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 |