Center for Applied NanoBioscience and Medicine, College of Medicine, University of Arizona, Phoenix, Arizona 85004, United States.
Department of Basic Medical Sciences, College of Medicine, The University of Arizona, 475 N 5th Street, Phoenix, Arizona 85004, United States.
Anal Chem. 2021 Jul 13;93(27):9337-9344. doi: 10.1021/acs.analchem.0c05278. Epub 2021 May 14.
is a Gram-negative bacterium that is the causative agent of plague and is widely recognized as a potential biological weapon. Due to the high fatality rate of plague when diagnosis is delayed, the development of rapid, sensitive, specific, and cost-effective methods is needed for its diagnosis. The low calcium response V (LcrV) protein has been identified as a potential microbial biomarker for the diagnosis of plague. In this paper, we present a highly sensitive, paper-based, vertical flow immunoassay (VFI) prototype for the detection of LcrV and the diagnosis of plague. An antigen-capture assay using monoclonal antibodies is employed to capture and detect the LcrV protein, using a colorimetric approach. In addition, the effect of miniaturizing the VFI device is explored based on two different sizes of VFI platforms, denoted as "large VFI" and "mini VFI." Also, a comparative analysis is performed between the VFI platform and a lateral flow immunoassay (LFI) platform to exhibit the improved assay sensitivity suitable for point-of-care (POC) diagnostics. The analytical sensitivity or limit of detection (LOD) in the mini VFI is approximately 0.025 ng/mL, that is, 10 times better than that of the large VFI platform or 80 times over a standard lateral flow configuration. The low LOD of the LcrV VFI appears to be highly suitable for testing clinical samples and potentially diagnosing plague at earlier time points. In addition, optimization of the gold nanoparticle (AuNP) concentration, nanomaterial plasmonic properties, and flow velocity analysis could improve the performance of the VFI. Furthermore, we developed automated image analysis software that shows potential for integrating the diagnostic system into a smartphone. These methods and findings demonstrate that the VFI platform is a highly sensitive device for detecting the LcrV and potentially many other biomarkers.
是一种革兰氏阴性细菌,是鼠疫的病原体,被广泛认为是一种潜在的生物武器。由于鼠疫的死亡率很高,如果诊断延迟,因此需要开发快速、敏感、特异和具有成本效益的方法来进行诊断。低钙反应 V(LcrV)蛋白已被确定为鼠疫诊断的潜在微生物生物标志物。在本文中,我们提出了一种基于纸的高度敏感的垂直流动免疫分析(VFI)原型,用于检测 LcrV 和鼠疫。使用单克隆抗体的抗原捕获测定法用于捕获和检测 LcrV 蛋白,使用比色法。此外,基于两种不同尺寸的 VFI 平台,即“大 VFI”和“小 VFI”,探索了微型化 VFI 装置的效果。还对 VFI 平台和侧向流动免疫分析(LFI)平台之间进行了比较分析,以展示适合即时护理(POC)诊断的改进的分析灵敏度。在 mini VFI 中的分析灵敏度或检测限(LOD)约为 0.025ng/mL,比大 VFI 平台好 10 倍,比标准的侧向流动配置好 80 倍。LcrV VFI 的低 LOD 似乎非常适合测试临床样本并有可能更早地诊断鼠疫。此外,优化金纳米颗粒(AuNP)浓度、纳米材料等离子体特性和流速分析可以提高 VFI 的性能。此外,我们开发了自动图像分析软件,该软件具有将诊断系统集成到智能手机中的潜力。这些方法和发现表明,VFI 平台是一种高度敏感的检测 LcrV 并可能检测许多其他生物标志物的设备。