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The biogeography of the mucosa-associated microbiome in health and disease.

作者信息

Sternes Peter R, Shah Ayesha, Ayala Pintos Camila, Fairlie Thomas, Koloski Natasha, Kang Seungha, Tousignant Kaylyn D, McIlroy Simon J, Morrison Mark, Tyson Gene W, Holtmann Gerald J

机构信息

Centre for Microbiome Research, School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute, Woolloongabba, QLD, Australia.

Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, QLD, Australia.

出版信息

Front Microbiol. 2024 Oct 14;15:1454910. doi: 10.3389/fmicb.2024.1454910. eCollection 2024.


DOI:10.3389/fmicb.2024.1454910
PMID:39469457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11513579/
Abstract

INTRODUCTION: Little is known about the biogeography of the mucosa associated microbiome (MAM) in patients with inflammatory bowel disease (IBD) versus controls in different segments of the gastrointestinal tract, as well as the links between the MAM, gastrointestinal symptoms, and use of proton pump inhibitors (PPI). METHODS: We recruited 59 controls (without structural abnormalities and gastrointestinal symptoms), 44 patients with ulcerative colitis (UC) and 31 with Crohn's disease (CD). Biopsies from various segments of the upper and lower gastrointestinal tract were collected. Microbial composition was assessed via 16S rRNA gene amplicon analysis and the bacterial load of the mucosal biopsies were assessed via qPCR. The MAM was examined in the context of disease status, PPI usage, the severity of gastrointestinal symptoms, and the symptom response to a standardised nutrient challenge (SNC). RESULTS: Microbial communities of the MAM in the upper and lower gastrointestinal tract differed. IBD patients were characterised by relative and absolute depletion of numerous genera known to produce butyrate and/or propionate, with the largest differentiation being the depletion of Faecalibacterium in the lower gastrointestinal tract of CD patients. Notably, PPI users exhibited an enrichment of Faecalibacterium in the lower gastrointestinal tract. The severity of gastrointestinal symptoms, as well as the symptom response to the SNC, were significantly associated with MAM composition in the gastrointestinal tract. CONCLUSION: The absolute and relative composition of the MAM is variable across different segments of the gastrointestinal tract. These quantitative changes indicates that MAM can be targeted in specific segments of the GI tract to improve patient outcomes.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/cb5fb882dd58/fmicb-15-1454910-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/5162cc7dfb9b/fmicb-15-1454910-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/6244ff184f9e/fmicb-15-1454910-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/6eec05497f5f/fmicb-15-1454910-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/6f75a9141e08/fmicb-15-1454910-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/1375e299666c/fmicb-15-1454910-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/cb5fb882dd58/fmicb-15-1454910-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/5162cc7dfb9b/fmicb-15-1454910-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/6244ff184f9e/fmicb-15-1454910-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/6eec05497f5f/fmicb-15-1454910-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/6f75a9141e08/fmicb-15-1454910-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/1375e299666c/fmicb-15-1454910-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d6/11513579/cb5fb882dd58/fmicb-15-1454910-g006.jpg

相似文献

[1]
The biogeography of the mucosa-associated microbiome in health and disease.

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[8]
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[9]
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[10]
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本文引用的文献

[1]
The duodenal mucosa associated microbiome, visceral sensory function, immune activation and psychological comorbidities in functional gastrointestinal disorders with and without self-reported non-celiac wheat sensitivity.

Gut Microbes. 2022

[2]
Alterations to the duodenal microbiota are linked to gastric emptying and symptoms in functional dyspepsia.

Gut. 2023-5

[3]
Current and Future Approaches for Diagnosing Small Intestinal Dysbiosis in Patients With Symptoms of Functional Dyspepsia.

Front Neurosci. 2022-5-6

[4]
Multivariable association discovery in population-scale meta-omics studies.

PLoS Comput Biol. 2021-11

[5]
A Review of Four Practice Guidelines of Inflammatory Bowel Disease.

Cureus. 2021-8-3

[6]
Concomitant Irritable Bowel Syndrome Does Not Influence the Response to Antimicrobial Therapy in Patients with Functional Dyspepsia.

Dig Dis Sci. 2022-6

[7]
Mechanisms of Food-Induced Symptom Induction and Dietary Management in Functional Dyspepsia.

Nutrients. 2021-3-28

[8]
Small Intestinal Bacterial Overgrowth in Functional Dyspepsia: A Systematic Review and Meta-Analysis.

Am J Gastroenterol. 2021-5-1

[9]
Primer, Pipelines, Parameters: Issues in 16S rRNA Gene Sequencing.

mSphere. 2021-2-24

[10]
Duodenal bacterial load as determined by quantitative polymerase chain reaction in asymptomatic controls, functional gastrointestinal disorders and inflammatory bowel disease.

Aliment Pharmacol Ther. 2020-5-15

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