Phytoplasmas are routinely detected by nucleic acid-based techniques. These approaches rely on enriched phytoplasma DNA extracts of good quality, following labor intensive and time-consuming purification protocols. Here we describe a very rapid, specific, sensitive, and reliable method for flavescence dorée phytoplasma detection, based on real-time Taqman® reverse transcription-PCR of the 16S rRNA. The protocol is particularly useful for large-scale screening of vineyards and nurseries, pathogen surveys, and field epidemiological studies

Reverse Transcription-PCR for Phytoplasma Detection Utilizing Crude Sap Extractions.

Margaria P;Palmano S
2013

Abstract

Phytoplasmas are routinely detected by nucleic acid-based techniques. These approaches rely on enriched phytoplasma DNA extracts of good quality, following labor intensive and time-consuming purification protocols. Here we describe a very rapid, specific, sensitive, and reliable method for flavescence dorée phytoplasma detection, based on real-time Taqman® reverse transcription-PCR of the 16S rRNA. The protocol is particularly useful for large-scale screening of vineyards and nurseries, pathogen surveys, and field epidemiological studies
2013
VIROLOGIA VEGETALE
Inglese
Dickinson M. and Hodgetts J.
Phytoplasma Methods and Protocols
283
289
7
http://link.springer.com/content/pdf/10.1007%2F978-1-62703-089-2_24
Springer Science+Business Media
Berlin, Heidelberg
GERMANIA
Sì, ma tipo non specificato
Crude sap
Grapevine
Real-time TaqMan ® reverse transcription-PCR
Ribosomal RNA
2
02 Contributo in Volume::02.01 Contributo in volume (Capitolo o Saggio)
268
none
Margaria, P; Palmano, S
info:eu-repo/semantics/bookPart
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/239634
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