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Diagnostic Performance of a Magnetic Field-Enhanced Agglutination Readout in Detecting Either Viral Genomes or Host Antibodies in Arbovirus Infection

Authors :
Jean-Jacques Vasseur
Elena Pinchon
Nevzat Temurok
Fanny Leon
Chantal Fournier-Wirth
Aurélien Daynes
Martine Clot
Vincent Foulongne
Philippe Van de Perre
François Morvan
Jean-François Cantaloube
Jean-Pierre Molès
Pathogénèse et contrôle des infections chroniques (PCCI)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre Hospitalier Universitaire de Montpellier (CHU Montpellier )
HORIBA Medical (HORIBA ABX SAS)
HORIBA Scientific [France]
Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM)
Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Pathogenesis and Control of Chronic and Emerging Infections (PCCEI)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Université des Antilles (UA)-Etablissement français du don du sang [Montpellier]
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Boutin, Marion
Source :
Microorganisms, Microorganisms, MDPI, 2021, 9 (4), pp.674. ⟨10.3390/microorganisms9040674⟩, Microorganisms, Vol 9, Iss 674, p 674 (2021), Microorganisms, 2021, 9 (4), pp.674. ⟨10.3390/microorganisms9040674⟩
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

Abstract

International audience; Arbovirus diagnostics on blood from donors and travelers returning from endemic areas is increasingly important for better patient management and epidemiological surveillance. We developed a flexible approach based on a magnetic field-enhanced agglutination (MFEA) readout to detect either genomes or host-derived antibodies. Dengue viruses (DENVs) were selected as models. For genome detection, a pan-flavivirus amplification was performed before capture of biotinylated amplicons between magnetic nanoparticles (MNPs) grafted with DENV probes and anti-biotin antibodies. Magnetization cycles accelerated this chaining process to within 5 min while simple turbidimetry measured the signal. This molecular MFEA readout was evaluated on 43 DENV RNA(+) and 32 DENV RNA(−) samples previously screened by real-time RT-PCR. The sensitivity and the specificity were 88.37% (95% CI, 78.76%–97.95%) and 96.87% (95% CI, 90.84%–100%), respectively. For anti-DENV antibody detection, 103 plasma samples from donors were first screened using ELISA assays. An immunological MFEA readout was then performed by adding MNPs grafted with viral antigens to the samples. Anti-DENV antibodies were detected with a sensitivity and specificity of 90.62% (95% CI, 83.50%–97.76%) and 97.44% (95% CI, 92.48%–100%), respectively. This adaptable approach offers flexibility to platforms dedicated to the screening of emerging infections

Details

Language :
English
ISSN :
20762607
Database :
OpenAIRE
Journal :
Microorganisms, Microorganisms, MDPI, 2021, 9 (4), pp.674. ⟨10.3390/microorganisms9040674⟩, Microorganisms, Vol 9, Iss 674, p 674 (2021), Microorganisms, 2021, 9 (4), pp.674. ⟨10.3390/microorganisms9040674⟩
Accession number :
edsair.doi.dedup.....6ac51ef28981a3e0baa360f7f70de582
Full Text :
https://doi.org/10.3390/microorganisms9040674⟩