Cargando…

Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers

High throughput sequencing technology has great promise for biodiversity studies. However, an underlying assumption is that the primers used in these studies are universal for the prokaryotic or eukaryotic groups of interest. Full primer universality is difficult or impossible to achieve and studies...

Descripción completa

Detalles Bibliográficos
Autores principales: Hadziavdic, Kenan, Lekang, Katrine, Lanzen, Anders, Jonassen, Inge, Thompson, Eric M., Troedsson, Christofer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917833/
https://www.ncbi.nlm.nih.gov/pubmed/24516555
http://dx.doi.org/10.1371/journal.pone.0087624
_version_ 1782302882967584768
author Hadziavdic, Kenan
Lekang, Katrine
Lanzen, Anders
Jonassen, Inge
Thompson, Eric M.
Troedsson, Christofer
author_facet Hadziavdic, Kenan
Lekang, Katrine
Lanzen, Anders
Jonassen, Inge
Thompson, Eric M.
Troedsson, Christofer
author_sort Hadziavdic, Kenan
collection PubMed
description High throughput sequencing technology has great promise for biodiversity studies. However, an underlying assumption is that the primers used in these studies are universal for the prokaryotic or eukaryotic groups of interest. Full primer universality is difficult or impossible to achieve and studies using different primer sets make biodiversity comparisons problematic. The aim of this study was to design and optimize universal eukaryotic primers that could be used as a standard in future biodiversity studies. Using the alignment of all eukaryotic sequences from the publicly available SILVA database, we generated a full characterization of variable versus conserved regions in the 18S rRNA gene. All variable regions within this gene were analyzed and our results suggested that the V2, V4 and V9 regions were best suited for biodiversity assessments. Previously published universal eukaryotic primers as well as a number of self-designed primers were mapped to the alignment. Primer selection will depend on sequencing technology used, and this study focused on the 454 pyrosequencing GS FLX Titanium platform. The results generated a primer pair yielding theoretical matches to 80% of the eukaryotic and 0% of the prokaryotic sequences in the SILVA database. An empirical test of marine sediments using the AmpliconNoise pipeline for analysis of the high throughput sequencing data yielded amplification of sequences for 71% of all eukaryotic phyla with no isolation of prokaryotic sequences. To our knowledge this is the first characterization of the complete 18S rRNA gene using all eukaryotes present in the SILVA database, providing a robust test for universal eukaryotic primers. Since both in silico and empirical tests using high throughput sequencing retained high inclusion of eukaryotic phyla and exclusion of prokaryotes, we conclude that these primers are well suited for assessing eukaryote diversity, and can be used as a standard in biodiversity studies.
format Online
Article
Text
id pubmed-3917833
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39178332014-02-10 Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers Hadziavdic, Kenan Lekang, Katrine Lanzen, Anders Jonassen, Inge Thompson, Eric M. Troedsson, Christofer PLoS One Research Article High throughput sequencing technology has great promise for biodiversity studies. However, an underlying assumption is that the primers used in these studies are universal for the prokaryotic or eukaryotic groups of interest. Full primer universality is difficult or impossible to achieve and studies using different primer sets make biodiversity comparisons problematic. The aim of this study was to design and optimize universal eukaryotic primers that could be used as a standard in future biodiversity studies. Using the alignment of all eukaryotic sequences from the publicly available SILVA database, we generated a full characterization of variable versus conserved regions in the 18S rRNA gene. All variable regions within this gene were analyzed and our results suggested that the V2, V4 and V9 regions were best suited for biodiversity assessments. Previously published universal eukaryotic primers as well as a number of self-designed primers were mapped to the alignment. Primer selection will depend on sequencing technology used, and this study focused on the 454 pyrosequencing GS FLX Titanium platform. The results generated a primer pair yielding theoretical matches to 80% of the eukaryotic and 0% of the prokaryotic sequences in the SILVA database. An empirical test of marine sediments using the AmpliconNoise pipeline for analysis of the high throughput sequencing data yielded amplification of sequences for 71% of all eukaryotic phyla with no isolation of prokaryotic sequences. To our knowledge this is the first characterization of the complete 18S rRNA gene using all eukaryotes present in the SILVA database, providing a robust test for universal eukaryotic primers. Since both in silico and empirical tests using high throughput sequencing retained high inclusion of eukaryotic phyla and exclusion of prokaryotes, we conclude that these primers are well suited for assessing eukaryote diversity, and can be used as a standard in biodiversity studies. Public Library of Science 2014-02-07 /pmc/articles/PMC3917833/ /pubmed/24516555 http://dx.doi.org/10.1371/journal.pone.0087624 Text en © 2014 Hadziavdic et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hadziavdic, Kenan
Lekang, Katrine
Lanzen, Anders
Jonassen, Inge
Thompson, Eric M.
Troedsson, Christofer
Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers
title Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers
title_full Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers
title_fullStr Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers
title_full_unstemmed Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers
title_short Characterization of the 18S rRNA Gene for Designing Universal Eukaryote Specific Primers
title_sort characterization of the 18s rrna gene for designing universal eukaryote specific primers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917833/
https://www.ncbi.nlm.nih.gov/pubmed/24516555
http://dx.doi.org/10.1371/journal.pone.0087624
work_keys_str_mv AT hadziavdickenan characterizationofthe18srrnagenefordesigninguniversaleukaryotespecificprimers
AT lekangkatrine characterizationofthe18srrnagenefordesigninguniversaleukaryotespecificprimers
AT lanzenanders characterizationofthe18srrnagenefordesigninguniversaleukaryotespecificprimers
AT jonasseninge characterizationofthe18srrnagenefordesigninguniversaleukaryotespecificprimers
AT thompsonericm characterizationofthe18srrnagenefordesigninguniversaleukaryotespecificprimers
AT troedssonchristofer characterizationofthe18srrnagenefordesigninguniversaleukaryotespecificprimers