Literature DB >> 26954709

Microbiome Heterogeneity Characterizing Intestinal Tissue and Inflammatory Bowel Disease Phenotype.

Andrea D Tyler1, Richard Kirsch, Raquel Milgrom, Joanne M Stempak, Boyko Kabakchiev, Mark S Silverberg.   

Abstract

Inflammatory bowel disease has been associated with differential abundance of numerous organisms when compared to healthy controls (HCs); however, few studies have investigated variability in the microbiome across intestinal locations and how this variability might be related to disease location and phenotype. In this study, we have analyzed the microbiome of a large cohort of individuals recruited at Mount Sinai Hospital in Toronto, Canada. Biopsies were taken from subjects with Crohn's disease, ulcerative colitis, and HC, and also individuals having undergone ileal pouch-anal anastomosis for treatment of ulcerative colitis or familial adenomatous polyposis. Microbial 16S rRNA was sequenced using the Illumina MiSeq platform. We observed a great deal of variability in the microbiome characterizing different sampling locations. Samples from pouch and afferent limb were comparable in microbial composition. When comparing sigmoid and terminal ileum samples, more differences were observed. The greatest number of differentially abundant microbes was observed when comparing either pouch or afferent limb samples to sigmoid or terminal ileum. Despite these differences, we were able to observe modest microbial variability between inflammatory bowel disease phenotypes and HCs, even when controlling for sampling location and additional experimental factors. Most detected associations were observed between HCs and Crohn's disease, with decreases in specific genera in the families Ruminococcaceae and Lachnospiraceae characterizing tissue samples from individuals with Crohn's disease. This study highlights important considerations when analyzing the composition of the microbiome and also provides useful insight into differences in the microbiome characterizing these seemingly related phenotypes.

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Year:  2016        PMID: 26954709      PMCID: PMC4812575          DOI: 10.1097/MIB.0000000000000674

Source DB:  PubMed          Journal:  Inflamm Bowel Dis        ISSN: 1078-0998            Impact factor:   5.325


  37 in total

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  11 in total

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Review 2.  Should We Divide Crohn's Disease Into Ileum-Dominant and Isolated Colonic Diseases?

Authors:  Parambir S Dulai; Siddharth Singh; Niels Vande Casteele; Brigid S Boland; Jesus Rivera-Nieves; Peter B Ernst; Lars Eckmann; Kim E Barrett; John T Chang; William J Sandborn
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Journal:  Front Immunol       Date:  2019-03-18       Impact factor: 7.561

5.  Mucosa-Associated Microbiota in Ileoanal Pouches May Contribute to Clinical Symptoms, Particularly Stool Frequency, Independent of Endoscopic Disease Activity.

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6.  Exploration of the Potential Relationship Between Gut Microbiota Remodeling Under the Influence of High-Protein Diet and Crohn's Disease.

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7.  Alginate Oligosaccharides Ameliorate DSS-Induced Colitis through Modulation of AMPK/NF-κB Pathway and Intestinal Microbiota.

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8.  Crohn's Disease Differentially Affects Region-Specific Composition and Aerotolerance Profiles of Mucosally Adherent Bacteria.

Authors:  Nur M Shahir; Jeremy R Wang; E Ashley Wolber; Matthew S Schaner; Daniel N Frank; Diana Ir; Charles E Robertson; Nicole Chaumont; Timothy S Sadiq; Mark J Koruda; Reza Rahbar; B Darren Nix; Rodney D Newberry; R Balfour Sartor; Shehzad Z Sheikh; Terrence S Furey
Journal:  Inflamm Bowel Dis       Date:  2020-11-19       Impact factor: 5.325

9.  Effects of Melatonin on Intestinal Microbiota and Oxidative Stress in Colitis Mice.

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Journal:  Biomed Res Int       Date:  2018-02-06       Impact factor: 3.411

10.  Astragalin Attenuates Dextran Sulfate Sodium (DSS)-Induced Acute Experimental Colitis by Alleviating Gut Microbiota Dysbiosis and Inhibiting NF-κB Activation in Mice.

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Journal:  Front Immunol       Date:  2020-09-15       Impact factor: 7.561

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