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Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets

Mortality, impaired development and metabolic dysfunctions of suckling low-birthweight piglets may be influenced by modulating the intestinal microbiome through glutamine supplementation. Therefore, this study examined whether glutamine supplementation may affect the colonic development and microbio...

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Autores principales: Schulze Holthausen, Johannes, Schregel, Johannes, Sciascia, Quentin L., Li, Zeyang, Tuchscherer, Armin, Vahjen, Wilfried, Metges, Cornelia C., Zentek, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612066/
https://www.ncbi.nlm.nih.gov/pubmed/36296176
http://dx.doi.org/10.3390/microorganisms10101899
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author Schulze Holthausen, Johannes
Schregel, Johannes
Sciascia, Quentin L.
Li, Zeyang
Tuchscherer, Armin
Vahjen, Wilfried
Metges, Cornelia C.
Zentek, Jürgen
author_facet Schulze Holthausen, Johannes
Schregel, Johannes
Sciascia, Quentin L.
Li, Zeyang
Tuchscherer, Armin
Vahjen, Wilfried
Metges, Cornelia C.
Zentek, Jürgen
author_sort Schulze Holthausen, Johannes
collection PubMed
description Mortality, impaired development and metabolic dysfunctions of suckling low-birthweight piglets may be influenced by modulating the intestinal microbiome through glutamine supplementation. Therefore, this study examined whether glutamine supplementation may affect the colonic development and microbiome composition of male low- and normal-birthweight piglets at 5 and 12 days of age. Suckling piglets were supplemented orally with glutamine or alanine. Colonic digesta samples were obtained for 16S rDNA sequencing, determination of bacterial metabolites and histomorphological tissue analyses. Glutamine-supplemented piglets had lower concentrations of cadaverine and spermidine in the colonic digesta (p < 0.05) and a higher number of CD3(+) colonic intraepithelial lymphocytes compared to alanine-supplemented piglets (p < 0.05). Low-birthweight piglets were characterised by a lower relative abundance of Firmicutes, the genera Negativibacillus and Faecalibacterium and a higher abundance of Alistipes (p < 0.05). Concentrations of cadaverine and total biogenic amines (p < 0.05) and CD3(+) intraepithelial lymphocytes (p < 0.05) were lower in low- compared with normal-birthweight piglets. In comparison to the factor age, glutamine supplementation and birthweight were associated with minor changes in microbial and histological characteristics of the colon, indicating that ontogenetic factors play a more important role in intestinal development.
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spelling pubmed-96120662022-10-28 Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets Schulze Holthausen, Johannes Schregel, Johannes Sciascia, Quentin L. Li, Zeyang Tuchscherer, Armin Vahjen, Wilfried Metges, Cornelia C. Zentek, Jürgen Microorganisms Article Mortality, impaired development and metabolic dysfunctions of suckling low-birthweight piglets may be influenced by modulating the intestinal microbiome through glutamine supplementation. Therefore, this study examined whether glutamine supplementation may affect the colonic development and microbiome composition of male low- and normal-birthweight piglets at 5 and 12 days of age. Suckling piglets were supplemented orally with glutamine or alanine. Colonic digesta samples were obtained for 16S rDNA sequencing, determination of bacterial metabolites and histomorphological tissue analyses. Glutamine-supplemented piglets had lower concentrations of cadaverine and spermidine in the colonic digesta (p < 0.05) and a higher number of CD3(+) colonic intraepithelial lymphocytes compared to alanine-supplemented piglets (p < 0.05). Low-birthweight piglets were characterised by a lower relative abundance of Firmicutes, the genera Negativibacillus and Faecalibacterium and a higher abundance of Alistipes (p < 0.05). Concentrations of cadaverine and total biogenic amines (p < 0.05) and CD3(+) intraepithelial lymphocytes (p < 0.05) were lower in low- compared with normal-birthweight piglets. In comparison to the factor age, glutamine supplementation and birthweight were associated with minor changes in microbial and histological characteristics of the colon, indicating that ontogenetic factors play a more important role in intestinal development. MDPI 2022-09-25 /pmc/articles/PMC9612066/ /pubmed/36296176 http://dx.doi.org/10.3390/microorganisms10101899 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
Schulze Holthausen, Johannes
Schregel, Johannes
Sciascia, Quentin L.
Li, Zeyang
Tuchscherer, Armin
Vahjen, Wilfried
Metges, Cornelia C.
Zentek, Jürgen
Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets
title Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets
title_full Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets
title_fullStr Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets
title_full_unstemmed Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets
title_short Effects of Oral Glutamine Supplementation, Birthweight and Age on Colonic Morphology and Microbiome Development in Male Suckling Piglets
title_sort effects of oral glutamine supplementation, birthweight and age on colonic morphology and microbiome development in male suckling piglets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612066/
https://www.ncbi.nlm.nih.gov/pubmed/36296176
http://dx.doi.org/10.3390/microorganisms10101899
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