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How hypoxia affects microbiota metabolism in mice

OBJECTIVE: To investigate the relationship between gut microbiota and the fecal metabolites of hypoxic environments in mice. METHODS: High-fat diet-induced obese mice (n = 20) and normal diet-fed mice (n = 20) were randomly divided into four groups: high altitude obese group (HOB), high altitude nor...

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Autores principales: Ailizire, Ainiwaer, Wang, Xiaojing, Ma, Yan, Yan, Xin, Li, Shiqi, Wu, Ziyi, Du, Wenqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569469/
https://www.ncbi.nlm.nih.gov/pubmed/37840721
http://dx.doi.org/10.3389/fmicb.2023.1244519
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author Ailizire, Ainiwaer
Wang, Xiaojing
Ma, Yan
Yan, Xin
Li, Shiqi
Wu, Ziyi
Du, Wenqi
author_facet Ailizire, Ainiwaer
Wang, Xiaojing
Ma, Yan
Yan, Xin
Li, Shiqi
Wu, Ziyi
Du, Wenqi
author_sort Ailizire, Ainiwaer
collection PubMed
description OBJECTIVE: To investigate the relationship between gut microbiota and the fecal metabolites of hypoxic environments in mice. METHODS: High-fat diet-induced obese mice (n = 20) and normal diet-fed mice (n = 20) were randomly divided into four groups: high altitude obese group (HOB), high altitude normal weight group (HN), low altitude obese group LOB (LOB), and low altitude normal weight group (LN). Fecal samples from each group were 16S rRNA gene sequenced, and five samples from each of the four groups above were selected for non-targeted fecal metabolomics analysis using liquid chromatography-mass spectrometry. The relationship between gut microbiota and fecal metabolites was analyzed using SIMCA 14.1, MetaboAnalyst 5.0 and R 4.1.11. RESULTS: (A) Body weight was significantly lower in the hypoxic obesity group than in the normoxic obesity group. (B) Differences in α-diversity and β-diversity were found in the fecal gut microbiota of mice of different body weights and altitude, and the diversity of gut microbiota was higher in the normal group than in the obese group; the results of the comparison between the two groups showed that Faecalibaculum, Romboutsia, Lactobacillus, and A2 were associated with obesity; Romboutsia was associated with hypoxia. (C) The metabolic profiles of fecal metabolites differed between groups: gut microbiota were associated with nucleotide and amino acid metabolism in the same body groups, while gut microbiota were associated with lipid and amino acid metabolism in the same oxygen concentration groups. CONCLUSION: (a) Gut microbiota diversity was reduced in obese groups. Romboutsia was the dominant microbiota in the hypoxia group. (b) Gut microbiota were associated with nucleotide and amino acid metabolism in the same body weight groups, while they were associated with lipid and amino acid metabolism in the same altitude groups.
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spelling pubmed-105694692023-10-13 How hypoxia affects microbiota metabolism in mice Ailizire, Ainiwaer Wang, Xiaojing Ma, Yan Yan, Xin Li, Shiqi Wu, Ziyi Du, Wenqi Front Microbiol Microbiology OBJECTIVE: To investigate the relationship between gut microbiota and the fecal metabolites of hypoxic environments in mice. METHODS: High-fat diet-induced obese mice (n = 20) and normal diet-fed mice (n = 20) were randomly divided into four groups: high altitude obese group (HOB), high altitude normal weight group (HN), low altitude obese group LOB (LOB), and low altitude normal weight group (LN). Fecal samples from each group were 16S rRNA gene sequenced, and five samples from each of the four groups above were selected for non-targeted fecal metabolomics analysis using liquid chromatography-mass spectrometry. The relationship between gut microbiota and fecal metabolites was analyzed using SIMCA 14.1, MetaboAnalyst 5.0 and R 4.1.11. RESULTS: (A) Body weight was significantly lower in the hypoxic obesity group than in the normoxic obesity group. (B) Differences in α-diversity and β-diversity were found in the fecal gut microbiota of mice of different body weights and altitude, and the diversity of gut microbiota was higher in the normal group than in the obese group; the results of the comparison between the two groups showed that Faecalibaculum, Romboutsia, Lactobacillus, and A2 were associated with obesity; Romboutsia was associated with hypoxia. (C) The metabolic profiles of fecal metabolites differed between groups: gut microbiota were associated with nucleotide and amino acid metabolism in the same body groups, while gut microbiota were associated with lipid and amino acid metabolism in the same oxygen concentration groups. CONCLUSION: (a) Gut microbiota diversity was reduced in obese groups. Romboutsia was the dominant microbiota in the hypoxia group. (b) Gut microbiota were associated with nucleotide and amino acid metabolism in the same body weight groups, while they were associated with lipid and amino acid metabolism in the same altitude groups. Frontiers Media S.A. 2023-09-28 /pmc/articles/PMC10569469/ /pubmed/37840721 http://dx.doi.org/10.3389/fmicb.2023.1244519 Text en Copyright © 2023 Ailizire, Wang, Ma, Yan, Li, Wu and Du. 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
Ailizire, Ainiwaer
Wang, Xiaojing
Ma, Yan
Yan, Xin
Li, Shiqi
Wu, Ziyi
Du, Wenqi
How hypoxia affects microbiota metabolism in mice
title How hypoxia affects microbiota metabolism in mice
title_full How hypoxia affects microbiota metabolism in mice
title_fullStr How hypoxia affects microbiota metabolism in mice
title_full_unstemmed How hypoxia affects microbiota metabolism in mice
title_short How hypoxia affects microbiota metabolism in mice
title_sort how hypoxia affects microbiota metabolism in mice
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569469/
https://www.ncbi.nlm.nih.gov/pubmed/37840721
http://dx.doi.org/10.3389/fmicb.2023.1244519
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