Genome-informed design of a LAMP assay for the specific detection of the strain of 'Candidatus Phytoplasma asteris' phytoplasma occurring in grapevines in South Africa

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dc.contributor.author Alic, Spela
dc.contributor.author Dermastia, Marina
dc.contributor.author Burger, Johan
dc.contributor.author Dickinson, Matthew
dc.contributor.author Pietersen, Gerhard
dc.contributor.author Pietersen, Gert
dc.contributor.author Dreo, Tanja
dc.date.accessioned 2023-01-30T11:47:30Z
dc.date.available 2023-01-30T11:47:30Z
dc.date.issued 2022-11
dc.description Supplementary File S1 : Experimental evaluation an optimisation of AY-SA LAMP assays en_US
dc.description Supplementary File S2 : Report on the results of the test performance study for molecular detection South African aster yellows en_US
dc.description Figure S1 : Synthetic target dsDNA standard curve data. Standard curves were performed as two and three technical repeats for LAMP and real-time PCR. A, standard curve for LAMP AY-SA_ftsH assay recorded on QuantStudio 3 Flex real-time PCR systems. B, standard curve for LAMP AY-SA_ftsH assay recorded on QuantStudio 7 Flex real-time PCR systems. C, standard curve for real-time PCR AY- SA_ftsH assay recorded on QuantStudio 3 Flex real-time PCR systems. D, standard curve for real-time PCR AY-SA_ftsH assay recorded on QuantStudio 7 Flex real-time PCR systems. One representative standard curve is shown for each instrument. en_US
dc.description Figure S2. Non-linear modeling of the probability of detection for the AY-SA-specific LAMP (A) and real-time AY-SA-specific PCR assays (B). For both assays two parameter Weibull function fitted the best to experimental data. Log concentration, expressed as log(target dsDNA molecules/ml); dotted line, 95% probability of detection. en_US
dc.description Table S1. List of genomes used as a negative data set input for pipeline analysis for the identification of the specific sequences using RUCS software. The list contains 73 complete or draft genomes of phytoplasma (18 genomes) and mycoplasma (55 genomes) derived from NCBI/Genbank database. en_US
dc.description Table S2. Nucleotide sequences of the target dsDNA (gBlock sequnces) used for experimental evaluation of LAMP assays. en_US
dc.description Table S3. Nucleotide sequences specific to AY-SA genomes and selected for LAMP primer design based on predefined criteria. en_US
dc.description Table S4. The list of designed LAMP assays selected for experimental evaluation. All the assays were designed on three different genomic sequences, named Seq1, Seq3 and Seq11, specific to AY-SA phytoplasma. Best performing assay, LAMP AY-SA_ftsH, was selected for validation. en_US
dc.description.abstract Grapevine yellows is one of the most damaging phytoplasma-associated diseases worldwide. It is linked to several phytoplasma species, which can vary regionally due to phytoplasma and insect-vector diversity. Specific, rapid, and reliable detection of the grapevine yellows pathogen has an important role in phytoplasma control. The purpose of this study was to develop and validate a specific loop-mediated isothermal amplification (LAMP) assay for detection of a distinct strain of grapevine ‘Candidatus Phytoplasma asteris’ that is present in South Africa, through implementation of a genome-informed test design approach. Several freely available, user-friendly, web-based tools were coupled to design the specific LAMP assays. The criteria for selection of the assays were set for each step of the process, which resulted in four experimentally operative LAMP assays that targeted the ftsH/hflB gene region, specific to the aster yellows phytoplasma strain from South Africa. A real-time PCR was developed, targeting the same genetic region, to provide extensive validation of the LAMP assay. The validated molecular assays are highly specific to the targeted aster yellows phytoplasma strain from South Africa, with good sensitivity and reproducibility. We show a genome-informed molecular test design and an efficient validation approach for molecular tests if reference and sample materials are sparse and hard to obtain. en_US
dc.description.department Microbiology and Plant Pathology en_US
dc.description.librarian hj2023 en_US
dc.description.sponsorship European Union Horizon 2020 Research and Innovation Programme and Javna Agencija za Raziskovalno Dejavnost RS. en_US
dc.description.uri https://apsjournals.apsnet.org/loi/pdis en_US
dc.identifier.citation Alič, Š., Dermastia, M., Burger, J., Dickinson, M., Pietersen, G., Pietersen, G., Dreo, T.. Genome-Informed Design of a LAMP Assay for the Specific Detection of the Strain of 'Candidatus Phytoplasma asteris' Phytoplasma Occurring in Grapevines in South Africa. Plant Disease. 106(11):2927-2939. doi: 10.1094/PDIS-10-21-2312-RE. en_US
dc.identifier.issn 0191-2917 (print)
dc.identifier.issn 1943-7692 (online)
dc.identifier.other 10.1094/PDIS-10-21-2312-RE
dc.identifier.uri https://repository.up.ac.za/handle/2263/89026
dc.language.iso en en_US
dc.publisher American Phytopathological Society en_US
dc.rights © 2022 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license. en_US
dc.subject Grapevine yellows (GY) en_US
dc.subject Loop-mediated isothermal amplification (LAMP) en_US
dc.subject Prokaryotes en_US
dc.subject Aster yellows en_US
dc.subject Fruit en_US
dc.subject Molecular detection en_US
dc.subject Pathogen detection en_US
dc.subject Phytoplasma en_US
dc.title Genome-informed design of a LAMP assay for the specific detection of the strain of 'Candidatus Phytoplasma asteris' phytoplasma occurring in grapevines in South Africa en_US
dc.type Article en_US


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