Comparing nucleic acid lateral flow and electrochemical genosensing for the simultaneous detection of foodborne pathogens

Due to the increasing need of rapid tests for application in low resource settings, WHO summarized their ideal features under the acronym ASSURED (Affordable, Sensitive, Specific, User-friendly, Rapid and Robust, Equipment-free, Delivered to those who need it). In this work, two different platforms...

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Detalles Bibliográficos
Autores: Ben Aissa Soler, Alejandra|||0000-0002-0419-0572, Jara, José Juan, Sebastián, Rosa María|||0000-0001-5519-9131, Vallribera, Adelina|||0000-0002-6452-4589, Campoy Sánchez, Susana|||0000-0003-1369-0197, Pividori, María Isabel|||0000-0002-5266-7873
Tipo de recurso: artículo
Fecha de publicación:2017
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:273775
Acceso en línea:https://ddd.uab.cat/record/273775
https://dx.doi.org/urn:doi:10.1016/j.bios.2016.08.046
Access Level:acceso abierto
Palabra clave:Nucleic acid lateral flow
Electrochemical magneto genosensing
Foodborne bacteria
Simultaneous detection
Magnetic particles
Descripción
Sumario:Due to the increasing need of rapid tests for application in low resource settings, WHO summarized their ideal features under the acronym ASSURED (Affordable, Sensitive, Specific, User-friendly, Rapid and Robust, Equipment-free, Delivered to those who need it). In this work, two different platforms for the rapid and simultaneous testing of the foodborne pathogens E. coli O157:H7 and Salmonella enterica, in detail a nucleic acid lateral flow and an electrochemical magneto-genosensor are presented and compared in terms of their analytical performance. The DNA of the bacteria was amplified by polymerase chain reaction using a quadruple-tagging set of primers specific for E. coli eaeA (151 bp) and Salmonella enterica yfiR (375 bp) genes. During the amplification, the amplicons were labelled at the same time with biotin/digoxigenin or biotin/fluorescein tags, respectively. The nucleic acid lateral flow assay was based on the use of streptavidin gold nanoparticles for the labelling of the tagged amplicon from E. coli and Salmonella. The visual readout was achieved when the gold-modified amplicons were captured by the specific antibodies. The features of this approach are discussed and compared with an electrochemical magneto-genosensor. Although nucleic acid lateral flow showed higher limit of detection, this strategy was able to clearly distinguish positive and negative samples of both bacteria being considered as a rapid and promising detection tool for bacteria screening.