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Portable bead-based fluorescence detection system for multiplex nucleic acid testing: a case study with Bacillus anthracis
Authors:Jean-François Gravel  Matthias Geissler  Sébastien Chapdelaine  Karel Boissinot  Benoît Voisin  Isabelle Charlebois  Hugo-Pierre Poirier-Richard  Alexandre Grégoire  Maurice Boissinot  Michel G Bergeron  Teodor Veres  Denis Boudreau
Affiliation:1. Département de chimie et centre d’optique, photonique et laser (COPL), Université Laval, Quebec, QC, G1V 0A6, Canada
2. Conseil national de recherches Canada (CNRC), Boucherville, QC, J4B 6Y4, Canada
3. Centre de recherche en infectiologie de l’Université Laval, Centre de recherche du CHUQ, Quebec, QC, G1V 4G2, Canada
Abstract:This paper describes the design, functioning and use of a portable detection platform for multiplex nucleic acid testing. The system features a bead-supported DNA hybridization assay performed inside a microfluidic cartridge. Polystyrene particles modified with DNA capture probes are confined in the detection area and exposed to a solution of fluorescently labeled target DNA strands. The cartridge, fabricated from inexpensive thermoplastic polymers, allows for conducting up to eight assays in parallel. The detection instrument is equipped with a pneumatic module and a manifold lid serving as an interface to mediate fluid displacement on the cartridge. The fluorescence signal deriving from each assay is recorded by a semi-confocal fluorescence reader embedded in the detection platform. The compact design of the instrument and its level of integration make it possible to obtain an analytical result in less than 15 min, while only few manual steps need to be performed in between. A proof-of-concept demonstration involving Cy3-labeled, PCR-amplified genomic DNA confirms the ability to detect Bacillus anthracis in a multiplexed single-assay format using lef and capC genes. Limits of quantification are on the order of 1 × 109 copies/μL for lef targets.
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