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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...
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Published in: | Scientific reports 2019-03, Vol.9 (1), p.4244-4244, Article 4244 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-019-40842-w |