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Critical evaluation of faecal microbiome preservation using metagenomic analysis

The ability to preserve microbial communities in faecal samples is essential as increasing numbers of studies seek to use the gut microbiome to identify biomarkers of disease. Here we use shotgun metagenomics to rigorously evaluate the technical and compositional reproducibility of five room tempera...

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Autores principales: Pribyl, Alena L., Parks, Donovan H., Angel, Nicola Z., Boyd, Joel A., Hasson, Alexander G., Fang, Liang, MacDonald, Samantha L., Wills, Blake A., Wood, David L. A., Krause, Lutz, Tyson, Gene W., Hugenholtz, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645250/
https://www.ncbi.nlm.nih.gov/pubmed/37938632
http://dx.doi.org/10.1038/s43705-021-00014-2
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author Pribyl, Alena L.
Parks, Donovan H.
Angel, Nicola Z.
Boyd, Joel A.
Hasson, Alexander G.
Fang, Liang
MacDonald, Samantha L.
Wills, Blake A.
Wood, David L. A.
Krause, Lutz
Tyson, Gene W.
Hugenholtz, Philip
author_facet Pribyl, Alena L.
Parks, Donovan H.
Angel, Nicola Z.
Boyd, Joel A.
Hasson, Alexander G.
Fang, Liang
MacDonald, Samantha L.
Wills, Blake A.
Wood, David L. A.
Krause, Lutz
Tyson, Gene W.
Hugenholtz, Philip
author_sort Pribyl, Alena L.
collection PubMed
description The ability to preserve microbial communities in faecal samples is essential as increasing numbers of studies seek to use the gut microbiome to identify biomarkers of disease. Here we use shotgun metagenomics to rigorously evaluate the technical and compositional reproducibility of five room temperature (RT) microbial stabilisation methods compared to the best practice of flash-freezing. These methods included RNALater, OMNIGene-GUT, a dry BBL swab, LifeGuard, and a novel method for preserving faecal samples, a Copan FLOQSwab in an active drying tube (FLOQSwab-ADT). Each method was assessed using six replicate faecal samples from five participants, totalling 180 samples. The FLOQSwab-ADT performed best for both technical and compositional reproducibility, followed by RNAlater and OMNIgene-GUT. LifeGuard and the BBL swab had unpredictable outgrowth of Escherichia species in at least one replicate from each participant. We further evaluated the FLOQSwab-ADT in an additional 239 samples across 10 individuals after storage at −20 °C, RT, and 50 °C for four weeks compared to fresh controls. The FLOQSwab-ADT maintained its performance across all temperatures, indicating this method is an excellent alternative to existing RT stabilisation methods.
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spelling pubmed-96452502023-01-04 Critical evaluation of faecal microbiome preservation using metagenomic analysis Pribyl, Alena L. Parks, Donovan H. Angel, Nicola Z. Boyd, Joel A. Hasson, Alexander G. Fang, Liang MacDonald, Samantha L. Wills, Blake A. Wood, David L. A. Krause, Lutz Tyson, Gene W. Hugenholtz, Philip ISME Commun Article The ability to preserve microbial communities in faecal samples is essential as increasing numbers of studies seek to use the gut microbiome to identify biomarkers of disease. Here we use shotgun metagenomics to rigorously evaluate the technical and compositional reproducibility of five room temperature (RT) microbial stabilisation methods compared to the best practice of flash-freezing. These methods included RNALater, OMNIGene-GUT, a dry BBL swab, LifeGuard, and a novel method for preserving faecal samples, a Copan FLOQSwab in an active drying tube (FLOQSwab-ADT). Each method was assessed using six replicate faecal samples from five participants, totalling 180 samples. The FLOQSwab-ADT performed best for both technical and compositional reproducibility, followed by RNAlater and OMNIgene-GUT. LifeGuard and the BBL swab had unpredictable outgrowth of Escherichia species in at least one replicate from each participant. We further evaluated the FLOQSwab-ADT in an additional 239 samples across 10 individuals after storage at −20 °C, RT, and 50 °C for four weeks compared to fresh controls. The FLOQSwab-ADT maintained its performance across all temperatures, indicating this method is an excellent alternative to existing RT stabilisation methods. Nature Publishing Group UK 2021-05-05 /pmc/articles/PMC9645250/ /pubmed/37938632 http://dx.doi.org/10.1038/s43705-021-00014-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pribyl, Alena L.
Parks, Donovan H.
Angel, Nicola Z.
Boyd, Joel A.
Hasson, Alexander G.
Fang, Liang
MacDonald, Samantha L.
Wills, Blake A.
Wood, David L. A.
Krause, Lutz
Tyson, Gene W.
Hugenholtz, Philip
Critical evaluation of faecal microbiome preservation using metagenomic analysis
title Critical evaluation of faecal microbiome preservation using metagenomic analysis
title_full Critical evaluation of faecal microbiome preservation using metagenomic analysis
title_fullStr Critical evaluation of faecal microbiome preservation using metagenomic analysis
title_full_unstemmed Critical evaluation of faecal microbiome preservation using metagenomic analysis
title_short Critical evaluation of faecal microbiome preservation using metagenomic analysis
title_sort critical evaluation of faecal microbiome preservation using metagenomic analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645250/
https://www.ncbi.nlm.nih.gov/pubmed/37938632
http://dx.doi.org/10.1038/s43705-021-00014-2
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