| Literature DB >> 21635923 |
D E Debreczeni1, S Ruiz-Ruiz, J Aramburu, C López, B Belliure, L Galipienso, S Soler, L Rubio.
Abstract
A quantitative real-time reverse transcription-polymerase chain reaction (RT-qPCR) procedure using a general primer set and three TaqMan(®)MGB probes was developed for general and genotype-specific detection and quantitation of the genomic M segment of Tomato spotted wilt virus (TSWV). Standard curves using RNA transcripts homologous to the three probes allowed reproducible quantitative assays with a wide dynamic range (10(3)-10(10) TSWV M segment RNA copies/ng of total RNA) and high sensitivity. This protocol was assayed with a battery of TSWV isolates, covering the range of the present known genetic variation, in single and/or mix infections in three plant hosts, as well as in the thrips vector Frankliniella occidentalis. This quantitative detection assay will be a valuable tool for molecular biology and epidemiology studies, diagnosis and disease control.Entities:
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Year: 2011 PMID: 21635923 DOI: 10.1016/j.jviromet.2011.05.027
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014