Cargando…

Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration

Glaucoma is a multifactorial, neurodegenerative disorder characterized by the loss of retinal ganglion cells (RGCs). Crosstalk between the gut microbiota and host is involved in the progression of many neurodegenerative diseases, although little is known about its role in glaucoma. To investigated t...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Yinglei, Zhou, Xujiao, Lu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411928/
https://www.ncbi.nlm.nih.gov/pubmed/36034713
http://dx.doi.org/10.3389/fcimb.2022.968992
_version_ 1784775375570599936
author Zhang, Yinglei
Zhou, Xujiao
Lu, Yi
author_facet Zhang, Yinglei
Zhou, Xujiao
Lu, Yi
author_sort Zhang, Yinglei
collection PubMed
description Glaucoma is a multifactorial, neurodegenerative disorder characterized by the loss of retinal ganglion cells (RGCs). Crosstalk between the gut microbiota and host is involved in the progression of many neurodegenerative diseases, although little is known about its role in glaucoma. To investigated the alterations of the gut microbiota and derived metabolites in glaucomatous rats, and the interaction with RGCs, we performed 16S rRNA (V1-V9) sequencing and untargeted metabolomic analyses. The microbial composition differed significantly between the two groups, and the diversity of cecal bacteria was dramatically reduced in glaucomatous rats. The Firmicutes/Bacteroidetes (F/B) ratio, Verrucomicrobia phylum, and some bacterial genera (Romboutsia, Akkermansia, and Bacteroides) were dramatically increased in the glaucomatous rat model compared with the control, which showed negative correlation with RGCs. Untargeted metabolomic analysis identified 284 differentially expressed metabolites, and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis revealed considerable enrichment mainly in bile secretion pathways. The relationships among the metabolites enriched in the bile secretion pathway, differentially expressed cecal microbiota, and RGCs were investigated, and glutathione (GSH) was found to be negatively correlated with Bacteroides and F/B and positively correlated with RGCs. Reduced GSH level in the blood of glaucoma rats is further established, and was negatively correlated with Romboutsia and the F/B ratio and positively correlated with RGCs. This finding suggests the potential role of the gut microbiota and derived metabolites in glaucoma, and GSH, a major antioxidant metabolite, was related to their effects, indicating the potential for the development of gut microbiota-targeted interventions for glaucoma.
format Online
Article
Text
id pubmed-9411928
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94119282022-08-27 Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration Zhang, Yinglei Zhou, Xujiao Lu, Yi Front Cell Infect Microbiol Cellular and Infection Microbiology Glaucoma is a multifactorial, neurodegenerative disorder characterized by the loss of retinal ganglion cells (RGCs). Crosstalk between the gut microbiota and host is involved in the progression of many neurodegenerative diseases, although little is known about its role in glaucoma. To investigated the alterations of the gut microbiota and derived metabolites in glaucomatous rats, and the interaction with RGCs, we performed 16S rRNA (V1-V9) sequencing and untargeted metabolomic analyses. The microbial composition differed significantly between the two groups, and the diversity of cecal bacteria was dramatically reduced in glaucomatous rats. The Firmicutes/Bacteroidetes (F/B) ratio, Verrucomicrobia phylum, and some bacterial genera (Romboutsia, Akkermansia, and Bacteroides) were dramatically increased in the glaucomatous rat model compared with the control, which showed negative correlation with RGCs. Untargeted metabolomic analysis identified 284 differentially expressed metabolites, and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis revealed considerable enrichment mainly in bile secretion pathways. The relationships among the metabolites enriched in the bile secretion pathway, differentially expressed cecal microbiota, and RGCs were investigated, and glutathione (GSH) was found to be negatively correlated with Bacteroides and F/B and positively correlated with RGCs. Reduced GSH level in the blood of glaucoma rats is further established, and was negatively correlated with Romboutsia and the F/B ratio and positively correlated with RGCs. This finding suggests the potential role of the gut microbiota and derived metabolites in glaucoma, and GSH, a major antioxidant metabolite, was related to their effects, indicating the potential for the development of gut microbiota-targeted interventions for glaucoma. Frontiers Media S.A. 2022-08-12 /pmc/articles/PMC9411928/ /pubmed/36034713 http://dx.doi.org/10.3389/fcimb.2022.968992 Text en Copyright © 2022 Zhang, Zhou and Lu 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 Cellular and Infection Microbiology
Zhang, Yinglei
Zhou, Xujiao
Lu, Yi
Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
title Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
title_full Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
title_fullStr Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
title_full_unstemmed Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
title_short Gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
title_sort gut microbiota and derived metabolomic profiling in glaucoma with progressive neurodegeneration
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411928/
https://www.ncbi.nlm.nih.gov/pubmed/36034713
http://dx.doi.org/10.3389/fcimb.2022.968992
work_keys_str_mv AT zhangyinglei gutmicrobiotaandderivedmetabolomicprofilinginglaucomawithprogressiveneurodegeneration
AT zhouxujiao gutmicrobiotaandderivedmetabolomicprofilinginglaucomawithprogressiveneurodegeneration
AT luyi gutmicrobiotaandderivedmetabolomicprofilinginglaucomawithprogressiveneurodegeneration