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Alterations of gut microbiota in a mouse model with partial small intestinal obstruction

INTRODUCTION: Changes in the gut microbiota of patients with partial small intestinal obstruction (PSIO) have not been widely clarified. We aimed to explore bacterial diversity in a PSIO mouse model. METHODS: A PSIO mouse model was established using male C57BL/6 mice, and feces samples from the dist...

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Autores principales: Wang, Yong, Zhang, Minzhong, Jiang, Lu, Gong, Yiming, Liu, Keqiang, Zhang, Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568644/
https://www.ncbi.nlm.nih.gov/pubmed/37840748
http://dx.doi.org/10.3389/fmicb.2023.1242650
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author Wang, Yong
Zhang, Minzhong
Jiang, Lu
Gong, Yiming
Liu, Keqiang
Zhang, Tian
author_facet Wang, Yong
Zhang, Minzhong
Jiang, Lu
Gong, Yiming
Liu, Keqiang
Zhang, Tian
author_sort Wang, Yong
collection PubMed
description INTRODUCTION: Changes in the gut microbiota of patients with partial small intestinal obstruction (PSIO) have not been widely clarified. We aimed to explore bacterial diversity in a PSIO mouse model. METHODS: A PSIO mouse model was established using male C57BL/6 mice, and feces samples from the distal ileum and ileum epithelium tissues were collected. MiSeq sequencing of the 16S rRNA gene was conducted to characterize microbiota diversity and composition. RNA sequencing for differences in transcriptomic programming of the ileum tissue was performed between the PSIO and (Control) Ctrl groups. RESULTS: Bacterial diversity in the PSIO group was significantly lower than that in the controls. Pseudomonadota was predominant in the feces of the PSIO group. Unclassified_Muribaculaceae (p = 0.008) and Akkermansia (p = 0.007) were more abundant in the Ctrl group than those in the PSIO group. Furthermore, Escherichia_Shigella (p = 0.008) was more predominant in the feces of the PSIO group. The Kyoto Encyclopedia of Genes and Genomes pathways related to metabolism were depleted in the PSIO group. Pathways associated with intestinal fibrosis, including extracellular matrix-receptor interaction, focal adhesion, phosphoinositide 3-kinase (PI3K)-Akt signaling pathway and transforming growth factor (TGF)-beta signaling pathway, which were enriched in ileum epithelial tissue in the PSIO group. CONCLUSION: PSIO can lead to changes in the predominant intestinal bacterial groups. Depleted functional profiles of the gut microbiota were identified in the PSIO group. Functional pathways associated with intestinal fibrosis were activated by PSIO. The potential regulation by the microbiota needs to be explored in the future.
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spelling pubmed-105686442023-10-13 Alterations of gut microbiota in a mouse model with partial small intestinal obstruction Wang, Yong Zhang, Minzhong Jiang, Lu Gong, Yiming Liu, Keqiang Zhang, Tian Front Microbiol Microbiology INTRODUCTION: Changes in the gut microbiota of patients with partial small intestinal obstruction (PSIO) have not been widely clarified. We aimed to explore bacterial diversity in a PSIO mouse model. METHODS: A PSIO mouse model was established using male C57BL/6 mice, and feces samples from the distal ileum and ileum epithelium tissues were collected. MiSeq sequencing of the 16S rRNA gene was conducted to characterize microbiota diversity and composition. RNA sequencing for differences in transcriptomic programming of the ileum tissue was performed between the PSIO and (Control) Ctrl groups. RESULTS: Bacterial diversity in the PSIO group was significantly lower than that in the controls. Pseudomonadota was predominant in the feces of the PSIO group. Unclassified_Muribaculaceae (p = 0.008) and Akkermansia (p = 0.007) were more abundant in the Ctrl group than those in the PSIO group. Furthermore, Escherichia_Shigella (p = 0.008) was more predominant in the feces of the PSIO group. The Kyoto Encyclopedia of Genes and Genomes pathways related to metabolism were depleted in the PSIO group. Pathways associated with intestinal fibrosis, including extracellular matrix-receptor interaction, focal adhesion, phosphoinositide 3-kinase (PI3K)-Akt signaling pathway and transforming growth factor (TGF)-beta signaling pathway, which were enriched in ileum epithelial tissue in the PSIO group. CONCLUSION: PSIO can lead to changes in the predominant intestinal bacterial groups. Depleted functional profiles of the gut microbiota were identified in the PSIO group. Functional pathways associated with intestinal fibrosis were activated by PSIO. The potential regulation by the microbiota needs to be explored in the future. Frontiers Media S.A. 2023-09-28 /pmc/articles/PMC10568644/ /pubmed/37840748 http://dx.doi.org/10.3389/fmicb.2023.1242650 Text en Copyright © 2023 Wang, Zhang, Jiang, Gong, Liu and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Yong
Zhang, Minzhong
Jiang, Lu
Gong, Yiming
Liu, Keqiang
Zhang, Tian
Alterations of gut microbiota in a mouse model with partial small intestinal obstruction
title Alterations of gut microbiota in a mouse model with partial small intestinal obstruction
title_full Alterations of gut microbiota in a mouse model with partial small intestinal obstruction
title_fullStr Alterations of gut microbiota in a mouse model with partial small intestinal obstruction
title_full_unstemmed Alterations of gut microbiota in a mouse model with partial small intestinal obstruction
title_short Alterations of gut microbiota in a mouse model with partial small intestinal obstruction
title_sort alterations of gut microbiota in a mouse model with partial small intestinal obstruction
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568644/
https://www.ncbi.nlm.nih.gov/pubmed/37840748
http://dx.doi.org/10.3389/fmicb.2023.1242650
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