Cargando…

Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides

Consumption of food contaminated by Listeria monocytogenes can result in Listeriosis, an illness with hospitalization rates of 94% and mortality rates up to 30%. As a result, U.S. regulatory agencies governing food safety retain zero-tolerance policies for L. monocytogenes. However, detection at suc...

Descripción completa

Detalles Bibliográficos
Autores principales: Armstrong, Cheryl M., Lee, Joe, Gehring, Andrew G., Capobianco, Joseph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198859/
https://www.ncbi.nlm.nih.gov/pubmed/34071528
http://dx.doi.org/10.3390/s21113754
_version_ 1783707239335329792
author Armstrong, Cheryl M.
Lee, Joe
Gehring, Andrew G.
Capobianco, Joseph A.
author_facet Armstrong, Cheryl M.
Lee, Joe
Gehring, Andrew G.
Capobianco, Joseph A.
author_sort Armstrong, Cheryl M.
collection PubMed
description Consumption of food contaminated by Listeria monocytogenes can result in Listeriosis, an illness with hospitalization rates of 94% and mortality rates up to 30%. As a result, U.S. regulatory agencies governing food safety retain zero-tolerance policies for L. monocytogenes. However, detection at such low concentrations often requires strategies such as increasing sample size or culture enrichment. A novel flow-through immunoelectrochemical biosensor has been developed for Escherichia coli O157:H7 detection in 1 L volumes without enrichment. The current work further augments this biosensor’s capabilities to (1) include detection of L. monocytogenes and (2) accommodate genetic detection to help overcome limitations based upon antibody availability and address specificity errors in phenotypic assays. Herein, the conjugation scheme for oligo attachment and the conditions necessary for genetic detection are laid forth while results of the present study demonstrate the sensor’s ability to distinguish L. monocytogenes DNA from L. innocua with a limit of detection of ~2 × 10(4) cells/mL, which agrees with prior studies. Total time for this assay can be constrained to <2.5 h because a timely culture enrichment period is not necessary. Furthermore, the electrochemical detection assay can be performed with hand-held electronics, allowing this platform to be adopted for near-line monitoring systems.
format Online
Article
Text
id pubmed-8198859
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81988592021-06-14 Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides Armstrong, Cheryl M. Lee, Joe Gehring, Andrew G. Capobianco, Joseph A. Sensors (Basel) Article Consumption of food contaminated by Listeria monocytogenes can result in Listeriosis, an illness with hospitalization rates of 94% and mortality rates up to 30%. As a result, U.S. regulatory agencies governing food safety retain zero-tolerance policies for L. monocytogenes. However, detection at such low concentrations often requires strategies such as increasing sample size or culture enrichment. A novel flow-through immunoelectrochemical biosensor has been developed for Escherichia coli O157:H7 detection in 1 L volumes without enrichment. The current work further augments this biosensor’s capabilities to (1) include detection of L. monocytogenes and (2) accommodate genetic detection to help overcome limitations based upon antibody availability and address specificity errors in phenotypic assays. Herein, the conjugation scheme for oligo attachment and the conditions necessary for genetic detection are laid forth while results of the present study demonstrate the sensor’s ability to distinguish L. monocytogenes DNA from L. innocua with a limit of detection of ~2 × 10(4) cells/mL, which agrees with prior studies. Total time for this assay can be constrained to <2.5 h because a timely culture enrichment period is not necessary. Furthermore, the electrochemical detection assay can be performed with hand-held electronics, allowing this platform to be adopted for near-line monitoring systems. MDPI 2021-05-28 /pmc/articles/PMC8198859/ /pubmed/34071528 http://dx.doi.org/10.3390/s21113754 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Armstrong, Cheryl M.
Lee, Joe
Gehring, Andrew G.
Capobianco, Joseph A.
Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides
title Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides
title_full Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides
title_fullStr Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides
title_full_unstemmed Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides
title_short Flow-Through Electrochemical Biosensor for the Detection of Listeria monocytogenes Using Oligonucleotides
title_sort flow-through electrochemical biosensor for the detection of listeria monocytogenes using oligonucleotides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198859/
https://www.ncbi.nlm.nih.gov/pubmed/34071528
http://dx.doi.org/10.3390/s21113754
work_keys_str_mv AT armstrongcherylm flowthroughelectrochemicalbiosensorforthedetectionoflisteriamonocytogenesusingoligonucleotides
AT leejoe flowthroughelectrochemicalbiosensorforthedetectionoflisteriamonocytogenesusingoligonucleotides
AT gehringandrewg flowthroughelectrochemicalbiosensorforthedetectionoflisteriamonocytogenesusingoligonucleotides
AT capobiancojosepha flowthroughelectrochemicalbiosensorforthedetectionoflisteriamonocytogenesusingoligonucleotides