Cargando…

Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus

Among the numerous molecular diagnostic methods, isothermal reverse transcription recombinase polymerase amplification (RT-RPA) is a simple method that has high sensitivity and avoids the use of expensive instruments. However, detection of amplified genomes often requires a fluorescence readout on c...

Descripción completa

Detalles Bibliográficos
Autores principales: Leon, Fanny, Pinchon, Elena, Mayran, Charly, Daynès, Aurélien, Morvan, François, Molès, Jean-Pierre, Cantaloube, Jean-François, Fournier-Wirth, Chantal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819590/
https://www.ncbi.nlm.nih.gov/pubmed/35141206
http://dx.doi.org/10.3389/fchem.2021.817246
_version_ 1784646088278409216
author Leon, Fanny
Pinchon, Elena
Mayran, Charly
Daynès, Aurélien
Morvan, François
Molès, Jean-Pierre
Cantaloube, Jean-François
Fournier-Wirth, Chantal
author_facet Leon, Fanny
Pinchon, Elena
Mayran, Charly
Daynès, Aurélien
Morvan, François
Molès, Jean-Pierre
Cantaloube, Jean-François
Fournier-Wirth, Chantal
author_sort Leon, Fanny
collection PubMed
description Among the numerous molecular diagnostic methods, isothermal reverse transcription recombinase polymerase amplification (RT-RPA) is a simple method that has high sensitivity and avoids the use of expensive instruments. However, detection of amplified genomes often requires a fluorescence readout on costly readers or migration on a lateral flow strip with a subjective visual reading. Aiming to establish a new approach to rapidly and sensitively detect viruses, we combined RT-RPA with a magnetic field-enhanced agglutination (MFEA) assay and assessed the ability of this method to detect the dengue virus (DENV). Magnetization cycles accelerated the capture of amplified DENV genomes between functionalized magnetic nanoparticles by a fast chaining process to less than 5 min; the agglutination was quantified by simple turbidimetry. A total of 37 DENV RNA(+) and 30 DENV RNA(−) samples were evaluated with this combined method. The sensitivity and specificity were 89.19% (95% CI, 72.75–100.00%) and 100% (95% CI, 81.74–100.00%), respectively. This approach provides a solution for developing innovative diagnostic assays for the molecular detection of emerging infections.
format Online
Article
Text
id pubmed-8819590
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88195902022-02-08 Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus Leon, Fanny Pinchon, Elena Mayran, Charly Daynès, Aurélien Morvan, François Molès, Jean-Pierre Cantaloube, Jean-François Fournier-Wirth, Chantal Front Chem Chemistry Among the numerous molecular diagnostic methods, isothermal reverse transcription recombinase polymerase amplification (RT-RPA) is a simple method that has high sensitivity and avoids the use of expensive instruments. However, detection of amplified genomes often requires a fluorescence readout on costly readers or migration on a lateral flow strip with a subjective visual reading. Aiming to establish a new approach to rapidly and sensitively detect viruses, we combined RT-RPA with a magnetic field-enhanced agglutination (MFEA) assay and assessed the ability of this method to detect the dengue virus (DENV). Magnetization cycles accelerated the capture of amplified DENV genomes between functionalized magnetic nanoparticles by a fast chaining process to less than 5 min; the agglutination was quantified by simple turbidimetry. A total of 37 DENV RNA(+) and 30 DENV RNA(−) samples were evaluated with this combined method. The sensitivity and specificity were 89.19% (95% CI, 72.75–100.00%) and 100% (95% CI, 81.74–100.00%), respectively. This approach provides a solution for developing innovative diagnostic assays for the molecular detection of emerging infections. Frontiers Media S.A. 2022-01-24 /pmc/articles/PMC8819590/ /pubmed/35141206 http://dx.doi.org/10.3389/fchem.2021.817246 Text en Copyright © 2022 Leon, Pinchon, Mayran, Daynès, Morvan, Molès, Cantaloube and Fournier-Wirth. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Leon, Fanny
Pinchon, Elena
Mayran, Charly
Daynès, Aurélien
Morvan, François
Molès, Jean-Pierre
Cantaloube, Jean-François
Fournier-Wirth, Chantal
Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus
title Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus
title_full Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus
title_fullStr Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus
title_full_unstemmed Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus
title_short Magnetic Field-Enhanced Agglutination Readout Combined With Isothermal Reverse Transcription Recombinase Polymerase Amplification for Rapid and Sensitive Molecular Detection of Dengue Virus
title_sort magnetic field-enhanced agglutination readout combined with isothermal reverse transcription recombinase polymerase amplification for rapid and sensitive molecular detection of dengue virus
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819590/
https://www.ncbi.nlm.nih.gov/pubmed/35141206
http://dx.doi.org/10.3389/fchem.2021.817246
work_keys_str_mv AT leonfanny magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT pinchonelena magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT mayrancharly magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT daynesaurelien magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT morvanfrancois magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT molesjeanpierre magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT cantaloubejeanfrancois magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus
AT fournierwirthchantal magneticfieldenhancedagglutinationreadoutcombinedwithisothermalreversetranscriptionrecombinasepolymeraseamplificationforrapidandsensitivemoleculardetectionofdenguevirus