数字农科院2.0

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

文献类型: 外文期刊

作者: Zhang, Zhonghui;Wang, Jinming;Niu, Qingli;Guan, Guiquan;Yin, Hong;Yang, Jifei

作者机构:

关键词: luminescent biosensor;African swine fever;antibodies;split-luciferase complementation assay;point-of-care test

期刊名称: JOURNAL OF CLINICAL MICROBIOLOGY

ISSN: 0095-1137

年卷期: 2024 年

页码:

收录情况: SCIE(2024版)

摘要: 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.IMPORTANCEThe 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. 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.

分类号:

  • 相关文献

[1]Antibody-Dependent Cellular Cytotoxicity Elicited by the Antibodies Against the E120R Protein of African Swine Fever Virus. Shengmei Chen,Jing Lan,Zhanhao Lu,Jia Li,Caoyuan Ma,Rui Luo,Qiang Fu,Yuan Sun,Tao Wang,Hua Ji Qiu. 2025

[2]Development of a Ready-To-Use Bioluminescence Immunosensor for the One-Step Sensitive Detection of Antibodies Against African Swine Fever Virus. Zhonghui Zhang,Xuesai Li,Qingli Niu,Jinming Wang,Yanghe Liu,Dossêh Jean Apôtre Afayibo,Wenting Chen,Songlin Yang,Hong Yin,Guiquan Guan,Jifei Yang. 2025

[3]Expression, purification, and characterization of recombinant NS-1, the porcine parvovirus non-structural protein. Qi, Ting,Cui, Shang-jin.

[4]Synthesis of empty capsid-like particles of Asia I foot-and-mouth disease virus in insect cells and their immunogenicity in guinea pigs. Cao, Yimei,Lu, Zengjun,Sun, Jiachuan,Bai, Xingwen,Sun, Pu,Bao, Huifang,Chen, Yingli,Guo, Jianhong,Li, Dong,Liu, Xiangtao,Liu, Zaixin.

[5]GhWRKY40 Interacts with an Asparaginase GhAPD6 Involved in Fiber Development in Upland Cotton (Gossypium hirsutum L.). Sujun Zhang,Xiao Cai,Jingyan Wei,Haitao Wang,Cunjing Liu,Xinghe Li,Liyuan Tang,Xiaodong Zhou,Jianhong Zhang. 2024

[6]Half-antibody spur one-to-one recognition mechanism can function with chemical-staining technology for next-generation lateral flow immunoassay. Xu, Jingke,Zhou, Jing,Liu, Kai,Bu, Tong,Dou, Leina,Shu, Rui,Liu, Sijie,Wang, Shaochi,Yin, Xuechi,Zhang, Daohong,Zhang, Ruiling,Cheng, Jie,Wang, Jianlong. 2024

[7]CRISPR/Cas14a1–enabled point–of–care test for sensitive detection of dibutyl phthalate in the environment and foods. Yuan Zhao,Xiaofeng Hu,Xiaoqian Tang,Peiwu Li,Zhaowei Zhang. 2025

[8]Seroprevalence of Toxoplasma gondii and Neospora caninum in Tarim Red Deer (Cervus elaphus yarkandensis) from Xinjiang Province, Northwest China. Meng, Q. L.,Qiao, J.,Wang, W. S.,Chen, C. F.,Zhang, Z. C.,Cai, K. J.,Tian, Z. Z.,Yang, L. H.,Cai, X. P.,Tian, G. F.. 2012

[9]Immunogenicity and protective efficacy in monkeys of purified inactivated Vero-cell SARS vaccine. Qin, E,Shi, HY,Tang, L,Wang, C,Chang, GH,Ding, ZF,Zhao, K,Wang, J,Chen, Z,Yu, M,Si, BY,Liu, JY,Wu, DL,Cheng, XJ,Yang, BA,Peng, WM,Meng, QW,Liu, BH,Han, WG,Yin, XA,Duan, HY,Zhan, DW,Tian, L,Li, SL,Wu, JS,Tan, G,Li, Y,Li, YC,Liu, YG,Liu, H,Lv, FS,Zhang, Y,Kong, XG,Fan, BC,Jiang, T,Xu, SL,Wang, XM,Li, CW,Wu, XH,Deng, YQ,Zhao, M,Zhu, QY.

[10]Development of blocking ELISA for detection of antibodies against H9N2 avian influenza viruses. Li, Zejun.

[11]Protective efficacy of commercial Newcastle disease vaccines against challenge of goose origin virulent Newcastle disease virus in geese. Dai, Yabin,Liu, Mei,Li, Wenliang.

[12]Field testing of Schistosoma japonicum DNA vaccines in cattle in China. Shi, FH,Zhang, YB,Lin, JJ,Zuo, X,Shen, W,Cai, YM,Ye, P,Bickle, QD,Taylor, MG.

[13]Serological detection of bovine ephemeral fever virus using an indirect ELISA based on antigenic site G(1) expressed in Pichia pastoris. Qiu, Chang-Qing.

[14]Fusion of C3d with hemagglutinin enhances protective immunity against swine influenza virus. Li, Guo-Xin,Tian, Zhi-Jun,Yu, Hai,Jin, Yuan-Yuan,Hou, Shao-Hua,Zhou, Yan-Jun,Liu, Tian-Qiang,Hu, Shou-Ping,Tong, Guang-Zhi,Li, Guo-Xin,Tong, Guang-Zhi,Li, Guo-Xin,Yu, Hai,Zhou, Yan-Jun,Tong, Guang-Zhi.

[15]Laboratory and field evaluation of Schistosoma japonicum DNA vaccines in sheep and water buffalo in China. Shi, FH,Zhang, YB,Ye, P,Lin, JJ,Cai, YM,Shen, W,Bickle, QD,Taylor, MG.

[16]Screening of strain-specific Actinobacillus pleuropneumoniae genes using a combination method. Lei, Liancheng,Wang, Jiaqi,Lei, Liancheng,Du, Chongtiao,Yang, Peng,Xie, Fang,Ou, Pingyang,Han, Wenyu.

[17]Plasmid containing CpG oligodeoxynucleotides can augment the immune responses of pigs immunized with porcine reproductive and respiratory syndrome killed virus vaccine. Quan, Zhang,Qin, Zhai Guo,Zhen, Wang,Feng, Xue Zheng,Hong, Jia,Fei, Zhu Hong.

[18]Positive role for rApxIVN in the immune protection of pigs against infection by Actinobacillus pleuropneumoniae. Wang, Chunlai,Wang, Yong,Shao, Meili,Si, Wei,Liu, Huifang,Chang, Yuehong,Peng, Wei,Kong, Xiangang,Liu, Siguo,Shao, Meili.

[19]Immune response in guinea pigs vaccinated with DNA vaccine of foot-and-mouth disease virus O/China99. Guo, HC,Liu, ZX,Sun, SQ,Bao, HF,Chen, YL,Liu, XT,Xie, QG.

[20]Immunoassay of chemical contaminants in milk: A review. Xu Fei,Liu Yi-ming,Li Xiu-bo,Ren Kang,Yang Yu-ze,Guo Jiang-peng,Lu Yong-qiang,Ma Guang-peng. 2015

作者其他论文 更多>>