Versatile and flexible microfluidic qPCR test for high-throughput SARS-CoV-2 and cellular response detection in nasopharyngeal swab samples.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 23 11 2020
accepted: 23 03 2021
entrez: 14 4 2021
pubmed: 15 4 2021
medline: 5 5 2021
Statut: epublish

Résumé

The emergence and quick spread of SARS-CoV-2 has pointed at a low capacity response for testing large populations in many countries, in line of material, technical and staff limitations. The traditional RT-qPCR diagnostic test remains the reference method and is by far the most widely used test. These assays are limited to a few probe sets, require large sample PCR reaction volumes, along with an expensive and time-consuming RNA extraction step. Here we describe a quantitative nanofluidic assay that overcomes some of these shortcomings, based on the BiomarkTM instrument from Fluidigm. This system offers the possibility of performing 4608 qPCR end-points in a single run, equivalent to 192 clinical samples combined with 12 pairs of primers/probe sets in duplicate, thus allowing the monitoring of SARS-CoV-2 including the detection of specific SARS-CoV-2 variants, as well as the detection other pathogens and/or host cellular responses (virus receptors, response markers, microRNAs). The 10 nL-range volume of BiomarkTM reactions is compatible with sensitive and reproducible reactions that can be easily and cost-effectively adapted to various RT-qPCR configurations and sets of primers/probe. Finally, we also evaluated the use of inactivating lysis buffers composed of various detergents in the presence or absence of proteinase K to assess the compatibility of these buffers with a direct reverse transcription enzymatic step and we propose several protocols, bypassing the need for RNA purification. We advocate that the combined utilization of an optimized processing buffer and a high-throughput real-time PCR device would contribute to improve the turn-around-time to deliver the test results to patients and increase the SARS-CoV-2 testing capacities.

Identifiants

pubmed: 33852580
doi: 10.1371/journal.pone.0243333
pii: PONE-D-20-36827
pmc: PMC8046349
doi:

Substances chimiques

DNA Primers 0
MicroRNAs 0
RNA, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0243333

Déclaration de conflit d'intérêts

The authors have read the journal’s policy and have the following competing interests: DR is a paid employee of Bayer SAS and VL is employed by LBM Bioesterel (LBM Bioesterel). There are no patents, products in development or marketed products associated with this research to declare. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Julien Fassy (J)

Université Côte d'Azur, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, FHU-OncoAge, Valbonne, France.

Caroline Lacoux (C)

Université Côte d'Azur, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, FHU-OncoAge, Valbonne, France.

Sylvie Leroy (S)

Université Côte d'Azur, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, FHU-OncoAge, Valbonne, France.
Département de Pneumologie, CHU-Nice, FHU-OncoAge, Université Côte d'Azur, Nice, France.

Latifa Noussair (L)

Assistance Publique-Hôpitaux de Paris, GHU Paris-Saclay, Garches, France.

Sylvain Hubac (S)

Institut de Recherche Criminelle de la Gendarmerie Nationale (IRCGN), Cergy, France.

Aurélien Degoutte (A)

Département de Pneumologie, CHU-Nice, FHU-OncoAge, Université Côte d'Azur, Nice, France.

Georges Vassaux (G)

Université Côte d'Azur, INSERM, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, Valbonne, France.

Vianney Leclercq (V)

LBM BIOESTEREL, Mouans-Sartoux, France.

David Rouquié (D)

Bayer SAS, Valbonne, France.

Charles-Hugo Marquette (CH)

Département de Pneumologie, CHU-Nice, FHU-OncoAge, Université Côte d'Azur, Nice, France.

Martin Rottman (M)

Assistance Publique-Hôpitaux de Paris, GHU Paris-Saclay, Garches, France.
Université Paris-Saclay, UVSQ, Inserm, Infection et inflammation, Montigny-Le-Bretonneux, France.

Patrick Touron (P)

Institut de Recherche Criminelle de la Gendarmerie Nationale (IRCGN), Cergy, France.

Antoinette Lemoine (A)

Assistance Publique-Hôpitaux de Paris, GHU Paris-Saclay, Garches, France.

Jean-Louis Herrmann (JL)

Assistance Publique-Hôpitaux de Paris, GHU Paris-Saclay, Garches, France.
Université Paris-Saclay, UVSQ, Inserm, Infection et inflammation, Montigny-Le-Bretonneux, France.

Pascal Barbry (P)

Université Côte d'Azur, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, FHU-OncoAge, Valbonne, France.

Jean-Louis Nahon (JL)

Université Côte d'Azur, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, FHU-OncoAge, Valbonne, France.

Laure-Emmanuelle Zaragosi (LE)

Université Côte d'Azur, INSERM, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, Valbonne, France.

Bernard Mari (B)

Université Côte d'Azur, CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, FHU-OncoAge, Valbonne, France.

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Classifications MeSH