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Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults
Longitudinal human gut microbiome datasets generated using community-level, sequence-based approaches often report a sub-set of long-lived “resident” taxa that rarely, if ever, are lost. This result contrasts with population-level turnover of resident clones on the order of months to years. We hypot...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776003/ https://www.ncbi.nlm.nih.gov/pubmed/31089259 http://dx.doi.org/10.1038/s41396-019-0435-7 |
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author | Martinson, Jonathan N. V. Pinkham, Nicholas V. Peters, Garrett W. Cho, Hanbyul Heng, Jeremy Rauch, Mychiel Broadaway, Susan C. Walk, Seth T. |
author_facet | Martinson, Jonathan N. V. Pinkham, Nicholas V. Peters, Garrett W. Cho, Hanbyul Heng, Jeremy Rauch, Mychiel Broadaway, Susan C. Walk, Seth T. |
author_sort | Martinson, Jonathan N. V. |
collection | PubMed |
description | Longitudinal human gut microbiome datasets generated using community-level, sequence-based approaches often report a sub-set of long-lived “resident” taxa that rarely, if ever, are lost. This result contrasts with population-level turnover of resident clones on the order of months to years. We hypothesized that the disconnect between these results is due to a relative lack of simultaneous discrimination of the human gut microbiome at both the community and population-levels. Here, we present results of a small, longitudinal cohort study (n = 8 participants) of healthy human adults that identifies static and dynamic members of the gut microbiome at the clone level based on cultivation/genetic discrimination and at the operational taxonomic unit/amplified sequence variant levels based on 16S rRNA sequencing. We provide evidence that there is little “stability” within resident clonal populations of the common gut microbiome bacterial family, Enterobacteriaceae. Given that clones can vary substantially in genome content and that evolutionary processes operate on the population level, these results question the biological relevance of apparent stability at higher taxonomic levels. |
format | Online Article Text |
id | pubmed-6776003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67760032019-10-04 Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults Martinson, Jonathan N. V. Pinkham, Nicholas V. Peters, Garrett W. Cho, Hanbyul Heng, Jeremy Rauch, Mychiel Broadaway, Susan C. Walk, Seth T. ISME J Article Longitudinal human gut microbiome datasets generated using community-level, sequence-based approaches often report a sub-set of long-lived “resident” taxa that rarely, if ever, are lost. This result contrasts with population-level turnover of resident clones on the order of months to years. We hypothesized that the disconnect between these results is due to a relative lack of simultaneous discrimination of the human gut microbiome at both the community and population-levels. Here, we present results of a small, longitudinal cohort study (n = 8 participants) of healthy human adults that identifies static and dynamic members of the gut microbiome at the clone level based on cultivation/genetic discrimination and at the operational taxonomic unit/amplified sequence variant levels based on 16S rRNA sequencing. We provide evidence that there is little “stability” within resident clonal populations of the common gut microbiome bacterial family, Enterobacteriaceae. Given that clones can vary substantially in genome content and that evolutionary processes operate on the population level, these results question the biological relevance of apparent stability at higher taxonomic levels. Nature Publishing Group UK 2019-05-14 2019-09 /pmc/articles/PMC6776003/ /pubmed/31089259 http://dx.doi.org/10.1038/s41396-019-0435-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Martinson, Jonathan N. V. Pinkham, Nicholas V. Peters, Garrett W. Cho, Hanbyul Heng, Jeremy Rauch, Mychiel Broadaway, Susan C. Walk, Seth T. Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults |
title | Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults |
title_full | Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults |
title_fullStr | Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults |
title_full_unstemmed | Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults |
title_short | Rethinking gut microbiome residency and the Enterobacteriaceae in healthy human adults |
title_sort | rethinking gut microbiome residency and the enterobacteriaceae in healthy human adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776003/ https://www.ncbi.nlm.nih.gov/pubmed/31089259 http://dx.doi.org/10.1038/s41396-019-0435-7 |
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