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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
- 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.
- Subjects :
- Streptavidin
SDG 16 - Peace
lcsh:QH426-470
padlock probes
[SDV]Life Sciences [q-bio]
lcsh:Biotechnology
Computational biology
Biology
amplification
Proteomics
Polymerase Chain Reaction
03 medical and health sciences
chemistry.chemical_compound
dna microarrays
biotin
lcsh:TP248.13-248.65
gene analysis
Genetics
streptavidin
Multiplex
phytophthora-ramorum
ComputingMilieux_MISCELLANEOUS
DNA Primers
030304 developmental biology
0303 health sciences
Biointeracties and Plant Health
Base Sequence
030306 microbiology
Oligonucleotide
Methodology Article
SDG 16 - Peace, Justice and Strong Institutions
Plants
assay
Molecular biology
quantification
Justice and Strong Institutions
communities
lcsh:Genetics
Real-time polymerase chain reaction
chemistry
Nucleic acid
PRI Biointeractions en Plantgezondheid
DNA microarray
Oligonucleotide Probes
Ligation
Biotechnology
Subjects
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