Dataset Information

Development and Validation of a New TaqMan Real-Time PCR for Detection of 'Candidatus Phytoplasma pruni'.

ABSTRACT: Phytoplasmas of the 16SrIII group are wide spread, and have a broad plant host range. Among these, 'Candidatus phytoplasma pruni' ('Ca. P. pruni'; phytoplasmas of 16SrIII subgroup A) can cause serious diseases in Prunus species and 'Ca. P. pruni'-related strains can infect other plant species, including grapevines. In this study, a new real-time PCR detection system was developed for 'Ca. P. pruni' using TaqMan chemistry. This test was designed to detect 'Ca. P. pruni', by amplifying the species-specific secY gene. In addition, a test to amplify the group-specific 16S rRNA gene region was also developed. The performances of both tests were evaluated. The test that amplifies the secY gene provided reliable and quick detection of 'Ca. P. pruni'. Using the newly developed and validated test, 'Ca. P. pruni' was not found in any of the 434 field samples collected from different plants species grown in different regions of Slovenia.

SUBMITTER: Kogej Z

PROVIDER: S-EPMC7459698 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Publications

Development and Validation of a New TaqMan Real-Time PCR for Detection of 'Candidatus Phytoplasma pruni'.

Kogej Zala Z Dermastia Marina M Mehle Nataša N

Pathogens (Basel, Switzerland) 20200807 8

Phytoplasmas of the 16SrIII group are wide spread, and have a broad plant host range. Among these, 'Candidatus phytoplasma pruni' ('Ca. P. pruni'; phytoplasmas of 16SrIII subgroup A) can cause serious diseases in Prunus species and 'Ca. P. pruni'-related strains can infect other plant species, including grapevines. In this study, a new real-time PCR detection system was developed for 'Ca. P. pruni' using TaqMan chemistry. This test was designed to detect 'Ca ...[more]

PMID: 32784551

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Project description:BackgroundDNA genotyping with mutation-specific TaqMan(R) probes (Applied Biosystems) is broadly used in detection of single-nucleotide polymorphisms but is less so for somatic mutations because of its limited selectivity for low-level mutations. We recently described coamplification at lower denaturation temperature-PCR (COLD-PCR), a method that amplifies minority alleles selectively from mixtures of wild-type and mutation-containing sequences during the PCR. We demonstrate that combining COLD-PCR with TaqMan technology provides TaqMan genotyping with the selectivity needed to detect low-level somatic mutations.MethodsMinor-groove binder-based or common TaqMan probes were designed to contain a nucleotide that matches the desired mutation approximately in the middle of the probe. The critical denaturation temperature (T(c)) of each amplicon was then experimentally determined. COLD-PCR/TaqMan genotyping was performed in 2 steps: denaturation at the T(c), followed by annealing and extension at a single temperature (fast COLD-PCR). The threshold cycle was used to identify mutations on the basis of serial dilutions of mutant DNA into wild-type DNA and to identify TP53 (tumor protein p53) and EGFR [epidermal growth factor receptor (erythroblastic leukemia viral (v-erb-b) oncogene homolog, avian)] mutations in tumors.ResultsCOLD-PCR/TaqMan genotyping identified G>A mutations within TP53 exon 8 (codon 273 mutation hot spot) and C>T mutations within the EGFR gene (drug-resistance mutation T790M) with a selectivity improvement of 15- to 30-fold over regular PCR/TaqMan genotyping. A second round of COLD-PCR/TaqMan genotyping improved the selectivity by another 15- to 30-fold and enabled detection of 1 mutant in 2000 wild-type alleles. Use of COLD-PCR/TaqMan genotyping allowed quantitative identification of low-level TP53 and T790 mutations in colon tumor samples and in non-small-cell lung cancer cell lines treated with kinase inhibitors.ConclusionsThe major improvement in selectivity provided by COLD-PCR enables the popular TaqMan genotyping method to become a powerful tool for detecting low-level mutations in clinical samples.

Dataset Information

Development and Validation of a New TaqMan Real-Time PCR for Detection of 'Candidatus Phytoplasma pruni'.

Publications

Development and Validation of a New TaqMan Real-Time PCR for Detection of '<i>Candidatus</i> Phytoplasma pruni'.

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