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Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp
BACKGROUND: Vibrio spp. are a diverse group of ecologically important marine bacteria responsible for several foodborne outbreaks of gastroenteritis around the world. Their detection and characterization are moving away from conventional culture-based methods towards next generation sequencing (NGS)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318669/ https://www.ncbi.nlm.nih.gov/pubmed/37403035 http://dx.doi.org/10.1186/s12864-023-09429-8 |
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author | Flütsch, Sabrina Wiestner, Fabian Butticaz, Lisa Moor, Dominik Stölting, Kai N. |
author_facet | Flütsch, Sabrina Wiestner, Fabian Butticaz, Lisa Moor, Dominik Stölting, Kai N. |
author_sort | Flütsch, Sabrina |
collection | PubMed |
description | BACKGROUND: Vibrio spp. are a diverse group of ecologically important marine bacteria responsible for several foodborne outbreaks of gastroenteritis around the world. Their detection and characterization are moving away from conventional culture-based methods towards next generation sequencing (NGS)-based approaches. However, genomic methods are relative in nature and suffer from technical biases arising from library preparation and sequencing. Here, we introduce a quantitative NGS-based method that enables the quantitation of Vibrio spp. at the limit of quantification (LOQ) through artificial DNA standards and their absolute quantification via digital PCR (dPCR). RESULTS: We developed six DNA standards, called Vibrio-Sequins, together with optimized TaqMan assays for their quantification in individually sequenced DNA libraries via dPCR. To enable Vibrio-Sequin quantification, we validated three duplex dPCR methods to quantify the six targets. LOQs were ranging from 20 to 120 cp/µl for the six standards, whereas the limit of detection (LOD) was ~ 10 cp/µl for all six assays. Subsequently, a quantitative genomics approach was applied to quantify Vibrio-DNA in a pooled DNA mixture derived from several Vibrio species in a proof-of-concept study, demonstrating the increased power of our quantitative genomic pipeline through the coupling of NGS and dPCR. CONCLUSIONS: We significantly advance existing quantitative (meta)genomic methods by ensuring metrological traceability of NGS-based DNA quantification. Our method represents a useful tool for future metagenomic studies aiming at quantifying microbial DNA in an absolute manner. The inclusion of dPCR into sequencing-based methods supports the development of statistical approaches for the estimation of measurement uncertainties (MU) for NGS, which is still in its infancy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09429-8. |
format | Online Article Text |
id | pubmed-10318669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103186692023-07-05 Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp Flütsch, Sabrina Wiestner, Fabian Butticaz, Lisa Moor, Dominik Stölting, Kai N. BMC Genomics Research BACKGROUND: Vibrio spp. are a diverse group of ecologically important marine bacteria responsible for several foodborne outbreaks of gastroenteritis around the world. Their detection and characterization are moving away from conventional culture-based methods towards next generation sequencing (NGS)-based approaches. However, genomic methods are relative in nature and suffer from technical biases arising from library preparation and sequencing. Here, we introduce a quantitative NGS-based method that enables the quantitation of Vibrio spp. at the limit of quantification (LOQ) through artificial DNA standards and their absolute quantification via digital PCR (dPCR). RESULTS: We developed six DNA standards, called Vibrio-Sequins, together with optimized TaqMan assays for their quantification in individually sequenced DNA libraries via dPCR. To enable Vibrio-Sequin quantification, we validated three duplex dPCR methods to quantify the six targets. LOQs were ranging from 20 to 120 cp/µl for the six standards, whereas the limit of detection (LOD) was ~ 10 cp/µl for all six assays. Subsequently, a quantitative genomics approach was applied to quantify Vibrio-DNA in a pooled DNA mixture derived from several Vibrio species in a proof-of-concept study, demonstrating the increased power of our quantitative genomic pipeline through the coupling of NGS and dPCR. CONCLUSIONS: We significantly advance existing quantitative (meta)genomic methods by ensuring metrological traceability of NGS-based DNA quantification. Our method represents a useful tool for future metagenomic studies aiming at quantifying microbial DNA in an absolute manner. The inclusion of dPCR into sequencing-based methods supports the development of statistical approaches for the estimation of measurement uncertainties (MU) for NGS, which is still in its infancy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09429-8. BioMed Central 2023-07-04 /pmc/articles/PMC10318669/ /pubmed/37403035 http://dx.doi.org/10.1186/s12864-023-09429-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Flütsch, Sabrina Wiestner, Fabian Butticaz, Lisa Moor, Dominik Stölting, Kai N. Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp |
title | Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp |
title_full | Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp |
title_fullStr | Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp |
title_full_unstemmed | Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp |
title_short | Vibrio-Sequins - dPCR-traceable DNA standards for quantitative genomics of Vibrio spp |
title_sort | vibrio-sequins - dpcr-traceable dna standards for quantitative genomics of vibrio spp |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318669/ https://www.ncbi.nlm.nih.gov/pubmed/37403035 http://dx.doi.org/10.1186/s12864-023-09429-8 |
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