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Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure

Clinical trial faecal collections present challenges through geographical spread and inexperienced participants. Collection techniques have been developed and tested to overcome these challenges, but previous studies investigating these techniques have demonstrated a highly variable capacity for sam...

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Autores principales: Watson, Emma-Jane, Giles, Jennifer, Scherer, Benjamin L., Blatchford, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856092/
https://www.ncbi.nlm.nih.gov/pubmed/31727963
http://dx.doi.org/10.1038/s41598-019-53183-5
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author Watson, Emma-Jane
Giles, Jennifer
Scherer, Benjamin L.
Blatchford, Paul
author_facet Watson, Emma-Jane
Giles, Jennifer
Scherer, Benjamin L.
Blatchford, Paul
author_sort Watson, Emma-Jane
collection PubMed
description Clinical trial faecal collections present challenges through geographical spread and inexperienced participants. Collection techniques have been developed and tested to overcome these challenges, but previous studies investigating these techniques have demonstrated a highly variable capacity for sample preservation. Furthermore, these studies typically only examine either preservation of genetic content or metabolites, not both. This study investigated the Stool Nucleic Acid Collection and Preservation Tube (Norgen BioTek Corp) for the preservation of both microbial DNA and microbial organic acid metabolites in human faecal samples when compared to frozen samples. Twenty six healthy adult participants were instructed to collect a bowel movement, subsample into collection tubes and immediately transfer the remaining bulk to −20 °C storage. Resulting organic acid concentrations remained comparable across methods when the preservation tubes were used correctly. The 16S rRNA gene sequencing data revealed twenty significantly different bacterial genera between the two collection methods. Ten Gram-negative genera were more abundant in the collection tubes, and ten Gram-positive genera were more abundant in the fresh frozen samples. This study has illustrated that faecal collection methods bias the microbial community profile according to Gram status and this should be considered when designing studies that collect and store human faecal samples.
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spelling pubmed-68560922019-11-19 Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure Watson, Emma-Jane Giles, Jennifer Scherer, Benjamin L. Blatchford, Paul Sci Rep Article Clinical trial faecal collections present challenges through geographical spread and inexperienced participants. Collection techniques have been developed and tested to overcome these challenges, but previous studies investigating these techniques have demonstrated a highly variable capacity for sample preservation. Furthermore, these studies typically only examine either preservation of genetic content or metabolites, not both. This study investigated the Stool Nucleic Acid Collection and Preservation Tube (Norgen BioTek Corp) for the preservation of both microbial DNA and microbial organic acid metabolites in human faecal samples when compared to frozen samples. Twenty six healthy adult participants were instructed to collect a bowel movement, subsample into collection tubes and immediately transfer the remaining bulk to −20 °C storage. Resulting organic acid concentrations remained comparable across methods when the preservation tubes were used correctly. The 16S rRNA gene sequencing data revealed twenty significantly different bacterial genera between the two collection methods. Ten Gram-negative genera were more abundant in the collection tubes, and ten Gram-positive genera were more abundant in the fresh frozen samples. This study has illustrated that faecal collection methods bias the microbial community profile according to Gram status and this should be considered when designing studies that collect and store human faecal samples. Nature Publishing Group UK 2019-11-14 /pmc/articles/PMC6856092/ /pubmed/31727963 http://dx.doi.org/10.1038/s41598-019-53183-5 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
Watson, Emma-Jane
Giles, Jennifer
Scherer, Benjamin L.
Blatchford, Paul
Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
title Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
title_full Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
title_fullStr Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
title_full_unstemmed Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
title_short Human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
title_sort human faecal collection methods demonstrate a bias in microbiome composition by cell wall structure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856092/
https://www.ncbi.nlm.nih.gov/pubmed/31727963
http://dx.doi.org/10.1038/s41598-019-53183-5
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