数字农科院2.0

A chemiluminescent magnetic microparticle immunoassay for the detection of antibody against African swine fever virus

文献类型： 外文期刊

作者： Shi, Zhengwang;Cao, Liyan;Luo, Juncong;Zhou, Gaijing;Zuo, Qingshan;Liu, XiangTao;Hu, Yonghao;Tian, Hong;Zheng, Haixue

作者机构：

关键词： Chemiluminescent magnetic microparticle immunoassay (CMIA);African swine fever virus (ASFV);p30 protein;Antibody detection;Serum

期刊名称： APPLIED MICROBIOLOGY AND BIOTECHNOLOGY

ISSN： 0175-7598

年卷期： 2023 年 107 卷 11 期

页码：

收录情况： SCIE（2023版） ; ; EI（2023版）

摘要： The p30 protein is abundantly expressed in the early stage of African swine fever virus (ASFV) infection. Thus, it is an ideal antigen candidate for serodiagnosis with the use of an immunoassay. In this study, a chemiluminescent magnetic microparticle immunoassay (CMIA) was developed for the detection of antibodies (Abs) against ASFV p30 protein in porcine serum. Purified p30 protein was coupled to magnetic beads, and the experimental conditions including concentration, temperature, incubation time, dilution ratio, buffers, and other relevant variables were evaluated and optimized. To evaluate the performance of the assay, a total of 178 pig serum samples (117 negative and 61 positive samples) were tested. According to receiver operator characteristic curve analysis, the cut-off value of the CMIA was 104,315 (area under the curve, 0.998; Youden's index, 0.974; 95% confidence interval: 99.45 to 100%). Sensitivity results showed that the dilution ratio of p30 Abs in ASFV-positive sera detected by the CMIA is much higher when compared to commercial blocking ELISA kit. Specificity testing showed that no cross-reactivity was observed with sera positive for other porcine disease viruses. The intraassay coefficient of variation (CV) was < 5%, and the interassay CV was < 10%. The p30-magnetic beads could be stored at 4 degrees C for more than 15 months without loss of activity. The kappa coefficient between CMIA and INGENASA blocking ELISA kit was 0.946, showing strong agreement. In conclusion, our method showed superiority with high sensitivity, specificity, reproducibility, and stability and potentialized its application in the development of a diagnostic kit for the detection of ASF in clinical samples. Key points center dot ASFV tag-free p30 was successfully purified. center dot High sensitivity, specificity, relatively simple, and time-saving to detect antibody against ASFV were developed. center dot The development of CMIA will help the clinical diagnosis of ASFV and will be useful for large-scale serological test.

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