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Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis

BACKGROUND: Inflammatory bowel disease (IBD) is characterized by gut dysbiosis. To date, the large bowel microbiota has been in focus. However, the microbiota of the small intestine may also be of importance, as the small bowel is a site for the induction and control of mucosal immune responses, whi...

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Autores principales: Sjöberg, Fei, Barkman, Cecilia, Nookaew, Intawat, Östman, Sofia, Adlerberth, Ingegerd, Saalman, Robert, Wold, Agnes E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648149/
https://www.ncbi.nlm.nih.gov/pubmed/29049404
http://dx.doi.org/10.1371/journal.pone.0186178
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author Sjöberg, Fei
Barkman, Cecilia
Nookaew, Intawat
Östman, Sofia
Adlerberth, Ingegerd
Saalman, Robert
Wold, Agnes E.
author_facet Sjöberg, Fei
Barkman, Cecilia
Nookaew, Intawat
Östman, Sofia
Adlerberth, Ingegerd
Saalman, Robert
Wold, Agnes E.
author_sort Sjöberg, Fei
collection PubMed
description BACKGROUND: Inflammatory bowel disease (IBD) is characterized by gut dysbiosis. To date, the large bowel microbiota has been in focus. However, the microbiota of the small intestine may also be of importance, as the small bowel is a site for the induction and control of mucosal immune responses, which can be modulated by constituents of the local microbiota. METHODS: Duodenal fluids were collected during diagnostic work-up of treatment-naïve children who were suspected of having IBD. The duodenal fluids were analyzed by pyrosequencing (average of 32,000 reads/sample, read length of 500 nucleotides). After diagnosis, the duodenal microbiota of subjects with ulcerative colitis (N = 8) or Crohn’s disease (N = 5), and non-IBD controls (N = 8) were compared. RESULTS: Pyrosequencing revealed that the duodenal microbiota of children with ulcerative colitis contained fewer Operational Taxonomic Units (OTUs) per individual than the duodenal microbiota of the controls (P = 0.005). This reduction in richness of the duodenal microbiota was seen for three major phyla: Firmicutes, Actinobacteria, and Bacteroidetes. Several bacterial genera were detected less frequently in the children with ulcerative colitis than in the non-IBD controls, including Collinsella (P = 0.001), Lactobacillus (P = 0.007), and Bacillus (P = 0.007), as well as a non-identified member of the order Sphingobacteriales (P = 0.007). CONCLUSIONS: In this pilot study, we show that the duodenal microbiota of children with ulcerative colitis exhibits reduced overall richness, despite the fact that the inflammation is primarily localized to the colon. These results should be corroborated in a larger study.
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spelling pubmed-56481492017-11-03 Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis Sjöberg, Fei Barkman, Cecilia Nookaew, Intawat Östman, Sofia Adlerberth, Ingegerd Saalman, Robert Wold, Agnes E. PLoS One Research Article BACKGROUND: Inflammatory bowel disease (IBD) is characterized by gut dysbiosis. To date, the large bowel microbiota has been in focus. However, the microbiota of the small intestine may also be of importance, as the small bowel is a site for the induction and control of mucosal immune responses, which can be modulated by constituents of the local microbiota. METHODS: Duodenal fluids were collected during diagnostic work-up of treatment-naïve children who were suspected of having IBD. The duodenal fluids were analyzed by pyrosequencing (average of 32,000 reads/sample, read length of 500 nucleotides). After diagnosis, the duodenal microbiota of subjects with ulcerative colitis (N = 8) or Crohn’s disease (N = 5), and non-IBD controls (N = 8) were compared. RESULTS: Pyrosequencing revealed that the duodenal microbiota of children with ulcerative colitis contained fewer Operational Taxonomic Units (OTUs) per individual than the duodenal microbiota of the controls (P = 0.005). This reduction in richness of the duodenal microbiota was seen for three major phyla: Firmicutes, Actinobacteria, and Bacteroidetes. Several bacterial genera were detected less frequently in the children with ulcerative colitis than in the non-IBD controls, including Collinsella (P = 0.001), Lactobacillus (P = 0.007), and Bacillus (P = 0.007), as well as a non-identified member of the order Sphingobacteriales (P = 0.007). CONCLUSIONS: In this pilot study, we show that the duodenal microbiota of children with ulcerative colitis exhibits reduced overall richness, despite the fact that the inflammation is primarily localized to the colon. These results should be corroborated in a larger study. Public Library of Science 2017-10-19 /pmc/articles/PMC5648149/ /pubmed/29049404 http://dx.doi.org/10.1371/journal.pone.0186178 Text en © 2017 Sjöberg et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sjöberg, Fei
Barkman, Cecilia
Nookaew, Intawat
Östman, Sofia
Adlerberth, Ingegerd
Saalman, Robert
Wold, Agnes E.
Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
title Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
title_full Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
title_fullStr Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
title_full_unstemmed Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
title_short Low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
title_sort low-complexity microbiota in the duodenum of children with newly diagnosed ulcerative colitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648149/
https://www.ncbi.nlm.nih.gov/pubmed/29049404
http://dx.doi.org/10.1371/journal.pone.0186178
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