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Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea
Enteral Nutrition-related Diarrhea (END) is an extremely common complication in Intensive Care Unit (ICU) patients. However, it is currently unclear whether the patient’s gut microbiota is disturbed. Our study aimed to explore the characteristics of gut microbiota changes in END patients. We divided...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722739/ https://www.ncbi.nlm.nih.gov/pubmed/36483214 http://dx.doi.org/10.3389/fmicb.2022.1051687 |
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author | Ni, Weiwei Jiao, Xinwei Zou, Huihuang Jing, Mengjuan Xia, Ming Zhu, Shichao Li, Liming |
author_facet | Ni, Weiwei Jiao, Xinwei Zou, Huihuang Jing, Mengjuan Xia, Ming Zhu, Shichao Li, Liming |
author_sort | Ni, Weiwei |
collection | PubMed |
description | Enteral Nutrition-related Diarrhea (END) is an extremely common complication in Intensive Care Unit (ICU) patients. However, it is currently unclear whether the patient’s gut microbiota is disturbed. Our study aimed to explore the characteristics of gut microbiota changes in END patients. We divided ICU patients into no-END group (n = 7) and END group (n = 7) according to whether they had END, then stool samples were collected separately. The V3-V4 region of stool bacterial 16S rRNA gene was amplified by PCR and sequenced on an Illumina MiSeq PE300 platform. Microbiome data obtained by quality control were analyzed, including microbial community composition, diversity and gene function prediction.The results showed that the dominant gut microbiota in ICU patients who were given total enteral nutrition were Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, and Verrucomicrobia. Bacterial richness and diversity in END patients were all significantly lower than those in no-END patients. In addition, END caused significant changes in bacterial composition. LEfSe found 34 biomarkers represented by Bacteroidetes and Subdoligranulum in the no-END group as well as 11 biomarkers represented by Enterococcus and Klebsiella in the END group. Finally, through PICRUST function prediction, we found that diarrhea led to abnormal changes in numerous KEGG pathways mainly related to immunity and metabolism. In short, ICU patients with END have severe gut dysbiosis, and our study provides a reliable experimental basis for the patient’s microbiota therapy. |
format | Online Article Text |
id | pubmed-9722739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97227392022-12-07 Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea Ni, Weiwei Jiao, Xinwei Zou, Huihuang Jing, Mengjuan Xia, Ming Zhu, Shichao Li, Liming Front Microbiol Microbiology Enteral Nutrition-related Diarrhea (END) is an extremely common complication in Intensive Care Unit (ICU) patients. However, it is currently unclear whether the patient’s gut microbiota is disturbed. Our study aimed to explore the characteristics of gut microbiota changes in END patients. We divided ICU patients into no-END group (n = 7) and END group (n = 7) according to whether they had END, then stool samples were collected separately. The V3-V4 region of stool bacterial 16S rRNA gene was amplified by PCR and sequenced on an Illumina MiSeq PE300 platform. Microbiome data obtained by quality control were analyzed, including microbial community composition, diversity and gene function prediction.The results showed that the dominant gut microbiota in ICU patients who were given total enteral nutrition were Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, and Verrucomicrobia. Bacterial richness and diversity in END patients were all significantly lower than those in no-END patients. In addition, END caused significant changes in bacterial composition. LEfSe found 34 biomarkers represented by Bacteroidetes and Subdoligranulum in the no-END group as well as 11 biomarkers represented by Enterococcus and Klebsiella in the END group. Finally, through PICRUST function prediction, we found that diarrhea led to abnormal changes in numerous KEGG pathways mainly related to immunity and metabolism. In short, ICU patients with END have severe gut dysbiosis, and our study provides a reliable experimental basis for the patient’s microbiota therapy. Frontiers Media S.A. 2022-11-22 /pmc/articles/PMC9722739/ /pubmed/36483214 http://dx.doi.org/10.3389/fmicb.2022.1051687 Text en Copyright © 2022 Ni, Jiao, Zou, Jing, Xia, Zhu and Li. 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 Ni, Weiwei Jiao, Xinwei Zou, Huihuang Jing, Mengjuan Xia, Ming Zhu, Shichao Li, Liming Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea |
title | Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea |
title_full | Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea |
title_fullStr | Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea |
title_full_unstemmed | Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea |
title_short | Gut microbiome alterations in ICU patients with enteral nutrition-related diarrhea |
title_sort | gut microbiome alterations in icu patients with enteral nutrition-related diarrhea |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722739/ https://www.ncbi.nlm.nih.gov/pubmed/36483214 http://dx.doi.org/10.3389/fmicb.2022.1051687 |
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