19
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      New universal ITS2 primers for high-resolution herbivory analyses using DNA metabarcoding in both tropical and temperate zones

      research-article

      Read this article at

          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          DNA metabarcoding is a rapidly growing technique for obtaining detailed dietary information. Current metabarcoding methods for herbivory, using a single locus, can lack taxonomic resolution for some applications. We present novel primers for the second internal transcribed spacer of nuclear ribosomal DNA (ITS2) designed for dietary studies in Mauritius and the UK, which have the potential to give unrivalled taxonomic coverage and resolution from a short-amplicon barcode. In silico testing used three databases of plant ITS2 sequences from UK and Mauritian floras (native and introduced) totalling 6561 sequences from 1790 species across 174 families. Our primers were well-matched in silico to 88% of species, providing taxonomic resolution of 86.1%, 99.4% and 99.9% at the species, genus and family levels, respectively. In vitro, the primers amplified 99% of Mauritian (n = 169) and 100% of UK (n = 33) species, and co-amplified multiple plant species from degraded faecal DNA from reptiles and birds in two case studies. For the ITS2 region, we advocate taxonomic assignment based on best sequence match instead of a clustering approach. With short amplicons of 187–387 bp, these primers are suitable for metabarcoding plant DNA from faecal samples, across a broad geographic range, whilst delivering unparalleled taxonomic resolution.

          Related collections

          Most cited references40

          • Record: found
          • Abstract: found
          • Article: not found

          A DNA barcode for land plants.

          DNA barcoding involves sequencing a standard region of DNA as a tool for species identification. However, there has been no agreement on which region(s) should be used for barcoding land plants. To provide a community recommendation on a standard plant barcode, we have compared the performance of 7 leading candidate plastid DNA regions (atpF-atpH spacer, matK gene, rbcL gene, rpoB gene, rpoC1 gene, psbK-psbI spacer, and trnH-psbA spacer). Based on assessments of recoverability, sequence quality, and levels of species discrimination, we recommend the 2-locus combination of rbcL+matK as the plant barcode. This core 2-locus barcode will provide a universal framework for the routine use of DNA sequence data to identify specimens and contribute toward the discovery of overlooked species of land plants.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            obitools: a unix-inspired software package for DNA metabarcoding.

            DNA metabarcoding offers new perspectives in biodiversity research. This recently developed approach to ecosystem study relies heavily on the use of next-generation sequencing (NGS) and thus calls upon the ability to deal with huge sequence data sets. The obitools package satisfies this requirement thanks to a set of programs specifically designed for analysing NGS data in a DNA metabarcoding context. Their capacity to filter and edit sequences while taking into account taxonomic annotation helps to set up tailor-made analysis pipelines for a broad range of DNA metabarcoding applications, including biodiversity surveys or diet analyses. The obitools package is distributed as an open source software available on the following website: http://metabarcoding.org/obitools. A Galaxy wrapper is available on the GenOuest core facility toolshed: http://toolshed.genouest.org.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              ITS as an environmental DNA barcode for fungi: an in silico approach reveals potential PCR biases

              Background During the last 15 years the internal transcribed spacer (ITS) of nuclear DNA has been used as a target for analyzing fungal diversity in environmental samples, and has recently been selected as the standard marker for fungal DNA barcoding. In this study we explored the potential amplification biases that various commonly utilized ITS primers might introduce during amplification of different parts of the ITS region in samples containing mixed templates ('environmental barcoding'). We performed in silico PCR analyses with commonly used primer combinations using various ITS datasets obtained from public databases as templates. Results Some of the ITS primers, such as ITS1-F, were hampered with a high proportion of mismatches relative to the target sequences, and most of them appeared to introduce taxonomic biases during PCR. Some primers, e.g. ITS1-F, ITS1 and ITS5, were biased towards amplification of basidiomycetes, whereas others, e.g. ITS2, ITS3 and ITS4, were biased towards ascomycetes. The assumed basidiomycete-specific primer ITS4-B only amplified a minor proportion of basidiomycete ITS sequences, even under relaxed PCR conditions. Due to systematic length differences in the ITS2 region as well as the entire ITS, we found that ascomycetes will more easily amplify than basidiomycetes using these regions as targets. This bias can be avoided by using primers amplifying ITS1 only, but this would imply preferential amplification of 'non-dikarya' fungi. Conclusions We conclude that ITS primers have to be selected carefully, especially when used for high-throughput sequencing of environmental samples. We suggest that different primer combinations or different parts of the ITS region should be analyzed in parallel, or that alternative ITS primers should be searched for.
                Bookmark

                Author and article information

                Contributors
                Moorhouse-GannRJ1@cardiff.ac.uk
                JDunn@lincoln.ac.uk
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                4 June 2018
                4 June 2018
                2018
                : 8
                : 8542
                Affiliations
                [1 ]ISNI 0000 0001 0807 5670, GRID grid.5600.3, School of Biosciences, , Cardiff University, The Sir Martin Evans Building, Museum Avenue, ; Cardiff, CF10 3AX UK
                [2 ]ISNI 0000 0001 2110 3189, GRID grid.421630.2, RSPB Centre for Conservation Science, , Royal Society for the Protection of Birds, The Lodge, Potton Road, ; Sandy, Bedfordshire SG19 2DL UK
                [3 ]ISNI 0000 0004 0420 4262, GRID grid.36511.30, School of Life Sciences, , University of Lincoln, Joseph Banks Laboratories, Green Lane, ; Lincoln, LN6 7TS UK
                [4 ]National Botanic Garden of Wales, Llanarthne, Carmarthenshire SA32 8HG UK
                [5 ]ISNI 0000000121682483, GRID grid.8186.7, Institute of Biological, , Environmental & Rural Sciences (IBERS), Aberystwyth University, Penglais, ; Aberystwyth, Ceredigion SY23 3DA UK
                [6 ]Mauritian Wildlife Foundation, Grannum Road, Vacoas, Mauritius
                [7 ]Durrell Wildlife Conservation Trust, Les Augrès Manor, La Profonde Rue, Trinity, JE3 5BP Jersey Channel Islands, UK
                [8 ]ISNI 0000 0004 1936 9262, GRID grid.11835.3e, NERC Biomolecular Analysis Facility, Department of Animal and Plant Sciences, , University of Sheffield, Western Bank, ; Sheffield, S10 2TN UK
                Author information
                http://orcid.org/0000-0002-6277-2781
                Article
                26648
                10.1038/s41598-018-26648-2
                5986805
                29867115
                5a294ecd-1eb2-432f-9700-72a82fd54ba1
                © The Author(s) 2018

                Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 28 November 2017
                : 15 May 2018
                Categories
                Article
                Custom metadata
                © The Author(s) 2018

                Uncategorized
                Uncategorized

                Comments

                Comment on this article