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Detection of Salmonella by Surface Plasmon Resonance

This study explores the possibility of simultaneous and specific detection of Salmonella serovars by surface plasmon resonance (SPR). The Plasmonic(®) SPR device was used to develop this rapid assay. The sandwich immunoassay involves the use of a polyclonal anti-Salmonella antibody to simultaneous c...

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Autores principales: Barlen, Benjamin, Mazumdar, Saikat Datta, Lezrich, Olga, Kämpfer, Peter, Keusgen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814861/
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author Barlen, Benjamin
Mazumdar, Saikat Datta
Lezrich, Olga
Kämpfer, Peter
Keusgen, Michael
author_facet Barlen, Benjamin
Mazumdar, Saikat Datta
Lezrich, Olga
Kämpfer, Peter
Keusgen, Michael
author_sort Barlen, Benjamin
collection PubMed
description This study explores the possibility of simultaneous and specific detection of Salmonella serovars by surface plasmon resonance (SPR). The Plasmonic(®) SPR device was used to develop this rapid assay. The sandwich immunoassay involves the use of a polyclonal anti-Salmonella antibody to simultaneous capture multiple Salmonella serovars present in a sample. This is followed by specific detection of the captured serovars using O-specific anti-Salmonella antibodies. Milk spiked with Salmonella Typhimurium and Salmonella Enteritidis was used as a model system to establish the assay. The assay was further extended to sequentially differentiate between the two Salmonella serovars on a single SPR chip in a single channel. The assay was proved to work without any additional dilution or clean-up steps. The sample volume requirement for the assay is only 10 μL. The lower limits of detection for Salmonella Typhimurium and Salmonella Enteritidis were 2.50×10(5) cells mL(−1) and 2.50×10(8) cells mL(−1), respectively.
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spelling pubmed-38148612013-11-04 Detection of Salmonella by Surface Plasmon Resonance Barlen, Benjamin Mazumdar, Saikat Datta Lezrich, Olga Kämpfer, Peter Keusgen, Michael Sensors (Basel) Full Research Paper This study explores the possibility of simultaneous and specific detection of Salmonella serovars by surface plasmon resonance (SPR). The Plasmonic(®) SPR device was used to develop this rapid assay. The sandwich immunoassay involves the use of a polyclonal anti-Salmonella antibody to simultaneous capture multiple Salmonella serovars present in a sample. This is followed by specific detection of the captured serovars using O-specific anti-Salmonella antibodies. Milk spiked with Salmonella Typhimurium and Salmonella Enteritidis was used as a model system to establish the assay. The assay was further extended to sequentially differentiate between the two Salmonella serovars on a single SPR chip in a single channel. The assay was proved to work without any additional dilution or clean-up steps. The sample volume requirement for the assay is only 10 μL. The lower limits of detection for Salmonella Typhimurium and Salmonella Enteritidis were 2.50×10(5) cells mL(−1) and 2.50×10(8) cells mL(−1), respectively. Molecular Diversity Preservation International (MDPI) 2007-08-07 /pmc/articles/PMC3814861/ Text en © 2007 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Full Research Paper
Barlen, Benjamin
Mazumdar, Saikat Datta
Lezrich, Olga
Kämpfer, Peter
Keusgen, Michael
Detection of Salmonella by Surface Plasmon Resonance
title Detection of Salmonella by Surface Plasmon Resonance
title_full Detection of Salmonella by Surface Plasmon Resonance
title_fullStr Detection of Salmonella by Surface Plasmon Resonance
title_full_unstemmed Detection of Salmonella by Surface Plasmon Resonance
title_short Detection of Salmonella by Surface Plasmon Resonance
title_sort detection of salmonella by surface plasmon resonance
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814861/
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