Panel of 23S rRNA Gene-Based Real-Time PCR Assays for Improved Universal and Group-Specific Detection of Phytoplasmas
Author:
Affiliation:
1. School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD, United Kingdom
2. Central Science Laboratory, Sand Hutton, York YO41 1LZ, United Kingdom
Abstract
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Link
https://journals.asm.org/doi/pdf/10.1128/AEM.02610-08
Reference22 articles.
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2. Angelini, E., G. L. Bianchi, L. Filippin, C. Morassutti, and M. Borgo. 2007. A new TaqMan method for the identification of phytoplasmas associated with grapevine yellows by real-time PCR assay. J. Microbiol. Methods68:613-622.
3. Baric, S., and J. Dalla-Via. 2004. A new approach to apple proliferation detection: a highly sensitive real-time PCR assay. J. Microbiol. Methods57:135-145.
4. Christensen, N. M., M. Nicolaisen, M. Hansen, and A. Schulz. 2004. Distribution of phytoplasmas in infected plants as revealed by real-time PCR and bioimaging. Mol. Plant-Microbe Interact.17:1175-1184.
5. Crosslin, J. M., G. J. Vandemark, and J. E. Munyaneza. 2006. Development of a real-time, quantitative PCR for detection of the Columbia basin potato purple top phytoplasma in plants and beet leafhoppers. Plant Dis.90:663-667.
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