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High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation

Low diversity intestinal dysbiosis has been associated with inflammatory bowel disease, including patients with ulcerative colitis with an ileo-anal pouch anastomosis. Furthermore, specific Escherichia coli phylogroups have been linked to inflammatory bowel disease. Our aim was to characterize the d...

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Autores principales: Petersen, Andreas Munk, Mirsepasi-Lauridsen, Hengameh Chloé, Vester-Andersen, Marianne K., Sørensen, Nikolaj, Krogfelt, Karen Angeliki, Bendtsen, Flemming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277091/
https://www.ncbi.nlm.nih.gov/pubmed/32397087
http://dx.doi.org/10.3390/antibiotics9050237
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author Petersen, Andreas Munk
Mirsepasi-Lauridsen, Hengameh Chloé
Vester-Andersen, Marianne K.
Sørensen, Nikolaj
Krogfelt, Karen Angeliki
Bendtsen, Flemming
author_facet Petersen, Andreas Munk
Mirsepasi-Lauridsen, Hengameh Chloé
Vester-Andersen, Marianne K.
Sørensen, Nikolaj
Krogfelt, Karen Angeliki
Bendtsen, Flemming
author_sort Petersen, Andreas Munk
collection PubMed
description Low diversity intestinal dysbiosis has been associated with inflammatory bowel disease, including patients with ulcerative colitis with an ileo-anal pouch anastomosis. Furthermore, specific Escherichia coli phylogroups have been linked to inflammatory bowel disease. Our aim was to characterize the differences among microbiota and E. coli phylogroups in active and inactive pouchitis. Disease activity was assessed using the modified pouch disease activity index and by fecal calprotectin. Microbiota diversity was assessed by 16S rDNA MiSeq sequencing. E. coli phylogroup was determined after triplex PCR. Twenty patients with ulcerative colitis with an ileo-anal pouch anastomosis were included, 10 of whom had active pouchitis. Ileo-anal pouch anastomosis patients had an increased abundance of Proteobacteria colonization compared to patients with ulcerative colitis or Crohn’s disease and healthy controls, p = 1.4·10(−5). No differences in E. coli phylogroup colonization could be determined between cases of active and inactive disease. No significant link was found between α-diversity and pouch inflammation. However, higher levels of Fusobacteria colonization were found in patients with a pouch with a fecal calprotectin level above 500, p = 0.02. In conclusion, patients with a pouch had an increased Proteobacteria abundance, but only Fusobacteria abundance was linked to inflammation.
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spelling pubmed-72770912020-06-15 High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation Petersen, Andreas Munk Mirsepasi-Lauridsen, Hengameh Chloé Vester-Andersen, Marianne K. Sørensen, Nikolaj Krogfelt, Karen Angeliki Bendtsen, Flemming Antibiotics (Basel) Article Low diversity intestinal dysbiosis has been associated with inflammatory bowel disease, including patients with ulcerative colitis with an ileo-anal pouch anastomosis. Furthermore, specific Escherichia coli phylogroups have been linked to inflammatory bowel disease. Our aim was to characterize the differences among microbiota and E. coli phylogroups in active and inactive pouchitis. Disease activity was assessed using the modified pouch disease activity index and by fecal calprotectin. Microbiota diversity was assessed by 16S rDNA MiSeq sequencing. E. coli phylogroup was determined after triplex PCR. Twenty patients with ulcerative colitis with an ileo-anal pouch anastomosis were included, 10 of whom had active pouchitis. Ileo-anal pouch anastomosis patients had an increased abundance of Proteobacteria colonization compared to patients with ulcerative colitis or Crohn’s disease and healthy controls, p = 1.4·10(−5). No differences in E. coli phylogroup colonization could be determined between cases of active and inactive disease. No significant link was found between α-diversity and pouch inflammation. However, higher levels of Fusobacteria colonization were found in patients with a pouch with a fecal calprotectin level above 500, p = 0.02. In conclusion, patients with a pouch had an increased Proteobacteria abundance, but only Fusobacteria abundance was linked to inflammation. MDPI 2020-05-08 /pmc/articles/PMC7277091/ /pubmed/32397087 http://dx.doi.org/10.3390/antibiotics9050237 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Petersen, Andreas Munk
Mirsepasi-Lauridsen, Hengameh Chloé
Vester-Andersen, Marianne K.
Sørensen, Nikolaj
Krogfelt, Karen Angeliki
Bendtsen, Flemming
High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation
title High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation
title_full High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation
title_fullStr High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation
title_full_unstemmed High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation
title_short High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation
title_sort high abundance of proteobacteria in ileo-anal pouch anastomosis and increased abundance of fusobacteria associated with increased pouch inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277091/
https://www.ncbi.nlm.nih.gov/pubmed/32397087
http://dx.doi.org/10.3390/antibiotics9050237
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