Dipartimento di Fisica Ettore Pancini, Università di Napoli Federico II, Via Cintia, 26 Ed. 6, 80126 Napoli, Italy.
Dipartimento di Scienze Mediche Traslazionali, Università di Napoli Federico II, Via Pansini, 5, 80131 Napoli, Italy.
ACS Sens. 2020 Oct 23;5(10):3043-3048. doi: 10.1021/acssensors.0c01742. Epub 2020 Oct 1.
Mass testing is fundamental to face the pandemic caused by the coronavirus SARS-CoV-2 discovered at the end of 2019. To this aim, it is necessary to establish reliable, fast, and cheap tools to detect viral particles in biological material so to identify the people capable of spreading the infection. We demonstrate that a colorimetric biosensor based on gold nanoparticle (AuNP) interaction induced by SARS-CoV-2 lends itself as an outstanding tool for detecting viral particles in nasal and throat swabs. The extinction spectrum of a colloidal solution of multiple viral-target gold nanoparticles-AuNPs functionalized with antibodies targeting three surface proteins of SARS-CoV-2 (spike, envelope, and membrane)-is red-shifted in few minutes when mixed with a solution containing the viral particle. The optical density of the mixed solution measured at 560 nm was compared to the threshold cycle () of a real-time PCR (gold standard for detecting the presence of viruses) finding that the colorimetric method is able to detect very low viral load with a detection limit approaching that of the real-time PCR. Since the method is sensitive to the infecting viral particle rather than to its RNA, the achievements reported here open a new perspective not only in the context of the current and possible future pandemics, but also in microbiology, as the biosensor proves itself to be a powerful though simple tool for measuring the viral particle concentration.
大规模检测对于应对 2019 年底发现的冠状病毒 SARS-CoV-2 引发的大流行至关重要。为此,有必要建立可靠、快速和廉价的工具来检测生物材料中的病毒颗粒,以确定有传播感染能力的人。我们证明,基于金纳米粒子(AuNP)与 SARS-CoV-2 相互作用的比色生物传感器可作为检测鼻拭子和咽拭子中病毒颗粒的出色工具。当与含有病毒颗粒的溶液混合时,胶体溶液中多个靶向病毒的 AuNPs(针对 SARS-CoV-2 的三种表面蛋白(刺突、包膜和膜)进行功能化的抗体)的消光谱在几分钟内发生红移。在 560nm 处测量混合溶液的光密度与实时 PCR 的阈值循环(检测病毒存在的金标准)进行比较,发现比色法能够以接近实时 PCR 的检测限检测到非常低的病毒载量。由于该方法对感染性病毒颗粒敏感,而不是其 RNA,因此这里报道的结果不仅为当前和可能未来的大流行开辟了新的视角,而且为微生物学开辟了新的视角,因为该生物传感器本身就是一种强大而简单的工具用于测量病毒颗粒浓度。