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Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study

Type 1 diabetes (T1D) is a chronic autoimmune metabolic disorder with onset in pediatric/adolescent age, characterized by insufficient insulin production, due to a progressive destruction of pancreatic β-cells. Evidence on the correlation between the human gut microbiota (GM) composition and T1D ins...

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Autores principales: Levi Mortera, Stefano, Marzano, Valeria, Vernocchi, Pamela, Matteoli, Maria Cristina, Guarrasi, Valerio, Gardini, Simone, Del Chierico, Federica, Rapini, Novella, Deodati, Annalisa, Fierabracci, Alessandra, Cianfarani, Stefano, Putignani, Lorenza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787575/
https://www.ncbi.nlm.nih.gov/pubmed/36555624
http://dx.doi.org/10.3390/ijms232415982
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author Levi Mortera, Stefano
Marzano, Valeria
Vernocchi, Pamela
Matteoli, Maria Cristina
Guarrasi, Valerio
Gardini, Simone
Del Chierico, Federica
Rapini, Novella
Deodati, Annalisa
Fierabracci, Alessandra
Cianfarani, Stefano
Putignani, Lorenza
author_facet Levi Mortera, Stefano
Marzano, Valeria
Vernocchi, Pamela
Matteoli, Maria Cristina
Guarrasi, Valerio
Gardini, Simone
Del Chierico, Federica
Rapini, Novella
Deodati, Annalisa
Fierabracci, Alessandra
Cianfarani, Stefano
Putignani, Lorenza
author_sort Levi Mortera, Stefano
collection PubMed
description Type 1 diabetes (T1D) is a chronic autoimmune metabolic disorder with onset in pediatric/adolescent age, characterized by insufficient insulin production, due to a progressive destruction of pancreatic β-cells. Evidence on the correlation between the human gut microbiota (GM) composition and T1D insurgence has been recently reported. In particular, 16S rRNA-based metagenomics has been intensively employed in the last decade in a number of investigations focused on GM representation in relation to a pre-disease state or to a response to clinical treatments. On the other hand, few works have been published using alternative functional omics, which is more suitable to provide a different interpretation of such a relationship. In this work, we pursued a comprehensive metaproteomic investigation on T1D children compared with a group of siblings (SIBL) and a reference control group (CTRL) composed of aged matched healthy subjects, with the aim of finding features in the T1D patients’ GM to be related with the onset of the disease. Modulated metaproteins were found either by comparing T1D with CTRL and SIBL or by stratifying T1D by insulin need (IN), as a proxy of β-cells damage, showing some functional and taxonomic traits of the GM, possibly related to the disease onset at different stages of severity.
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spelling pubmed-97875752022-12-24 Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study Levi Mortera, Stefano Marzano, Valeria Vernocchi, Pamela Matteoli, Maria Cristina Guarrasi, Valerio Gardini, Simone Del Chierico, Federica Rapini, Novella Deodati, Annalisa Fierabracci, Alessandra Cianfarani, Stefano Putignani, Lorenza Int J Mol Sci Article Type 1 diabetes (T1D) is a chronic autoimmune metabolic disorder with onset in pediatric/adolescent age, characterized by insufficient insulin production, due to a progressive destruction of pancreatic β-cells. Evidence on the correlation between the human gut microbiota (GM) composition and T1D insurgence has been recently reported. In particular, 16S rRNA-based metagenomics has been intensively employed in the last decade in a number of investigations focused on GM representation in relation to a pre-disease state or to a response to clinical treatments. On the other hand, few works have been published using alternative functional omics, which is more suitable to provide a different interpretation of such a relationship. In this work, we pursued a comprehensive metaproteomic investigation on T1D children compared with a group of siblings (SIBL) and a reference control group (CTRL) composed of aged matched healthy subjects, with the aim of finding features in the T1D patients’ GM to be related with the onset of the disease. Modulated metaproteins were found either by comparing T1D with CTRL and SIBL or by stratifying T1D by insulin need (IN), as a proxy of β-cells damage, showing some functional and taxonomic traits of the GM, possibly related to the disease onset at different stages of severity. MDPI 2022-12-15 /pmc/articles/PMC9787575/ /pubmed/36555624 http://dx.doi.org/10.3390/ijms232415982 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Levi Mortera, Stefano
Marzano, Valeria
Vernocchi, Pamela
Matteoli, Maria Cristina
Guarrasi, Valerio
Gardini, Simone
Del Chierico, Federica
Rapini, Novella
Deodati, Annalisa
Fierabracci, Alessandra
Cianfarani, Stefano
Putignani, Lorenza
Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study
title Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study
title_full Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study
title_fullStr Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study
title_full_unstemmed Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study
title_short Functional and Taxonomic Traits of the Gut Microbiota in Type 1 Diabetes Children at the Onset: A Metaproteomic Study
title_sort functional and taxonomic traits of the gut microbiota in type 1 diabetes children at the onset: a metaproteomic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787575/
https://www.ncbi.nlm.nih.gov/pubmed/36555624
http://dx.doi.org/10.3390/ijms232415982
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