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Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography

The emetic toxin cereulide is a 1.2 kDa dodecadepsipeptide produced by the food pathogen Bacillus cereus. As cereulide poses a serious health risk to humans, sensitive and specific detection, as well as toxin purification and quantification, methods are of utmost importance. Recently, a stable isoto...

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Autores principales: Kalbhenn, Eva Maria, Bauer, Tobias, Stark, Timo D., Knüpfer, Mandy, Grass, Gregor, Ehling-Schulz, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915282/
https://www.ncbi.nlm.nih.gov/pubmed/33557428
http://dx.doi.org/10.3390/toxins13020115
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author Kalbhenn, Eva Maria
Bauer, Tobias
Stark, Timo D.
Knüpfer, Mandy
Grass, Gregor
Ehling-Schulz, Monika
author_facet Kalbhenn, Eva Maria
Bauer, Tobias
Stark, Timo D.
Knüpfer, Mandy
Grass, Gregor
Ehling-Schulz, Monika
author_sort Kalbhenn, Eva Maria
collection PubMed
description The emetic toxin cereulide is a 1.2 kDa dodecadepsipeptide produced by the food pathogen Bacillus cereus. As cereulide poses a serious health risk to humans, sensitive and specific detection, as well as toxin purification and quantification, methods are of utmost importance. Recently, a stable isotope dilution assay tandem mass spectrometry (SIDA–MS/MS)-based method has been described, and an method for the quantitation of cereulide in foods was established by the International Organization for Standardization (ISO). However, although this SIDA–MS/MS method is highly accurate, the sophisticated high-end MS equipment required for such measurements limits the method’s suitability for microbiological and molecular research. Thus, we aimed to develop a method for cereulide toxin detection and isolation using equipment commonly available in microbiological and biochemical research laboratories. Reproducible detection and relative quantification of cereulide was achieved, employing reversed phase chromatography (RPC). Chromatographic signals were cross validated by ultraperformance liquid chromatography–mass spectrometry (UPLC–MS/MS). The specificity of the RPC method was tested using a test panel of strains that included non-emetic representatives of the B. cereus group, emetic B. cereus strains, and cereulide-deficient isogenic mutants. In summary, the new method represents a robust, economical, and easily accessible research tool that complements existing diagnostics for the detection and quantification of cereulide.
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spelling pubmed-79152822021-03-01 Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography Kalbhenn, Eva Maria Bauer, Tobias Stark, Timo D. Knüpfer, Mandy Grass, Gregor Ehling-Schulz, Monika Toxins (Basel) Communication The emetic toxin cereulide is a 1.2 kDa dodecadepsipeptide produced by the food pathogen Bacillus cereus. As cereulide poses a serious health risk to humans, sensitive and specific detection, as well as toxin purification and quantification, methods are of utmost importance. Recently, a stable isotope dilution assay tandem mass spectrometry (SIDA–MS/MS)-based method has been described, and an method for the quantitation of cereulide in foods was established by the International Organization for Standardization (ISO). However, although this SIDA–MS/MS method is highly accurate, the sophisticated high-end MS equipment required for such measurements limits the method’s suitability for microbiological and molecular research. Thus, we aimed to develop a method for cereulide toxin detection and isolation using equipment commonly available in microbiological and biochemical research laboratories. Reproducible detection and relative quantification of cereulide was achieved, employing reversed phase chromatography (RPC). Chromatographic signals were cross validated by ultraperformance liquid chromatography–mass spectrometry (UPLC–MS/MS). The specificity of the RPC method was tested using a test panel of strains that included non-emetic representatives of the B. cereus group, emetic B. cereus strains, and cereulide-deficient isogenic mutants. In summary, the new method represents a robust, economical, and easily accessible research tool that complements existing diagnostics for the detection and quantification of cereulide. MDPI 2021-02-04 /pmc/articles/PMC7915282/ /pubmed/33557428 http://dx.doi.org/10.3390/toxins13020115 Text en © 2021 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Kalbhenn, Eva Maria
Bauer, Tobias
Stark, Timo D.
Knüpfer, Mandy
Grass, Gregor
Ehling-Schulz, Monika
Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography
title Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography
title_full Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography
title_fullStr Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography
title_full_unstemmed Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography
title_short Detection and Isolation of Emetic Bacillus cereus Toxin Cereulide by Reversed Phase Chromatography
title_sort detection and isolation of emetic bacillus cereus toxin cereulide by reversed phase chromatography
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915282/
https://www.ncbi.nlm.nih.gov/pubmed/33557428
http://dx.doi.org/10.3390/toxins13020115
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