出了巨大贡献。非洲猪瘟是家猪和野猪中最具毁灭性的传染病,近年来严重威胁着全球养猪业。在此,我们开发了一种基于分裂荧光素酶系统的快速、简单、灵敏的免疫测定方法,用于检测非洲猪瘟病毒(ASFV)的 IgG 抗体。在这种检测方法中,ASFV 的 p30 蛋白与纳米荧光素酶的 LgBiT 和 SmBiT 亚基通过基因耦合,用作特异性抗体的融合探针。探针的靶向啮合导致功能性纳米荧光素酶的重组,从而进一步催化生物发光反应。我们设计并研究了 LgBiT 和 SmBiT-p30 融合探针的不同取向,并确定 N-LgBiT/p30 和 N-SmBiT/p30 是在特异性抗体存在下重组活性纳米荧光素酶的理想探针对。经过优化后,这种分裂荧光素酶互补测定在检测 ASFV 抗体方面显示出了高灵敏度和特异性。通过检测连续稀释的血清,该测定的分析灵敏度是阻断酶联免疫吸附测定(ELISA)的 16 倍,而且没有观察到与其他猪病原体的交叉反应。在临床样本中证明,其性能与商业 ELISA 试剂盒高度一致,吻合率高达 98.19%。该检测方法简便易行,为临床应用中 ASFV 抗体的测定提供了一种更灵活、更有效的方法:重要意义:本研究涉及一种用于抗体检测的均相裂解荧光素酶测定法。该研究设计了用于检测 ASFV 抗体的分离式纳米荧光素酶生物传感器。该传感器平台能够灵敏、特异地检测抗体。分裂荧光素酶检测法简单、快速、易于使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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