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First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity

Gluten-related disorders (GRDs) are common chronic enteropathies and increasing evidence suggests an involvement of the gut microbiota. We examined the gut microbiota in Mexican people afflicted with GRDs. Ultra-high-throughput 16S marker sequencing was used to deeply describe the duodenal and fecal...

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Autores principales: Garcia-Mazcorro, Jose F., Rivera-Gutierrez, Xaira, Cobos-Quevedo, Orestes De Jesus, Grube-Pagola, Peter, Meixueiro-Daza, Arturo, Hernandez-Flores, Karina, Cabrera-Jorge, Francisco J., Vivanco-Cid, Hector, Dowd, Scot E., Remes-Troche, Jose M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266755/
https://www.ncbi.nlm.nih.gov/pubmed/30400238
http://dx.doi.org/10.3390/nu10111641
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author Garcia-Mazcorro, Jose F.
Rivera-Gutierrez, Xaira
Cobos-Quevedo, Orestes De Jesus
Grube-Pagola, Peter
Meixueiro-Daza, Arturo
Hernandez-Flores, Karina
Cabrera-Jorge, Francisco J.
Vivanco-Cid, Hector
Dowd, Scot E.
Remes-Troche, Jose M.
author_facet Garcia-Mazcorro, Jose F.
Rivera-Gutierrez, Xaira
Cobos-Quevedo, Orestes De Jesus
Grube-Pagola, Peter
Meixueiro-Daza, Arturo
Hernandez-Flores, Karina
Cabrera-Jorge, Francisco J.
Vivanco-Cid, Hector
Dowd, Scot E.
Remes-Troche, Jose M.
author_sort Garcia-Mazcorro, Jose F.
collection PubMed
description Gluten-related disorders (GRDs) are common chronic enteropathies and increasing evidence suggests an involvement of the gut microbiota. We examined the gut microbiota in Mexican people afflicted with GRDs. Ultra-high-throughput 16S marker sequencing was used to deeply describe the duodenal and fecal microbiota of patients with celiac disease (CD, n = 6), non-celiac gluten sensitivity (NCGS, n = 12), and healthy subjects (n = 12) from our local area. Additionally, we also investigated the changes in gut microbiota after four weeks on a gluten-free diet (GFD) in a subset of patients from whom paired samples were available. Despite a high inter-individual variability, significant differences in various microbial populations were identified. The linear discriminant analysis (LDA) effect size (LEfSe) method revealed that the genus Actinobacillus and the family Ruminococcaceae were higher in the duodenal and fecal microbiota of NCGS patients, respectively, while Novispirillum was higher in the duodenum of CD patients (p < 0.05, LDA score > 3.5). Interestingly, paired samples from NCGS patients showed a significant difference in duodenal Pseudomonas between the baseline period (median: 1.3%; min/max: 0.47–6.8%) and the period after four weeks on GFD (14.8%; 2.3–38.5%, p < 0.01, Wilcoxon signed-rank test). These results encourage more research on GRDs in México.
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spelling pubmed-62667552018-12-06 First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity Garcia-Mazcorro, Jose F. Rivera-Gutierrez, Xaira Cobos-Quevedo, Orestes De Jesus Grube-Pagola, Peter Meixueiro-Daza, Arturo Hernandez-Flores, Karina Cabrera-Jorge, Francisco J. Vivanco-Cid, Hector Dowd, Scot E. Remes-Troche, Jose M. Nutrients Article Gluten-related disorders (GRDs) are common chronic enteropathies and increasing evidence suggests an involvement of the gut microbiota. We examined the gut microbiota in Mexican people afflicted with GRDs. Ultra-high-throughput 16S marker sequencing was used to deeply describe the duodenal and fecal microbiota of patients with celiac disease (CD, n = 6), non-celiac gluten sensitivity (NCGS, n = 12), and healthy subjects (n = 12) from our local area. Additionally, we also investigated the changes in gut microbiota after four weeks on a gluten-free diet (GFD) in a subset of patients from whom paired samples were available. Despite a high inter-individual variability, significant differences in various microbial populations were identified. The linear discriminant analysis (LDA) effect size (LEfSe) method revealed that the genus Actinobacillus and the family Ruminococcaceae were higher in the duodenal and fecal microbiota of NCGS patients, respectively, while Novispirillum was higher in the duodenum of CD patients (p < 0.05, LDA score > 3.5). Interestingly, paired samples from NCGS patients showed a significant difference in duodenal Pseudomonas between the baseline period (median: 1.3%; min/max: 0.47–6.8%) and the period after four weeks on GFD (14.8%; 2.3–38.5%, p < 0.01, Wilcoxon signed-rank test). These results encourage more research on GRDs in México. MDPI 2018-11-02 /pmc/articles/PMC6266755/ /pubmed/30400238 http://dx.doi.org/10.3390/nu10111641 Text en © 2018 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
Garcia-Mazcorro, Jose F.
Rivera-Gutierrez, Xaira
Cobos-Quevedo, Orestes De Jesus
Grube-Pagola, Peter
Meixueiro-Daza, Arturo
Hernandez-Flores, Karina
Cabrera-Jorge, Francisco J.
Vivanco-Cid, Hector
Dowd, Scot E.
Remes-Troche, Jose M.
First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity
title First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity
title_full First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity
title_fullStr First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity
title_full_unstemmed First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity
title_short First Insights into the Gut Microbiota of Mexican Patients with Celiac Disease and Non-Celiac Gluten Sensitivity
title_sort first insights into the gut microbiota of mexican patients with celiac disease and non-celiac gluten sensitivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266755/
https://www.ncbi.nlm.nih.gov/pubmed/30400238
http://dx.doi.org/10.3390/nu10111641
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