4.5 Article

Frequency of different CYP51-haplotypes of Mycosphaerella graminicola and their impact on epoxiconazole-sensitivity and -field efficacy

Journal

CROP PROTECTION
Volume 27, Issue 11, Pages 1448-1456

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cropro.2008.07.007

Keywords

14 alpha-Demethylase; CYP51; Demethylation inhibitor; Epoxiconazole; Field efficacy; Microtitre assay; Mycosphaerella graminicola; Pyrosequencing; Septoria leaf blotch

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After development of Qol resistance in Mycosphaerella graminicola in intensive European wheat growing areas, demethylation inhibitors (DMIs) have become the most important fungicides for control of this disease. The sensitivity of M. graminicola towards DMIs has been monitored in recent years and a shift in the population to slightly reduced sensitivities in vitro was determined, which has now reached a plateau. As one reason for this shift, mutations in the target protein 14 alpha-demethylase (CYP51) have been discussed, mainly the amino acid exchanges V136A, A379G, 1381 V, and mutations or deletions at the amino acid positions 459-462 of CYP51. Comparison of the CYP51-haplotypes of 615 isolates from different European regions for their in vitro sensitivity towards the triazole epoxiconazole nevertheless showed that the influence of the CYP51-haplotypes on sensitivity is limited. There was no correlation between in vitro sensitivity or CYP51-haplotype pattern and field performance of epoxiconazole detectable at different trials sites. Equally high levels of efficacy were achieved at sites where the mutations 1381V or A379G, i.e. mutations conferring the highest reduction of efficacy in vitro, were dominant as well as where they were less frequent. Consequently, epoxiconazole treatments did not differentiate between isolates with different mutations. The European survey provides an overview of the distribution of the frequency of different CYP51-haplotypes in Europe indicating a heterogeneous population in Europe and the different regions, and even in a single field. (C) 2008 Elsevier Ltd. All rights reserved.

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