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Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish
BACKGROUND: The majority of animal associated microorganisms are present in digestive tract communities. These intestinal communities arise from selective pressures of the gut habitats as well as host's genotype are regarded as an extra ‘organ’ regulate functions that have not evolved wholly on...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261916/ https://www.ncbi.nlm.nih.gov/pubmed/22276219 http://dx.doi.org/10.1371/journal.pone.0030603 |
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author | Yan, Qingyun van der Gast, Christopher J. Yu, Yuhe |
author_facet | Yan, Qingyun van der Gast, Christopher J. Yu, Yuhe |
author_sort | Yan, Qingyun |
collection | PubMed |
description | BACKGROUND: The majority of animal associated microorganisms are present in digestive tract communities. These intestinal communities arise from selective pressures of the gut habitats as well as host's genotype are regarded as an extra ‘organ’ regulate functions that have not evolved wholly on the host. They are functionally essential in providing nourishment, regulating epithelial development, and influencing immunity in the vertebrate host. As vertebrates are born free of microorganisms, what is poorly understood is how intestinal bacterial communities assemble and develop in conjunction with the development of the host. METHODOLOGY/PRINCIPAL FINDINGS: Set within an ecological framework, we investigated the bacterial community assembly and turnover within the intestinal habitats of developing zebrafish (from larvae to adult animals). Spatial and temporal species-richness relationships and Mantel and partial Mantel tests revealed that turnover was low and that richness and composition was best predicted by time and not intestinal volume (habitat size) or changes in food diet. We also observed that bacterial communities within the zebrafish intestines were deterministically assembled (reflected by the observed low turnover) switching to stochastic assembly in the later stages of zebrafish development. CONCLUSIONS/SIGNIFICANCE: This study is of importance as it provides a novel insight into how intestinal bacterial communities assemble in tandem with the host's development (from early to adult stages). It is our hope that by studying intestinal microbiota of this vertebrate model with such or some more refined approaches in the future could well provide ecological insights for clinical benefit. In addition, this study also adds to our still fledgling knowledge of how spatial and temporal species-richness relationships are shaped and provides further mounting evidence that bacterial community assembly and dynamics are shaped by both deterministic and stochastic considerations. |
format | Online Article Text |
id | pubmed-3261916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32619162012-01-24 Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish Yan, Qingyun van der Gast, Christopher J. Yu, Yuhe PLoS One Research Article BACKGROUND: The majority of animal associated microorganisms are present in digestive tract communities. These intestinal communities arise from selective pressures of the gut habitats as well as host's genotype are regarded as an extra ‘organ’ regulate functions that have not evolved wholly on the host. They are functionally essential in providing nourishment, regulating epithelial development, and influencing immunity in the vertebrate host. As vertebrates are born free of microorganisms, what is poorly understood is how intestinal bacterial communities assemble and develop in conjunction with the development of the host. METHODOLOGY/PRINCIPAL FINDINGS: Set within an ecological framework, we investigated the bacterial community assembly and turnover within the intestinal habitats of developing zebrafish (from larvae to adult animals). Spatial and temporal species-richness relationships and Mantel and partial Mantel tests revealed that turnover was low and that richness and composition was best predicted by time and not intestinal volume (habitat size) or changes in food diet. We also observed that bacterial communities within the zebrafish intestines were deterministically assembled (reflected by the observed low turnover) switching to stochastic assembly in the later stages of zebrafish development. CONCLUSIONS/SIGNIFICANCE: This study is of importance as it provides a novel insight into how intestinal bacterial communities assemble in tandem with the host's development (from early to adult stages). It is our hope that by studying intestinal microbiota of this vertebrate model with such or some more refined approaches in the future could well provide ecological insights for clinical benefit. In addition, this study also adds to our still fledgling knowledge of how spatial and temporal species-richness relationships are shaped and provides further mounting evidence that bacterial community assembly and dynamics are shaped by both deterministic and stochastic considerations. Public Library of Science 2012-01-19 /pmc/articles/PMC3261916/ /pubmed/22276219 http://dx.doi.org/10.1371/journal.pone.0030603 Text en Yan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Yan, Qingyun van der Gast, Christopher J. Yu, Yuhe Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish |
title | Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish |
title_full | Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish |
title_fullStr | Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish |
title_full_unstemmed | Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish |
title_short | Bacterial Community Assembly and Turnover within the Intestines of Developing Zebrafish |
title_sort | bacterial community assembly and turnover within the intestines of developing zebrafish |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261916/ https://www.ncbi.nlm.nih.gov/pubmed/22276219 http://dx.doi.org/10.1371/journal.pone.0030603 |
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