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Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients

A life-long dietary intervention can affect the substrates’ availability for gut fermentation in metabolic diseases such as the glycogen-storage diseases (GSD). Besides drug consumption, the main treatment of types GSD-Ia and Ib to prevent metabolic complications is a specific diet with definite nut...

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Autores principales: Ceccarani, Camilla, Bassanini, Giulia, Montanari, Chiara, Casiraghi, Maria Cristina, Ottaviano, Emerenziana, Morace, Giulia, Biasucci, Giacomo, Paci, Sabrina, Borghi, Elisa, Verduci, Elvira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240959/
https://www.ncbi.nlm.nih.gov/pubmed/32235604
http://dx.doi.org/10.3390/metabo10040133
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author Ceccarani, Camilla
Bassanini, Giulia
Montanari, Chiara
Casiraghi, Maria Cristina
Ottaviano, Emerenziana
Morace, Giulia
Biasucci, Giacomo
Paci, Sabrina
Borghi, Elisa
Verduci, Elvira
author_facet Ceccarani, Camilla
Bassanini, Giulia
Montanari, Chiara
Casiraghi, Maria Cristina
Ottaviano, Emerenziana
Morace, Giulia
Biasucci, Giacomo
Paci, Sabrina
Borghi, Elisa
Verduci, Elvira
author_sort Ceccarani, Camilla
collection PubMed
description A life-long dietary intervention can affect the substrates’ availability for gut fermentation in metabolic diseases such as the glycogen-storage diseases (GSD). Besides drug consumption, the main treatment of types GSD-Ia and Ib to prevent metabolic complications is a specific diet with definite nutrient intakes. In order to evaluate how deeply this dietary treatment affects gut bacteria, we compared the gut microbiota of nine GSD-I subjects and 12 healthy controls (HC) through 16S rRNA gene sequencing; we assessed their dietary intake and nutrients, their microbial short chain fatty acids (SCFAs) via gas chromatography and their hematic values. Both alpha-diversity and phylogenetic analysis revealed a significant biodiversity reduction in the GSD group compared to the HC group, and highlighted profound differences of their gut microbiota. GSD subjects were characterized by an increase in the relative abundance of Enterobacteriaceae and Veillonellaceae families, while the beneficial genera Faecalibacterium and Oscillospira were significantly reduced. SCFA quantification revealed a significant increase of fecal acetate and propionate in GSD subjects, but with a beneficial role probably reduced due to unbalanced bacterial interactions; nutritional values correlated to bacterial genera were significantly different between experimental groups, with nearly opposite cohort trends.
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spelling pubmed-72409592020-06-11 Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients Ceccarani, Camilla Bassanini, Giulia Montanari, Chiara Casiraghi, Maria Cristina Ottaviano, Emerenziana Morace, Giulia Biasucci, Giacomo Paci, Sabrina Borghi, Elisa Verduci, Elvira Metabolites Article A life-long dietary intervention can affect the substrates’ availability for gut fermentation in metabolic diseases such as the glycogen-storage diseases (GSD). Besides drug consumption, the main treatment of types GSD-Ia and Ib to prevent metabolic complications is a specific diet with definite nutrient intakes. In order to evaluate how deeply this dietary treatment affects gut bacteria, we compared the gut microbiota of nine GSD-I subjects and 12 healthy controls (HC) through 16S rRNA gene sequencing; we assessed their dietary intake and nutrients, their microbial short chain fatty acids (SCFAs) via gas chromatography and their hematic values. Both alpha-diversity and phylogenetic analysis revealed a significant biodiversity reduction in the GSD group compared to the HC group, and highlighted profound differences of their gut microbiota. GSD subjects were characterized by an increase in the relative abundance of Enterobacteriaceae and Veillonellaceae families, while the beneficial genera Faecalibacterium and Oscillospira were significantly reduced. SCFA quantification revealed a significant increase of fecal acetate and propionate in GSD subjects, but with a beneficial role probably reduced due to unbalanced bacterial interactions; nutritional values correlated to bacterial genera were significantly different between experimental groups, with nearly opposite cohort trends. MDPI 2020-03-30 /pmc/articles/PMC7240959/ /pubmed/32235604 http://dx.doi.org/10.3390/metabo10040133 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ceccarani, Camilla
Bassanini, Giulia
Montanari, Chiara
Casiraghi, Maria Cristina
Ottaviano, Emerenziana
Morace, Giulia
Biasucci, Giacomo
Paci, Sabrina
Borghi, Elisa
Verduci, Elvira
Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients
title Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients
title_full Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients
title_fullStr Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients
title_full_unstemmed Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients
title_short Proteobacteria Overgrowth and Butyrate-Producing Taxa Depletion in the Gut Microbiota of Glycogen Storage Disease Type 1 Patients
title_sort proteobacteria overgrowth and butyrate-producing taxa depletion in the gut microbiota of glycogen storage disease type 1 patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240959/
https://www.ncbi.nlm.nih.gov/pubmed/32235604
http://dx.doi.org/10.3390/metabo10040133
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