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Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis

BACKGROUND: Prokaryotic 16S ribosomal RNA (rRNA) sequences are widely used in environmental microbiology and molecular evolution as reliable markers for the taxonomic classification and phylogenetic analysis of microbes. Restricted by current sequencing techniques, the massive sequencing of 16S rRNA...

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Autores principales: Yang, Bo, Wang, Yong, Qian, Pei-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802574/
https://www.ncbi.nlm.nih.gov/pubmed/27000765
http://dx.doi.org/10.1186/s12859-016-0992-y
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author Yang, Bo
Wang, Yong
Qian, Pei-Yuan
author_facet Yang, Bo
Wang, Yong
Qian, Pei-Yuan
author_sort Yang, Bo
collection PubMed
description BACKGROUND: Prokaryotic 16S ribosomal RNA (rRNA) sequences are widely used in environmental microbiology and molecular evolution as reliable markers for the taxonomic classification and phylogenetic analysis of microbes. Restricted by current sequencing techniques, the massive sequencing of 16S rRNA gene amplicons encompassing the full length of genes is not yet feasible. Thus, the selection of the most efficient hypervariable regions for phylogenetic analysis and taxonomic classification is still debated. In the present study, several bioinformatics tools were integrated to build an in silico pipeline to evaluate the phylogenetic sensitivity of the hypervariable regions compared with the corresponding full-length sequences. RESULTS: The correlation of seven sub-regions was inferred from the geodesic distance, a parameter that is applied to quantitatively compare the topology of different phylogenetic trees constructed using the sequences from different sub-regions. The relationship between different sub-regions based on the geodesic distance indicated that V4-V6 were the most reliable regions for representing the full-length 16S rRNA sequences in the phylogenetic analysis of most bacterial phyla, while V2 and V8 were the least reliable regions. CONCLUSIONS: Our results suggest that V4-V6 might be optimal sub-regions for the design of universal primers with superior phylogenetic resolution for bacterial phyla. A potential relationship between function and the evolution of 16S rRNA is also discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-0992-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-48025742016-03-22 Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis Yang, Bo Wang, Yong Qian, Pei-Yuan BMC Bioinformatics Research Article BACKGROUND: Prokaryotic 16S ribosomal RNA (rRNA) sequences are widely used in environmental microbiology and molecular evolution as reliable markers for the taxonomic classification and phylogenetic analysis of microbes. Restricted by current sequencing techniques, the massive sequencing of 16S rRNA gene amplicons encompassing the full length of genes is not yet feasible. Thus, the selection of the most efficient hypervariable regions for phylogenetic analysis and taxonomic classification is still debated. In the present study, several bioinformatics tools were integrated to build an in silico pipeline to evaluate the phylogenetic sensitivity of the hypervariable regions compared with the corresponding full-length sequences. RESULTS: The correlation of seven sub-regions was inferred from the geodesic distance, a parameter that is applied to quantitatively compare the topology of different phylogenetic trees constructed using the sequences from different sub-regions. The relationship between different sub-regions based on the geodesic distance indicated that V4-V6 were the most reliable regions for representing the full-length 16S rRNA sequences in the phylogenetic analysis of most bacterial phyla, while V2 and V8 were the least reliable regions. CONCLUSIONS: Our results suggest that V4-V6 might be optimal sub-regions for the design of universal primers with superior phylogenetic resolution for bacterial phyla. A potential relationship between function and the evolution of 16S rRNA is also discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-0992-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-22 /pmc/articles/PMC4802574/ /pubmed/27000765 http://dx.doi.org/10.1186/s12859-016-0992-y Text en © Yang et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yang, Bo
Wang, Yong
Qian, Pei-Yuan
Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis
title Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis
title_full Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis
title_fullStr Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis
title_full_unstemmed Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis
title_short Sensitivity and correlation of hypervariable regions in 16S rRNA genes in phylogenetic analysis
title_sort sensitivity and correlation of hypervariable regions in 16s rrna genes in phylogenetic analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802574/
https://www.ncbi.nlm.nih.gov/pubmed/27000765
http://dx.doi.org/10.1186/s12859-016-0992-y
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