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Fungal community analysis by high-throughput sequencing of amplified markers - a user's guide

Journal

NEW PHYTOLOGIST
Volume 199, Issue 1, Pages 288-299

Publisher

WILEY
DOI: 10.1111/nph.12243

Keywords

454-pyrosequencing; bioinformatics; barcoding; environmental sequencing; internal transcribed spacer (ITS) region; PCR

Categories

Funding

  1. Nord-Forsk
  2. 'NEFOM'
  3. European Forest Institute
  4. Swedish Research Council FORMAS

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Novel high-throughput sequencing methods outperform earlier approaches in terms of resolution and magnitude. They enable identification and relative quantification of community members and offer new insights into fungal community ecology. These methods are currently taking over as the primary tool to assess fungal communities of plant-associated endophytes, pathogens, and mycorrhizal symbionts, as well as free-living saprotrophs. Taking advantage of the collective experience of six research groups, we here review the different stages involved in fungal community analysis, from field sampling via laboratory procedures to bioinformatics and data interpretation. We discuss potential pitfalls, alternatives, and solutions. Highlighted topics are challenges involved in: obtaining representative DNA/RNA samples and replicates that encompass the targeted variation in community composition, selection of marker regions and primers, options for amplification and multiplexing, handling of sequencing errors, and taxonomic identification. Without awareness of methodological biases, limitations of markers, and bioinformatics challenges, large-scale sequencing projects risk yielding artificial results and misleading conclusions.

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