Moustakim Hamza, Amine Aziz, Mohammadi Hasna
Chemical Analysis and Biosensors Research Group, Laboratory of Process Engineering and Environment, Faculty of Sciences and Techniques, Hassan II University of Casablanca, Morocco.
Chemical Analysis and Biosensors Research Group, Laboratory of Process Engineering and Environment, Faculty of Sciences and Techniques, Hassan II University of Casablanca, Morocco.
Enzyme Microb Technol. 2025 Feb;183:110549. doi: 10.1016/j.enzmictec.2024.110549. Epub 2024 Nov 21.
The ongoing challenge of infectious pathogens highlights the need for accurate and accessible methods to discern their genetic signatures, especially in resource-limited settings. In response to this crucial requirement, we introduce an affordable large-scale screening platform for infectious pathogen detection, using Hepatitis B virus (HBV) as a fundamental model. This proposed biosensor integrates an exonuclease III-assisted target recycling amplification strategy within a high-throughput 96-well microplate format. The HBV DNA target binds to a capture probe DNA and exonuclease III digests the probe to release the target. This mechanism enables the target to engage in binding cycles with new probes, each digested in turn, increasing detection sensitivity for even small quantities of HBV DNA. The implemented approach incorporates a biotin-streptavidin interaction allowing the undigested capture probe DNA to bind to a 5'-biotin-modified detection probe for effective HBV DNA quantification. This interaction generates a signal that, following the enzyme-substrate reaction, can be detected on-site using a smartphone, offering either optical or electrochemical readouts. The developed biosensor was capable of detecting HBV DNA with a detection limit of 5.62 fM and provided a considerable linear range covering concentrations from 100 fM to 100 nM. The determination of HBV DNA quantities in spiked human serum was achieved with a recovery of 90.0 % - 107.4 % as well. The results suggest that the developed dual-mode biosensor offers an adaptable and cost-effective approach for detecting infectious diseases, with promising applications in medical diagnostics and environmental monitoring to support public health efforts.
传染性病原体带来的持续挑战凸显了对准确且易于使用的方法来识别其基因特征的需求,尤其是在资源有限的环境中。为满足这一关键需求,我们引入了一种用于检测传染性病原体的经济实惠的大规模筛查平台,以乙型肝炎病毒(HBV)作为基础模型。该新型生物传感器在高通量96孔微孔板形式中集成了核酸外切酶III辅助的靶标循环扩增策略。HBV DNA靶标与捕获探针DNA结合,核酸外切酶III消化探针以释放靶标。这种机制使靶标能够与新的探针进行结合循环,每个探针依次被消化,从而提高了对少量HBV DNA的检测灵敏度。所采用的方法结合了生物素 - 链霉亲和素相互作用,使未消化的捕获探针DNA能够与5' - 生物素修饰的检测探针结合,以实现有效的HBV DNA定量。这种相互作用产生一个信号,在酶 - 底物反应后,可以使用智能手机进行现场检测,提供光学或电化学读数。所开发的生物传感器能够检测HBV DNA,检测限为5.62 fM,并提供了相当大的线性范围,涵盖从100 fM到100 nM的浓度。加标人血清中HBV DNA量的测定回收率也达到了90.0% - 107.4%。结果表明,所开发的双模式生物传感器为检测传染病提供了一种适应性强且经济高效的方法,在医学诊断和环境监测中具有广阔的应用前景,有助于公共卫生事业。