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Proteotyping as alternate typing method to differentiate Campylobacter coli clades

Besides Campylobacter jejuni, Campylobacter coli is the most common bacterial cause of gastroenteritis worldwide. C. coli is subdivided into three clades, which are associated with sample source. Clade 1 isolates are associated with acute diarrhea in humans whereas clade 2 and 3 isolates are more co...

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Autores principales: Emele, Matthias Frederik, Možina, Sonja Smole, Lugert, Raimond, Bohne, Wolfgang, Masanta, Wycliffe Omurwa, Riedel, Thomas, Groß, Uwe, Bader, Oliver, Zautner, Andreas Erich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414644/
https://www.ncbi.nlm.nih.gov/pubmed/30862911
http://dx.doi.org/10.1038/s41598-019-40842-w
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author Emele, Matthias Frederik
Možina, Sonja Smole
Lugert, Raimond
Bohne, Wolfgang
Masanta, Wycliffe Omurwa
Riedel, Thomas
Groß, Uwe
Bader, Oliver
Zautner, Andreas Erich
author_facet Emele, Matthias Frederik
Možina, Sonja Smole
Lugert, Raimond
Bohne, Wolfgang
Masanta, Wycliffe Omurwa
Riedel, Thomas
Groß, Uwe
Bader, Oliver
Zautner, Andreas Erich
author_sort Emele, Matthias Frederik
collection PubMed
description Besides Campylobacter jejuni, Campylobacter coli is the most common bacterial cause of gastroenteritis worldwide. C. coli is subdivided into three clades, which are associated with sample source. Clade 1 isolates are associated with acute diarrhea in humans whereas clade 2 and 3 isolates are more commonly obtained from environmental waters. The phylogenetic classification of an isolate is commonly done using laborious multilocus sequence typing (MLST). The aim of this study was to establish a proteotyping scheme using MALDI-TOF MS to offer an alternative to sequence-based methods. A total of 97 clade-representative C. coli isolates were analyzed by MALDI-TOF-based intact cell mass spectrometry (ICMS) and evaluated to establish a C. coli proteotyping scheme. MLST was used as reference method. Different isoforms of the detectable biomarkers, resulting in biomarker mass shifts, were associated with their amino acid sequences and included into the C. coli proteotyping scheme. In total, we identified 16 biomarkers to differentiate C. coli into the three clades and three additional sub-clades of clade 1. In this study, proteotyping has been successfully adapted to C. coli. The established C. coli clades and sub-clades can be discriminated using this method. Especially the clinically relevant clade 1 isolates can be differentiated clearly.
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spelling pubmed-64146442019-03-14 Proteotyping as alternate typing method to differentiate Campylobacter coli clades Emele, Matthias Frederik Možina, Sonja Smole Lugert, Raimond Bohne, Wolfgang Masanta, Wycliffe Omurwa Riedel, Thomas Groß, Uwe Bader, Oliver Zautner, Andreas Erich Sci Rep Article Besides Campylobacter jejuni, Campylobacter coli is the most common bacterial cause of gastroenteritis worldwide. C. coli is subdivided into three clades, which are associated with sample source. Clade 1 isolates are associated with acute diarrhea in humans whereas clade 2 and 3 isolates are more commonly obtained from environmental waters. The phylogenetic classification of an isolate is commonly done using laborious multilocus sequence typing (MLST). The aim of this study was to establish a proteotyping scheme using MALDI-TOF MS to offer an alternative to sequence-based methods. A total of 97 clade-representative C. coli isolates were analyzed by MALDI-TOF-based intact cell mass spectrometry (ICMS) and evaluated to establish a C. coli proteotyping scheme. MLST was used as reference method. Different isoforms of the detectable biomarkers, resulting in biomarker mass shifts, were associated with their amino acid sequences and included into the C. coli proteotyping scheme. In total, we identified 16 biomarkers to differentiate C. coli into the three clades and three additional sub-clades of clade 1. In this study, proteotyping has been successfully adapted to C. coli. The established C. coli clades and sub-clades can be discriminated using this method. Especially the clinically relevant clade 1 isolates can be differentiated clearly. Nature Publishing Group UK 2019-03-12 /pmc/articles/PMC6414644/ /pubmed/30862911 http://dx.doi.org/10.1038/s41598-019-40842-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Emele, Matthias Frederik
Možina, Sonja Smole
Lugert, Raimond
Bohne, Wolfgang
Masanta, Wycliffe Omurwa
Riedel, Thomas
Groß, Uwe
Bader, Oliver
Zautner, Andreas Erich
Proteotyping as alternate typing method to differentiate Campylobacter coli clades
title Proteotyping as alternate typing method to differentiate Campylobacter coli clades
title_full Proteotyping as alternate typing method to differentiate Campylobacter coli clades
title_fullStr Proteotyping as alternate typing method to differentiate Campylobacter coli clades
title_full_unstemmed Proteotyping as alternate typing method to differentiate Campylobacter coli clades
title_short Proteotyping as alternate typing method to differentiate Campylobacter coli clades
title_sort proteotyping as alternate typing method to differentiate campylobacter coli clades
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414644/
https://www.ncbi.nlm.nih.gov/pubmed/30862911
http://dx.doi.org/10.1038/s41598-019-40842-w
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