A safe, cost-effective, and high-throughput SARS-CoV-2 antigen capture ELISA suitable for large-scale screening in low-resource settings

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Journal of virological methods Pub Date : 2024-07-06 DOI:10.1016/j.jviromet.2024.114995
Ashutosh Singh , Upasana Sahu , Pratik M. Kulkarni , Rupali Yadav , Sandeep Bhatia , Harshad Vinayakrao Murugkar , Madhusudan Hosamani , Suresh Basagoudanavar , Gaurav Kumar Sharma , Praveen Kumar Gupta , Naveen Kumar , Aniket Sanyal , Naveen Kumar
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Abstract

Diagnostics employing multiple modalities have been essential for controlling and managing COVID-19, caused by SARS-CoV-2. However, scaling up Reverse Transcription–Quantitative Polymerase Chain Reaction (RT-qPCR), the gold standard for SARS-CoV-2 detection, remains challenging in low and middle-income countries. Cost-effective and high-throughput alternatives like enzyme-linked immunosorbent assay (ELISA) could address this issue. We developed an in-house SARS-CoV-2 nucleocapsid capture ELISA, and validated on 271 nasopharyngeal swab samples from humans (n = 252), bovines (n = 10), and dogs (n = 9). This ELISA has a detection limit of 195 pg/100 µL of nucleocapsid protein and does not cross-react with related coronaviruses, ensuring high specificity to SARS-CoV-2. Diagnostic performance was evaluated using receiver operating characteristic curve analysis, showing a diagnostic sensitivity of 67.78 % and specificity of 100 %. Sensitivity improved to 74.32 % when excluding positive clinical samples with RT-qPCR Ct values > 25. Furthermore, inter-rater reliability analysis demonstrated substantial agreement (κ values = 0.73–0.80) with the VIRALDTECT II Multiplex RT-qPCR kit and perfect agreement with the CoVeasy™ COVID-19 rapid antigen self-test (κ values = 0.89–0.93). Our findings demonstrated that the in-house nucleocapsid capture ELISA is suitable for SARS-CoV-2 testing in humans and animals, meeting the necessary sensitivity and specificity thresholds for cost-effective, large-scale screening.

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安全、经济、高通量的 SARS-CoV-2 抗原捕获酶联免疫吸附试验,适合在低资源环境中进行大规模筛查。
采用多种模式的诊断方法对于控制和管理由 SARS-CoV-2 引起的 COVID-19 至关重要。然而,在中低收入国家,扩大反转录-定量聚合酶链反应(RT-qPCR)这一检测 SARS-CoV-2 的黄金标准仍具有挑战性。酶联免疫吸附试验(ELISA)等具有成本效益和高通量的替代方法可以解决这一问题。我们开发了一种内部 SARS-CoV-2 核头壳捕获酶联免疫吸附测定法,并在 271 份鼻咽拭子样本中进行了验证,这些样本分别来自人类(n = 252)、牛(n = 10)和狗(n = 9)。该酶联免疫吸附试验的 N 蛋白检测限为 195pg/100µL,不会与相关冠状病毒发生交叉反应,确保了对 SARS-CoV-2 的高度特异性。使用 ROC 曲线分析评估了诊断性能,结果显示诊断灵敏度为 67.78%,特异性为 100%。当排除 RT-qPCR Ct 值大于 25 的阳性临床样本时,灵敏度提高到 74.32%。此外,评分者之间的可靠性分析表明,VIRALDTECT II Multiplex RT-qPCR 试剂盒和 CoVeasyTM COVID-19 快速抗原自我检测(κ值=0.89-0.93)之间的一致性非常好(κ值=0.73-0.80)。我们的研究结果表明,内部核苷酸捕获酶联免疫吸附试验适用于人类和动物的 SARS-CoV-2 检测,符合成本效益高的大规模筛查所需的灵敏度和特异性阈值。
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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
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