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Optimisation of sample storage and DNA extraction for human gut microbiota studies
BACKGROUND: New developments in next-generation sequencing technologies and massive data received from this approach open wide prospects for personalised medicine and nutrition studies. Metagenomic analysis of the gut microbiota is paramount for the characterization of human health and wellbeing. De...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164492/ https://www.ncbi.nlm.nih.gov/pubmed/34051731 http://dx.doi.org/10.1186/s12866-021-02233-y |
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author | Kazantseva, Jekaterina Malv, Esther Kaleda, Aleksei Kallastu, Aili Meikas, Anne |
author_facet | Kazantseva, Jekaterina Malv, Esther Kaleda, Aleksei Kallastu, Aili Meikas, Anne |
author_sort | Kazantseva, Jekaterina |
collection | PubMed |
description | BACKGROUND: New developments in next-generation sequencing technologies and massive data received from this approach open wide prospects for personalised medicine and nutrition studies. Metagenomic analysis of the gut microbiota is paramount for the characterization of human health and wellbeing. Despite the intensive research, there is a huge gap and inconsistency between different studies due to the non-standardised and biased pipeline. Methodical and systemic understanding of every stage in the process is necessary to overcome all bottlenecks and grey zones of gut microbiota studies, where all details and interactions between processes are important. RESULTS: Here we show that an inexpensive, but reliable iSeq 100 platform is an excellent tool to perform the analysis of the human gut microbiota by amplicon sequencing of the 16 S rRNA gene. Two commercial DNA extraction kits and different starting materials performed similarly regarding the taxonomic distribution of identified bacteria. DNA/RNA Shield reagent proved to be a reliable solution for stool samples collection, preservation, and storage, as the storage of faecal material in DNA/RNA Shield for three weeks at different temperatures and thawing cycles had a low impact on the bacterial distribution. CONCLUSIONS: Altogether, a thoroughly elaborated pipeline with close attention to details ensures high reproducibility with significant biological but not technical variations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02233-y. |
format | Online Article Text |
id | pubmed-8164492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81644922021-06-01 Optimisation of sample storage and DNA extraction for human gut microbiota studies Kazantseva, Jekaterina Malv, Esther Kaleda, Aleksei Kallastu, Aili Meikas, Anne BMC Microbiol Research Article BACKGROUND: New developments in next-generation sequencing technologies and massive data received from this approach open wide prospects for personalised medicine and nutrition studies. Metagenomic analysis of the gut microbiota is paramount for the characterization of human health and wellbeing. Despite the intensive research, there is a huge gap and inconsistency between different studies due to the non-standardised and biased pipeline. Methodical and systemic understanding of every stage in the process is necessary to overcome all bottlenecks and grey zones of gut microbiota studies, where all details and interactions between processes are important. RESULTS: Here we show that an inexpensive, but reliable iSeq 100 platform is an excellent tool to perform the analysis of the human gut microbiota by amplicon sequencing of the 16 S rRNA gene. Two commercial DNA extraction kits and different starting materials performed similarly regarding the taxonomic distribution of identified bacteria. DNA/RNA Shield reagent proved to be a reliable solution for stool samples collection, preservation, and storage, as the storage of faecal material in DNA/RNA Shield for three weeks at different temperatures and thawing cycles had a low impact on the bacterial distribution. CONCLUSIONS: Altogether, a thoroughly elaborated pipeline with close attention to details ensures high reproducibility with significant biological but not technical variations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02233-y. BioMed Central 2021-05-29 /pmc/articles/PMC8164492/ /pubmed/34051731 http://dx.doi.org/10.1186/s12866-021-02233-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Kazantseva, Jekaterina Malv, Esther Kaleda, Aleksei Kallastu, Aili Meikas, Anne Optimisation of sample storage and DNA extraction for human gut microbiota studies |
title | Optimisation of sample storage and DNA extraction for human gut microbiota studies |
title_full | Optimisation of sample storage and DNA extraction for human gut microbiota studies |
title_fullStr | Optimisation of sample storage and DNA extraction for human gut microbiota studies |
title_full_unstemmed | Optimisation of sample storage and DNA extraction for human gut microbiota studies |
title_short | Optimisation of sample storage and DNA extraction for human gut microbiota studies |
title_sort | optimisation of sample storage and dna extraction for human gut microbiota studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164492/ https://www.ncbi.nlm.nih.gov/pubmed/34051731 http://dx.doi.org/10.1186/s12866-021-02233-y |
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