State Key Laboratory for Animal Disease Control and Prevention, African Swine Fever Regional Laboratory of China (Lanzhou), Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu, China.
Jiangsu Co-Innovation Center for the Prevention and Control of Important Animal Infectious Disease and Zoonosis, Yangzhou University, Yangzhou, Jiangsu, China.
J Clin Microbiol. 2024 Oct 16;62(10):e0046324. doi: 10.1128/jcm.00463-24. Epub 2024 Sep 5.
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.
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.
血清学检测抗体的方法对传染病的诊断和控制起到了重要作用。非洲猪瘟是家猪和野猪最具破坏性的传染病,近年来严重威胁着全球的养猪业。在这里,我们开发了一种基于荧光素酶系统的快速、简单和灵敏的免疫分析方法,用于检测抗非洲猪瘟病毒(ASFV)的 IgG 抗体。在该测定中,ASFV 的 p30 蛋白与纳米荧光素酶的 LgBiT 和 SmBiT 亚基发生基因融合,作为融合探针用于特异性抗体。探针的靶标结合导致功能型纳米荧光素酶的重新组装,进一步催化生物发光反应。设计并研究了 LgBiT 和 SmBiT-p30 融合传感器的不同取向,发现 N-LgBiT/p30 和 N-SmBiT/p30 是在存在特异性抗体时用于重新构建活性纳米荧光素酶的有前途的传感器对。经过优化,该荧光素酶互补测定法对 ASFV 抗体的检测具有很高的灵敏度和特异性。通过检测血清的系列稀释液,该测定法的分析灵敏度比阻断酶联免疫吸附测定(ELISA)高 16 倍,并且与其他猪病原体没有交叉反应。在临床样本中的结果表明,其性能与商业 ELISA 试剂盒高度一致,符合率为 98.19%。该测定法简单易用,为临床应用中 ASFV 抗体的测量提供了更灵活高效的方法。
本研究涉及用于抗体检测的均相荧光素酶分析。设计了用于检测 ASFV 抗体的分裂纳米荧光素酶生物传感器。该传感器平台能够灵敏且特异性地检测抗体。荧光素酶分析简单、快速且易于使用。