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

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          Abstract

          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.

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          Most cited references31

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          Group-specific primer and probe sets to detect methanogenic communities using quantitative real-time polymerase chain reaction.

          Real-time polymerase chain reaction (PCR) is a highly sensitive method that can be used for the detection and quantification of microbial populations without cultivating them in anaerobic processes and environmental samples. This work was conducted to design primer and probe sets for the detection of methanogens using a real-time PCR with the TaqMan system. Six group-specific methanogenic primer and probe sets were designed. These sets separately detect four orders (Methanococcales, Methanobacteriales, Methanomicrobiales, and Methanosarcinales) along with two families (Methanosarcinaceae and Methanosaetaceae) of the order Methanosarcinales. We also designed the universal primer and probe sets that specifically detect the 16S rDNA of prokaryotes and of the domain Bacteria and Archaea, and which are fully compatible with the TaqMan real-time PCR system. Target-group specificity of each primer and probe set was empirically verified by testing DNA isolated from 28 archaeal cultures and by analyzing potential false results. In general, each primer and probe set was very specific to the target group. The primer and probe sets designed in this study can be used to detect and quantify the order-level (family-level in the case of Methanosarcinales) methanogenic groups in anaerobic biological processes and various environments.
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            Defining a healthy human gut microbiome: current concepts, future directions, and clinical applications.

            Indigenous microbiota are an essential component in the modern concept of human health, but the composition and functional characteristics of a healthy microbiome remain to be precisely defined. Patterns of microbial colonization associated with disease states have been documented, but the health-associated microbial patterns and their functional characteristics are less clear. A healthy microbiome, considered in the context of body habitat or body site, could be described in terms of ecologic stability (i.e., ability to resist community structure change under stress or to rapidly return to baseline following a stress-related change), by an idealized (presumably health-associated) composition or by a desirable functional profile (including metabolic and trophic provisions to the host). Elucidation of the properties of healthy microbiota would provide a target for dietary interventions and/or microbial modifications aimed at sustaining health in generally healthy populations and improving the health of individuals exhibiting disrupted microbiota and associated diseases. Copyright © 2012 Elsevier Inc. All rights reserved.
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              Identification of an Intestinal Microbiota Signature Associated With Severity of Irritable Bowel Syndrome.

              We have limited knowledge about the association between the composition of the intestinal microbiota and clinical features of irritable bowel syndrome (IBS). We collected information on the fecal and mucosa-associated microbiota of patients with IBS and evaluated whether these were associated with symptoms.
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                Author and article information

                Contributors
                +45 47 32 29 52 , Lrk@dadlnet.dk
                Journal
                Clin Transl Gastroenterol
                Clin Transl Gastroenterol
                Clinical and Translational Gastroenterology
                Nature Publishing Group US (New York )
                2155-384X
                19 June 2018
                June 2018
                : 9
                : 6
                : 161
                Affiliations
                [1 ]GRID grid.476266.7, Department of Gastroenterology, , Zealand University Hospital, ; Lykkebækvej 1, DK–4600 Køge, Denmark
                [2 ]ISNI 0000 0001 0674 042X, GRID grid.5254.6, Department of Clinical Medicine, , University of Copenhagen, ; København, Denmark
                [3 ]ISNI 0000 0004 0417 4147, GRID grid.6203.7, Department of Bacteria, Parasites & Fungi, , Statens Serum Institut, ; Artillerivej 5, DK–2300 Copenhagen S, Denmark
                [4 ]ISNI 0000 0004 0646 7373, GRID grid.4973.9, Department of Clinical Microbiology, , Copenhagen University Hospital, ; Kettegård Alle 30, DK–2560 Hvidovre, Denmark
                Article
                27
                10.1038/s41424-018-0027-2
                6006308
                29915224
                1415ae83-2c97-4a81-bd1a-4fbb69ccce3c
                © 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/.

                History
                : 5 February 2018
                : 23 March 2018
                : 9 April 2018
                Categories
                Article
                Custom metadata
                © The Author(s) 2018

                Gastroenterology & Hepatology
                Gastroenterology & Hepatology

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