Nunez Freddy A, Castro Ana C H, de Oliveira Vivian L, Lima Ariane C, Oliveira Jamille R, de Medeiros Giuliana X, Sasahara Greyce L, Santos Keity S, Lanfredi Alexandre J C, Alves Wendel A
Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Av. dos Estados, 5001, Santo André, São Paulo 09210-580, Brazil.
Laboratório de Imunologia, LIM19, Instituto do Coração (InCor), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), Av. Dr. Arnaldo, 44, São Paulo, São Paulo 05403-900, Brazil.
ACS Biomater Sci Eng. 2023 Jan 9;9(1):458-473. doi: 10.1021/acsbiomaterials.2c00509. Epub 2022 Sep 1.
Even after over 2 years of the COVID-19 pandemic, research on rapid, inexpensive, and accurate tests remains essential for controlling and avoiding the global spread of SARS-CoV-2 across the planet during a potential reappearance in future global waves or regional outbreaks. Assessment of serological responses for COVID-19 can be beneficial for population-level surveillance purposes, supporting the development of novel vaccines and evaluating the efficacy of different immunization programs. This can be especially relevant for broadly used inactivated whole virus vaccines, such as CoronaVac, which produced lower titers of neutralizing antibodies. and showed lower efficacy for specific groups such as the elderly and immunocompromised. We developed an impedimetric biosensor based on the immobilization of SARS-CoV-2 recombinant trimeric spike protein (S protein) on zinc oxide nanorod (ZnONR)-modified fluorine-doped tin oxide substrates for COVID-19 serology testing. Due to electrostatic interactions, the negatively charged S protein was immobilized via physical adsorption. The electrochemical response of the immunosensor was measured at each modification step and characterized by scanning electron microscopy and electrochemical techniques. We successfully evaluated the applicability of the modified ZnONR electrodes using serum samples from COVID-19 convalescent individuals, CoronaVac-vaccinated with or without positive results for SARS-CoV-2 infection, and pre-pandemic samples from healthy volunteers as controls. ELISA for IgG anti-SARS-CoV-2 spike protein was performed for comparison, and ELISA for IgG anti-RBDs of seasonal coronavirus (HCoVs) was used to test the specificity of immunosensor detection. No cross-reactivity with HCoVs was detected using the ZnONR immunosensor, and more interestingly, the sensor presented higher sensitivity when compared to negative ELISA results. The results demonstrate that the ZnONRs/spike-modified electrode displayed sensitive results for convalescents and vaccinated samples and shows excellent potential as a tool for the population's assessment and monitoring of seroconversion and seroprevalence.
即使在新冠疫情爆发两年多之后,对于快速、廉价且准确的检测方法的研究,对于在未来全球疫情卷土重来或局部爆发期间控制和避免新冠病毒在全球范围内传播而言,仍然至关重要。评估新冠病毒的血清学反应,对于人群层面的监测目的、支持新型疫苗的研发以及评估不同免疫计划的效果可能会有所助益。这对于广泛使用的灭活全病毒疫苗(如科兴新冠疫苗)尤其重要,该疫苗产生的中和抗体滴度较低,并且对老年人和免疫功能低下等特定群体显示出较低的效力。我们开发了一种基于将新冠病毒重组三聚体刺突蛋白(S蛋白)固定在氧化锌纳米棒(ZnONR)修饰的氟掺杂氧化锡基底上的阻抗生物传感器,用于新冠病毒血清学检测。由于静电相互作用,带负电荷的S蛋白通过物理吸附被固定。在每个修饰步骤测量免疫传感器的电化学响应,并通过扫描电子显微镜和电化学技术进行表征。我们使用新冠康复者的血清样本、接种科兴新冠疫苗且有或无新冠病毒感染阳性结果的样本,以及来自健康志愿者的疫情前样本作为对照,成功评估了修饰后的ZnONR电极的适用性。进行了针对抗新冠病毒刺突蛋白IgG的酶联免疫吸附测定(ELISA)以作比较,并使用针对季节性冠状病毒(HCoV)抗受体结合域(RBD)IgG的ELISA来测试免疫传感器检测的特异性。使用ZnONR免疫传感器未检测到与HCoV的交叉反应,更有趣的是,与ELISA阴性结果相比,该传感器表现出更高的灵敏度。结果表明,ZnONRs/刺突修饰电极对康复者和接种疫苗的样本显示出灵敏的结果,并显示出作为人群血清转化和血清阳性率评估及监测工具的巨大潜力。