| Literature DB >> 33780549 |
Zuzana Kolaříková1, Renata Slavíková1, Claudia Krüger1, Manuela Krüger1, Petr Kohout1,2,3.
Abstract
There is no consensus barcoding region for determination of arbuscular mycorrhizal fungal (AMF) taxa. To overcome this obstacle, we have developed an approach to sequence an AMF marker within the ribosome-encoding operon (rDNA) that covers all three widely applied variable molecular markers. Using a nested PCR approach specific to AMF, we amplified a part (c. 2.5 kb) of the rDNA spanning the majority of the small subunit rRNA (SSU) gene, the complete internal transcribed spacer (ITS) region and a part of the large subunit (LSU) rRNA gene. The PCR products were sequenced on the PacBio platform utilizing Single Molecule Real Time (SMRT) sequencing. Employing this method for selected environmental DNA samples, we were able to describe complex AMF communities consisting of various glomeromycotan lineages. We demonstrate the applicability of this new 2.5 kb approach to provide robust phylogenetic assignment of AMF lineages without known sequences from pure cultures and to consolidate information about AMF taxon distributions coming from three widely used barcoding regions into one integrative dataset.Keywords: Archaeosporales; Glomeromycota; PacBio; long-read metabarcoding; mycorrhizal fungi distribution; third-generation sequencing
Year: 2021 PMID: 33780549 DOI: 10.1111/nph.17372
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151