Cargando…

Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome

OBJECTIVE: A low prevalence of intestinal parasites has been identified in individuals with irritable bowel syndrome (IBS), but potential associations with alterations in the bacterial microbiome remain largely unexplored. We aimed to investigate the relationship between parasites and bacteria in in...

Descripción completa

Detalles Bibliográficos
Autores principales: Krogsgaard, Laura Rindom, Andersen, Lee O ‘Brien, Johannesen, Thor Bech, Engsbro, Anne Line, Stensvold, Christen Rune, Nielsen, Henrik Vedel, Bytzer, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006308/
https://www.ncbi.nlm.nih.gov/pubmed/29915224
http://dx.doi.org/10.1038/s41424-018-0027-2
_version_ 1783332814173765632
author Krogsgaard, Laura Rindom
Andersen, Lee O ‘Brien
Johannesen, Thor Bech
Engsbro, Anne Line
Stensvold, Christen Rune
Nielsen, Henrik Vedel
Bytzer, Peter
author_facet Krogsgaard, Laura Rindom
Andersen, Lee O ‘Brien
Johannesen, Thor Bech
Engsbro, Anne Line
Stensvold, Christen Rune
Nielsen, Henrik Vedel
Bytzer, Peter
author_sort Krogsgaard, Laura Rindom
collection PubMed
description OBJECTIVE: A low prevalence of intestinal parasites has been identified in individuals with irritable bowel syndrome (IBS), but potential associations with alterations in the bacterial microbiome remain largely unexplored. We aimed to investigate the relationship between parasites and bacteria in individuals with IBS in order to identify potential trans-kingdom microbial characteristics. DESIGN: Stool samples were collected from the Danish background population classified into IBS (n = 119), unspecific gastrointestinal (GI) symptoms (n = 114), and asymptomatic controls (n = 186) based on the Rome III criteria for IBS. Bacterial (16S) and eukaryotic (18S) ribosomal DNA was sequenced, and 18S data were merged with data from conventional parasite laboratory tests. The bacterial microbiome was analyzed according to symptom group and parasite colonization status. RESULTS: Bacterial richness and diversity were similar for IBS and controls but higher in those with unspecific GI symptoms. A higher abundance of Bacteroides and a lower abundance of Faecalibacterium were detected in individuals with IBS and unspecific GI symptoms compared with controls. Principal component analyses indicated differences in bacterial composition related to parasite colonization rather than symptom group. Parasites were detected at the lowest frequency in the IBS group (39%) and in samples dominated by Bacteroides. Higher bacterial richness and diversity were found in parasite-positive samples from controls and those with unspecific GI symptoms but not in individuals with IBS. CONCLUSION: Parasite colonization, rather than bacterial composition, differed between individuals with IBS and healthy controls. Parasite colonization was associated to a rich and diverse bacterial microbiome; however, this association was altered in IBS.
format Online
Article
Text
id pubmed-6006308
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group US
record_format MEDLINE/PubMed
spelling pubmed-60063082018-06-20 Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome Krogsgaard, Laura Rindom Andersen, Lee O ‘Brien Johannesen, Thor Bech Engsbro, Anne Line Stensvold, Christen Rune Nielsen, Henrik Vedel Bytzer, Peter Clin Transl Gastroenterol Article OBJECTIVE: A low prevalence of intestinal parasites has been identified in individuals with irritable bowel syndrome (IBS), but potential associations with alterations in the bacterial microbiome remain largely unexplored. We aimed to investigate the relationship between parasites and bacteria in individuals with IBS in order to identify potential trans-kingdom microbial characteristics. DESIGN: Stool samples were collected from the Danish background population classified into IBS (n = 119), unspecific gastrointestinal (GI) symptoms (n = 114), and asymptomatic controls (n = 186) based on the Rome III criteria for IBS. Bacterial (16S) and eukaryotic (18S) ribosomal DNA was sequenced, and 18S data were merged with data from conventional parasite laboratory tests. The bacterial microbiome was analyzed according to symptom group and parasite colonization status. RESULTS: Bacterial richness and diversity were similar for IBS and controls but higher in those with unspecific GI symptoms. A higher abundance of Bacteroides and a lower abundance of Faecalibacterium were detected in individuals with IBS and unspecific GI symptoms compared with controls. Principal component analyses indicated differences in bacterial composition related to parasite colonization rather than symptom group. Parasites were detected at the lowest frequency in the IBS group (39%) and in samples dominated by Bacteroides. Higher bacterial richness and diversity were found in parasite-positive samples from controls and those with unspecific GI symptoms but not in individuals with IBS. CONCLUSION: Parasite colonization, rather than bacterial composition, differed between individuals with IBS and healthy controls. Parasite colonization was associated to a rich and diverse bacterial microbiome; however, this association was altered in IBS. Nature Publishing Group US 2018-06-19 /pmc/articles/PMC6006308/ /pubmed/29915224 http://dx.doi.org/10.1038/s41424-018-0027-2 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
Krogsgaard, Laura Rindom
Andersen, Lee O ‘Brien
Johannesen, Thor Bech
Engsbro, Anne Line
Stensvold, Christen Rune
Nielsen, Henrik Vedel
Bytzer, Peter
Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
title Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
title_full Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
title_fullStr Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
title_full_unstemmed Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
title_short Characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
title_sort characteristics of the bacterial microbiome in association with common intestinal parasites in irritable bowel syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006308/
https://www.ncbi.nlm.nih.gov/pubmed/29915224
http://dx.doi.org/10.1038/s41424-018-0027-2
work_keys_str_mv AT krogsgaardlaurarindom characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome
AT andersenleeobrien characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome
AT johannesenthorbech characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome
AT engsbroanneline characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome
AT stensvoldchristenrune characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome
AT nielsenhenrikvedel characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome
AT bytzerpeter characteristicsofthebacterialmicrobiomeinassociationwithcommonintestinalparasitesinirritablebowelsyndrome