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Microvolume DNA extraction methods for microscale amplicon and metagenomic studies
Investigating the composition and metabolic capacity of aquatic microbial assemblages usually requires the filtration of multi-litre samples, which are up to 1 million-fold larger than the microenvironments within which microbes are predicted to be spatially organised. To determine if community prof...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723667/ https://www.ncbi.nlm.nih.gov/pubmed/37938281 http://dx.doi.org/10.1038/s43705-021-00079-z |
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author | Bramucci, Anna R. Focardi, Amaranta Rinke, Christian Hugenholtz, Philip Tyson, Gene W. Seymour, Justin R. Raina, Jean-Baptiste |
author_facet | Bramucci, Anna R. Focardi, Amaranta Rinke, Christian Hugenholtz, Philip Tyson, Gene W. Seymour, Justin R. Raina, Jean-Baptiste |
author_sort | Bramucci, Anna R. |
collection | PubMed |
description | Investigating the composition and metabolic capacity of aquatic microbial assemblages usually requires the filtration of multi-litre samples, which are up to 1 million-fold larger than the microenvironments within which microbes are predicted to be spatially organised. To determine if community profiles can be reliably generated from microlitre volumes, we sampled seawater at a coastal and an oceanic site, filtered and homogenised them, and extracted DNA from bulk samples (2 L) and microvolumes (100, 10 and 1 μL) using two new approaches. These microvolume DNA extraction methods involve either physical or chemical lysis (through pH/thermal shock and lytic enzymes/surfactants, respectively), directly followed by the capture of DNA on magnetic beads. Downstream analysis of extracted DNA using both amplicon sequencing and metagenomics, revealed strong correlation with standard large volume approaches, demonstrating the fidelity of taxonomic and functional profiles of microbial communities in as little as 1 μL of seawater. This volume is six orders of magnitude smaller than most standard operating procedures for marine metagenomics, which will allow precise sampling of the heterogenous landscape that microbes inhabit. |
format | Online Article Text |
id | pubmed-9723667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97236672023-01-04 Microvolume DNA extraction methods for microscale amplicon and metagenomic studies Bramucci, Anna R. Focardi, Amaranta Rinke, Christian Hugenholtz, Philip Tyson, Gene W. Seymour, Justin R. Raina, Jean-Baptiste ISME Commun Brief Communication Investigating the composition and metabolic capacity of aquatic microbial assemblages usually requires the filtration of multi-litre samples, which are up to 1 million-fold larger than the microenvironments within which microbes are predicted to be spatially organised. To determine if community profiles can be reliably generated from microlitre volumes, we sampled seawater at a coastal and an oceanic site, filtered and homogenised them, and extracted DNA from bulk samples (2 L) and microvolumes (100, 10 and 1 μL) using two new approaches. These microvolume DNA extraction methods involve either physical or chemical lysis (through pH/thermal shock and lytic enzymes/surfactants, respectively), directly followed by the capture of DNA on magnetic beads. Downstream analysis of extracted DNA using both amplicon sequencing and metagenomics, revealed strong correlation with standard large volume approaches, demonstrating the fidelity of taxonomic and functional profiles of microbial communities in as little as 1 μL of seawater. This volume is six orders of magnitude smaller than most standard operating procedures for marine metagenomics, which will allow precise sampling of the heterogenous landscape that microbes inhabit. Nature Publishing Group UK 2021-12-17 /pmc/articles/PMC9723667/ /pubmed/37938281 http://dx.doi.org/10.1038/s43705-021-00079-z 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/) |
spellingShingle | Brief Communication Bramucci, Anna R. Focardi, Amaranta Rinke, Christian Hugenholtz, Philip Tyson, Gene W. Seymour, Justin R. Raina, Jean-Baptiste Microvolume DNA extraction methods for microscale amplicon and metagenomic studies |
title | Microvolume DNA extraction methods for microscale amplicon and metagenomic studies |
title_full | Microvolume DNA extraction methods for microscale amplicon and metagenomic studies |
title_fullStr | Microvolume DNA extraction methods for microscale amplicon and metagenomic studies |
title_full_unstemmed | Microvolume DNA extraction methods for microscale amplicon and metagenomic studies |
title_short | Microvolume DNA extraction methods for microscale amplicon and metagenomic studies |
title_sort | microvolume dna extraction methods for microscale amplicon and metagenomic studies |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723667/ https://www.ncbi.nlm.nih.gov/pubmed/37938281 http://dx.doi.org/10.1038/s43705-021-00079-z |
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