Quantification of potato common scab pathogens in soil by quantitative competitive PCR with fluorescent quenching-based probes

• Published in: Plant pathology Vol. 57; no. 5; pp. 887 - 896
• Main Authors: Manome, A, Kageyama, A, Kurata, S, Yokomaku, T, Koyama, O, Kanagawa, T, Tamaki, H, Tagawa, M, Kamagata, Y
• Format: Journal Article
• Language: English
• Published: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01-10-2008; Blackwell Publishing Ltd; Blackwell
• Subjects: Bacterial plant pathogens; Biological and medical sciences; common scab of potato; Fundamental and applied biological sciences. Psychology; nec1 gene; Phytopathology. Animal pests. Plant and forest protection; quantitative competitive quenching probe PCR; real-time PCR; soilborne disease; Solanum tuberosum; Streptomyces; Streptomyces spp; soilborne disease; Plant pathology; Plant pathogen; Disease; Competitiveness; common scab of potato; real-time PCR; Probe; Actinomycetales; necl gene; quantitative competitive quenching probe PCR; Gene; Pathogenic; Streptomyces spp; Bacteria; Quantitative analysis; Soilborne transmission; Streptomycetaceae; Streptomyces scabiei; Real time; Polymerase chain reaction; Soils; Actinomycetes; Transmission mode; Molecular biology; Fluorescent compound
• ISSN: 0032-0862; 1365-3059
• DOI: 10.1111/j.1365-3059.2008.01881.x

Common scab of potato tubers caused by pathogenic Streptomyces spp. is a cause of serious economic loss worldwide. For the rapid and accurate quantification of pathogenic Streptomyces spp. residing in soil, a new competitive real-time PCR method using fluorescent quenching-based probes (quantitative competitive quenching probe PCR: QCQP-PCR) was developed. The virulence gene of pathogenic Streptomyces spp., nec1, was selected as the target for QCQP-PCR. A specific primer set to amplify the nec1 gene, and a fluorescently labelled probe that specifically hybridizes with the nec1 amplicon were designed. For QCQP-PCR, an internal standard DNA (IS DNA) that is identical to the nec1 amplicon but has a 4-base mismatch in the probe-hybridizing region, and a fluorescently labelled probe IS, which specifically hybridizes with IS DNA at the mutagenized region, were PCR-synthesized. The target nec1 gene was co-amplified with the known copy number of IS DNA by PCR using the same primer set in the presence of the specific probes. The PCR products were monitored in real-time by measuring the fluorescence intensity (quenching) of each probe. The initial amount of the nec1 gene was quantified based on the ratio of the PCR products of the same PCR cycle. The results revealed that QCQP-PCR could be used to precisely quantify the nec1 gene, even in the presence of PCR inhibitors in the soil samples examined. The lower limit of quantification was 20 copies per tube, which corresponded to 1500 copies per g dry soil. The quantification achieved by this method was completed within 5 h, i.e. the duration of the entire analysis. These results demonstrate the usefulness of the present method for monitoring pathogenic Streptomyces species in soil.