Norouzi Masoud, Truong Thang, Jaenes Katariina, Warner Bryce M, Vendramelli Robert, Tierney Kevin, Kobasa Darwyn, Tailor Nikesh, Plant Pamela, Dos Santos Claudia, Babiuk Shawn, Ambagala Aruna, Pardee Keith
Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada.
Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Microbiol Spectr. 2023 Jan 31;11(2):e0245722. doi: 10.1128/spectrum.02457-22.
Since its emergence in late 2019, the coronavirus disease 2019 (COVID-19) pandemic has caused severe disruption to key aspects of human life globally and highlighted the need for timely, adaptive, and accessible pandemic response strategies. Here, we introduce the cell-free dot blot (CFDB) method, a practical and ultra-low-cost immune diagnostic platform capable of rapid response and mass immunity screening for the current and future pandemics. Similar in mechanism to the widely used enzyme-linked immunosorbent assays (ELISAs), our method is novel and advantageous in that (i) it uses linear DNA to produce the target viral antigen fused to a SpyTag peptide in a cell-free expression system without the need for traditional cloning and antigen purification, (ii) it uses SpyCatcher2-Apex2, an Escherichia coli-produced peroxidase conjugate as a universal secondary detection reagent, obviating the need for commercial or sophisticated enzyme conjugates, and (iii) sera are spotted directly on a nitrocellulose membrane, enabling a simple "dipping" mechanism for downstream incubation and washing steps, as opposed to individual processing of wells in a multiwell plate. To demonstrate the utility of our method, we performed CFDB to detect anti-severe acute respiratory syndrome coronavirus 2 nucleocapsid protein antibodies in precharacterized human sera (23 negative and 36 positive for COVID-19) and hamster sera (16 negative and 36 positive for COVID-19), including independent testing at a collaborating laboratory, and we show assay performance comparable to that of conventional ELISAs. At a similar capacity to 96-well plate ELISA kits, one CFDB assay costs only ~$3 USD. We believe that CFDB can become a valuable pandemic response tool for adaptive and accessible sero-surveillance in human and animal populations. The recent COVID-19 pandemic has highlighted the need for diagnostic platforms that are rapidly adaptable, affordable, and accessible globally, especially for low-resource settings. To address this need, we describe the development and functional validation of a novel immunoassay technique termed the cell-free dot blot (CFDB) method. Based on the principles of cell-free synthetic biology and alternative dot blotting procedures, our CFDB immunoassay is designed to provide for timely, practical, and low-cost responses to existing and emerging public health threats, such as the COVID-19 pandemic, at a similar throughput and comparable performance as conventional ELISAs. Notably, the molecular detection reagents used in CFDB can be produced rapidly in-house, using established protocols and basic laboratory infrastructure, minimizing reliance on strained commercial reagents. In addition, the materials and imaging instruments required for CFDB are the same as those used for common Western blotting experiments, further expanding the reach of CFDB in decentralized facilities.
自2019年末出现以来,2019冠状病毒病(COVID-19)大流行给全球人类生活的关键方面造成了严重破坏,并凸显了及时、适应性强且易于获取的大流行应对策略的必要性。在此,我们介绍无细胞斑点印迹(CFDB)方法,这是一种实用且超低成本的免疫诊断平台,能够对当前及未来的大流行进行快速响应和大规模免疫筛查。我们的方法在机制上与广泛使用的酶联免疫吸附测定(ELISA)相似,具有新颖性和优势,具体如下:(i)它利用线性DNA在无细胞表达系统中产生与SpyTag肽融合的目标病毒抗原,无需传统克隆和抗原纯化;(ii)它使用大肠杆菌产生的过氧化物酶偶联物SpyCatcher2-Apex2作为通用的二级检测试剂,无需商业或复杂的酶偶联物;(iii)血清直接点样在硝酸纤维素膜上,对于下游孵育和洗涤步骤采用简单的“浸泡”机制,而不是对多孔板中的孔进行逐个处理。为证明我们方法的实用性,我们进行了CFDB检测,以检测预先分类的人类血清(23份COVID-19阴性和36份阳性)和仓鼠血清(16份COVID-19阴性和36份阳性)中的抗严重急性呼吸综合征冠状病毒2核衣壳蛋白抗体,包括在合作实验室进行的独立检测,我们展示了与传统ELISA相当的检测性能。在与96孔板ELISA试剂盒类似的检测能力下,一次CFDB检测成本仅约3美元。我们相信CFDB可以成为一种有价值的大流行应对工具,用于对人类和动物群体进行适应性强且易于获取的血清监测。最近的COVID-19大流行凸显了对快速适应、价格合理且全球可及的诊断平台的需求,特别是对于资源匮乏地区。为满足这一需求,我们描述了一种名为无细胞斑点印迹(CFDB)方法的新型免疫测定技术的开发和功能验证。基于无细胞合成生物学原理和替代斑点印迹程序,我们的CFDB免疫测定旨在以与传统ELISA相似的通量和相当的性能,对现有和新出现的公共卫生威胁(如COVID-19大流行)提供及时、实用且低成本的应对措施。值得注意的是,CFDB中使用的分子检测试剂可以使用既定方案和基本实验室基础设施在内部快速生产,最大限度地减少对紧张的商业试剂的依赖。此外,CFDB所需的材料和成像仪器与普通蛋白质印迹实验相同,进一步扩大了CFDB在分散设施中的应用范围。