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Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig

Weaning is a period of environmental changes and stress that results in significant alterations to the piglet gut microbiome and is associated with a predisposition to disease, making potential interventions of interest to the swine industry. In other animals, interactions between the bacteriome and...

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Autores principales: Arfken, Ann M., Frey, Juli Foster, Summers, Katie Lynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356342/
https://www.ncbi.nlm.nih.gov/pubmed/32526857
http://dx.doi.org/10.3390/microorganisms8060868
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author Arfken, Ann M.
Frey, Juli Foster
Summers, Katie Lynn
author_facet Arfken, Ann M.
Frey, Juli Foster
Summers, Katie Lynn
author_sort Arfken, Ann M.
collection PubMed
description Weaning is a period of environmental changes and stress that results in significant alterations to the piglet gut microbiome and is associated with a predisposition to disease, making potential interventions of interest to the swine industry. In other animals, interactions between the bacteriome and mycobiome can result in altered nutrient absorption and susceptibility to disease, but these interactions remain poorly understood in pigs. Recently, we assessed the colonization dynamics of fungi and bacteria in the gastrointestinal tract of piglets at a single time point post-weaning (day 35) and inferred interactions were found between fungal and bacterial members of the porcine gut ecosystem. In this study, we performed a longitudinal assessment of the fecal bacteriome and mycobiome of piglets from birth through the weaning transition. Piglet feces in this study showed a dramatic shift over time in the bacterial and fungal communities, as well as an increase in network connectivity between the two kingdoms. The piglet fecal bacteriome showed a relatively stable and predictable pattern of development from Bacteroidaceae to Prevotellaceae, as seen in other studies, while the mycobiome demonstrated a loss in diversity over time with a post-weaning population dominated by Saccharomycetaceae. The mycobiome demonstrated a more transient community that is likely driven by factors such as diet or environmental exposure rather than an organized pattern of colonization and succession evidenced by fecal sample taxonomic clustering with nursey feed samples post-weaning. Due to the potential tractability of the community, the mycobiome may be a viable candidate for potential microbial interventions that will alter piglet health and growth during the weaning transition.
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spelling pubmed-73563422020-07-30 Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig Arfken, Ann M. Frey, Juli Foster Summers, Katie Lynn Microorganisms Article Weaning is a period of environmental changes and stress that results in significant alterations to the piglet gut microbiome and is associated with a predisposition to disease, making potential interventions of interest to the swine industry. In other animals, interactions between the bacteriome and mycobiome can result in altered nutrient absorption and susceptibility to disease, but these interactions remain poorly understood in pigs. Recently, we assessed the colonization dynamics of fungi and bacteria in the gastrointestinal tract of piglets at a single time point post-weaning (day 35) and inferred interactions were found between fungal and bacterial members of the porcine gut ecosystem. In this study, we performed a longitudinal assessment of the fecal bacteriome and mycobiome of piglets from birth through the weaning transition. Piglet feces in this study showed a dramatic shift over time in the bacterial and fungal communities, as well as an increase in network connectivity between the two kingdoms. The piglet fecal bacteriome showed a relatively stable and predictable pattern of development from Bacteroidaceae to Prevotellaceae, as seen in other studies, while the mycobiome demonstrated a loss in diversity over time with a post-weaning population dominated by Saccharomycetaceae. The mycobiome demonstrated a more transient community that is likely driven by factors such as diet or environmental exposure rather than an organized pattern of colonization and succession evidenced by fecal sample taxonomic clustering with nursey feed samples post-weaning. Due to the potential tractability of the community, the mycobiome may be a viable candidate for potential microbial interventions that will alter piglet health and growth during the weaning transition. MDPI 2020-06-09 /pmc/articles/PMC7356342/ /pubmed/32526857 http://dx.doi.org/10.3390/microorganisms8060868 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
Arfken, Ann M.
Frey, Juli Foster
Summers, Katie Lynn
Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig
title Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig
title_full Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig
title_fullStr Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig
title_full_unstemmed Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig
title_short Temporal Dynamics of the Gut Bacteriome and Mycobiome in the Weanling Pig
title_sort temporal dynamics of the gut bacteriome and mycobiome in the weanling pig
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356342/
https://www.ncbi.nlm.nih.gov/pubmed/32526857
http://dx.doi.org/10.3390/microorganisms8060868
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