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GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity
INTRODUCTION: A precise fecal microbiome analysis requires normalized methods for microbiome sampling, transport and manipulation in order to obtain a representative snapshot of the microbial community. GutAlive(®) is the unique stool collection kit that generates an anaerobic atmosphere enabling ox...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117842/ https://www.ncbi.nlm.nih.gov/pubmed/37089545 http://dx.doi.org/10.3389/fmicb.2023.1118291 |
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author | Montero, Ignacio Barrientos, Desirée Hidalgo-Cantabrana, Claudio Martínez-Álvarez, Noelia |
author_facet | Montero, Ignacio Barrientos, Desirée Hidalgo-Cantabrana, Claudio Martínez-Álvarez, Noelia |
author_sort | Montero, Ignacio |
collection | PubMed |
description | INTRODUCTION: A precise fecal microbiome analysis requires normalized methods for microbiome sampling, transport and manipulation in order to obtain a representative snapshot of the microbial community. GutAlive(®) is the unique stool collection kit that generates an anaerobic atmosphere enabling oxygen sensitive bacteria to survive, maintaining the original microbiome composition and diversity. METHODS: Five stool samples from different donors were collected using two different sampling devices, GutAlive(®) and Zymo DNA/RNA Shield(®), and processed at four different time points. Shotgun metagenomics was used to evaluate the influence of the device and the processing timing on the microbial populations to unravel the potential fluctuations on the composition and diversity of the fecal microbiome and the metabolic pathways profiling. Additionally, RT-qPCR was used to quantify bacterial cell viability for downstream applications of microbiota samples beyond metagenomics. RESULTS: Our results show that GutAlive(®) enables bacterial cell viability overtime preserving DNA integrity, obtaining high-quantity and high-quality DNA to perform microbiome analysis using shotgun metagenomics. Based on the taxonomic profiling, metabolic pathways analysis, phylogeny and metagenome-assembled genomes, GutAlive(®) displayed greater performance without significant variability over time, showcasing the stabilization of the microbiome preserving the original composition and diversity. Indeed, this DNA stabilization is enabled with the preservation of bacterial viability on an anaerobic environment inside of the sampling device, without the addition of any reagents that interact directly with sample. CONCLUSION: All the above makes GutAlive(®) an user-friendly kit for self-collection of biological samples, suitable for microbiome analysis, diagnostics, fecal microbiota transplant and bacterial isolation, maintaining the stability and bacterial viability over time, preserving the original composition and diversity of the microbiome. |
format | Online Article Text |
id | pubmed-10117842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101178422023-04-21 GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity Montero, Ignacio Barrientos, Desirée Hidalgo-Cantabrana, Claudio Martínez-Álvarez, Noelia Front Microbiol Microbiology INTRODUCTION: A precise fecal microbiome analysis requires normalized methods for microbiome sampling, transport and manipulation in order to obtain a representative snapshot of the microbial community. GutAlive(®) is the unique stool collection kit that generates an anaerobic atmosphere enabling oxygen sensitive bacteria to survive, maintaining the original microbiome composition and diversity. METHODS: Five stool samples from different donors were collected using two different sampling devices, GutAlive(®) and Zymo DNA/RNA Shield(®), and processed at four different time points. Shotgun metagenomics was used to evaluate the influence of the device and the processing timing on the microbial populations to unravel the potential fluctuations on the composition and diversity of the fecal microbiome and the metabolic pathways profiling. Additionally, RT-qPCR was used to quantify bacterial cell viability for downstream applications of microbiota samples beyond metagenomics. RESULTS: Our results show that GutAlive(®) enables bacterial cell viability overtime preserving DNA integrity, obtaining high-quantity and high-quality DNA to perform microbiome analysis using shotgun metagenomics. Based on the taxonomic profiling, metabolic pathways analysis, phylogeny and metagenome-assembled genomes, GutAlive(®) displayed greater performance without significant variability over time, showcasing the stabilization of the microbiome preserving the original composition and diversity. Indeed, this DNA stabilization is enabled with the preservation of bacterial viability on an anaerobic environment inside of the sampling device, without the addition of any reagents that interact directly with sample. CONCLUSION: All the above makes GutAlive(®) an user-friendly kit for self-collection of biological samples, suitable for microbiome analysis, diagnostics, fecal microbiota transplant and bacterial isolation, maintaining the stability and bacterial viability over time, preserving the original composition and diversity of the microbiome. Frontiers Media S.A. 2023-04-06 /pmc/articles/PMC10117842/ /pubmed/37089545 http://dx.doi.org/10.3389/fmicb.2023.1118291 Text en Copyright © 2023 Montero, Barrientos, Hidalgo-Cantabrana and Martínez-Álvarez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Montero, Ignacio Barrientos, Desirée Hidalgo-Cantabrana, Claudio Martínez-Álvarez, Noelia GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity |
title | GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity |
title_full | GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity |
title_fullStr | GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity |
title_full_unstemmed | GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity |
title_short | GutAlive(®) enables DNA-based microbiome analysis without disrupting the original composition and diversity |
title_sort | gutalive(®) enables dna-based microbiome analysis without disrupting the original composition and diversity |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117842/ https://www.ncbi.nlm.nih.gov/pubmed/37089545 http://dx.doi.org/10.3389/fmicb.2023.1118291 |
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