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Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)

PREMISE OF THE STUDY: Arbuscular mycorrhizal fungi (AMF) are globally important root symbioses that enhance plant growth and nutrition and influence ecosystem structure and function. To better characterize levels of AMF diversity relevant to ecosystem function, deeper sequencing depth in environment...

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Detalles Bibliográficos
Autores principales: Morgan, Benjamin S. T., Egerton-Warburton, Louise M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Botanical Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584815/
https://www.ncbi.nlm.nih.gov/pubmed/28924511
http://dx.doi.org/10.3732/apps.1700017
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author Morgan, Benjamin S. T.
Egerton-Warburton, Louise M.
author_facet Morgan, Benjamin S. T.
Egerton-Warburton, Louise M.
author_sort Morgan, Benjamin S. T.
collection PubMed
description PREMISE OF THE STUDY: Arbuscular mycorrhizal fungi (AMF) are globally important root symbioses that enhance plant growth and nutrition and influence ecosystem structure and function. To better characterize levels of AMF diversity relevant to ecosystem function, deeper sequencing depth in environmental samples is needed. In this study, Illumina barcoded primers and a bioinformatics pipeline were developed and applied to study AMF diversity and community structure in environmental samples. METHODS: Libraries of small subunit ribosomal RNA fragment amplicons were amplified from environmental DNA using a single-step PCR reaction with barcoded NS31/AML2 primers. Amplicons were sequenced on an Illumina MiSeq sequencer using version 2, 2 × 250-bp paired-end chemistry, and analyzed using QIIME and RDP Classifier. RESULTS: Sequencing captured 196 to 6416 operational taxonomic units (OTUs; depending on clustering parameters) representing nine AMF genera. Regardless of clustering parameters, ∼20 OTUs dominated AMF communities (78–87% reads) with the remaining reads distributed among other OTUs. Analyses also showed significant biogeographic differences in AMF communities and that community composition could be linked to specific edaphic factors. DISCUSSION: Barcoded NS31/AML2 primers and Illumina MiSeq sequencing provide a powerful approach to address AMF diversity and variations in fungal assemblages across host plants, ecosystems, and responses to environmental drivers including global change.
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spelling pubmed-55848152017-09-18 Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1) Morgan, Benjamin S. T. Egerton-Warburton, Louise M. Appl Plant Sci Application Article PREMISE OF THE STUDY: Arbuscular mycorrhizal fungi (AMF) are globally important root symbioses that enhance plant growth and nutrition and influence ecosystem structure and function. To better characterize levels of AMF diversity relevant to ecosystem function, deeper sequencing depth in environmental samples is needed. In this study, Illumina barcoded primers and a bioinformatics pipeline were developed and applied to study AMF diversity and community structure in environmental samples. METHODS: Libraries of small subunit ribosomal RNA fragment amplicons were amplified from environmental DNA using a single-step PCR reaction with barcoded NS31/AML2 primers. Amplicons were sequenced on an Illumina MiSeq sequencer using version 2, 2 × 250-bp paired-end chemistry, and analyzed using QIIME and RDP Classifier. RESULTS: Sequencing captured 196 to 6416 operational taxonomic units (OTUs; depending on clustering parameters) representing nine AMF genera. Regardless of clustering parameters, ∼20 OTUs dominated AMF communities (78–87% reads) with the remaining reads distributed among other OTUs. Analyses also showed significant biogeographic differences in AMF communities and that community composition could be linked to specific edaphic factors. DISCUSSION: Barcoded NS31/AML2 primers and Illumina MiSeq sequencing provide a powerful approach to address AMF diversity and variations in fungal assemblages across host plants, ecosystems, and responses to environmental drivers including global change. Botanical Society of America 2017-08-24 /pmc/articles/PMC5584815/ /pubmed/28924511 http://dx.doi.org/10.3732/apps.1700017 Text en © 2017 Morgan and Egerton-Warburton. Published by the Botanical Society of America https://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (CC-BY-NC-SA 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/) ), which permits unrestricted noncommercial use and redistribution provided that the original author and source are credited and the new work is distributed under the same license as the original.
spellingShingle Application Article
Morgan, Benjamin S. T.
Egerton-Warburton, Louise M.
Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
title Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
title_full Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
title_fullStr Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
title_full_unstemmed Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
title_short Barcoded NS31/AML2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
title_sort barcoded ns31/aml2 primers for sequencing of arbuscular mycorrhizal communities in environmental samples(1)
topic Application Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584815/
https://www.ncbi.nlm.nih.gov/pubmed/28924511
http://dx.doi.org/10.3732/apps.1700017
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