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The gut microbiome: a core regulator of metabolism

The human body is inhabited by numerous bacteria, fungi, and viruses, and each part has a unique microbial community structure. The gastrointestinal tract harbors approximately 100 trillion strains comprising more than 1000 bacterial species that maintain symbiotic relationships with the host. The g...

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Detalles Bibliográficos
Autores principales: Fujisaka, Shiho, Watanabe, Yoshiyuki, Tobe, Kazuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874984/
https://www.ncbi.nlm.nih.gov/pubmed/36458804
http://dx.doi.org/10.1530/JOE-22-0111
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author Fujisaka, Shiho
Watanabe, Yoshiyuki
Tobe, Kazuyuki
author_facet Fujisaka, Shiho
Watanabe, Yoshiyuki
Tobe, Kazuyuki
author_sort Fujisaka, Shiho
collection PubMed
description The human body is inhabited by numerous bacteria, fungi, and viruses, and each part has a unique microbial community structure. The gastrointestinal tract harbors approximately 100 trillion strains comprising more than 1000 bacterial species that maintain symbiotic relationships with the host. The gut microbiota consists mainly of the phyla Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria. Of these, Firmicutes and Bacteroidetes constitute 70–90% of the total abundance. Gut microbiota utilize nutrients ingested by the host, interact with other bacterial species, and help maintain healthy homeostasis in the host. In recent years, it has become increasingly clear that a breakdown of the microbial structure and its functions, known as dysbiosis, is associated with the development of allergies, autoimmune diseases, cancers, and arteriosclerosis, among others. Metabolic diseases, such as obesity and diabetes, also have a causal relationship with dysbiosis. The present review provides a brief overview of the general roles of the gut microbiota and their relationship with metabolic disorders.
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spelling pubmed-98749842023-02-06 The gut microbiome: a core regulator of metabolism Fujisaka, Shiho Watanabe, Yoshiyuki Tobe, Kazuyuki J Endocrinol Review The human body is inhabited by numerous bacteria, fungi, and viruses, and each part has a unique microbial community structure. The gastrointestinal tract harbors approximately 100 trillion strains comprising more than 1000 bacterial species that maintain symbiotic relationships with the host. The gut microbiota consists mainly of the phyla Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria. Of these, Firmicutes and Bacteroidetes constitute 70–90% of the total abundance. Gut microbiota utilize nutrients ingested by the host, interact with other bacterial species, and help maintain healthy homeostasis in the host. In recent years, it has become increasingly clear that a breakdown of the microbial structure and its functions, known as dysbiosis, is associated with the development of allergies, autoimmune diseases, cancers, and arteriosclerosis, among others. Metabolic diseases, such as obesity and diabetes, also have a causal relationship with dysbiosis. The present review provides a brief overview of the general roles of the gut microbiota and their relationship with metabolic disorders. Bioscientifica Ltd 2022-12-02 /pmc/articles/PMC9874984/ /pubmed/36458804 http://dx.doi.org/10.1530/JOE-22-0111 Text en © The authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Review
Fujisaka, Shiho
Watanabe, Yoshiyuki
Tobe, Kazuyuki
The gut microbiome: a core regulator of metabolism
title The gut microbiome: a core regulator of metabolism
title_full The gut microbiome: a core regulator of metabolism
title_fullStr The gut microbiome: a core regulator of metabolism
title_full_unstemmed The gut microbiome: a core regulator of metabolism
title_short The gut microbiome: a core regulator of metabolism
title_sort gut microbiome: a core regulator of metabolism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874984/
https://www.ncbi.nlm.nih.gov/pubmed/36458804
http://dx.doi.org/10.1530/JOE-22-0111
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