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Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization
PURPOSE: Choroidal neovascularization (CNV) is the defining feature of neovascular age-related macular degeneration (nAMD). Gut microbiota might be deeply involved in the pathogenesis of nAMD. This study aimed to reveal the roles of the gut microbiome and fecal metabolome in a mouse model of laser-i...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427291/ https://www.ncbi.nlm.nih.gov/pubmed/34512615 http://dx.doi.org/10.3389/fmicb.2021.738796 |
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author | Li, Yun Cai, Yuting Huang, Qian Tan, Wei Li, Bingyan Zhou, Haixiang Wang, Zicong Zou, Jingling Ding, Chun Jiang, Bing Yoshida, Shigeo Zhou, Yedi |
author_facet | Li, Yun Cai, Yuting Huang, Qian Tan, Wei Li, Bingyan Zhou, Haixiang Wang, Zicong Zou, Jingling Ding, Chun Jiang, Bing Yoshida, Shigeo Zhou, Yedi |
author_sort | Li, Yun |
collection | PubMed |
description | PURPOSE: Choroidal neovascularization (CNV) is the defining feature of neovascular age-related macular degeneration (nAMD). Gut microbiota might be deeply involved in the pathogenesis of nAMD. This study aimed to reveal the roles of the gut microbiome and fecal metabolome in a mouse model of laser-induced CNV. METHODS: The feces of C57BL/6J mice with or without laser-induced CNV were collected. Multi-omics analyses, including 16S rRNA gene sequencing and untargeted metabolomics, were conducted to analyze the changes in the gut microbial composition and the fecal metabolomic profiles in CNV mice. RESULTS: The gut microbiota was significantly altered in CNV mice. The abundance of Candidatus_Saccharimonas was significantly upregulated in the feces of CNV mice, while 16 genera, including Prevotellaceae_NK3B31_group, Candidatus_Soleaferrea, and Truepera, were significantly more abundant in the controls than in the CNV group. Fecal metabolomics identified 73 altered metabolites (including 52 strongly significantly altered metabolites) in CNV mice compared to control mice. Correlation analysis indicated significant correlations between the altered fecal metabolites and gut microbiota genera, such as Lachnospiraceae_UCG-001 and Candidatus_Saccharimonas. Moreover, KEGG analysis revealed six pathways associated with these altered metabolites, such as the ABC transporter, primary bile acid biosynthesis and steroid hormone biosynthesis pathways. CONCLUSION: The study identified an altered fecal microbiome and metabolome in a CNV mouse model. The altered microbes, metabolites and the involved pathways might be associated with the pathogenesis of nAMD. |
format | Online Article Text |
id | pubmed-8427291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84272912021-09-10 Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization Li, Yun Cai, Yuting Huang, Qian Tan, Wei Li, Bingyan Zhou, Haixiang Wang, Zicong Zou, Jingling Ding, Chun Jiang, Bing Yoshida, Shigeo Zhou, Yedi Front Microbiol Microbiology PURPOSE: Choroidal neovascularization (CNV) is the defining feature of neovascular age-related macular degeneration (nAMD). Gut microbiota might be deeply involved in the pathogenesis of nAMD. This study aimed to reveal the roles of the gut microbiome and fecal metabolome in a mouse model of laser-induced CNV. METHODS: The feces of C57BL/6J mice with or without laser-induced CNV were collected. Multi-omics analyses, including 16S rRNA gene sequencing and untargeted metabolomics, were conducted to analyze the changes in the gut microbial composition and the fecal metabolomic profiles in CNV mice. RESULTS: The gut microbiota was significantly altered in CNV mice. The abundance of Candidatus_Saccharimonas was significantly upregulated in the feces of CNV mice, while 16 genera, including Prevotellaceae_NK3B31_group, Candidatus_Soleaferrea, and Truepera, were significantly more abundant in the controls than in the CNV group. Fecal metabolomics identified 73 altered metabolites (including 52 strongly significantly altered metabolites) in CNV mice compared to control mice. Correlation analysis indicated significant correlations between the altered fecal metabolites and gut microbiota genera, such as Lachnospiraceae_UCG-001 and Candidatus_Saccharimonas. Moreover, KEGG analysis revealed six pathways associated with these altered metabolites, such as the ABC transporter, primary bile acid biosynthesis and steroid hormone biosynthesis pathways. CONCLUSION: The study identified an altered fecal microbiome and metabolome in a CNV mouse model. The altered microbes, metabolites and the involved pathways might be associated with the pathogenesis of nAMD. Frontiers Media S.A. 2021-08-26 /pmc/articles/PMC8427291/ /pubmed/34512615 http://dx.doi.org/10.3389/fmicb.2021.738796 Text en Copyright © 2021 Li, Cai, Huang, Tan, Li, Zhou, Wang, Zou, Ding, Jiang, Yoshida and Zhou. 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 Li, Yun Cai, Yuting Huang, Qian Tan, Wei Li, Bingyan Zhou, Haixiang Wang, Zicong Zou, Jingling Ding, Chun Jiang, Bing Yoshida, Shigeo Zhou, Yedi Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization |
title | Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization |
title_full | Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization |
title_fullStr | Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization |
title_full_unstemmed | Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization |
title_short | Altered Fecal Microbiome and Metabolome in a Mouse Model of Choroidal Neovascularization |
title_sort | altered fecal microbiome and metabolome in a mouse model of choroidal neovascularization |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427291/ https://www.ncbi.nlm.nih.gov/pubmed/34512615 http://dx.doi.org/10.3389/fmicb.2021.738796 |
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