Detection of Leaf Blotches - Causal Agents in Barley Leaves and Grains

Gubiš, Jozef; Hudcovicová, Martina; Klčová, Lenka; Červená, Viera; Bojnanská, Katarína; Kraic, Ján

doi:10.17221/3708-cjgpb

Cited by 5 publications

(1 citation statement)

References 13 publications

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“…nih.gov/BLAST). The PCR analysis of R. secalis was done as described previously (GUBIŠ et al 2004). Electrophoretic detection of PCR products was performed in 3% agarose gels stained with ethidium bromide.…”

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Rapid Detection and Quantification of Rhynchosporium secalis in Barley Using a Polymerase Chain Reaction

Gubiš¹,

Hudcovicová²,

Gubišová³

2006

CZECH J GENET PLANT

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PCR primers for diagnosis of Rhynchosporium secalis in seed samples of barley were developed. For the quantification of the pathogen in seed samples a real-time PCR with SYBR Green approach was used. Amounts from 1.8 to 419.1 pg of R. secalis DNA per 100 ng of total DNA were detected in 18 samples of barley seeds contaminated by R. secalis in field conditions. The correctness of this quantitative analysis was checked using an artificial infection of seeds with 1, 2, 5 and 20% level of infection by R. secalis. The level of contamination of artificially infected samples decreased with a lowering amount of added seed powder contaminated by the pathogen, the correlation coefficient for this analysis was 0.98. While the primer pair used in these analyses shows cross-reactions with other pathogens (P. teres, Drechslera tritici-repentis, F. culmorum and F. poe), it is recommended to check the products of RT-PCR by agarose-gel electrophoresis, in which these pathogens are easily distinguishable from R. secalis by different lengths of the amplified fragments.

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confidence: 99%