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Integrity of the Human Faecal Microbiota following Long-Term Sample Storage

In studies of the human microbiome, faecal samples are frequently used as a non-invasive proxy for the study of the intestinal microbiota. To obtain reliable insights, the need for bacterial DNA of high quality and integrity following appropriate faecal sample collection and preservation steps is pa...

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Autores principales: Kia, Elahe, Wagner Mackenzie, Brett, Middleton, Danielle, Lau, Anna, Waite, David W., Lewis, Gillian, Chan, Yih-Kai, Silvestre, Marta, Cooper, Garth J. S., Poppitt, Sally D., Taylor, Michael W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049846/
https://www.ncbi.nlm.nih.gov/pubmed/27701448
http://dx.doi.org/10.1371/journal.pone.0163666
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author Kia, Elahe
Wagner Mackenzie, Brett
Middleton, Danielle
Lau, Anna
Waite, David W.
Lewis, Gillian
Chan, Yih-Kai
Silvestre, Marta
Cooper, Garth J. S.
Poppitt, Sally D.
Taylor, Michael W.
author_facet Kia, Elahe
Wagner Mackenzie, Brett
Middleton, Danielle
Lau, Anna
Waite, David W.
Lewis, Gillian
Chan, Yih-Kai
Silvestre, Marta
Cooper, Garth J. S.
Poppitt, Sally D.
Taylor, Michael W.
author_sort Kia, Elahe
collection PubMed
description In studies of the human microbiome, faecal samples are frequently used as a non-invasive proxy for the study of the intestinal microbiota. To obtain reliable insights, the need for bacterial DNA of high quality and integrity following appropriate faecal sample collection and preservation steps is paramount. In a study of dietary mineral balance in the context of type 2 diabetes (T2D), faecal samples were collected from healthy and T2D individuals throughout a 13-day residential trial. These samples were freeze-dried, then stored mostly at -20°C from the trial date in 2000/2001 until the current research in 2014. Given the relative antiquity of these samples (~14 years), we sought to evaluate DNA quality and comparability to freshly collected human faecal samples. Following the extraction of bacterial DNA, gel electrophoresis indicated that our DNA extracts were more sheared than extracts made from freshly collected faecal samples, but still of sufficiently high molecular weight to support amplicon-based studies. Likewise, spectrophotometric assessment of extracts revealed that they were of high quality and quantity. A subset of bacterial 16S rRNA gene amplicons were sequenced using Illumina MiSeq and compared against publicly available sequence data representing a similar cohort analysed by the American Gut Project (AGP). Notably, our bacterial community profiles were highly consistent with those from the AGP data. Our results suggest that when faecal specimens are stored appropriately, the microbial profiles are preserved and robust to extended storage periods.
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spelling pubmed-50498462016-10-27 Integrity of the Human Faecal Microbiota following Long-Term Sample Storage Kia, Elahe Wagner Mackenzie, Brett Middleton, Danielle Lau, Anna Waite, David W. Lewis, Gillian Chan, Yih-Kai Silvestre, Marta Cooper, Garth J. S. Poppitt, Sally D. Taylor, Michael W. PLoS One Research Article In studies of the human microbiome, faecal samples are frequently used as a non-invasive proxy for the study of the intestinal microbiota. To obtain reliable insights, the need for bacterial DNA of high quality and integrity following appropriate faecal sample collection and preservation steps is paramount. In a study of dietary mineral balance in the context of type 2 diabetes (T2D), faecal samples were collected from healthy and T2D individuals throughout a 13-day residential trial. These samples were freeze-dried, then stored mostly at -20°C from the trial date in 2000/2001 until the current research in 2014. Given the relative antiquity of these samples (~14 years), we sought to evaluate DNA quality and comparability to freshly collected human faecal samples. Following the extraction of bacterial DNA, gel electrophoresis indicated that our DNA extracts were more sheared than extracts made from freshly collected faecal samples, but still of sufficiently high molecular weight to support amplicon-based studies. Likewise, spectrophotometric assessment of extracts revealed that they were of high quality and quantity. A subset of bacterial 16S rRNA gene amplicons were sequenced using Illumina MiSeq and compared against publicly available sequence data representing a similar cohort analysed by the American Gut Project (AGP). Notably, our bacterial community profiles were highly consistent with those from the AGP data. Our results suggest that when faecal specimens are stored appropriately, the microbial profiles are preserved and robust to extended storage periods. Public Library of Science 2016-10-04 /pmc/articles/PMC5049846/ /pubmed/27701448 http://dx.doi.org/10.1371/journal.pone.0163666 Text en © 2016 Kia 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kia, Elahe
Wagner Mackenzie, Brett
Middleton, Danielle
Lau, Anna
Waite, David W.
Lewis, Gillian
Chan, Yih-Kai
Silvestre, Marta
Cooper, Garth J. S.
Poppitt, Sally D.
Taylor, Michael W.
Integrity of the Human Faecal Microbiota following Long-Term Sample Storage
title Integrity of the Human Faecal Microbiota following Long-Term Sample Storage
title_full Integrity of the Human Faecal Microbiota following Long-Term Sample Storage
title_fullStr Integrity of the Human Faecal Microbiota following Long-Term Sample Storage
title_full_unstemmed Integrity of the Human Faecal Microbiota following Long-Term Sample Storage
title_short Integrity of the Human Faecal Microbiota following Long-Term Sample Storage
title_sort integrity of the human faecal microbiota following long-term sample storage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049846/
https://www.ncbi.nlm.nih.gov/pubmed/27701448
http://dx.doi.org/10.1371/journal.pone.0163666
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