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基于核衣壳蛋白的阻断 ELISA 检测方法的建立及其用于猪德尔塔冠状病毒抗体的检测

Development of a Nucleocapsid Protein-Based Blocking ELISA for the Detection of Porcine Deltacoronavirus Antibodies.

机构信息

Key Laboratory of Animal Epidemiology of Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.

出版信息

Viruses. 2022 Aug 18;14(8):1815. doi: 10.3390/v14081815.

Abstract

Porcine deltacoronavirus (PDCoV) is an emerging enteropathogen which mainly causes diarrhea, dehydration and death in nursing piglets, threatening the global swine industry. Moreover, it can infect multiple animal species and humans. Hence, reliable diagnostic assays are needed to better control this zoonotic pathogen. Here, a blocking ELISA was developed using a recombinant nucleocapsid (N) protein as the coating antigen paired with an N-specific monoclonal antibody (mAb) as the detection antibody. The percent inhibition (PI) of the ELISA was determined using 384 swine serum samples, with an indirect immunofluorescence assay (IFA) as the reference method. Through receiver operating characteristic analysis in conjunction with Youden's index, the optimal PI cut-off value was determined to be 51.65%, which corresponded to a diagnostic sensitivity of 98.79% and a diagnostic specificity of 100%. Of the 330 serum samples tested positive via IFA, 326 and 4 were tested positive and negative via the ELISA, respectively, while the 54 serum samples tested negative via IFA were all negative via the ELISA. The overall coincidence rate between the two assays was 98.96% (380/384). The ELISA exhibited good repeatability and did not cross-react with antisera against other swine pathogens. Overall, this is the first report on developing a blocking ELISA for PDCoV serodiagnosis.

摘要

猪德尔塔冠状病毒(PDCoV)是一种新兴的肠道病原体,主要导致哺乳仔猪腹泻、脱水和死亡,对全球养猪业构成威胁。此外,它还可以感染多种动物和人类。因此,需要可靠的诊断检测方法来更好地控制这种人畜共患病原体。本研究采用重组核衣壳(N)蛋白作为包被抗原,结合 N 特异性单克隆抗体(mAb)作为检测抗体,建立了一种阻断 ELISA。通过对 384 份猪血清样本的抑制率(PI)进行检测,以间接免疫荧光试验(IFA)为参考方法。通过结合受试者工作特征分析和 Youden 指数,确定最佳 PI 截断值为 51.65%,对应的诊断敏感性为 98.79%,诊断特异性为 100%。在 330 份经 IFA 检测阳性的血清样本中,ELISA 检测阳性和阴性的分别为 326 份和 4 份,而在 54 份经 IFA 检测阴性的血清样本中,ELISA 检测均为阴性。两种检测方法的总符合率为 98.96%(380/384)。ELISA 具有良好的重复性,与针对其他猪病原体的抗血清无交叉反应。综上所述,本研究首次报道了用于 PDCoV 血清学诊断的阻断 ELISA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f0/9412986/19bfa645515b/viruses-14-01815-g001.jpg

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