Vedelago Courtney, Li Junrong, Lowry Kym, Howard Christopher, Wuethrich Alain, Trau Matt
Centre for Personalised Nanomedicine, Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD 4072, Australia.
The Queensland Paediatric Infectious Diseases (QIPD) Sakzewski Research Group, Queensland Children's Hospital, Brisbane, QLD 4101, Australia.
ACS Sens. 2023 Apr 28;8(4):1648-1657. doi: 10.1021/acssensors.2c02782. Epub 2023 Apr 7.
Severe acute respiratory syndrome coronavirus 2 variants play an important role in predicting patient outcome during postinfection, and with growing fears of COVID-19 reservoirs in domestic and wild animals, it is necessary to adapt detection systems for variant detection. However, variant-specific detection remains challenging. Surface-enhanced Raman scattering is a sensitive and multiplexing technique that allows the simultaneous detection of multiple targets for accurate identification. Here we propose the development of a multiplex SERS microassay to detect both the spike and nucleocapsid structural proteins of SARS-CoV-2. The designed SERS microassay integrates gold-silver hollow nanobox barcodes and electrohydrodynamically induced nanomixing which in combination enables highly specific and sensitive detection of SARS-CoV-2 and the S-protein epitopes to delineate between ancestral prevariant strains with the newer variants of concern, Delta and Omicron. The microassay allows detection from as low as 20 virus/μL and 50 pg/mL RBD protein and can clearly identify the virus among infected versus healthy nasopharyngeal swabs, with the potential to identify between variants. The detection of both S- and N-proteins of SARS-CoV-2 and the differentiation of variants on the SERS microassay can aid the early detection of COVID-19 to reduce transmission rates and lead into adequate treatments for those severely affected by the virus.
严重急性呼吸综合征冠状病毒2变体在预测感染后患者的预后方面发挥着重要作用,并且随着人们对新冠病毒在 domestic 和野生动物中储存库的担忧日益增加,有必要调整检测系统以进行变体检测。然而,特定变体的检测仍然具有挑战性。表面增强拉曼散射是一种灵敏的多路复用技术,能够同时检测多个目标以进行准确识别。在此,我们提出开发一种多路复用表面增强拉曼散射微测定法,以检测严重急性呼吸综合征冠状病毒2的刺突蛋白和核衣壳结构蛋白。所设计的表面增强拉曼散射微测定法集成了金银中空纳米盒条形码和电流体动力学诱导的纳米混合,二者结合能够对严重急性呼吸综合征冠状病毒2和S蛋白表位进行高度特异性和灵敏的检测,从而区分具有新的关注变体(德尔塔和奥密克戎)的祖先前变体菌株。该微测定法能够检测低至20个病毒/微升和50皮克/毫升的受体结合域蛋白,并且能够在受感染的鼻咽拭子与健康的鼻咽拭子之间清晰地识别出病毒,还有识别不同变体的潜力。在表面增强拉曼散射微测定法上对严重急性呼吸综合征冠状病毒2的S蛋白和N蛋白进行检测以及区分变体,有助于早期检测新冠病毒,以降低传播率,并为那些受该病毒严重影响的患者带来适当的治疗。