SARS-CoV-2 detection using a nanobody-functionalized voltammetric device

严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 唾液 2019年冠状病毒病(COVID-19) 穗蛋白 病毒学 冠状病毒 病毒 生物 医学 生物化学 疾病 病理 传染病(医学专业)
作者
Quentin Pagneux,Alain Roussel,Hiba Saada,Christian Cambillau,Béatrice Amigues,Vincent Delauzun,Ilka Engelmann,Enagnon Kazali Alidjinou,Judith Ogiez,Anne‐Sophie Rolland,Emmanuel Faure,Julien Poissy,Alain Duhamel,Rabah Boukherroub,David Devos,Sabine Szunerits
出处
期刊:Communications medicine [Springer Nature]
卷期号:2 (1) 被引量:22
标识
DOI:10.1038/s43856-022-00113-8
摘要

An ongoing need during the COVID-19 pandemic has been the requirement for accurate and efficient point-of-care testing platforms to distinguish infected from non-infected people, and to differentiate SARS-CoV-2 infections from other viruses. Electrochemical platforms can detect the virus via its envelope spike protein by recording changes in voltammetric signals between samples. However, this remains challenging due to the limited sensitivity of these sensing platforms.Here, we report on a nanobody-functionalized electrochemical platform for the rapid detection of whole SARS-CoV-2 viral particles in complex media such as saliva and nasopharyngeal swab samples. The sensor relies on the functionalization of gold electrode surface with highly-oriented Llama nanobodies specific to the spike protein receptor binding domain (RBD). The device provides results in 10 min of exposure to 200 µL of unprocessed samples with high specificity to SARS-CoV-2 viral particles in human saliva and nasopharyngeal swab samples.The developed sensor could discriminate between different human coronavirus strains and other respiratory viruses, with 90% positive and 90% negative percentage agreement on 80 clinical samples, as compared to RT-qPCR.We believe this diagnostic concept, also validated for RBD mutants and successfully tested on Delta variant samples, to be a powerful tool to detect patients' infection status, easily extendable to other viruses and capable of overcoming sensing-related mutation effects.

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