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Campylobacter concisus – A New Player in Intestinal Disease

Over the last decade Campylobacter concisus, a highly fastidious member of the Campylobacter genus has been described as an emergent pathogen of the human intestinal tract. Historically, C. concisus was associated with the human oral cavity and has been linked with periodontal lesions, including gin...

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Autores principales: Kaakoush, Nadeem Omar, Mitchell, Hazel Marjory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3417403/
https://www.ncbi.nlm.nih.gov/pubmed/22919596
http://dx.doi.org/10.3389/fcimb.2012.00004
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author Kaakoush, Nadeem Omar
Mitchell, Hazel Marjory
author_facet Kaakoush, Nadeem Omar
Mitchell, Hazel Marjory
author_sort Kaakoush, Nadeem Omar
collection PubMed
description Over the last decade Campylobacter concisus, a highly fastidious member of the Campylobacter genus has been described as an emergent pathogen of the human intestinal tract. Historically, C. concisus was associated with the human oral cavity and has been linked with periodontal lesions, including gingivitis and periodontitis, although currently its role as an oral pathogen remains contentious. Evidence to support the role of C. concisus in acute intestinal disease has come from studies that have detected or isolated C. concisus as sole pathogen in fecal samples from diarrheic patients. C. concisus has also been associated with chronic intestinal disease, its prevalence being significantly higher in children with newly diagnosed Crohn’s disease (CD) and adults with ulcerative colitis than in controls. Further C. concisus has been isolated from biopsy specimens of patients with CD. While such studies support the role of C. concisus as an intestinal pathogen, its isolation from healthy individuals, and failure of some studies to show a significant difference in C. concisus prevalence in subjects with diarrhea and healthy controls has raised contention as to its role in intestinal disease. Such findings could argue against the role of C. concisus in intestinal disease, however, the fact that C. concisus strains are genetically diverse raises the possibility that differences exist in their pathogenic potential. Evidence to support this view comes from studies showing strain specific differences in the ability of C. concisus to attach to and invade cells and produce virulence factors, including toxins and hemolytic phospholipase A. Further, sequencing of the genome of a C. concisus strain isolated from a child with CD (UNSWCD) and comparison of this with the only other fully sequenced strain (BAA-1457) would suggest that major differences exist in the genetic make-up of this species which could explain different outcomes of C. concisus infection.
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spelling pubmed-34174032012-08-23 Campylobacter concisus – A New Player in Intestinal Disease Kaakoush, Nadeem Omar Mitchell, Hazel Marjory Front Cell Infect Microbiol Microbiology Over the last decade Campylobacter concisus, a highly fastidious member of the Campylobacter genus has been described as an emergent pathogen of the human intestinal tract. Historically, C. concisus was associated with the human oral cavity and has been linked with periodontal lesions, including gingivitis and periodontitis, although currently its role as an oral pathogen remains contentious. Evidence to support the role of C. concisus in acute intestinal disease has come from studies that have detected or isolated C. concisus as sole pathogen in fecal samples from diarrheic patients. C. concisus has also been associated with chronic intestinal disease, its prevalence being significantly higher in children with newly diagnosed Crohn’s disease (CD) and adults with ulcerative colitis than in controls. Further C. concisus has been isolated from biopsy specimens of patients with CD. While such studies support the role of C. concisus as an intestinal pathogen, its isolation from healthy individuals, and failure of some studies to show a significant difference in C. concisus prevalence in subjects with diarrhea and healthy controls has raised contention as to its role in intestinal disease. Such findings could argue against the role of C. concisus in intestinal disease, however, the fact that C. concisus strains are genetically diverse raises the possibility that differences exist in their pathogenic potential. Evidence to support this view comes from studies showing strain specific differences in the ability of C. concisus to attach to and invade cells and produce virulence factors, including toxins and hemolytic phospholipase A. Further, sequencing of the genome of a C. concisus strain isolated from a child with CD (UNSWCD) and comparison of this with the only other fully sequenced strain (BAA-1457) would suggest that major differences exist in the genetic make-up of this species which could explain different outcomes of C. concisus infection. Frontiers Research Foundation 2012-02-03 /pmc/articles/PMC3417403/ /pubmed/22919596 http://dx.doi.org/10.3389/fcimb.2012.00004 Text en Copyright © 2012 Kaakoush and Mitchell. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Microbiology
Kaakoush, Nadeem Omar
Mitchell, Hazel Marjory
Campylobacter concisus – A New Player in Intestinal Disease
title Campylobacter concisus – A New Player in Intestinal Disease
title_full Campylobacter concisus – A New Player in Intestinal Disease
title_fullStr Campylobacter concisus – A New Player in Intestinal Disease
title_full_unstemmed Campylobacter concisus – A New Player in Intestinal Disease
title_short Campylobacter concisus – A New Player in Intestinal Disease
title_sort campylobacter concisus – a new player in intestinal disease
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3417403/
https://www.ncbi.nlm.nih.gov/pubmed/22919596
http://dx.doi.org/10.3389/fcimb.2012.00004
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