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A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics

Shiga toxin-producing Escherichia coli (STEC) are a cause of severe human illness and are frequently associated with haemolytic uraemic syndrome (HUS) in children. It remains difficult to identify virulence factors for STEC that absolutely predict the potential to cause human disease. In addition to...

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Autores principales: Jaudou, Sandra, Deneke, Carlus, Tran, Mai-Lan, Schuh, Elisabeth, Goehler, André, Vorimore, Fabien, Malorny, Burkhard, Fach, Patrick, Grützke, Josephine, Delannoy, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836091/
https://www.ncbi.nlm.nih.gov/pubmed/36748417
http://dx.doi.org/10.1099/mgen.0.000911
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author Jaudou, Sandra
Deneke, Carlus
Tran, Mai-Lan
Schuh, Elisabeth
Goehler, André
Vorimore, Fabien
Malorny, Burkhard
Fach, Patrick
Grützke, Josephine
Delannoy, Sabine
author_facet Jaudou, Sandra
Deneke, Carlus
Tran, Mai-Lan
Schuh, Elisabeth
Goehler, André
Vorimore, Fabien
Malorny, Burkhard
Fach, Patrick
Grützke, Josephine
Delannoy, Sabine
author_sort Jaudou, Sandra
collection PubMed
description Shiga toxin-producing Escherichia coli (STEC) are a cause of severe human illness and are frequently associated with haemolytic uraemic syndrome (HUS) in children. It remains difficult to identify virulence factors for STEC that absolutely predict the potential to cause human disease. In addition to the Shiga-toxin (stx genes), many additional factors have been reported, such as intimin (eae gene), which is clearly an aggravating factor for developing HUS. Current STEC detection methods classically rely on real-time PCR (qPCR) to detect the presence of the key virulence markers (stx and eae). Although qPCR gives an insight into the presence of these virulence markers, it is not appropriate for confirming their presence in the same strain. Therefore, isolation steps are necessary to confirm STEC viability and characterize STEC genomes. While STEC isolation is laborious and time-consuming, metagenomics has the potential to accelerate the STEC characterization process in an isolation-free manner. Recently, short-read sequencing metagenomics have been applied for this purpose, but assembly quality and contiguity suffer from the high proportion of mobile genetic elements occurring in STEC strains. To circumvent this problem, we used long-read sequencing metagenomics for identifying eae-positive STEC strains using raw cow's milk as a causative matrix for STEC food-borne outbreaks. By comparing enrichment conditions, optimizing library preparation for MinION sequencing and generating an easy-to-use STEC characterization pipeline, the direct identification of an eae-positive STEC strain was successful after enrichment of artificially contaminated raw cow's milk samples at a contamination level as low as 5 c.f.u. ml(−1). Our newly developed method combines optimized enrichment conditions of STEC in raw milk in combination with a complete STEC analysis pipeline from long-read sequencing metagenomics data. This study shows the potential of the innovative methodology for characterizing STEC strains from complex matrices. Further developments will nonetheless be necessary for this method to be applied in STEC surveillance.
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spelling pubmed-98360912023-01-13 A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics Jaudou, Sandra Deneke, Carlus Tran, Mai-Lan Schuh, Elisabeth Goehler, André Vorimore, Fabien Malorny, Burkhard Fach, Patrick Grützke, Josephine Delannoy, Sabine Microb Genom Research Articles Shiga toxin-producing Escherichia coli (STEC) are a cause of severe human illness and are frequently associated with haemolytic uraemic syndrome (HUS) in children. It remains difficult to identify virulence factors for STEC that absolutely predict the potential to cause human disease. In addition to the Shiga-toxin (stx genes), many additional factors have been reported, such as intimin (eae gene), which is clearly an aggravating factor for developing HUS. Current STEC detection methods classically rely on real-time PCR (qPCR) to detect the presence of the key virulence markers (stx and eae). Although qPCR gives an insight into the presence of these virulence markers, it is not appropriate for confirming their presence in the same strain. Therefore, isolation steps are necessary to confirm STEC viability and characterize STEC genomes. While STEC isolation is laborious and time-consuming, metagenomics has the potential to accelerate the STEC characterization process in an isolation-free manner. Recently, short-read sequencing metagenomics have been applied for this purpose, but assembly quality and contiguity suffer from the high proportion of mobile genetic elements occurring in STEC strains. To circumvent this problem, we used long-read sequencing metagenomics for identifying eae-positive STEC strains using raw cow's milk as a causative matrix for STEC food-borne outbreaks. By comparing enrichment conditions, optimizing library preparation for MinION sequencing and generating an easy-to-use STEC characterization pipeline, the direct identification of an eae-positive STEC strain was successful after enrichment of artificially contaminated raw cow's milk samples at a contamination level as low as 5 c.f.u. ml(−1). Our newly developed method combines optimized enrichment conditions of STEC in raw milk in combination with a complete STEC analysis pipeline from long-read sequencing metagenomics data. This study shows the potential of the innovative methodology for characterizing STEC strains from complex matrices. Further developments will nonetheless be necessary for this method to be applied in STEC surveillance. Microbiology Society 2022-11-24 /pmc/articles/PMC9836091/ /pubmed/36748417 http://dx.doi.org/10.1099/mgen.0.000911 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License.
spellingShingle Research Articles
Jaudou, Sandra
Deneke, Carlus
Tran, Mai-Lan
Schuh, Elisabeth
Goehler, André
Vorimore, Fabien
Malorny, Burkhard
Fach, Patrick
Grützke, Josephine
Delannoy, Sabine
A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics
title A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics
title_full A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics
title_fullStr A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics
title_full_unstemmed A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics
title_short A step forward for Shiga toxin-producing Escherichia coli identification and characterization in raw milk using long-read metagenomics
title_sort step forward for shiga toxin-producing escherichia coli identification and characterization in raw milk using long-read metagenomics
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836091/
https://www.ncbi.nlm.nih.gov/pubmed/36748417
http://dx.doi.org/10.1099/mgen.0.000911
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