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Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer

BACKGROUND: The miniaturised and portable DNA sequencer MinION™ has been released to the scientific community within the framework of an early access programme to evaluate its application for a wide variety of genetic approaches. This technology has demonstrated great potential, especially in genome...

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Autores principales: Benítez-Páez, Alfonso, Portune, Kevin J., Sanz, Yolanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730766/
https://www.ncbi.nlm.nih.gov/pubmed/26823973
http://dx.doi.org/10.1186/s13742-016-0111-z
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author Benítez-Páez, Alfonso
Portune, Kevin J.
Sanz, Yolanda
author_facet Benítez-Páez, Alfonso
Portune, Kevin J.
Sanz, Yolanda
author_sort Benítez-Páez, Alfonso
collection PubMed
description BACKGROUND: The miniaturised and portable DNA sequencer MinION™ has been released to the scientific community within the framework of an early access programme to evaluate its application for a wide variety of genetic approaches. This technology has demonstrated great potential, especially in genome-wide analyses. In this study, we tested the ability of the MinION™ system to perform amplicon sequencing in order to design new approaches to study microbial diversity using nearly full-length 16S rDNA sequences. RESULTS: Using R7.3 chemistry, we generated more than 3.8 million events (nt) during a single sequencing run. These data were sufficient to reconstruct more than 90 % of the 16S rRNA gene sequences for 20 different species present in a mock reference community. After read mapping and 16S rRNA gene assembly, consensus sequences and 2d reads were recovered to assign taxonomic classification down to the species level. Additionally, we were able to measure the relative abundance of all the species present in a mock community and detected a biased species distribution originating from the PCR reaction using ‘universal’ primers. CONCLUSIONS: Although nanopore-based sequencing produces reads with lower per-base accuracy compared with other platforms, the MinION™ DNA sequencer is valuable for both high taxonomic resolution and microbial diversity analysis. Improvements in nanopore chemistry, such as minimising base-calling errors and the nucleotide bias reported here for 16S amplicon sequencing, will further deliver more reliable information that is useful for the specific detection of microbial species and strains in complex ecosystems.
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spelling pubmed-47307662016-01-29 Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer Benítez-Páez, Alfonso Portune, Kevin J. Sanz, Yolanda Gigascience Research BACKGROUND: The miniaturised and portable DNA sequencer MinION™ has been released to the scientific community within the framework of an early access programme to evaluate its application for a wide variety of genetic approaches. This technology has demonstrated great potential, especially in genome-wide analyses. In this study, we tested the ability of the MinION™ system to perform amplicon sequencing in order to design new approaches to study microbial diversity using nearly full-length 16S rDNA sequences. RESULTS: Using R7.3 chemistry, we generated more than 3.8 million events (nt) during a single sequencing run. These data were sufficient to reconstruct more than 90 % of the 16S rRNA gene sequences for 20 different species present in a mock reference community. After read mapping and 16S rRNA gene assembly, consensus sequences and 2d reads were recovered to assign taxonomic classification down to the species level. Additionally, we were able to measure the relative abundance of all the species present in a mock community and detected a biased species distribution originating from the PCR reaction using ‘universal’ primers. CONCLUSIONS: Although nanopore-based sequencing produces reads with lower per-base accuracy compared with other platforms, the MinION™ DNA sequencer is valuable for both high taxonomic resolution and microbial diversity analysis. Improvements in nanopore chemistry, such as minimising base-calling errors and the nucleotide bias reported here for 16S amplicon sequencing, will further deliver more reliable information that is useful for the specific detection of microbial species and strains in complex ecosystems. BioMed Central 2016-01-28 /pmc/articles/PMC4730766/ /pubmed/26823973 http://dx.doi.org/10.1186/s13742-016-0111-z Text en © Benítez-Páez et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Benítez-Páez, Alfonso
Portune, Kevin J.
Sanz, Yolanda
Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer
title Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer
title_full Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer
title_fullStr Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer
title_full_unstemmed Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer
title_short Species-level resolution of 16S rRNA gene amplicons sequenced through the MinION™ portable nanopore sequencer
title_sort species-level resolution of 16s rrna gene amplicons sequenced through the minion™ portable nanopore sequencer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730766/
https://www.ncbi.nlm.nih.gov/pubmed/26823973
http://dx.doi.org/10.1186/s13742-016-0111-z
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