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An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region

The Internal Transcribed Spacer 2 (ITS2) rRNA gene is a commonly targeted genetic marker to assess diversity of Symbiodinium, a dinoflagellate genus of algal endosymbionts that is pervasively associated with marine invertebrates, and notably reef-building corals. Here we tested three commonly used I...

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Autores principales: Hume, Benjamin C.C., Ziegler, Maren, Poulain, Julie, Pochon, Xavier, Romac, Sarah, Boissin, Emilie, de Vargas, Colomban, Planes, Serge, Wincker, Patrick, Voolstra, Christian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970565/
https://www.ncbi.nlm.nih.gov/pubmed/29844969
http://dx.doi.org/10.7717/peerj.4816
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author Hume, Benjamin C.C.
Ziegler, Maren
Poulain, Julie
Pochon, Xavier
Romac, Sarah
Boissin, Emilie
de Vargas, Colomban
Planes, Serge
Wincker, Patrick
Voolstra, Christian R.
author_facet Hume, Benjamin C.C.
Ziegler, Maren
Poulain, Julie
Pochon, Xavier
Romac, Sarah
Boissin, Emilie
de Vargas, Colomban
Planes, Serge
Wincker, Patrick
Voolstra, Christian R.
author_sort Hume, Benjamin C.C.
collection PubMed
description The Internal Transcribed Spacer 2 (ITS2) rRNA gene is a commonly targeted genetic marker to assess diversity of Symbiodinium, a dinoflagellate genus of algal endosymbionts that is pervasively associated with marine invertebrates, and notably reef-building corals. Here we tested three commonly used ITS2 primer pairs (SYM_VAR_5.8S2/SYM_VAR_REV, ITSintfor2/ITSReverse, and ITS-DINO/ITS2Rev2) with regard to amplification specificity and sensitivity towards Symbiodinium, as well as sub-genera taxonomic bias. We tested these primers over a range of sample types including three coral species, coral surrounding water, reef surface water, and open ocean water to assess their suitability for use in large-scale next generation sequencing projects and to develop a standardised PCR protocol. We found the SYM_VAR_5.8S2/SYM_VAR_REV primers to perform superior to the other tested ITS2 primers. We therefore used this primer pair to develop a standardised PCR protocol. To do this, we tested the effect of PCR-to-PCR variation, annealing temperature, cycle number, and different polymerase systems on the PCR efficacy. The Symbiodinium ITS2 PCR protocol developed here delivers improved specificity and sensitivity towards Symbiodinium with apparent minimal sub-genera taxonomic bias across all sample types. In particular, the protocol’s ability to amplify Symbiodinium from a range of environmental sources will facilitate the study of Symbiodinium populations across biomes.
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spelling pubmed-59705652018-05-29 An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region Hume, Benjamin C.C. Ziegler, Maren Poulain, Julie Pochon, Xavier Romac, Sarah Boissin, Emilie de Vargas, Colomban Planes, Serge Wincker, Patrick Voolstra, Christian R. PeerJ Biodiversity The Internal Transcribed Spacer 2 (ITS2) rRNA gene is a commonly targeted genetic marker to assess diversity of Symbiodinium, a dinoflagellate genus of algal endosymbionts that is pervasively associated with marine invertebrates, and notably reef-building corals. Here we tested three commonly used ITS2 primer pairs (SYM_VAR_5.8S2/SYM_VAR_REV, ITSintfor2/ITSReverse, and ITS-DINO/ITS2Rev2) with regard to amplification specificity and sensitivity towards Symbiodinium, as well as sub-genera taxonomic bias. We tested these primers over a range of sample types including three coral species, coral surrounding water, reef surface water, and open ocean water to assess their suitability for use in large-scale next generation sequencing projects and to develop a standardised PCR protocol. We found the SYM_VAR_5.8S2/SYM_VAR_REV primers to perform superior to the other tested ITS2 primers. We therefore used this primer pair to develop a standardised PCR protocol. To do this, we tested the effect of PCR-to-PCR variation, annealing temperature, cycle number, and different polymerase systems on the PCR efficacy. The Symbiodinium ITS2 PCR protocol developed here delivers improved specificity and sensitivity towards Symbiodinium with apparent minimal sub-genera taxonomic bias across all sample types. In particular, the protocol’s ability to amplify Symbiodinium from a range of environmental sources will facilitate the study of Symbiodinium populations across biomes. PeerJ Inc. 2018-05-23 /pmc/articles/PMC5970565/ /pubmed/29844969 http://dx.doi.org/10.7717/peerj.4816 Text en © 2018 Hume 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biodiversity
Hume, Benjamin C.C.
Ziegler, Maren
Poulain, Julie
Pochon, Xavier
Romac, Sarah
Boissin, Emilie
de Vargas, Colomban
Planes, Serge
Wincker, Patrick
Voolstra, Christian R.
An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region
title An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region
title_full An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region
title_fullStr An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region
title_full_unstemmed An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region
title_short An improved primer set and amplification protocol with increased specificity and sensitivity targeting the Symbiodinium ITS2 region
title_sort improved primer set and amplification protocol with increased specificity and sensitivity targeting the symbiodinium its2 region
topic Biodiversity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970565/
https://www.ncbi.nlm.nih.gov/pubmed/29844969
http://dx.doi.org/10.7717/peerj.4816
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