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Moving pictures of the human microbiome
BACKGROUND: Understanding the normal temporal variation in the human microbiome is critical to developing treatments for putative microbiome-related afflictions such as obesity, Crohn's disease, inflammatory bowel disease and malnutrition. Sequencing and computational technologies, however, hav...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271711/ https://www.ncbi.nlm.nih.gov/pubmed/21624126 http://dx.doi.org/10.1186/gb-2011-12-5-r50 |
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author | Caporaso, J Gregory Lauber, Christian L Costello, Elizabeth K Berg-Lyons, Donna Gonzalez, Antonio Stombaugh, Jesse Knights, Dan Gajer, Pawel Ravel, Jacques Fierer, Noah Gordon, Jeffrey I Knight, Rob |
author_facet | Caporaso, J Gregory Lauber, Christian L Costello, Elizabeth K Berg-Lyons, Donna Gonzalez, Antonio Stombaugh, Jesse Knights, Dan Gajer, Pawel Ravel, Jacques Fierer, Noah Gordon, Jeffrey I Knight, Rob |
author_sort | Caporaso, J Gregory |
collection | PubMed |
description | BACKGROUND: Understanding the normal temporal variation in the human microbiome is critical to developing treatments for putative microbiome-related afflictions such as obesity, Crohn's disease, inflammatory bowel disease and malnutrition. Sequencing and computational technologies, however, have been a limiting factor in performing dense time series analysis of the human microbiome. Here, we present the largest human microbiota time series analysis to date, covering two individuals at four body sites over 396 timepoints. RESULTS: We find that despite stable differences between body sites and individuals, there is pronounced variability in an individual's microbiota across months, weeks and even days. Additionally, only a small fraction of the total taxa found within a single body site appear to be present across all time points, suggesting that no core temporal microbiome exists at high abundance (although some microbes may be present but drop below the detection threshold). Many more taxa appear to be persistent but non-permanent community members. CONCLUSIONS: DNA sequencing and computational advances described here provide the ability to go beyond infrequent snapshots of our human-associated microbial ecology to high-resolution assessments of temporal variations over protracted periods, within and between body habitats and individuals. This capacity will allow us to define normal variation and pathologic states, and assess responses to therapeutic interventions. |
format | Online Article Text |
id | pubmed-3271711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32717112012-02-04 Moving pictures of the human microbiome Caporaso, J Gregory Lauber, Christian L Costello, Elizabeth K Berg-Lyons, Donna Gonzalez, Antonio Stombaugh, Jesse Knights, Dan Gajer, Pawel Ravel, Jacques Fierer, Noah Gordon, Jeffrey I Knight, Rob Genome Biol Research BACKGROUND: Understanding the normal temporal variation in the human microbiome is critical to developing treatments for putative microbiome-related afflictions such as obesity, Crohn's disease, inflammatory bowel disease and malnutrition. Sequencing and computational technologies, however, have been a limiting factor in performing dense time series analysis of the human microbiome. Here, we present the largest human microbiota time series analysis to date, covering two individuals at four body sites over 396 timepoints. RESULTS: We find that despite stable differences between body sites and individuals, there is pronounced variability in an individual's microbiota across months, weeks and even days. Additionally, only a small fraction of the total taxa found within a single body site appear to be present across all time points, suggesting that no core temporal microbiome exists at high abundance (although some microbes may be present but drop below the detection threshold). Many more taxa appear to be persistent but non-permanent community members. CONCLUSIONS: DNA sequencing and computational advances described here provide the ability to go beyond infrequent snapshots of our human-associated microbial ecology to high-resolution assessments of temporal variations over protracted periods, within and between body habitats and individuals. This capacity will allow us to define normal variation and pathologic states, and assess responses to therapeutic interventions. BioMed Central 2011 2011-05-30 /pmc/articles/PMC3271711/ /pubmed/21624126 http://dx.doi.org/10.1186/gb-2011-12-5-r50 Text en Copyright ©2011 Caporaso et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Caporaso, J Gregory Lauber, Christian L Costello, Elizabeth K Berg-Lyons, Donna Gonzalez, Antonio Stombaugh, Jesse Knights, Dan Gajer, Pawel Ravel, Jacques Fierer, Noah Gordon, Jeffrey I Knight, Rob Moving pictures of the human microbiome |
title | Moving pictures of the human microbiome |
title_full | Moving pictures of the human microbiome |
title_fullStr | Moving pictures of the human microbiome |
title_full_unstemmed | Moving pictures of the human microbiome |
title_short | Moving pictures of the human microbiome |
title_sort | moving pictures of the human microbiome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271711/ https://www.ncbi.nlm.nih.gov/pubmed/21624126 http://dx.doi.org/10.1186/gb-2011-12-5-r50 |
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