Real-Time PCR Assays for the Detection of Puccinia psidii

Puccinia psidii (Myrtle rust) is an emerging pathogen that has a wide host range in the Myrtaceae family; it continues to show an increase in geographic range and is considered to be a significant threat to Myrtaceae plants worldwide. In this study, we describe the development and validation of thre...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Plant disease. - 1997. - 100(2016), 3 vom: 21. März, Seite 617-624
1. Verfasser: Baskarathevan, J (VerfasserIn)
Weitere Verfasser: Taylor, R K, Ho, W, McDougal, R L, Shivas, R G, Alexander, B J R
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2016
Zugriff auf das übergeordnete Werk:Plant disease
Schlagworte:Journal Article
LEADER 01000naa a22002652 4500
001 NLM293159157
003 DE-627
005 20231225074715.0
007 cr uuu---uuuuu
008 231225s2016 xx |||||o 00| ||eng c
024 7 |a 10.1094/PDIS-08-15-0851-RE  |2 doi 
028 5 2 |a pubmed24n0977.xml 
035 |a (DE-627)NLM293159157 
035 |a (NLM)30688594 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Baskarathevan, J  |e verfasserin  |4 aut 
245 1 0 |a Real-Time PCR Assays for the Detection of Puccinia psidii 
264 1 |c 2016 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Revised 20.11.2019 
500 |a published: Print-Electronic 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a Puccinia psidii (Myrtle rust) is an emerging pathogen that has a wide host range in the Myrtaceae family; it continues to show an increase in geographic range and is considered to be a significant threat to Myrtaceae plants worldwide. In this study, we describe the development and validation of three novel real-time polymerase reaction (qPCR) assays using ribosomal DNA and β-tubulin gene sequences to detect P. psidii. All qPCR assays were able to detect P. psidii DNA extracted from urediniospores and from infected plants, including asymptomatic leaf tissues. Depending on the gene target, qPCR was able to detect down to 0.011 pg of P. psidii DNA. The most optimum qPCR assay was shown to be highly specific, repeatable, and reproducible following testing using different qPCR reagents and real-time PCR platforms in different laboratories. In addition, a duplex qPCR assay was developed to allow coamplification of the cytochrome oxidase gene from host plants for use as an internal PCR control. The most optimum qPCR assay proved to be faster and more sensitive than the previously published nested PCR assay and will be particularly useful for high-throughput testing and to detect P. psidii at the early stages of infection, before the development of sporulating rust pustules 
650 4 |a Journal Article 
700 1 |a Taylor, R K  |e verfasserin  |4 aut 
700 1 |a Ho, W  |e verfasserin  |4 aut 
700 1 |a McDougal, R L  |e verfasserin  |4 aut 
700 1 |a Shivas, R G  |e verfasserin  |4 aut 
700 1 |a Alexander, B J R  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Plant disease  |d 1997  |g 100(2016), 3 vom: 21. März, Seite 617-624  |w (DE-627)NLM098181742  |x 0191-2917  |7 nnns 
773 1 8 |g volume:100  |g year:2016  |g number:3  |g day:21  |g month:03  |g pages:617-624 
856 4 0 |u http://dx.doi.org/10.1094/PDIS-08-15-0851-RE  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 100  |j 2016  |e 3  |b 21  |c 03  |h 617-624