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Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples
BACKGROUND: Detection and quantification of plant pathogens in the presence of inhibitory substances can be a challenge especially with plant and environmental samples. Real-time quantitative PCR has enabled high-throughput detection and quantification of pathogens; however, its quantitative use is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307183/ https://www.ncbi.nlm.nih.gov/pubmed/25628753 http://dx.doi.org/10.1186/s13007-014-0042-6 |
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author | Rački, Nejc Dreo, Tanja Gutierrez-Aguirre, Ion Blejec, Andrej Ravnikar, Maja |
author_facet | Rački, Nejc Dreo, Tanja Gutierrez-Aguirre, Ion Blejec, Andrej Ravnikar, Maja |
author_sort | Rački, Nejc |
collection | PubMed |
description | BACKGROUND: Detection and quantification of plant pathogens in the presence of inhibitory substances can be a challenge especially with plant and environmental samples. Real-time quantitative PCR has enabled high-throughput detection and quantification of pathogens; however, its quantitative use is linked to standardized reference materials, and its sensitivity to inhibitors can lead to lower quantification accuracy. Droplet digital PCR has been proposed as a method to overcome these drawbacks. Its absolute quantification does not rely on standards and its tolerance to inhibitors has been demonstrated mostly in clinical samples. Such features would be of great use in agricultural and environmental fields, therefore our study compared the performance of droplet digital PCR method when challenged with inhibitors common to plant and environmental samples and compared it with quantitative PCR. RESULTS: Transfer of an existing Pepper mild mottle virus assay from reverse transcription real-time quantitative PCR to reverse transcription droplet digital PCR was straight forward. When challenged with complex matrices (seeds, plants, soil, wastewater) and selected purified inhibitors droplet digital PCR showed higher resilience to inhibition for the quantification of an RNA virus (Pepper mild mottle virus), compared to reverse transcription real-time quantitative PCR. CONCLUSIONS: This study confirms the improved detection and quantification of the PMMoV RT-ddPCR in the presence of inhibitors that are commonly found in samples of seeds, plant material, soil, and wastewater. Together with absolute quantification, independent of standard reference materials, this makes droplet digital PCR a valuable tool for detection and quantification of pathogens in inhibition prone samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13007-014-0042-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4307183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43071832015-01-28 Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples Rački, Nejc Dreo, Tanja Gutierrez-Aguirre, Ion Blejec, Andrej Ravnikar, Maja Plant Methods Methodology BACKGROUND: Detection and quantification of plant pathogens in the presence of inhibitory substances can be a challenge especially with plant and environmental samples. Real-time quantitative PCR has enabled high-throughput detection and quantification of pathogens; however, its quantitative use is linked to standardized reference materials, and its sensitivity to inhibitors can lead to lower quantification accuracy. Droplet digital PCR has been proposed as a method to overcome these drawbacks. Its absolute quantification does not rely on standards and its tolerance to inhibitors has been demonstrated mostly in clinical samples. Such features would be of great use in agricultural and environmental fields, therefore our study compared the performance of droplet digital PCR method when challenged with inhibitors common to plant and environmental samples and compared it with quantitative PCR. RESULTS: Transfer of an existing Pepper mild mottle virus assay from reverse transcription real-time quantitative PCR to reverse transcription droplet digital PCR was straight forward. When challenged with complex matrices (seeds, plants, soil, wastewater) and selected purified inhibitors droplet digital PCR showed higher resilience to inhibition for the quantification of an RNA virus (Pepper mild mottle virus), compared to reverse transcription real-time quantitative PCR. CONCLUSIONS: This study confirms the improved detection and quantification of the PMMoV RT-ddPCR in the presence of inhibitors that are commonly found in samples of seeds, plant material, soil, and wastewater. Together with absolute quantification, independent of standard reference materials, this makes droplet digital PCR a valuable tool for detection and quantification of pathogens in inhibition prone samples. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13007-014-0042-6) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-31 /pmc/articles/PMC4307183/ /pubmed/25628753 http://dx.doi.org/10.1186/s13007-014-0042-6 Text en © Racki et al.; licensee BioMed Central. 2014 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 work is properly credited. 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 | Methodology Rački, Nejc Dreo, Tanja Gutierrez-Aguirre, Ion Blejec, Andrej Ravnikar, Maja Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples |
title | Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples |
title_full | Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples |
title_fullStr | Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples |
title_full_unstemmed | Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples |
title_short | Reverse transcriptase droplet digital PCR shows high resilience to PCR inhibitors from plant, soil and water samples |
title_sort | reverse transcriptase droplet digital pcr shows high resilience to pcr inhibitors from plant, soil and water samples |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307183/ https://www.ncbi.nlm.nih.gov/pubmed/25628753 http://dx.doi.org/10.1186/s13007-014-0042-6 |
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