This study was conducted to investigate the relationship between the recent increase in the frequency of drought conditions and Root-Crown Rot (Fusarium pseudograminearum, Fusarium culmorum) in rainfed wheat growing areas of Central Anatolia. In 2018, the experiment was established in the greenhouse of Konya Bahri Dağdaş International Agricultural Research Institute using 25 registered wheat varieties in a randomised block split-plot experimental design with 4 replications. Irrigation levels (100% field capacity and 50% field capacity) were designed as main plots, inoculation (+ and -) as subplots and varieties as sub-subplots. In the study, the response of the cultivars to inoculation under artificial drought conditions was evaluated by measuring Crown Score (CR), Lesion Length (LL), Number of Diseased Leaves from outside to inside (NDL) and Plant Height (PH) from five plants in each pot. Statistically, the differences between inoculation, irrigation, NDL and LL were found to be significant at P<0.0001 level, while the differences between varieties were found to be significant at P<0.001 level for the CR parameter. On the other hand, when the interactions were evaluated for the NDL parameter, the differences were found to be significant at P<0.0001 level for all three interactions of cultivar*inoculation, cultivar*irrigation and cultivar*inoculation*irrigation. When the effect of reduced water application intended to be used in resistance breeding was evaluated for 25 different varieties under Fusarium culmorum inoculation, there was an increase in CR from 41,7% (Gerek-79) to 487,5% (Altay-2000), NDL from 7,14% (Kirgiz-95) to 200% (Alpu-2001), LL from -36,84% (Karahan-99) to 283,33% (Altay-2000) and in PH reduction from 12,41% (Seval) to 32,22% (Kirgiz-95). The results showed that drought-stressed plants were already weakened and therefore more easily and severely infected by pathogens. According to these results, it has been determined that it is very important for the region to obtain resistance to drought and crown rot diseases, which have such an obvious relationship, in breeding studies.

Fusarium culmorum is predominating causal agent of head blight (HB) and root rot (RR) in cereals worldwide. Since F. culmorum has a great level of genetic diversity and the parasexual stage is assumed for this phytopathogen, characterization of isolates from different regions is significant step in food safety and controlling the HB. In this study, it was aimed to characterize totally 37 F. culmorum isolates from Turkey via sequence related amplified polymorphism (SRAP) marker based genotyping. MAT-1/MAT-2 type assay was also used in order to reveal intraspecific variation in F. culmorum. MAT-1 and MAT-2 specific primer pairs for mating assays resulted in 210 and 260 bp bands, respectively. 11 of isolates were belonged to MAT-1 type whereas 19 samples were of MAT-2. Remaining 7 samples yielded both amplicons. Totally 9 SRAP primer sets yielded amplicons from all isolates. Genetic similarity values were ranged from 39 to 94.7%. Total band number was 127 and PCR product sizes were in the range of 0.1-2.5 kb. Amplicon numbers for individuals were ranged from 1 to 16. According to data obtained from current study, SRAP based genotyping is powerful tool for supporting the data obtained from investigations including phenotypic and agro-ecological characteristics. Findings showed that SRAP-based markers could be useful in F. culmorum characterization.

Fusarium culmorum is predominating causal agent of head blight (HB) and root rot (RR) in cereals worldwide. Since F. culmorum has a great level of genetic diversity and the parasexual stage is assumed for this phytopathogen, characterization of isolates from different regions is significant step in food safety and controlling the HB. In this study, it was aimed to characterize totally 37 F. culmorum isolates from Turkey via sequence related amplified polymorphism (SRAP) marker based genotyping. MAT-1/MAT-2 type assay was also used in order to reveal intraspecific variation in F. culmorum. MAT-1 and MAT-2 specific primer pairs for mating assays resulted in 210 and 260 bp bands, respectively. 11 of isolates were belonged to MAT-1 type whereas 19 samples were of MAT-2. Remaining 7 samples yielded both amplicons. Totally 9 SRAP primer sets yielded amplicons from all isolates. Genetic similarity values were ranged from 39 to 94.7%. Total band number was 127 and PCR product sizes were in the range of 0.1-2.5 kb. Amplicon numbers for individuals were ranged from 1 to 16. According to data obtained from current study, SRAP based genotyping is powerful tool for supporting the data obtained from investigations including phenotypic and agro-ecological characteristics. Findings showed that SRAP-based markers could be useful in F. culmorum characterization.

The use of antagonist microorganisms against pathogenic organisms in organic agricultural systems was promising for biological control approach. The aim of this study was to determination of the potential biological control of some fungal isolates which characterized as endophytic and antagonistic against soil borne Fusarium culmorum (FC) and F. oxysporum f.sp. radicis lycopersici (FORL) pathogens. For this, seven isolates of endophytic Acremonium spp. that isolated from healthy wheat plants and eight isolates of antagonist Trichoderma spp., isolated from soil of organic vegetable areas, were performed as biological control agents (BCA). The agar media with hypha and mycelia of the BCAs and spore suspensions (106 spores/ml) of FC and FORL were treated for inoculation of wheat seeds and tomato seedlings. The harvested plants were statistically analyzed by some parameters (severity of crown rot disease (%DS and scale), plant lengths (cm) etc.). In conclusion, the Acremonium isolates (47.5%) were lower means of disease severity than Trichoderma isolates (74.6%) for FC and FORL assessments in wheat experiment. In tomato, the averages of disease severity between Acremonium and Trichoderma were similar while their means were lower than positive control (The Scale of DS=0.67