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Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession

The fine‐scale temporal dynamics of the chicken gut microbiome are unexplored, but thought to be critical for chicken health and productivity. Here, we monitored the fecal microbiome of healthy chickens on days 1–7, 10, 14, 21, 28, and 35 after hatching, and performed 16S rRNA amplicon sequencing in...

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Autores principales: Jurburg, Stephanie D., Brouwer, Michael S. M., Ceccarelli, Daniela, van der Goot, Jeanet, Jansman, Alfons J. M., Bossers, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741130/
https://www.ncbi.nlm.nih.gov/pubmed/30828985
http://dx.doi.org/10.1002/mbo3.821
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author Jurburg, Stephanie D.
Brouwer, Michael S. M.
Ceccarelli, Daniela
van der Goot, Jeanet
Jansman, Alfons J. M.
Bossers, Alex
author_facet Jurburg, Stephanie D.
Brouwer, Michael S. M.
Ceccarelli, Daniela
van der Goot, Jeanet
Jansman, Alfons J. M.
Bossers, Alex
author_sort Jurburg, Stephanie D.
collection PubMed
description The fine‐scale temporal dynamics of the chicken gut microbiome are unexplored, but thought to be critical for chicken health and productivity. Here, we monitored the fecal microbiome of healthy chickens on days 1–7, 10, 14, 21, 28, and 35 after hatching, and performed 16S rRNA amplicon sequencing in order to obtain a high‐resolution census of the fecal microbiome over time. In the period studied, the fecal microbiomes of the developing chickens showed a linear‐log increase in community richness and consistent shifts in community composition. Three successional stages were detected: the first stage was dominated by vertically transmitted or rapidly colonizing taxa including Streptococcus and Escherichia/Shigella; in the second stage beginning on day 4, these taxa were displaced by rapid‐growing taxa including Lachnospiraceae and Ruminococcus‐like species variants; and in the third stage, starting on day 10, slow‐growing, specialist taxa including Candidatus Arthrobacter and Romboutsia were detected. The patterns of displacement and the previously reported ecological characteristics of many of the dominant taxa observed suggest that resource competition plays an important role in regulating successional dynamics in the developing chicken gut. We propose that the boundaries between successional stages (3–4 and 14–21 days after hatching) may be optimal times for microbiome interventions.
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spelling pubmed-67411302019-09-13 Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession Jurburg, Stephanie D. Brouwer, Michael S. M. Ceccarelli, Daniela van der Goot, Jeanet Jansman, Alfons J. M. Bossers, Alex Microbiologyopen Original Articles The fine‐scale temporal dynamics of the chicken gut microbiome are unexplored, but thought to be critical for chicken health and productivity. Here, we monitored the fecal microbiome of healthy chickens on days 1–7, 10, 14, 21, 28, and 35 after hatching, and performed 16S rRNA amplicon sequencing in order to obtain a high‐resolution census of the fecal microbiome over time. In the period studied, the fecal microbiomes of the developing chickens showed a linear‐log increase in community richness and consistent shifts in community composition. Three successional stages were detected: the first stage was dominated by vertically transmitted or rapidly colonizing taxa including Streptococcus and Escherichia/Shigella; in the second stage beginning on day 4, these taxa were displaced by rapid‐growing taxa including Lachnospiraceae and Ruminococcus‐like species variants; and in the third stage, starting on day 10, slow‐growing, specialist taxa including Candidatus Arthrobacter and Romboutsia were detected. The patterns of displacement and the previously reported ecological characteristics of many of the dominant taxa observed suggest that resource competition plays an important role in regulating successional dynamics in the developing chicken gut. We propose that the boundaries between successional stages (3–4 and 14–21 days after hatching) may be optimal times for microbiome interventions. John Wiley and Sons Inc. 2019-03-03 /pmc/articles/PMC6741130/ /pubmed/30828985 http://dx.doi.org/10.1002/mbo3.821 Text en © 2019 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Jurburg, Stephanie D.
Brouwer, Michael S. M.
Ceccarelli, Daniela
van der Goot, Jeanet
Jansman, Alfons J. M.
Bossers, Alex
Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
title Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
title_full Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
title_fullStr Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
title_full_unstemmed Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
title_short Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
title_sort patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741130/
https://www.ncbi.nlm.nih.gov/pubmed/30828985
http://dx.doi.org/10.1002/mbo3.821
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