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Bipolaris sorokiniana is a dangerous pathogen of plants from Poaceae family. A secondary metabolite with carcinogenic properties produced by this fungus is sterigmatocystin. A field experiment with inoculation of the grain of 9 spring barley genotypes with B. sorokiniana No. 36 was carried out in the years 2012–2014 in the Zamość region. Field observations revealed leaf spot caused by B. sorokiniana in all studied genotypes. In 2012, values of the leaf infection index varied from 21.88 (Oberek) to 48.12 (Hajduczek), in 2013 from 25.31 (Skald, Oberek) to 50.00 (STH 7910) and in 2014 from 21.88 (Oberek) to 50.00 (Hajduczek). In the experimental combination with B. sorokiniana, colonies of this fungus in the years 2012–2014 accounted for: 81.22%, 93.11% and 71.78%, respectively, and in control combination: 40.06%, 32.26% and 33.72%, respectively. The chemical analysis of grain of 9 barley genotypes obtained from plants in an experimental combination with B. sorokiniana in 2014, revealed the presence of sterigmatocystin in the genotypes: Hajduczek, Kormoran, Stratus and STH 7910. The sterigmatocystin concentration ranged from 5.39 ng·g–1 (STH 7910) to 67.05 ng·g–1 (Hajduczek). A statistically significant correlation was found between the value of the leaf infection index and the concentration of sterigmatocystin in the grain.
In this study the pathogenicity of Rhizoctonia spp. isolates towards wheat seedlings in laboratory and greenhouse conditions was evaluated. In both experiments seven features were examined: plant height, roots weight, the percentage of infected stems and leaf sheaths and also the degree of stem and leaf sheaths infection. Isolates R1, R29, R39 and R59 were the most pathogenic. Percentage of infected stems ranged from 25.3 to 82.5 and roots from 35 to 82.3. The amplification of internal transcribed spacer regions (ITS1 and ITS2) between 18S, 5.8S and 28S rRNA genes and sequence analysis of these regions have been shown to be sufficiently variable to resolve two Rhizoctonia species. Random amplified polymorphic DNA (RAPD) was used to assess genetic variability among isolates. The suitability of RAPD method for isolates differentiation at intraspecific level was shown. Using seven arbitrary primers in polymerase chain reaction (PCR) thirty-three RAPD markers were generated. Clustering analysis from RAPD data resolved two groups of R. cerealis isolates at the 36% similarity level. Moreover, significant associations between molecular markers and pathogenicity of R. cerealis isolates were found.
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