Prado Isis Campos, Carvalho João Pedro Rangel da Silva, Araujo André Souza, Napoleão-Pêgo Paloma, De-Simone Salvatore Giovanni
Center for Technological Development in Health (CDTS)/National Institute of Science and Technology for Innovation in Neglected Population Diseases (INCT-IDPN), Oswaldo Cruz Foundation (FIOCRUZ), Rio de Janeiro 21040-900, RJ, Brazil.
Program of Post-Graduation on Science and Biotechnology, Biology Institute, Federal Fluminense University, Niteroi 24020-141, RJ, Brazil.
Biosensors (Basel). 2025 Apr 8;15(4):236. doi: 10.3390/bios15040236.
Dengue is a neglected disease mainly affecting tropical and subtropical countries. The diagnosis of dengue fever is still a problem since most of it is made from whole or recombinant DENV proteins, which present cross-reactions with other members of the Flavivirus family. Therefore, there is still a huge demand for new diagnostic methods that provide rapid, low-cost, easy-to-use confirmation. Thus, in this study, we developed an affordable electrochemical biosensor for rapidly detecting immunoglobulin G (IgG) serological antibodies in the sera of DENV-infected patients. An identified linear B-cell epitope (DENV/18) specific for DENV 1-4 serotypes recognized by IgG in patient sera was selected as a target molecule after a microarray of peptides using the SPOT-synthesis methodology. After chemical synthesis, the DENV/18-peptide was immobilized on the surface of the working electrode of a commercially available screen-printed gold electrode (SPGE). The capture of DENV-specific IgG allowed for the formation of an immunocomplex that was measured by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) using a potassium ferrocyanide/ferricyanide ([Fe(CN)]) electrochemical probe. An evaluation of the biosensor's performance showed a detection limit of 100 µg mL for the synthetic peptides (DENV/18) and 1.21 ng mL in CV and 0.43 ng mL in DPV for human serum, with a sensitivity of 7.21 µA in CV and 8.79 µA in DPV. The differentiation of infected and uninfected individuals was possible even at a high dilution factor that reduced the required sample volumes to a few microliters. The final device proved suitable for diagnosing DENV by analyzing real serum samples, and the results showed good agreement with molecular biology diagnostics. The flexibility to conjugate other antigenic peptides to SPEs suggests that this technology could be rapidly adapted to diagnose other pathogens.
登革热是一种主要影响热带和亚热带国家的被忽视疾病。登革热的诊断仍然是一个问题,因为大多数诊断是基于完整或重组的登革病毒(DENV)蛋白,这些蛋白会与黄病毒科的其他成员发生交叉反应。因此,对于能够提供快速、低成本、易于使用的确诊方法的新诊断手段仍有巨大需求。因此,在本研究中,我们开发了一种经济实惠的电化学生物传感器,用于快速检测登革病毒感染患者血清中的免疫球蛋白G(IgG)血清学抗体。在使用SPOT合成方法进行肽微阵列分析后,从患者血清中被IgG识别的、对登革病毒1 - 4血清型具有特异性的已鉴定线性B细胞表位(DENV/18)被选为靶分子。化学合成后,将DENV/18肽固定在市售丝网印刷金电极(SPGE)工作电极的表面。捕获登革病毒特异性IgG可形成免疫复合物,该复合物使用亚铁氰化钾/铁氰化钾([Fe(CN)])电化学探针通过循环伏安法(CV)和差分脉冲伏安法(DPV)进行测量。对该生物传感器性能的评估表明,合成肽(DENV/18)的检测限为100 µg/mL,人血清在CV中的检测限为1.21 ng/mL,在DPV中的检测限为0.43 ng/mL,CV中的灵敏度为7.21 µA,DPV中的灵敏度为8.79 µA。即使在高稀释倍数下,也能够区分感染和未感染个体,这将所需样本体积减少到了几微升。最终的装置被证明适用于通过分析实际血清样本诊断登革病毒,结果与分子生物学诊断显示出良好的一致性。将其他抗原肽偶联到丝网印刷电极上的灵活性表明,该技术可以快速适用于诊断其他病原体。