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Species Level Description of the Human Ileal Bacterial Microbiota
The small bowel is responsible for most of the body’s nutritional uptake and for the development of intestinal and systemic tolerance towards microbes. Nevertheless, the human small bowel microbiota has remained poorly characterized, mainly owing to sampling difficulties. Sample collection directly...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856834/ https://www.ncbi.nlm.nih.gov/pubmed/29549283 http://dx.doi.org/10.1038/s41598-018-23198-5 |
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author | Villmones, Heidi Cecilie Haug, Erik Skaaheim Ulvestad, Elling Grude, Nils Stenstad, Tore Halland, Adrian Kommedal, Øyvind |
author_facet | Villmones, Heidi Cecilie Haug, Erik Skaaheim Ulvestad, Elling Grude, Nils Stenstad, Tore Halland, Adrian Kommedal, Øyvind |
author_sort | Villmones, Heidi Cecilie |
collection | PubMed |
description | The small bowel is responsible for most of the body’s nutritional uptake and for the development of intestinal and systemic tolerance towards microbes. Nevertheless, the human small bowel microbiota has remained poorly characterized, mainly owing to sampling difficulties. Sample collection directly from the distal ileum was performed during radical cystectomy with urinary diversion. Material from the ileal mucosa were analysed using massive parallel sequencing of the 16S rRNA gene. Samples from 27 Caucasian patients were included. In total 280 unique Operational Taxonomic Units were identified, whereof 229 could be assigned to a species or a species group. The most frequently detected bacteria belonged to the genera Streptococcus, Granulicatella, Actinomyces, Solobacterium, Rothia, Gemella and TM7(G-1). Among these, the most abundant species were typically streptococci within the mitis and sanguinis groups, Streptococcus salivarius, Rothia mucilaginosa and Actinomyces from the A. meyeri/odontolyticus group. The amounts of Proteobacteria and strict anaerobes were low. The microbiota of the distal part of the human ileum is oral-like and strikingly different from the colonic microbiota. Although our patient population is elderly and hospitalized with a high prevalence of chronic conditions, our results provide new and valuable insights into a lesser explored part of the human intestinal ecosystem. |
format | Online Article Text |
id | pubmed-5856834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58568342018-03-22 Species Level Description of the Human Ileal Bacterial Microbiota Villmones, Heidi Cecilie Haug, Erik Skaaheim Ulvestad, Elling Grude, Nils Stenstad, Tore Halland, Adrian Kommedal, Øyvind Sci Rep Article The small bowel is responsible for most of the body’s nutritional uptake and for the development of intestinal and systemic tolerance towards microbes. Nevertheless, the human small bowel microbiota has remained poorly characterized, mainly owing to sampling difficulties. Sample collection directly from the distal ileum was performed during radical cystectomy with urinary diversion. Material from the ileal mucosa were analysed using massive parallel sequencing of the 16S rRNA gene. Samples from 27 Caucasian patients were included. In total 280 unique Operational Taxonomic Units were identified, whereof 229 could be assigned to a species or a species group. The most frequently detected bacteria belonged to the genera Streptococcus, Granulicatella, Actinomyces, Solobacterium, Rothia, Gemella and TM7(G-1). Among these, the most abundant species were typically streptococci within the mitis and sanguinis groups, Streptococcus salivarius, Rothia mucilaginosa and Actinomyces from the A. meyeri/odontolyticus group. The amounts of Proteobacteria and strict anaerobes were low. The microbiota of the distal part of the human ileum is oral-like and strikingly different from the colonic microbiota. Although our patient population is elderly and hospitalized with a high prevalence of chronic conditions, our results provide new and valuable insights into a lesser explored part of the human intestinal ecosystem. Nature Publishing Group UK 2018-03-16 /pmc/articles/PMC5856834/ /pubmed/29549283 http://dx.doi.org/10.1038/s41598-018-23198-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Villmones, Heidi Cecilie Haug, Erik Skaaheim Ulvestad, Elling Grude, Nils Stenstad, Tore Halland, Adrian Kommedal, Øyvind Species Level Description of the Human Ileal Bacterial Microbiota |
title | Species Level Description of the Human Ileal Bacterial Microbiota |
title_full | Species Level Description of the Human Ileal Bacterial Microbiota |
title_fullStr | Species Level Description of the Human Ileal Bacterial Microbiota |
title_full_unstemmed | Species Level Description of the Human Ileal Bacterial Microbiota |
title_short | Species Level Description of the Human Ileal Bacterial Microbiota |
title_sort | species level description of the human ileal bacterial microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856834/ https://www.ncbi.nlm.nih.gov/pubmed/29549283 http://dx.doi.org/10.1038/s41598-018-23198-5 |
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