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Targeted recovery of novel phylogenetic diversity from next-generation sequence data
Next-generation sequencing technologies have led to recognition of a so-called ‘rare biosphere'. These microbial operational taxonomic units (OTUs) are defined by low relative abundance and may be specifically adapted to maintaining low population sizes. We hypothesized that mining of low-abund...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475379/ https://www.ncbi.nlm.nih.gov/pubmed/22791239 http://dx.doi.org/10.1038/ismej.2012.50 |
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author | Lynch, Michael D J Bartram, Andrea K Neufeld, Josh D |
author_facet | Lynch, Michael D J Bartram, Andrea K Neufeld, Josh D |
author_sort | Lynch, Michael D J |
collection | PubMed |
description | Next-generation sequencing technologies have led to recognition of a so-called ‘rare biosphere'. These microbial operational taxonomic units (OTUs) are defined by low relative abundance and may be specifically adapted to maintaining low population sizes. We hypothesized that mining of low-abundance next-generation 16S ribosomal RNA (rRNA) gene data would lead to the discovery of novel phylogenetic diversity, reflecting microorganisms not yet discovered by previous sampling efforts. Here, we test this hypothesis by combining molecular and bioinformatic approaches for targeted retrieval of phylogenetic novelty within rare biosphere OTUs. We combined BLASTN network analysis, phylogenetics and targeted primer design to amplify 16S rRNA gene sequences from unique potential bacterial lineages, comprising part of the rare biosphere from a multi-million sequence data set from an Arctic tundra soil sample. Demonstrating the feasibility of the protocol developed here, three of seven recovered phylogenetic lineages represented extremely divergent taxonomic entities. These divergent target sequences correspond to (a) a previously unknown lineage within the BRC1 candidate phylum, (b) a sister group to the early diverging and currently recognized monospecific Cyanobacteria Gloeobacter, a genus containing multiple plesiomorphic traits and (c) a highly divergent lineage phylogenetically resolved within mitochondria. A comparison to twelve next-generation data sets from additional soils suggested persistent low-abundance distributions of these novel 16S rRNA genes. The results demonstrate this sequence analysis and retrieval pipeline as applicable for exploring underrepresented phylogenetic novelty and recovering taxa that may represent significant steps in bacterial evolution. |
format | Online Article Text |
id | pubmed-3475379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34753792012-11-01 Targeted recovery of novel phylogenetic diversity from next-generation sequence data Lynch, Michael D J Bartram, Andrea K Neufeld, Josh D ISME J Original Article Next-generation sequencing technologies have led to recognition of a so-called ‘rare biosphere'. These microbial operational taxonomic units (OTUs) are defined by low relative abundance and may be specifically adapted to maintaining low population sizes. We hypothesized that mining of low-abundance next-generation 16S ribosomal RNA (rRNA) gene data would lead to the discovery of novel phylogenetic diversity, reflecting microorganisms not yet discovered by previous sampling efforts. Here, we test this hypothesis by combining molecular and bioinformatic approaches for targeted retrieval of phylogenetic novelty within rare biosphere OTUs. We combined BLASTN network analysis, phylogenetics and targeted primer design to amplify 16S rRNA gene sequences from unique potential bacterial lineages, comprising part of the rare biosphere from a multi-million sequence data set from an Arctic tundra soil sample. Demonstrating the feasibility of the protocol developed here, three of seven recovered phylogenetic lineages represented extremely divergent taxonomic entities. These divergent target sequences correspond to (a) a previously unknown lineage within the BRC1 candidate phylum, (b) a sister group to the early diverging and currently recognized monospecific Cyanobacteria Gloeobacter, a genus containing multiple plesiomorphic traits and (c) a highly divergent lineage phylogenetically resolved within mitochondria. A comparison to twelve next-generation data sets from additional soils suggested persistent low-abundance distributions of these novel 16S rRNA genes. The results demonstrate this sequence analysis and retrieval pipeline as applicable for exploring underrepresented phylogenetic novelty and recovering taxa that may represent significant steps in bacterial evolution. Nature Publishing Group 2012-11 2012-07-12 /pmc/articles/PMC3475379/ /pubmed/22791239 http://dx.doi.org/10.1038/ismej.2012.50 Text en Copyright © 2012 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Lynch, Michael D J Bartram, Andrea K Neufeld, Josh D Targeted recovery of novel phylogenetic diversity from next-generation sequence data |
title | Targeted recovery of novel phylogenetic diversity from next-generation sequence data |
title_full | Targeted recovery of novel phylogenetic diversity from next-generation sequence data |
title_fullStr | Targeted recovery of novel phylogenetic diversity from next-generation sequence data |
title_full_unstemmed | Targeted recovery of novel phylogenetic diversity from next-generation sequence data |
title_short | Targeted recovery of novel phylogenetic diversity from next-generation sequence data |
title_sort | targeted recovery of novel phylogenetic diversity from next-generation sequence data |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475379/ https://www.ncbi.nlm.nih.gov/pubmed/22791239 http://dx.doi.org/10.1038/ismej.2012.50 |
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