http://www.cnr.it/ontology/cnr/individuo/prodotto/ID180484
Rapid Differentiation and Identification of Potential Severe Strains of Citrus tristeza virus by Real-Time Reverse Transcription-Polymerase Chain Reaction Assays (Articolo in rivista)
- Type
- Label
- Rapid Differentiation and Identification of Potential Severe Strains of Citrus tristeza virus by Real-Time Reverse Transcription-Polymerase Chain Reaction Assays (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1094/PHYTO-100-4-0319 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- R. K. Yokomi; M. Saponari; P. J. Sieburth (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- United States Department of Agriculture-Agricultural Research Service (USDA-ARS), Parlier, CA 93648;
Bureau of Citrus Budwood Registration, Florida Department of Agriculture and Consumer Services, Division of Plant Industry, Winter Haven, FL 33881. (literal)
- Titolo
- Rapid Differentiation and Identification of Potential Severe Strains of Citrus tristeza virus by Real-Time Reverse Transcription-Polymerase Chain Reaction Assays (literal)
- Abstract
- A multiplex Taqman-based real-time reverse transcription (RT)
polymerase chain reaction (PCR) assay was developed to identify
potential severe strains of Citrus tristeza virus (CTV) and separate
genotypes that react with the monoclonal antibody MCA13. Three strainspecific
probes were developed using intergene sequences between the
major and minor coat protein genes (CPi) in a multiplex reaction. Probe
CPi-VT3 was designed for VT and T3 genotypes; probe CPi-T36 for T36
genotypes; and probe CPi-T36-NS to identify isolates in an outgroup
clade of T36-like genotypes mild in California. Total nucleic acids
extracted by chromatography on silica particles, sodium dodecyl sulfatepotassium
acetate, and CTV virion immunocapture all yielded high
quality templates for real-time PCR detection of CTV. These assays successfully
differentiated CTV isolates from California, Florida, and a large
panel of CTV isolates from an international collection maintained in
Beltsville, MD. The utility of the assay was validated using field isolates
collected in California and Florida. (literal)
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