| Literature DB >> 19270148 |
Jennifer Hodgetts1, Neil Boonham, Rick Mumford, Matthew Dickinson.
Abstract
Primers and probes based on the 23S rRNA gene have been utilized to design a range of real-time PCR assays for routine phytoplasma diagnostics. These assays have been authenticated as phytoplasma specific and shown to be at least as sensitive as nested PCR. A universal assay to detect all phytoplasmas has been developed, along with a multiplex assay to discriminate 16SrI group phytoplasmas from members of all of the other 16Sr groups. Assays for the 16SrII, 16SrIV, and 16SrXII groups have also been developed to confirm that the 23S rRNA gene can be used to design group-specific assays.Mesh:
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Year: 2009 PMID: 19270148 PMCID: PMC2681720 DOI: 10.1128/AEM.02610-08
Source DB: PubMed Journal: Appl Environ Microbiol ISSN: 0099-2240 Impact factor: 4.792