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p54-Fc-Labeled Gold Nanoparticle-Based Lateral Flow Strip-Assisted Portable Devices for Rapid and Quantitative Point-of-Care Detection of ASFV Antibodies

文献类型： 外文期刊

作者： Yang, Yang 1 ; Li, Yuhao 1 ; Wang, Ziyang 1 ; Tong, Minglong 2 ; Zhu, Pengcheng 2 ; Deng, Juanxian 3 ; Li, Zongjie 1 ; Liu, Ke 1 ; Li, Beibei 1 ; Shao, Donghua 1 ; Zhou, Zhongren 4 ; Qiu, Yafeng 1 ; Ma, Zhiyong 1 ; Wei, Jianchao 1 ;

作者机构： 1.Chinese Acad Agr Sci, Shanghai Vet Res Inst, Shanghai 200241, Peoples R China

2.Yixing Customs, Yixing 214200, Peoples R China

3.Nanjing Customs, Nanjing 210001, Peoples R China

4.Shanghai Quicking Biotech Co, Shanghai 201314, Peoples R China

关键词： immunochromatographic (IC) test; SPA; Fc fusion protein; ASFV; field rapid detection

期刊名称：BIOSENSORS-BASEL （ 影响因子：5.6； 五年影响因子：5.7 ）

ISSN：

年卷期： 2025 年 15 卷 1 期

页码：

收录情况： SCI

摘要： In this study, a novel rapid immunochromatographic (IC) test for African swine fever virus (ASFV) antibodies is presented. An immunochromatographic test (IC) is a detection technique that combines membrane chromatography with immunolabeling. This approach saves time for antibody preparation, resulting in a shorter production cycle. p54 is an important structural protein of African swine fever, and an ideal protein for serotype diagnosis. Gold nanoparticles are attached to the ASFV p54-Fc fusion protein, and the ASFV-specific antigen p54 and Staphylococcus aureus protein A (SPA) are labeled on a nitrocellulose membrane, at positions T and C, respectively. We developed a SPA double sandwich IC test strip, and assessed its feasibility using ASFV p54 and p54-Fc fusion proteins as antigens. ASFV p54 and p54-Fc fusion proteins were expressed and purified. A sandwich cross-flow detection method for p54, which is the primary structural protein of ASFV, was established, using colloidal gold conjugation. Our method can detect ASFV antibodies in field serum samples in about 15 min using a portable colloidal gold detector, demonstrating high specificity and sensitivity (1:320), and the coincidence rate was 98% using a commercial ELISA kit. The dilution of the serum sample can be determined by substituting the absorbance (T-line) interpreted by portable devices into the calibration curve function formula of an African swine fever virus standard serum. In summary, our method is rapid, cost-effective, precise, and highly selective. Additionally, it introduces a new approach for constructing IC test strips using SPA protein without antibody preparation, making it a reliable on-site antibody test for ASFV.

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