Patterns of Splash Dispersed Conidia of Fusarium poae and Fusarium culmorum

Splash dispersal of Fusarium culmorum and Fusarium poae spores was studied, using inoculated straw placed on tiles as the inoculum source to infect agar strips and artificially produced leaves. In addition, patterns of spread were studied with spores from inoculated artificial leaves onto agar strips. Observed patterns of spore dispersal for each species were indistinguishable, although F. culmorum produced fewer colonies than F. poae. Furthermore, spore dispersal from inoculated straw and artificial leaves were essentially identical, with one exception; colonies arose from single conidia when spread from artificial leaves, but consisted of clumps of conidia when derived from inoculated straw. Splash dispersal patterns of both species onto the upper- and undersides of artificial leaves were different. On the upperside of the leaf, most colonies were found at the tip, while on the underside of the leaf most colonies were found at the base of the leaf. This is the first time that artificially produced leaves have been used in splash dispersal experiments.     

Antifungal Activity Toward Fusarium culmorum in Soluble Wheat Extracts

ABSTRACT This study investigated antifungal activity in soluble extracts from seed of a range of wheat cultivars differing in susceptibility to Fusarium head blight. Antifungal activity was assessed in terms of beta-D-glucuronidase (GUS) activity of a Fusarium culmorum GUS transformant using a sensitive laboratory assay. Significant antifungal activity was detected in seed extracts from WEK0609, CM 820036, and Arina. Initial characterization of the Arina seed extract indicated that it contained antifungal proteinaceous compounds. The Arina extract yielded two (60 and 80%) ammonium sulfate fractions containing inhibitory compounds. Gel filtration chromatography and subsequent sodium dodecyl sulfate-polyacrylamide gel electrophoresis of antifungal fractions showed that the antifungal activities detected in the Arina 60 and 80% ammonium sulfate fractions were associated with putative proteinaceous compounds with apparent molecular masses of approximately 60 and 28 kDa, respectively.     

Deal stem disease of asparagus caused by Fusarium culmorum

Deal stem disease in asparagus is characterized by yellow dead stems with reddish lesions, mostly at soil level. There are two types of infection. The first one with lesions on the base of the stem at soil level, as a result of which the stem dies off. In the second type of infection the lesions appear higher up on the stems, while stems remain mostly green. The disease was proved to be caused byFusarium culmorum. This fungus is mainly spread through the soil. Air dispersal was demonstrated but seems of little importance to disease incidence.     

Untersuchungen zur systemischen Infektion von Fusarium culmorum an Winterweizen in Schleswig-Holstein

In north-west Germany Fusarium head blight of wheat (FHB) is frequently caused by Fusarium culmorum and F. graminearum. This damage has, however, mainly been caused by infections during flowering; the incidence of FHB has increased steadily for many years in crop rotations without maize. The authors postulate that F. culmorum can cause systemic infections in wheat. In 2003 they used real-time PCR to analyse more than 1?100 tissue samples from wheat fields in order to determine whether F. culmorum was present in the internodes and spikes of the wheat plants. More than 30% of all analysed samples contained F. culmorum-DNA, and many wheat stems were completely or nearly completely systemically colonized by F. culmorum. These findings are consistent with those of other researchers who have detected a systemic growth of F. culmorum during experiments under controlled conditions. It cannot be automatically assumed that the fungus spreads from the wheat head during flowering; the plant could have become infected through chlamydospores or mycelium on residual plant debris in the soil. Therefore this pathogen must be regarded as a crop rotation disease. F. culmorum is able to severely infect wheat through the roots and stem bases, especially when the soil is dry and warm. Thus, spraying fungicides during flowering is ineffective.     

Role of Deoxynivalenol in Aggressiveness of Fusarium graminearum and F. culmorum and in Resistance to Fusarium Head Blight

The data available indicate that aggressiveness of Fusarium graminearum and F. culmorum depends on their deoxynivalenol (DON) and nivalenol-producing capacity: toxin-producing ability correlated closely with the level of aggressiveness measured. This agrees well with other literature findings. However, the resistance of a cultivar influenced DON production significantly. In the most resistant genotypes, toxin contamination remained near zero, whereas the same isolates and inoculum produced very high toxin levels in susceptible cultivars. As toxin levels were correlated with the ratio of Fusarium-damaged kernels (FDK) and this ratio is very low in highly resistant cultivars, the conclusion is that the level of resistance level is more important in governing DON accumulation in a given cultivar than is the aggressiveness of an isolate. In susceptible cultivars, DON producing ability is decisive, but in highly resistant cultivars resistance is the major factor in suppressing disease development and DON accumulation. In different years, the same FDK values were associated with different DON concentrations and this depended very much on the precipitation towards the end of May, the time of inoculation.     

Zearalenone production in Fusarium culmorum after transformation with DNA of F. graminearum

Total DNA from a cycloheximide-resistant mutant of Fusarium graminearum producing zearalenone was incubated with the protoplasts of a non-zearalenone-producing cycloheximide-susceptible isolate of F. culmorum. The regenerated protoplasts were inoculated on a 5-mM cycloheximide medium. The cultures which developed were examined for zearalenone production. Sixty-five cycloheximide-resistant isolates, including two isolates producing zearalenone, were obtained from approximately 3.6 × 10⁴ viable F. culmorum protoplasts. Similar incubations with homologous F. culmorum DNA and non-fungal DNA did not elicit zearalenone production. The results suggest the transformation of F. culmorum by the genetic factors responsible for cycloheximide resistance and zearalenone production from F. graminearum. The epidemiological and taxonomic significance of these observations is discussed.     

Head blight and biosynthesis of Fusarium toxins in barley kernels field inoculated withFusarium culmorum

Heads of 12 spring barley genotypes (eight cultivars, four lines) were inoculated with conidial suspensions of twoFusarium culmorum isolates (I₁ and I₂). Both isolates caused the following significant reductions (%) when compared with the control: number of kernels head^–1 12 and 16, weight of 1000 kernels 47 and 24, yield 49 and 37, for I₁ and I₂ respectively. Both isolates were able to produce average levels (mg kg^–1) of deoxynivalenol of 67.1 and 13.9, 3-acetyldeoxynivalenol of 9.4 and 1.4 and zearalenone of 0.3 and 0.4 for I₁ and I₂ respectively. In kernels of three genotypes inoculated with the same isolates, 15-acetyldeoxynivalenol at an average level (mg kg^–1) of 1.3 and 1.5 was detected, while in kernels of six genotypes inoculated with I₂, 0.2 of nivalenol was found. A significant correlation for yield and toxin level was found for less pathogenicF. culmorum isolate I₂.     

Screening for fungal antagonists of seed-borne Fusarium culmorum on wheat using in vivo tests

A screening system is described for identifying fungal antagonists from soil which are effective in controlling seed-borne Fusarium culmorum on wheat (T. aestivum L.). The procedure comprised three consecutive in vivo tests done under controlled conditions using three different plant growing media. Altogether 1701 fungal isolates from Finnish field soils were screened for biocontrol activity. 210 fungal isolates that had advanced to various stages in the screening system were also included in a field experiment. The isolates that were the most effective in controlling seedling blight under natural conditions belonged to the genus Gliocladium. The screening tests separated Gliocladium spp. rather clearly from the rest of test fungi and thus the overall agreement among the results was good. The assays run under controlled conditions did not efficiently predict which of the Gliocladium isolates would be best in protecting wheat seedlings under field conditions.     

Deoxynivalenol and Nivalenol Production by Fusarium culmorum Isolates Differing in Aggressiveness Toward Winter Rye

ABSTRACT A susceptible synthetic winter rye population was inoculated with 42 isolates of Fusarium culmorum, originating from nine European countries and Australia, at two field locations in Germany. Significant (P = 0.01) genetic variation in aggressiveness of isolates of F. culmorum was observed across both field locations. Field samples were used to determine deoxynivalenol (DON), nivalenol (NIV), and ergosterol (ERG) contents. The 42 isolates also were incubated on rye grain in vitro, and DON and NIV contents were analyzed. Thirty-four isolates produced DON, and seven isolates produced NIV at both field locations and in vitro. Mean DON contents ranged from 0.5 to 64.6 mg/kg in grain from field trials and from 0.3 to 376.3 mg/kg in grain incubated in vitro; mean NIV contents ranged from 17.6 to 30.4 mg/kg in grain from field trials and from 0.8 to 381.0 mg/kg in grain incubated in vitro. No correlation was found between the DON content of field-grown grain and grain incubated in vitro. NIV-producing isolates originated from the Netherlands, Germany, Italy, and Australia. More aggressive isolates produced higher mean DON contents in grain in field trials (r = 0.69; P = 0.01). However, DON production rate per unit of fungal biomass, estimated as the DON/ERG ratio at harvest, was not correlated with aggressiveness. Toxin production seemed to be a common feature in F. culmorum. In vitro assays reliably distinguished DON- and NIV-producing types of F. culmorum; however, these assays could not predict production of DON by these isolates in the field.     

Repression of deoxynivalenol accumulation and expression of Tri genes in Fusarium culmorum by fungicides in vitro

A defined medium was developed in which to monitor deoxynivalenol (DON) accumulation, fungal growth and expression of genes involved in trichothecene biosynthesis (designated Tri genes). In liquid culture, DON accumulated shortly after maximum expression of Tri6 and coincident with expression of Tri5. This was generally 96 h after inoculation. The effects of sublethal concentrations of the fungicides azoxystrobin, trifloxystrobin, kresoxim-methyl and tebuconazole on biosynthesis of the trichothecene DON by Fusarium culmorum were studied using this medium. The strobilurin fungicides trifloxystrobin and azoxystrobin significantly reduced the accumulation of DON in culture medium at a range of concentrations. Kresoxim-methyl, also a strobilurin, and tebuconazole, a triazole, did not significantly reduce the accumulation of DON, although levels were lower than those in nonamended cultures. Trifloxystrobin significantly reduced the accumulation of DON when added to cultures before initiation of trichothecene biosynthesis. RT-PCR assays of the expression of Tri6 and Tri5 genes indicated that trifloxystrobin acted by inhibiting the initiation of trichothecene biosynthesis.     

Parasitism of macroconidia, chlamydospores and hyphae of Fusarium culmorum by mycoparasitic Pythium species

Parasitism of macroconidia and endoconidial chlamydospores of Fusarium culmorum by Pythium oligandrum was studied on water agar (WA), corn-meal agar (CMA) and glass slides. Loss of cytoplasmic content in F. culmorum spores was followed by complete degradation, and P. oligandrum produced an abundance of oogonia on the parasitized macroconidia. A simple method for assessing the relative aggressiveness of isolates is presented, based on the percentage of macroconidial cells devoid of cytoplasm. Parasitism of macroconidia by P. acanthophoron , P. oligandrum and P. periplocum , but not by the plant pathogenic species, P. tracheiphilum , was demonstrated by this method. Interactions between hyphae of P. oligandrum and F. culmorum on WA resulted in an increase in the number of oogonia of P. oligandrum and a decrease in the sporulation of F. culmorum . The ability of isolates of P. oligandrum , P. periplocum , P. acanthophoron and P. mycoparasiticum to suppress disease symptoms caused by F. culmorum on barley seedlings was demonstrated in a greenhouse test.     

The contribution of ground-level inoculum of Fusarium culmorum to ear blight of winter wheat

In a series of field experiments in eastern England over 5 years, severe ear blight developed only in plots of winter wheat that were inoculated by spraying with conidial suspensions of Fusarium culmorum during anthesis, and in which infection was encouraged by rainfall or mist irrigation. In the absence of artificial inoculation of the ears, F. culmorum caused less extensive ear blight, and only where soil-surface inoculum was available after its application on infested plant material (colonized oat grains) up to 3–4 weeks before anthesis; it then developed most where significant rainfall occurred close to the time of anthesis. A warm, dry period following application of inoculum to the ground in late March contributed to increased infection of grain by F. culmorum , although ear blight was not increased. Ear infection therefore depended on adequate viable inoculum on infested plant debris within the crop, and conditions tending to favour brown foot rot development as well as, subsequently, rainfall and moist conditions during anthesis. These conditions did not occur together naturally during this period. Seedling infection by F. culmorum or Microdochium nivale made no significant contribution to ear blight. Inoculation of ears at anthesis with M. nivale or a locally obtained isolate of F. langsethiae did not produce ear blight symptoms. Possibilities for minimizing the availability of inoculum of F. culmorum and the implications for various options for ear-blight control are discussed.     

Suppression of wheat-seedling diseases caused by Fusarium culmorum and Microdochium nivale using bacterial seed treatment

Snow mould, caused by Microdochium nivale , and seedling blight caused by members of the Fusarium complex, are cereal diseases of great economic importance in many temperate zones. In a glasshouse bioassay designed to enhance disease, about 600 plant-associated bacterial isolates obtained by different methods were screened for suppressive effects in wheat against infection caused by Fusarium culmorum . Although most of the isolates tested had a neutral effect on test plants and disease development, a few were synergistic to the pathogen and about one-fifth showed > 80% disease suppression. During five consecutive growing seasons, 164 bacterial isolates were tested in field experiments against both F. culmorum and M. nivale as causal agents of seedling blight. Tests for effects on yield in experiments with spring and winter wheat, performed in different climatic regions of Sweden, showed that disease-suppressive effects were repeatable. The most efficient isolates, three fluorescent pseudomonads and a species of Pantoea , suppressed disease equal to that of the fungicide guazatine, both with respect to crop stand and yield. Seed treatment with Pantoea sp. (isolate MF 626) increased yield by an average of more than 500 kg ha⁻¹ in six field experiments.     

Genetic Variability and Population Structure of the Wheat Foot Rot Fungus, Fusarium culmorum, in Tunisia

The random amplified polymorphic DNA (RAPD) method was used to investigate the genetic variability and population structure of Fusarium culmorum isolated from wheat stem bases. A total of 108 isolates, representing seven geographically distinct populations, was collected from five climatic regions in Tunisia. Pseudo-allelic frequencies were estimated at each of the 25 putative RAPD loci analyzed by scoring for the presence or absence of amplified fragments; 92 haplotypes were found among the 108 strains. The analysis of the population structure did not reveal any trend with regard to geographic origin. Total gene diversity (H_T ^* = 0.318) was mostly attributable to diversity within populations (H_S ^* = 0.308). Analysis of molecular variance confirmed that most of the genetic variability was within populations. Genetic differentiation among populations was low to moderate (G_ST ^* ranged from 0 to 0.190 and averaged 0.041 over all loci). Cluster analysis with UPGMA using genetic distances did not reveal any spatial clustering of the isolates collected from the different geographic regions. Based on these results, we conclude that the F. culmorum isolates recovered from different regions in Tunisia might be part of a single population pool.     

Effect of temperature on head blight of wheat caused by Fusarium culmorum and F. graminearum

The effect of small temperature differentials (16 vs. 20°C) on the pathogenicity of deoxynivalenol producing single isolates of Fusarium culmorum and F. graminearum and on the fusarium head blight (FHB) response of eight wheat cultivars was examined. Fusarium culmorum inoculation caused greater visual disease symptoms at 20°C than at 16°C, both overall and on an individual cultivar basis (overall AUDPC = 13·5 and 9·6, respectively) ( P  < 0·05). In contrast, F. graminearum inoculation caused greater overall visual disease symptoms at 16°C than at 20°C, both overall and at the individual cultivar level (overall AUDPC = 12·8 and 10·9, respectively) ( P  < 0·05). Results showed both F. culmorum and F. graminearum inoculations caused a greater loss in yield at 20°C (54·3 and 46·9% relative 1000-grain weight, respectively) compared with 16°C (73·3 and 66·9% relative 1000-grain weight, respectively) ( P  < 0·05). Fusarium culmorum -inoculated heads contained similar amounts of fungal DNA at both 16 and 20°C (1·9 and 1·7 ng mg⁻¹ of plant material, respectively) (not significant), while for F. graminearum inoculation, plants contained higher amounts of fungal DNA at 20°C (2·0 and 1·0 ng mg⁻¹ of plant material, respectively) ( P  < 0·05). Overall, there was a significant negative correlation between AUDPC and percentage relative 1000-grain weight at both 16 and 20°C ( r  =−0·693 and −0·794, respectively, P  < 0·01).     

Competition Effects Among Isolates of Fusarium culmorum Differing in Aggressiveness and Mycotoxin Production on Heads of Winter Rye

Fusarium culmorum is a phytopathogenic, toxigenic fungus causing seedling diseases, foot rot and head blight of cereals. For estimating competition effects in mixtures of two single-spore isolates, two winter rye single crosses were tested with either four isolates individually or four 1 : 1 mixtures of the same isolates in six field environments. Two isolates (FC46, FC64) were highly aggressive deoxynivalenol (DON) and 3-acetyl DON-producers, the other two (FC30, FC71) were medium aggressive nivalenol-producers. Rye heads were inoculated during flowering with conidia of pairs of isolates expressing similar (FC46 + FC64, FC30 + FC71) or contrary (FC46 + FC71, FC30 + FC64) levels of aggressiveness and similar or different concentrations and chemotypes of mycotoxins, respectively. Head blight rating and yield components relative to the non-inoculated plots were recorded as aggressiveness traits. Additionally, mycotoxin concentrations were measured in the rye grain. Random pathogen samples were re-isolated from heads at the onset of symptom development and analysed by molecular markers (RAPD–PCR) in one environment. Aggressiveness of the isolate mixtures was significantly lower than that of the isolates applied individually on both rye genotypes. Similarly, mycotoxin concentrations were significantly lower in the mixtures in seven out of eleven comparisons. Among the re-isolates, the component genotypes of a mixture significantly deviated from the inoculated 1 : 1 ratio when a particular isolate (FC46) was present in the mixture. This isolate displayed a superior competitive ability irrespective of the aggressiveness or mycotoxin profile of the mixing partner illustrating that pathogenic fitness is caused by additional factors that have not, as yet, been identified.     

Evaluation and characterization of resistance to fusarium head blight caused by Fusarium culmorum in UK winter wheat cultivars

Fusarium head blight (FHB) resistance of 50 cultivars from the National List of winter wheat cultivars approved for sale (or were undergoing trails for approval in 2003) in the UK was compared with 21 reference cultivars from continental Europe which had previously been characterized for resistance. Only three UK National List cultivars (Soissons, Spark and Vector) had stable resistance over trial sites that was significantly greater than that of the FHB susceptible cultivar Wizard. In addition, under moderate disease pressure, 21 of the National List cultivars had levels of the trichothecene mycotoxin deoxynivalenol (DON) above the proposed European Union limit of 1·25 ppm in grain. Surveys show that levels of FHB and DON in the UK crop are currently very low, however, should disease pressure increase for any reason, then an improvement in the overall levels of FHB resistance of UK winter wheat germplasm will be required. In order to infer the origin of resistance and to identify potentially novel resistance, allele sizes of microsatellite (simple sequence repeat, SSR) markers linked to quantitative trait loci (QTL) for FHB resistance were compared between the test cultivars and known, characterized resistance sources. The major FHB resistance QTL from the Chinese cv. Sumai-3 (3BS, 5A and 6B), the Romanian cv. Fundulea F201R (1B and 5A) and the French cv. Renan (5AL) were screened with 17 SSRs. No National List cultivar had haplotypes similar to any of these QTL. However, the highly resistant German reference cultivar Petrus had an identical haplotype to cv. Fundulea F201R on 1B indicating that this cultivar has an allelic FHB resistance QTL at that location.