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Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract

Interactions between the bacteria and fungi in the gut microbiome can result in altered nutrition, pathogenicity of infection, and host development, making them a crucial component in host health. Associations between the mycobiome and bacteriome in the piglet gut, in the context of weaning, remain...

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Autores principales: Arfken, Ann M., Frey, Juli Foster, Ramsay, Timothy G., Summers, Katie Lynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792466/
https://www.ncbi.nlm.nih.gov/pubmed/31649634
http://dx.doi.org/10.3389/fmicb.2019.02286
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author Arfken, Ann M.
Frey, Juli Foster
Ramsay, Timothy G.
Summers, Katie Lynn
author_facet Arfken, Ann M.
Frey, Juli Foster
Ramsay, Timothy G.
Summers, Katie Lynn
author_sort Arfken, Ann M.
collection PubMed
description Interactions between the bacteria and fungi in the gut microbiome can result in altered nutrition, pathogenicity of infection, and host development, making them a crucial component in host health. Associations between the mycobiome and bacteriome in the piglet gut, in the context of weaning, remain unknown. Weaning is a time of significant stress, dietary changes, microbial alterations, and a predisposition to infection. The loss of animal health and growth makes potential microbial interventions of interest to the swine industry. Recent studies have demonstrated the diversity and development of the microbiome in the gastrointestinal (GI) tract of piglets during weaning, resulting from the dietary and physiological changes. Despite these advances, the role of the mycobiota in piglet health and its contribution to overall microbiome development remains mostly unknown. In this study we investigated the bacteriome and the mycobiome after weaning in the GI tract organs and feces from 35-day old piglets. Following weaning, the α-diversity and amplicon sequence variants (ASVs) counts of the bacteriome increased, proximally to distally, from the stomach to the feces along the GI tract, while the mycobiome α-diversity and ASV counts were highest in the porcine stomach. β-diversity analyses show distinct clusters based on organ type in the bacteriome and mycobiome, but dispersion remained relatively constant in the mycobiome between organ/fecal sites. Bacteroidetes, Firmicutes, and Epsilonbacteraeota were the most abundant bacterial phyla present in the GI tract and feces based on mean taxonomic composition with high variation of composition found in the stomach. In the mycobiome, the dominant phyla were Ascomycota and Basidiomycota, and the stomach mycobiome did not demonstrate the same high level of variation observed in the bacteriome. Potential interactions between genera were found in the lower piglet GI bacteriome and mycobiome with positive correlations found between the fungus, Kazachstania, and several bacterial species, including Lactobacillus. Aspergillus demonstrated negative correlations with the short chain fatty acid-producing bacteria Butyricoccus, Subdoligranulum, and Fusicatenibacter. This study demonstrates the distinct colonization dynamics between fungi and bacteria in the GI tract and feces of piglets directly following weaning and the potential interactions of these microbes in the porcine gut ecosystem.
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spelling pubmed-67924662019-10-24 Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract Arfken, Ann M. Frey, Juli Foster Ramsay, Timothy G. Summers, Katie Lynn Front Microbiol Microbiology Interactions between the bacteria and fungi in the gut microbiome can result in altered nutrition, pathogenicity of infection, and host development, making them a crucial component in host health. Associations between the mycobiome and bacteriome in the piglet gut, in the context of weaning, remain unknown. Weaning is a time of significant stress, dietary changes, microbial alterations, and a predisposition to infection. The loss of animal health and growth makes potential microbial interventions of interest to the swine industry. Recent studies have demonstrated the diversity and development of the microbiome in the gastrointestinal (GI) tract of piglets during weaning, resulting from the dietary and physiological changes. Despite these advances, the role of the mycobiota in piglet health and its contribution to overall microbiome development remains mostly unknown. In this study we investigated the bacteriome and the mycobiome after weaning in the GI tract organs and feces from 35-day old piglets. Following weaning, the α-diversity and amplicon sequence variants (ASVs) counts of the bacteriome increased, proximally to distally, from the stomach to the feces along the GI tract, while the mycobiome α-diversity and ASV counts were highest in the porcine stomach. β-diversity analyses show distinct clusters based on organ type in the bacteriome and mycobiome, but dispersion remained relatively constant in the mycobiome between organ/fecal sites. Bacteroidetes, Firmicutes, and Epsilonbacteraeota were the most abundant bacterial phyla present in the GI tract and feces based on mean taxonomic composition with high variation of composition found in the stomach. In the mycobiome, the dominant phyla were Ascomycota and Basidiomycota, and the stomach mycobiome did not demonstrate the same high level of variation observed in the bacteriome. Potential interactions between genera were found in the lower piglet GI bacteriome and mycobiome with positive correlations found between the fungus, Kazachstania, and several bacterial species, including Lactobacillus. Aspergillus demonstrated negative correlations with the short chain fatty acid-producing bacteria Butyricoccus, Subdoligranulum, and Fusicatenibacter. This study demonstrates the distinct colonization dynamics between fungi and bacteria in the GI tract and feces of piglets directly following weaning and the potential interactions of these microbes in the porcine gut ecosystem. Frontiers Media S.A. 2019-10-08 /pmc/articles/PMC6792466/ /pubmed/31649634 http://dx.doi.org/10.3389/fmicb.2019.02286 Text en Copyright © 2019 Arfken, Frey, Ramsay and Summers. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Arfken, Ann M.
Frey, Juli Foster
Ramsay, Timothy G.
Summers, Katie Lynn
Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract
title Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract
title_full Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract
title_fullStr Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract
title_full_unstemmed Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract
title_short Yeasts of Burden: Exploring the Mycobiome–Bacteriome of the Piglet GI Tract
title_sort yeasts of burden: exploring the mycobiome–bacteriome of the piglet gi tract
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792466/
https://www.ncbi.nlm.nih.gov/pubmed/31649634
http://dx.doi.org/10.3389/fmicb.2019.02286
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