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Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?

BACKGROUND: Inflammatory bowel disease (IBD) refers to a diverse group of chronic gastrointestinal diseases, and gut microbial dysbiosis has been proposed as a modulating factor in its pathogenesis. Several studies have investigated the gut microbial ecology of dogs with IBD but it is yet unclear if...

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Autores principales: Xu, Jia, Verbrugghe, Adronie, Lourenço, Marta, Janssens, Geert P. J., Liu, Daisy J. X., Van de Wiele, Tom, Eeckhaut, Venessa, Van Immerseel, Filip, Van de Maele, Isabel, Niu, Yufeng, Bosch, Guido, Junius, Greet, Wuyts, Brigitte, Hesta, Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910228/
https://www.ncbi.nlm.nih.gov/pubmed/27306031
http://dx.doi.org/10.1186/s12917-016-0736-2
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author Xu, Jia
Verbrugghe, Adronie
Lourenço, Marta
Janssens, Geert P. J.
Liu, Daisy J. X.
Van de Wiele, Tom
Eeckhaut, Venessa
Van Immerseel, Filip
Van de Maele, Isabel
Niu, Yufeng
Bosch, Guido
Junius, Greet
Wuyts, Brigitte
Hesta, Myriam
author_facet Xu, Jia
Verbrugghe, Adronie
Lourenço, Marta
Janssens, Geert P. J.
Liu, Daisy J. X.
Van de Wiele, Tom
Eeckhaut, Venessa
Van Immerseel, Filip
Van de Maele, Isabel
Niu, Yufeng
Bosch, Guido
Junius, Greet
Wuyts, Brigitte
Hesta, Myriam
author_sort Xu, Jia
collection PubMed
description BACKGROUND: Inflammatory bowel disease (IBD) refers to a diverse group of chronic gastrointestinal diseases, and gut microbial dysbiosis has been proposed as a modulating factor in its pathogenesis. Several studies have investigated the gut microbial ecology of dogs with IBD but it is yet unclear if this microbial profile can alter the nutrient metabolism of the host. The aim of the present study was to characterize the faecal bacterial profile and functionality as well as to determine host metabolic changes in IBD dogs. Twenty-three dogs diagnosed with IBD and ten healthy control dogs were included. Dogs with IBD were given a clinical score using the canine chronic enteropathy clinical activity index (CCECAI). Faecal short-chain fatty acids (SCFA) and ammonia concentrations were measured and quantitative PCR was performed. The concentration of plasma amino acids, acylcarnitines, serum folate, cobalamin, and indoxyl sulfate was determined. RESULTS: No significant differences in the abundance of a selection of bacterial groups and fermentation metabolites were observed between the IBD and control groups. However, significant negative correlations were found between CCECAI and the faecal proportion of Lactobacillus as well as between CCECAI and total SCFA concentration. Serum folate and plasma citrulline were decreased and plasma valine was increased in IBD compared to control dogs. Increased plasma free carnitine and total acylcarnitines were observed in IBD compared with control dogs, whereas short-chain acylcarnitines (butyrylcarnitine + isobutyrylcarnitine and, methylmalonylcarnitine) to free carnitine ratios decreased. Dogs with IBD had a higher 3-hydroxyisovalerylcarnitine + isovalerylcarnitine to leucine ratio compared to control dogs. CONCLUSIONS: Canine IBD induced a wide range of changes in metabolic profile, especially for the plasma concentrations of short-chain acylcarnitines and amino acids, which could have evolved from tissue damage and alteration in host metabolism. In addition, dogs with more severe IBD were characterised by a decrease in faecal proportion of Lactobacillus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-016-0736-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-49102282016-06-17 Does canine inflammatory bowel disease influence gut microbial profile and host metabolism? Xu, Jia Verbrugghe, Adronie Lourenço, Marta Janssens, Geert P. J. Liu, Daisy J. X. Van de Wiele, Tom Eeckhaut, Venessa Van Immerseel, Filip Van de Maele, Isabel Niu, Yufeng Bosch, Guido Junius, Greet Wuyts, Brigitte Hesta, Myriam BMC Vet Res Research Article BACKGROUND: Inflammatory bowel disease (IBD) refers to a diverse group of chronic gastrointestinal diseases, and gut microbial dysbiosis has been proposed as a modulating factor in its pathogenesis. Several studies have investigated the gut microbial ecology of dogs with IBD but it is yet unclear if this microbial profile can alter the nutrient metabolism of the host. The aim of the present study was to characterize the faecal bacterial profile and functionality as well as to determine host metabolic changes in IBD dogs. Twenty-three dogs diagnosed with IBD and ten healthy control dogs were included. Dogs with IBD were given a clinical score using the canine chronic enteropathy clinical activity index (CCECAI). Faecal short-chain fatty acids (SCFA) and ammonia concentrations were measured and quantitative PCR was performed. The concentration of plasma amino acids, acylcarnitines, serum folate, cobalamin, and indoxyl sulfate was determined. RESULTS: No significant differences in the abundance of a selection of bacterial groups and fermentation metabolites were observed between the IBD and control groups. However, significant negative correlations were found between CCECAI and the faecal proportion of Lactobacillus as well as between CCECAI and total SCFA concentration. Serum folate and plasma citrulline were decreased and plasma valine was increased in IBD compared to control dogs. Increased plasma free carnitine and total acylcarnitines were observed in IBD compared with control dogs, whereas short-chain acylcarnitines (butyrylcarnitine + isobutyrylcarnitine and, methylmalonylcarnitine) to free carnitine ratios decreased. Dogs with IBD had a higher 3-hydroxyisovalerylcarnitine + isovalerylcarnitine to leucine ratio compared to control dogs. CONCLUSIONS: Canine IBD induced a wide range of changes in metabolic profile, especially for the plasma concentrations of short-chain acylcarnitines and amino acids, which could have evolved from tissue damage and alteration in host metabolism. In addition, dogs with more severe IBD were characterised by a decrease in faecal proportion of Lactobacillus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-016-0736-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-16 /pmc/articles/PMC4910228/ /pubmed/27306031 http://dx.doi.org/10.1186/s12917-016-0736-2 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Xu, Jia
Verbrugghe, Adronie
Lourenço, Marta
Janssens, Geert P. J.
Liu, Daisy J. X.
Van de Wiele, Tom
Eeckhaut, Venessa
Van Immerseel, Filip
Van de Maele, Isabel
Niu, Yufeng
Bosch, Guido
Junius, Greet
Wuyts, Brigitte
Hesta, Myriam
Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
title Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
title_full Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
title_fullStr Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
title_full_unstemmed Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
title_short Does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
title_sort does canine inflammatory bowel disease influence gut microbial profile and host metabolism?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910228/
https://www.ncbi.nlm.nih.gov/pubmed/27306031
http://dx.doi.org/10.1186/s12917-016-0736-2
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