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Rapid‐cycle PCR detection of Pyrenophora graminea from barley seed
Author(s) -
Taylor E. J. A.,
Stevens E. A.,
Bates J. A.,
Morreale G.,
Lee D.,
Kenyon D. M.,
Thomas J. E.
Publication year - 2001
Publication title -
plant pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.928
H-Index - 85
eISSN - 1365-3059
pISSN - 0032-0862
DOI - 10.1046/j.1365-3059.2001.00563.x
Subject(s) - biology , sybr green i , primer (cosmetics) , pyrenophora , polymerase chain reaction , hordeum vulgare , melting curve analysis , botany , microbiology and biotechnology , poaceae , genetics , gene , cultivar , chemistry , organic chemistry
Sixty RAPD primers were used to screen for a diagnostic marker that could be used to identify Pyrenophora graminea , a fungal seedborne pathogen that causes leaf stripe on barley. Primer pairs were designed to differentiate P. graminea from other Pyrenophora spp. using a sequence‐characterized amplified region (SCAR) approach. A pair of P. graminea ‐specific primers (PG2 F/R) was obtained that amplified a single fragment from 37 isolates of P. graminea tested, but not from 29 isolates of other Pyrenophora spp. or 12 saprophytes isolated from barley seed. Rapid PCR detection was achieved using a LightCycler, in which the emission of fluorescence from the binding of SYBR Green I dye to the PCR products is measured. The P. graminea ‐specific product resulting from amplification with PG2 F/R can be distinguished from any nonspecific products by post‐PCR melting point analysis. The PCR assay involves 40 amplification cycles of PCR, and the total PCR test including melting point analysis takes 25 min to complete. The rapidity of this test, combined with the closed ‘in‐tube’ detection of PCR products, which reduces the potential for contamination, offers significant advantages compared with conventional laboratory and PCR analyses.