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Optimized metabarcoding with Pacific biosciences enables semi-quantitative analysis of fungal communities.
Castaño, Carles; Berlin, Anna; Brandström Durling, Mikael; Ihrmark, Katharina; Lindahl, Björn D; Stenlid, Jan; Clemmensen, Karina E; Olson, Åke.
Afiliación
  • Castaño C; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Berlin A; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Brandström Durling M; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Ihrmark K; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Lindahl BD; Department of Soil and Environment, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Stenlid J; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Clemmensen KE; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
  • Olson Å; Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, SE-75007, Sweden.
New Phytol ; 228(3)2020 11.
Article en En | MEDLINE | ID: mdl-32531109
Recent studies have questioned the use of high-throughput sequencing of the nuclear ribosomal internal transcribed spacer (ITS) region to derive a semi-quantitative representation of fungal community composition. However, comprehensive studies that quantify biases occurring during PCR and sequencing of ITS amplicons are still lacking. We used artificially assembled communities consisting of 10 ITS-like fragments of varying lengths and guanine-cytosine (GC) contents to evaluate and quantify biases during PCR and sequencing with Illumina MiSeq, PacBio RS II and PacBio Sequel I technologies. Fragment length variation was the main source of bias in observed community composition relative to the template, with longer fragments generally being under-represented for all sequencing platforms. This bias was three times higher for Illumina MiSeq than for PacBio RS II and Sequel I. All 10 fragments in the artificial community were recovered when sequenced with PacBio technologies, whereas the three longest fragments (> 447 bases) were lost when sequenced with Illumina MiSeq. Fragment length bias also increased linearly with increasing number of PCR cycles but could be mitigated by optimization of the PCR setup. No significant biases related to GC content were observed. Despite lower sequencing output, PacBio sequencing was better able to reflect the community composition of the template than Illumina MiSeq sequencing.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Micobioma Idioma: En Revista: New Phytol Asunto de la revista: BOTANICA Año: 2020 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Micobioma Idioma: En Revista: New Phytol Asunto de la revista: BOTANICA Año: 2020 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Reino Unido