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Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota
Alterations in the composition of commensal bacterial populations, a phenomenon known as dysbiosis, are linked to multiple gastrointestinal disorders, such as inflammatory bowel disease and irritable bowel syndrome, or to infections by diverse enteric pathogens. Blastocystis is one of the most commo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857090/ https://www.ncbi.nlm.nih.gov/pubmed/27147260 http://dx.doi.org/10.1038/srep25255 |
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author | Audebert, Christophe Even, Gaël Cian, Amandine Loywick, Alexandre Merlin, Sophie Viscogliosi, Eric Chabé, Magali |
author_facet | Audebert, Christophe Even, Gaël Cian, Amandine Loywick, Alexandre Merlin, Sophie Viscogliosi, Eric Chabé, Magali |
author_sort | Audebert, Christophe |
collection | PubMed |
description | Alterations in the composition of commensal bacterial populations, a phenomenon known as dysbiosis, are linked to multiple gastrointestinal disorders, such as inflammatory bowel disease and irritable bowel syndrome, or to infections by diverse enteric pathogens. Blastocystis is one of the most common single-celled eukaryotes detected in human faecal samples. However, the clinical significance of this widespread colonization remains unclear, and its pathogenic potential is controversial. To address the issue of Blastocystis pathogenicity, we investigated the impact of colonization by this protist on the composition of the human gut microbiota. For that purpose, we conducted a cross-sectional study including 48 Blastocystis-colonized patients and 48 Blastocystis-free subjects and performed an Ion Torrent 16S rDNA gene sequencing to decipher the Blastocystis-associated gut microbiota. Here, we report a higher bacterial diversity in faecal microbiota of Blastocystis colonized patients, a higher abundance of Clostridia as well as a lower abundance of Enterobacteriaceae. Our results contribute to suggesting that Blastocystis colonization is usually associated with a healthy gut microbiota, rather than with gut dysbiosis generally observed in metabolic or infectious inflammatory diseases of the lower gastrointestinal tract. |
format | Online Article Text |
id | pubmed-4857090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48570902016-05-18 Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota Audebert, Christophe Even, Gaël Cian, Amandine Loywick, Alexandre Merlin, Sophie Viscogliosi, Eric Chabé, Magali Sci Rep Article Alterations in the composition of commensal bacterial populations, a phenomenon known as dysbiosis, are linked to multiple gastrointestinal disorders, such as inflammatory bowel disease and irritable bowel syndrome, or to infections by diverse enteric pathogens. Blastocystis is one of the most common single-celled eukaryotes detected in human faecal samples. However, the clinical significance of this widespread colonization remains unclear, and its pathogenic potential is controversial. To address the issue of Blastocystis pathogenicity, we investigated the impact of colonization by this protist on the composition of the human gut microbiota. For that purpose, we conducted a cross-sectional study including 48 Blastocystis-colonized patients and 48 Blastocystis-free subjects and performed an Ion Torrent 16S rDNA gene sequencing to decipher the Blastocystis-associated gut microbiota. Here, we report a higher bacterial diversity in faecal microbiota of Blastocystis colonized patients, a higher abundance of Clostridia as well as a lower abundance of Enterobacteriaceae. Our results contribute to suggesting that Blastocystis colonization is usually associated with a healthy gut microbiota, rather than with gut dysbiosis generally observed in metabolic or infectious inflammatory diseases of the lower gastrointestinal tract. Nature Publishing Group 2016-05-05 /pmc/articles/PMC4857090/ /pubmed/27147260 http://dx.doi.org/10.1038/srep25255 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Audebert, Christophe Even, Gaël Cian, Amandine Loywick, Alexandre Merlin, Sophie Viscogliosi, Eric Chabé, Magali Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota |
title | Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota |
title_full | Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota |
title_fullStr | Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota |
title_full_unstemmed | Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota |
title_short | Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota |
title_sort | colonization with the enteric protozoa blastocystis is associated with increased diversity of human gut bacterial microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857090/ https://www.ncbi.nlm.nih.gov/pubmed/27147260 http://dx.doi.org/10.1038/srep25255 |
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