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Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach
BACKGROUND: Meta-barcoding of mixed pollen samples constitutes a suitable alternative to conventional pollen identification via light microscopy. Current approaches however have limitations in practicability due to low sample throughput and/or inefficient processing methods, e.g. separate steps for...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509727/ https://www.ncbi.nlm.nih.gov/pubmed/26194794 http://dx.doi.org/10.1186/s12898-015-0051-y |
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author | Sickel, Wiebke Ankenbrand, Markus J Grimmer, Gudrun Holzschuh, Andrea Härtel, Stephan Lanzen, Jonathan Steffan-Dewenter, Ingolf Keller, Alexander |
author_facet | Sickel, Wiebke Ankenbrand, Markus J Grimmer, Gudrun Holzschuh, Andrea Härtel, Stephan Lanzen, Jonathan Steffan-Dewenter, Ingolf Keller, Alexander |
author_sort | Sickel, Wiebke |
collection | PubMed |
description | BACKGROUND: Meta-barcoding of mixed pollen samples constitutes a suitable alternative to conventional pollen identification via light microscopy. Current approaches however have limitations in practicability due to low sample throughput and/or inefficient processing methods, e.g. separate steps for amplification and sample indexing. RESULTS: We thus developed a new primer-adapter design for high throughput sequencing with the Illumina technology that remedies these issues. It uses a dual-indexing strategy, where sample-specific combinations of forward and reverse identifiers attached to the barcode marker allow high sample throughput with a single sequencing run. It does not require further adapter ligation steps after amplification. We applied this protocol to 384 pollen samples collected by solitary bees and sequenced all samples together on a single Illumina MiSeq v2 flow cell. According to rarefaction curves, 2,000–3,000 high quality reads per sample were sufficient to assess the complete diversity of 95% of the samples. We were able to detect 650 different plant taxa in total, of which 95% were classified at the species level. Together with the laboratory protocol, we also present an update of the reference database used by the classifier software, which increases the total number of covered global plant species included in the database from 37,403 to 72,325 (93% increase). CONCLUSIONS: This study thus offers improvements for the laboratory and bioinformatical workflow to existing approaches regarding data quantity and quality as well as processing effort and cost-effectiveness. Although only tested for pollen samples, it is furthermore applicable to other research questions requiring plant identification in mixed and challenging samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12898-015-0051-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4509727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45097272015-07-22 Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach Sickel, Wiebke Ankenbrand, Markus J Grimmer, Gudrun Holzschuh, Andrea Härtel, Stephan Lanzen, Jonathan Steffan-Dewenter, Ingolf Keller, Alexander BMC Ecol Methodology Article BACKGROUND: Meta-barcoding of mixed pollen samples constitutes a suitable alternative to conventional pollen identification via light microscopy. Current approaches however have limitations in practicability due to low sample throughput and/or inefficient processing methods, e.g. separate steps for amplification and sample indexing. RESULTS: We thus developed a new primer-adapter design for high throughput sequencing with the Illumina technology that remedies these issues. It uses a dual-indexing strategy, where sample-specific combinations of forward and reverse identifiers attached to the barcode marker allow high sample throughput with a single sequencing run. It does not require further adapter ligation steps after amplification. We applied this protocol to 384 pollen samples collected by solitary bees and sequenced all samples together on a single Illumina MiSeq v2 flow cell. According to rarefaction curves, 2,000–3,000 high quality reads per sample were sufficient to assess the complete diversity of 95% of the samples. We were able to detect 650 different plant taxa in total, of which 95% were classified at the species level. Together with the laboratory protocol, we also present an update of the reference database used by the classifier software, which increases the total number of covered global plant species included in the database from 37,403 to 72,325 (93% increase). CONCLUSIONS: This study thus offers improvements for the laboratory and bioinformatical workflow to existing approaches regarding data quantity and quality as well as processing effort and cost-effectiveness. Although only tested for pollen samples, it is furthermore applicable to other research questions requiring plant identification in mixed and challenging samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12898-015-0051-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-22 /pmc/articles/PMC4509727/ /pubmed/26194794 http://dx.doi.org/10.1186/s12898-015-0051-y Text en © Sickel et al. 2015 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 | Methodology Article Sickel, Wiebke Ankenbrand, Markus J Grimmer, Gudrun Holzschuh, Andrea Härtel, Stephan Lanzen, Jonathan Steffan-Dewenter, Ingolf Keller, Alexander Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
title | Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
title_full | Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
title_fullStr | Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
title_full_unstemmed | Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
title_short | Increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
title_sort | increased efficiency in identifying mixed pollen samples by meta-barcoding with a dual-indexing approach |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509727/ https://www.ncbi.nlm.nih.gov/pubmed/26194794 http://dx.doi.org/10.1186/s12898-015-0051-y |
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