| Title: | Highly specific qPCR and amplicon sequencing method for detection of quarantine citrus pathogen Phyllosticta citricarpaapplicable for air samples |
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| Authors: | ID Zajc, Janja (Author)
ID Kogej Zwitter, Zala (Author)
ID Fišer, Sara (Author)
ID Gostinčar, Cene (Author)
ID Vicent, Antonio (Author)
ID Galvañ Domenech, Anaïs (Author)
ID Riccioni, Luca (Author)
ID Boonham, Neil (Author)
ID Ravnikar, Maja (Author)
ID Kogovšek, Polona (Author) |
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| Files: |  URL - Source URL, visit https://doi.org/10.1111/ppa.13679
 PDF - Presentation file, download (1,49 MB)
MD5: 88FD8DBB0D128A1105CCA95420E40048
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| Language: | English |
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| Typology: | 1.01 - Original Scientific Article |
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| Organization: |  NIB - National Institute of Biology
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| Abstract: | The fungus Phyllosticta citricarpa is a quarantine pathogen in the EU and is of high economic importance in many parts of the world where favourable climate conditions drive the development of citrus black spot (CBS) disease. Disease symptoms include necrotic lesions on leaves and fruits. Low disease pressure can reduce crop market-ability, while higher disease pressure can cause premature fruit drop, significantly increasing crop losses. The wind-dispersed spores of P. citricarpa are especially prob-lematic for rapid pathogen dispersal, but also provide an opportunity for early detec-tion of the disease spreading into a new area. In this study we have developed and validated a quantitative PCR (qPCR) assay based on the TEF1-α sequence. Specificity testing demonstrated that it is currently the only qPCR assay that does not cross- react with closely related Phyllosticta species. The assay is sensitive and can detect a single copy of the TEF1 gene in a reaction, it is highly repeatable and reproducible and can be used for testing of the sticky tapes from spore traps as well as citrus fruit sam-ples. High-throughput sequencing (HTS) of the DNA barcodes ITS1 and TEF1 was also explored for the detection and discrimination of P. citricarpa. The limit of detection of the HTS was 1000 spores on a daily spore trap tape. This study makes an important improvement to the diagnostics of the CBS and the methods developed can also be applied to improve the surveillance and early detection of the pathogen when linked to spore samplers in the field. |
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| Keywords: | detection, fungal spore sampling, internal transcribed region (ITS), translation elongation factor 1-α (TEF1) |
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| Publication status: | Published |
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| Publication version: | Version of Record |
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| Publication date: | 17.11.2022 |
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| Year of publishing: | 2023 |
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| Number of pages: | str. 548-563 |
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| Numbering: | Vol. 3, Vol. 72 |
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| PID: | 20.500.12556/DiRROS-19244  |
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| UDC: | 632 |
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| ISSN on article: | 1365-3059 |
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| DOI: | 10.1111/ppa.13679 |
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| COBISS.SI-ID: | 136443139 |
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| Note: | Ostali avtorji: Zala Kogej Zwitter, Sara Fišer, Cene Gostinčar, Antonio Vicent, Anaïs Galvañ Domenech, Luca Riccioni, Neil Boonham, Maja Ravnikar, Polona Kogovšek;
Nasl. z nasl. zaslona;
Opis vira z dne 5. 1. 2023;
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| Publication date in DiRROS: | 12.07.2024 |
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| Views: | 308 |
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| Downloads: | 258 |
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