ArticleBMC microbiology2012
Epidemiological association of Campylobacter jejuni groups with pathogenicity-associated genetic markers.
Article in BMC microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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14 citing papers in PubMed, 30 citations in OpenAlex.
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- Genomic Epidemiology and Evolution of Diverse Lineages of Clinical Campylobacter jejuni Cocirculating in New Hampshire, USA, 2017.Journal of clinical microbiology · 2020Article
- Unexpected differential metabolic responses of Campylobacter jejuni to the abundant presence of glutamate and fucose.Metabolomics : Official journal of the Metabolomic Society · 2018Article
- Monomorphic genotypes within a generalist lineage ofMicrobial genomics · 2016Article
- Association ofEuropean journal of microbiology & immunology · 2016Article
- Glucose Metabolism via the Entner-Doudoroff Pathway inFrontiers in microbiology · 2016Article
- Mass Spectrometry-based PhyloProteomics (MSPP): A novel microbial typing Method.Scientific reports · 2015Article
- Colonisation of a phage susceptible Campylobacter jejuni population in two phage positive broiler flocks.PloS one · 2014Article
- The periplasmic enzyme, AnsB, of Shigella flexneri modulates bacterial adherence to host epithelial cells.PloS one · 2014Article
- Discrimination of multilocus sequence typing-based Campylobacter jejuni subgroups by MALDI-TOF mass spectrometry.BMC microbiology · 2013Article
- Modification of intestinal microbiota and its consequences for innate immune response in the pathogenesis of campylobacteriosis.Clinical & developmental immunology · 2013Review
- The Campylobacter jejuni Cj0268c protein is required for adhesion and invasion in vitro.PloS one · 2013Article
- Operationalising factors that explain the emergence of infectious diseases: a case study of the human campylobacteriosis epidemic.PloS one · 2013Article
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5 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundCampylobacter jejuni, the most leading cause for bacterial gastroenteritis worldwide, shows a high genetic diversity among its isolates. Recently, we demonstrated the existence of six C. jejuni-groups by combining MLST with six genetic markers. These groups were further characterized by the detection of cj1321-cj1326, fucP, cj0178, cj0755/cfrA, ceuE, pldA, cstII, and cstIII in order (I.) to show further associations between these different genetic markers and MLST CCs. Moreover, different studies were able to associate several of these markers: a sialylated lipoologosaccharide (cstII/III(+)), the gamma-glytamyl-transpeptidase (ggt(+)), and the absence of a certain allele of the enterochelin-uptake-binding-protein (ceuE(11168)(-)) with severe campylobacteriosis, bloody diarrhea and unpleasant outcome. Additionally more than half of human Campylobacter-isolates were assigned to a non-livestock clade associated with the absence of cj1321-cj1326. These isolates were considered as mere colonizers.From the combination of marker genes, the ratio of human isolates in a specific group, and clinical data (II.) it should be demonstrated to which of the previous defined groups these Campylobacter-subpopulations, associated with higher virulence, correspond.
resultsBesides the marker gene pldA, all new estimated genetic markers show significant differences in their distribution among the various MLST-based groups. Especially the genes for cj1321-cj1326, fucP, cj0178, cj0755/cfrA are widely associated with each other and split the study population into two major and seven intermediate groups substantiating the previous group-definition, whereas cstII and cstIII indicate at least three groups following an independent distribution pattern.
conclusionsBased on these data a group of C. jejuni-isolates characterized by the presence of ansB, dmsA, ggt, and the absence of cj1365c, cj1585c, cj1321-cj1326, fucP, cj0178, cj0755/cfrA, and cstII/III was associated with a higher prevalence in human campylobacteriosis, bloody diarrhea as well as hospitalization and bears obviously a higher virulence for humans. In contrast to that better livestock-adapted groups characterized by the ability to utilize L-fucose and the presence of all of the five identified putative C. jejuni iron-uptake systems as well as cj1321-cj1326, cj1365c, cj1585c, and cstII and/or cstIII (sialylated lipoologosaccharide) is more prevalent in animal hosts and was secondary associated with less severe campylobacteriosis.
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