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Covariation of ergot severity and alkaloid content measured by HPLC and one ELISA method in inoculated winter rye across three isolates and three European countries

Zugehörigkeit
State Plant Breeding Institute, University of Hohenheim, Stuttgart, Germany
Kodisch, Anna;
Zugehörigkeit
Austrian Agency for Health and Food Safety (AGES), Institute for Sustainable Plant Production, Austria
Oberforster, Michael;
Zugehörigkeit
Austrian Agency for Health and Food Safety (AGES), Institute for Sustainable Plant Production, Austria
Raditschnig, Armin;
GND
122207777
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute of Plant Protection in Field Crops and Grassland, Germany
Rodemann, Bernd;
Zugehörigkeit
Institute of Plant Protection-National Research Institute, 60-318 Poznań, Poland
Tratwal, Anna;
Zugehörigkeit
Institute of Plant Protection-National Research Institute, 60-318 Poznań, Poland
Danielewicz, Jakub;
Zugehörigkeit
Institute of Plant Protection-National Research Institute, 60-318 Poznań, Poland
Korbas, Marek;
Zugehörigkeit
KWS LOCHOW GMBH, Bergen, Germany
Schmiedchen, Brigitta;
Zugehörigkeit
KWS LOCHOW GMBH, Bergen, Germany
Eifler, Jakob;
Zugehörigkeit
KWS LOCHOW GMBH, Bergen, Germany
Gordillo, Andres;
Zugehörigkeit
HYBRO Saatzucht GmbH & Co. KG, Schenkenberg, Germany
Siekmann, Dörthe;
Zugehörigkeit
HYBRO Saatzucht GmbH & Co. KG, Schenkenberg, Germany
Fromme, Franz Joachim;
Zugehörigkeit
LCTech GmbH, 84419 Obertaufkirchen, Germany
Wuppermann, Frederik N.;
Zugehörigkeit
Austria
Wieser, Franz;
Zugehörigkeit
Austria
Zechner, Elisabeth; Niewińska, Małgorzata;
Zugehörigkeit
State Plant Breeding Institute, University of Hohenheim, Stuttgart, Germany
Miedaner, Thomas

Ergot caused by Claviceps purpurea is a problem for food and feed security in rye due to the occurrence of toxic ergot alkaloids (EAs). For grain elevators and breeders, a quick, easy-to-handle, and cheap screening assay would have a high economic impact. The study was performed to reveal (1) the covariation of ergot severity (= percentage of sclerotia in harvested grain) and the content of 12 EAs determined by high performance liquid chromatography (HPLC) and (2) the covariation between these traits and results of one commercial enzyme linked immunosorbent assays (ELISA). In total, 372 winter rye samples consisting of a diverse set of genotypes, locations from Germany, Austria, and Poland over two years, and three isolates were analyzed. Ergocornine and α-ergocryptine were detected as major EAs. Ergocristinine occurred as a minor component. Claviceps isolates from different countries showed a similar EA spectrum, but different quantities of individual EAs. A moderate, positive covariation between ergot severity and EA content determined by HPLC was observed across two years (r = 0.53, p < 0.01), but large deviation from the regression was detected. ELISA values did neither correlate with the HPLC results nor with ergot severity. In conclusion, a reliable prediction of the EA content based on ergot severity is, at present, not possible.

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