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Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species

Reliable species identification methods are important for industrial environmental monitoring programs. Probe based real-time quantitative polymerase chain reaction (qPCR) provides an accurate, cost-effective and high-throughput method for species identification. Here we present the development and...

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Autores principales: Hulley, Emily N., Tharmalingam, Sujeenthar, Zarnke, Andrew, Boreham, Douglas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353101/
https://www.ncbi.nlm.nih.gov/pubmed/30699146
http://dx.doi.org/10.1371/journal.pone.0210165
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author Hulley, Emily N.
Tharmalingam, Sujeenthar
Zarnke, Andrew
Boreham, Douglas R.
author_facet Hulley, Emily N.
Tharmalingam, Sujeenthar
Zarnke, Andrew
Boreham, Douglas R.
author_sort Hulley, Emily N.
collection PubMed
description Reliable species identification methods are important for industrial environmental monitoring programs. Probe based real-time quantitative polymerase chain reaction (qPCR) provides an accurate, cost-effective and high-throughput method for species identification. Here we present the development and validation of species-specific primers and probes for the cytochrome c oxidase (COI) gene for the identification of eight ecologically and economically important freshwater fish species: lake whitefish (Coregonus clupeaformis), yellow perch (Perca flavescens), rainbow smelt (Osmerus mordax), brook trout (Salvelinus fontinalis), smallmouth bass (Micropterus dolomieu), round whitefish (Prosopium cylindraceum), spottail shiner (Notropis hudsonius) and deepwater sculpin (Myoxocephalus thompsonii). In order to identify novel primer-probe sets with maximum species-specificity, two separate primer-probe design criteria were employed. Highest ranked primer-probe sets from both methods were assayed to identify sequences that demonstrated highest specificity. Specificity was determined using control species from same genus and non-target species from different genus. Selected primer-probe sets were optimized for annealing temperature and primer-probe concentrations to identify minimum reagent parameters. The selected primer-probe sets were highly sensitive, with DNA concentrations as low as 1 ng adequate for positive species identification. A decoder algorithm was developed based on the cumulative qPCR results that allowed for full automation of species identification. Blinded experiments revealed that the combination of the species-specific primer/probes sets with the automated species decoder resulted in target species identification with 100% accuracy. We also conducted a cost/time comparison analysis between the qPCR assays established in this study with other species identification methods. The qPCR technique was the most cost-effective and least time consuming method of species identification. In summary, probe-based multiplex qPCR assays provide a rapid and accurate method for freshwater fish species identification, and the methodology established in this study can be utilized for various other species identification initiatives.
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spelling pubmed-63531012019-02-15 Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species Hulley, Emily N. Tharmalingam, Sujeenthar Zarnke, Andrew Boreham, Douglas R. PLoS One Research Article Reliable species identification methods are important for industrial environmental monitoring programs. Probe based real-time quantitative polymerase chain reaction (qPCR) provides an accurate, cost-effective and high-throughput method for species identification. Here we present the development and validation of species-specific primers and probes for the cytochrome c oxidase (COI) gene for the identification of eight ecologically and economically important freshwater fish species: lake whitefish (Coregonus clupeaformis), yellow perch (Perca flavescens), rainbow smelt (Osmerus mordax), brook trout (Salvelinus fontinalis), smallmouth bass (Micropterus dolomieu), round whitefish (Prosopium cylindraceum), spottail shiner (Notropis hudsonius) and deepwater sculpin (Myoxocephalus thompsonii). In order to identify novel primer-probe sets with maximum species-specificity, two separate primer-probe design criteria were employed. Highest ranked primer-probe sets from both methods were assayed to identify sequences that demonstrated highest specificity. Specificity was determined using control species from same genus and non-target species from different genus. Selected primer-probe sets were optimized for annealing temperature and primer-probe concentrations to identify minimum reagent parameters. The selected primer-probe sets were highly sensitive, with DNA concentrations as low as 1 ng adequate for positive species identification. A decoder algorithm was developed based on the cumulative qPCR results that allowed for full automation of species identification. Blinded experiments revealed that the combination of the species-specific primer/probes sets with the automated species decoder resulted in target species identification with 100% accuracy. We also conducted a cost/time comparison analysis between the qPCR assays established in this study with other species identification methods. The qPCR technique was the most cost-effective and least time consuming method of species identification. In summary, probe-based multiplex qPCR assays provide a rapid and accurate method for freshwater fish species identification, and the methodology established in this study can be utilized for various other species identification initiatives. Public Library of Science 2019-01-30 /pmc/articles/PMC6353101/ /pubmed/30699146 http://dx.doi.org/10.1371/journal.pone.0210165 Text en © 2019 Hulley 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, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hulley, Emily N.
Tharmalingam, Sujeenthar
Zarnke, Andrew
Boreham, Douglas R.
Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species
title Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species
title_full Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species
title_fullStr Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species
title_full_unstemmed Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species
title_short Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species
title_sort development and validation of probe-based multiplex real-time pcr assays for the rapid and accurate detection of freshwater fish species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353101/
https://www.ncbi.nlm.nih.gov/pubmed/30699146
http://dx.doi.org/10.1371/journal.pone.0210165
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