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Quantitative multiplex detection of plant pathogens using a novel ligation probe-based system coupled with universal, high-throughput real-time PCR on OpenArraysTM

Authors :
Elen Ortenberg
Peter J. M. Bonants
C.D. Schoen
Marianna Szemes
Joana Falcão Salles
George A. Kowalchuk
Ronald van Doorn
Systems Ecology
Laboratoire d'Ecologie Microbienne - UMR 5557 (LEM)
Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Ecole Nationale Vétérinaire de Lyon (ENVL)
Terrestrial Microbial Ecology (TME)
Source :
BMC Genomics 8 (2007), BMC Genomics, 8, van Doorn, R, Szemes, M, Bonants, P, Kowalchuk, G A, Sallas, J, Ortenberg, E & Schoen, C D 2007, ' Quantitative multiplex detection of plant pathogens using a novel ligation probe-based system coupled with universal, high-throughput real-time PCR on OpenArraysTM. ', BMC Genomics, vol. 8, pp. Art. 276 . https://doi.org/10.1186/1471-2164-8-276, BMC Genomics, 8. BioMed Central, BMC Genomics, BMC Genomics, Vol 8, Iss 1, p 276 (2007), BMC Genomics, BioMed Central, 2007, 8 (1), pp.276. ⟨10.1186/1471-2164-8-276⟩
Publication Year :
2007
Publisher :
BioMed Central, 2007.

Abstract

Background Diagnostics and disease-management strategies require technologies to enable the simultaneous detection and quantification of a wide range of pathogenic microorganisms. Most multiplex, quantitative detection methods available suffer from compromises between the level of multiplexing, throughput and accuracy of quantification. Here, we demonstrate the efficacy of a novel, high-throughput, ligation-based assay for simultaneous quantitative detection of multiple plant pathogens. The ligation probes, designated Plant Research International-lock probes (PRI-lock probes), are long oligonucleotides with target complementary regions at their 5' and 3' ends. Upon perfect target hybridization, the PRI-lock probes are circularized via enzymatic ligation, subsequently serving as template for individual, standardized amplification via unique probe-specific primers. Adaptation to OpenArrays™, which can accommodate up to 3072 33 nl PCR amplifications, allowed high-throughput real-time quantification. The assay combines the multiplex capabilities and specificity of ligation reactions with high-throughput real-time PCR in the OpenArray™, resulting in a flexible, quantitative multiplex diagnostic system. Results The performance of the PRI-lock detection system was demonstrated using 13 probes targeting several significant plant pathogens at different taxonomic levels. All probes specifically detected their corresponding targets and provided perfect discrimination against non-target organisms with very similar ligation target sites. The nucleic acid targets could be reliably quantified over 5 orders of magnitude with a dynamic detection range of more than 104. Pathogen quantification was equally robust in single target versus mixed target assays. Conclusion This novel assay enables very specific, high-throughput, quantitative detection of multiple pathogens over a wide range of target concentrations and should be easily adaptable for versatile diagnostic purposes.

Details

Language :
English
ISSN :
14712164
Volume :
8
Database :
OpenAIRE
Journal :
BMC Genomics
Accession number :
edsair.doi.dedup.....df5f4b01e4b5df7f792bf4647897b1e5
Full Text :
https://doi.org/10.1186/1471-2164-8-276