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Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study

Obesity is a multifactorial disorder, and the gut microbiome has been suggested to contribute to its onset. In order to better clarify the role of the microbiome in obesity, we evaluated the metatranscriptome in duodenal biopsies from a cohort of 23 adult severely obese and lean control subjects usi...

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Autores principales: Granata, Ilaria, Nardelli, Carmela, D’Argenio, Valeria, Tramontano, Salvatore, Compare, Debora, Guarracino, Mario Rosario, Nardone, Gerardo, Pilone, Vincenzo, Sacchetti, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698607/
https://www.ncbi.nlm.nih.gov/pubmed/33213098
http://dx.doi.org/10.3390/microorganisms8111811
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author Granata, Ilaria
Nardelli, Carmela
D’Argenio, Valeria
Tramontano, Salvatore
Compare, Debora
Guarracino, Mario Rosario
Nardone, Gerardo
Pilone, Vincenzo
Sacchetti, Lucia
author_facet Granata, Ilaria
Nardelli, Carmela
D’Argenio, Valeria
Tramontano, Salvatore
Compare, Debora
Guarracino, Mario Rosario
Nardone, Gerardo
Pilone, Vincenzo
Sacchetti, Lucia
author_sort Granata, Ilaria
collection PubMed
description Obesity is a multifactorial disorder, and the gut microbiome has been suggested to contribute to its onset. In order to better clarify the role of the microbiome in obesity, we evaluated the metatranscriptome in duodenal biopsies from a cohort of 23 adult severely obese and lean control subjects using next generation sequencing. Our aim was to provide a general picture of the duodenal metatranscriptome associated with severe obesity. We found altered expressions of human and microbial genes in the obese compared to lean subjects, with most of the gene alterations being present in the carbohydrate, protein, and lipid metabolic pathways. Defects were also present in several human genes involved in epithelial intestinal cells differentiation and function, as well as in the immunity/inflammation pathways. Moreover, the microbial taxa abundance inferred by our transcriptomic data differed in part from the data that we previously evaluated by 16S rRNA in 13/23 individuals of our cohort, particularly concerning the Firmicutes and Proteobacteria phyla abundances. In conclusion, our pilot study provides the first taxonomic and functional characterization of duodenal microbiota in severely obese subjects and lean controls. Our findings suggest that duodenal microbiome and human genes both play a role in deregulating metabolic pathways, likely affecting energy metabolism and thus contributing to the obese phenotype.
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spelling pubmed-76986072020-11-29 Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study Granata, Ilaria Nardelli, Carmela D’Argenio, Valeria Tramontano, Salvatore Compare, Debora Guarracino, Mario Rosario Nardone, Gerardo Pilone, Vincenzo Sacchetti, Lucia Microorganisms Article Obesity is a multifactorial disorder, and the gut microbiome has been suggested to contribute to its onset. In order to better clarify the role of the microbiome in obesity, we evaluated the metatranscriptome in duodenal biopsies from a cohort of 23 adult severely obese and lean control subjects using next generation sequencing. Our aim was to provide a general picture of the duodenal metatranscriptome associated with severe obesity. We found altered expressions of human and microbial genes in the obese compared to lean subjects, with most of the gene alterations being present in the carbohydrate, protein, and lipid metabolic pathways. Defects were also present in several human genes involved in epithelial intestinal cells differentiation and function, as well as in the immunity/inflammation pathways. Moreover, the microbial taxa abundance inferred by our transcriptomic data differed in part from the data that we previously evaluated by 16S rRNA in 13/23 individuals of our cohort, particularly concerning the Firmicutes and Proteobacteria phyla abundances. In conclusion, our pilot study provides the first taxonomic and functional characterization of duodenal microbiota in severely obese subjects and lean controls. Our findings suggest that duodenal microbiome and human genes both play a role in deregulating metabolic pathways, likely affecting energy metabolism and thus contributing to the obese phenotype. MDPI 2020-11-17 /pmc/articles/PMC7698607/ /pubmed/33213098 http://dx.doi.org/10.3390/microorganisms8111811 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
Granata, Ilaria
Nardelli, Carmela
D’Argenio, Valeria
Tramontano, Salvatore
Compare, Debora
Guarracino, Mario Rosario
Nardone, Gerardo
Pilone, Vincenzo
Sacchetti, Lucia
Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study
title Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study
title_full Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study
title_fullStr Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study
title_full_unstemmed Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study
title_short Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study
title_sort duodenal metatranscriptomics to define human and microbial functional alterations associated with severe obesity: a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698607/
https://www.ncbi.nlm.nih.gov/pubmed/33213098
http://dx.doi.org/10.3390/microorganisms8111811
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