Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession
Abstract 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 sequ...
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doaj-4685f5a3ab0d42c58ee9ea89ea3ab2072020-11-25T01:53:47ZengWileyMicrobiologyOpen2045-88272019-09-0189n/an/a10.1002/mbo3.821Patterns of community assembly in the developing chicken microbiome reveal rapid primary successionStephanie D. Jurburg0Michael S. M. Brouwer1Daniela Ceccarelli2Jeanet van derGoot3Alfons J. M. Jansman4Alex Bossers5Department of Infection Biology Wageningen Bioveterinary Research Lelystad The NetherlandsDepartment of Bacteriology and Epidemiology Wageningen Bioveterinary Research Lelystad The NetherlandsDepartment of Bacteriology and Epidemiology Wageningen Bioveterinary Research Lelystad The NetherlandsDepartment of Bacteriology and Epidemiology Wageningen Bioveterinary Research Lelystad The NetherlandsWageningen Livestock Research Wageningen The NetherlandsDepartment of Infection Biology Wageningen Bioveterinary Research Lelystad The NetherlandsAbstract 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.https://doi.org/10.1002/mbo3.821broilerchicken microbiomecommunity assemblyfecal microbiomeprimary succession |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stephanie D. Jurburg Michael S. M. Brouwer Daniela Ceccarelli Jeanet van derGoot Alfons J. M. Jansman Alex Bossers |
spellingShingle |
Stephanie D. Jurburg Michael S. M. Brouwer Daniela Ceccarelli Jeanet van derGoot Alfons J. M. Jansman Alex Bossers Patterns of community assembly in the developing chicken microbiome reveal rapid primary succession MicrobiologyOpen broiler chicken microbiome community assembly fecal microbiome primary succession |
author_facet |
Stephanie D. Jurburg Michael S. M. Brouwer Daniela Ceccarelli Jeanet van derGoot Alfons J. M. Jansman Alex Bossers |
author_sort |
Stephanie D. Jurburg |
title |
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_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_sort |
patterns of community assembly in the developing chicken microbiome reveal rapid primary succession |
publisher |
Wiley |
series |
MicrobiologyOpen |
issn |
2045-8827 |
publishDate |
2019-09-01 |
description |
Abstract 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. |
topic |
broiler chicken microbiome community assembly fecal microbiome primary succession |
url |
https://doi.org/10.1002/mbo3.821 |
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