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SARS-CoV-2 detection using a nanobody-functionalized voltammetric device.
Pagneux, Quentin; Roussel, Alain; Saada, Hiba; Cambillau, Christian; Amigues, Béatrice; Delauzun, Vincent; Engelmann, Ilka; Alidjinou, Enagnon Kazali; Ogiez, Judith; Rolland, Anne Sophie; Faure, Emmanuel; Poissy, Julien; Duhamel, Alain; Boukherroub, Rabah; Devos, David; Szunerits, Sabine.
  • Pagneux Q; Univ. Lille, CNRS, Centrale Lille, Univ. Polytechnique Hauts-de-France, UMR 8520 - IEMN, Lille, France.
  • Roussel A; Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), Institut de Microbiologie, Bioénergies et Biotechnologie (IM2B), Aix-Marseille Université - CNRS, UMR, Marseille, France.
  • Saada H; Univ. Lille, CNRS, Centrale Lille, Univ. Polytechnique Hauts-de-France, UMR 8520 - IEMN, Lille, France.
  • Cambillau C; Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), Institut de Microbiologie, Bioénergies et Biotechnologie (IM2B), Aix-Marseille Université - CNRS, UMR, Marseille, France.
  • Amigues B; Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), Institut de Microbiologie, Bioénergies et Biotechnologie (IM2B), Aix-Marseille Université - CNRS, UMR, Marseille, France.
  • Delauzun V; Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), Institut de Microbiologie, Bioénergies et Biotechnologie (IM2B), Aix-Marseille Université - CNRS, UMR, Marseille, France.
  • Engelmann I; Univ Lille, CHU Lille, Laboratoire de Virologie ULR3610, Lille, France.
  • Alidjinou EK; Univ Lille, CHU Lille, Laboratoire de Virologie ULR3610, Lille, France.
  • Ogiez J; Univ Lille, CHU Lille, Laboratoire de Virologie ULR3610, Lille, France.
  • Rolland AS; Univ. Lille, CHU-Lille, Inserm, U1172, Lille Neuroscience & Cognition, LICEND, Lille, France.
  • Faure E; Service Universitaire de maladies infectieuses - Hôpital Hutiez, CHU de Lille, Lille, France.
  • Poissy J; UMR8204 U1019, Centre infection et immunité de Lille, Equipe Opinfield, Institut Pasteur de Lille, Lille, France.
  • Duhamel A; Univ. Lille, Inserm U1285, CHU Lille, Pôle de réanimation, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, Lille, France.
  • Boukherroub R; Univ. Lille, CHU Lille, ULR2694 METRICS: évaluation des technologies de santé et des pratiques médicales, Lille, France.
  • Devos D; Univ. Lille, CNRS, Centrale Lille, Univ. Polytechnique Hauts-de-France, UMR 8520 - IEMN, Lille, France.
  • Szunerits S; Univ. Lille, CHU-Lille, Inserm, U1172, Lille Neuroscience & Cognition, LICEND, Lille, France.
Commun Med (Lond) ; 2: 56, 2022.
Article in English | MEDLINE | ID: covidwho-1947553
ABSTRACT

Background:

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.

Methods:

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.

Results:

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.

Conclusions:

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.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Prognostic study Topics: Variants Language: English Journal: Commun Med (Lond) Year: 2022 Document Type: Article Affiliation country: S43856-022-00113-8

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Prognostic study Topics: Variants Language: English Journal: Commun Med (Lond) Year: 2022 Document Type: Article Affiliation country: S43856-022-00113-8