This review of Fusarium ear blight (scab) of small grain cereals has shown that up to 17 causal organisms have been associated with the disease, which occurs in most cereal‐growing areas of the world. The most common species were Fusarium graminearum (Gibberella zeae), F. culmorum, F, avenaceum (G, avenacea), F, poae and Microdochium nivale (Monographella nivalis). The disease was recorded most frequently under hot, wet climatic conditions where significant yield losses and mycotoxin accumulation in grain were reported. Possible sources of inoculum were reported as crop debris, alternative hosts and Fusarium seedling blight and foot rot of cereals. The mode of dispiersal of inoculum to ears remains unclear, but contaminated arthropod vectors, systemic fungal growth through plants, and wind and rain‐splash dispersal of spores have been proposed. Infection of wheat ears was shown to occur mainly during anthesis, and it has been demonstrated that fungal growth stimulants may be present in anthers. Despite the importance of the disease, particularly during epidemic years, control methods are limited. Much effort has gone into breeding resistant wheat varieties and into improving our understanding of the possible mechanisms and genetic basis of resistance, with only moderate success. There are also surprisingly few reports of successful fungicidal or biological control of the disease in the field.
Two years of field sampling aimed to establish the predominance and association among the fungal pathogens causing Fusarium ear blight (FEB) in four European countries (Hungary, Ireland, Italy and the UK). A PCR-based method was used to detect four Fusarium species and two varieties of Microdochium nivale present in the samples. The prevalence of FEB pathogens differed significantly between countries. Overall, all pathogens were commonly detected in Ireland and to a lesser extent in the UK. In contrast, only two species, F. graminearum and F. poae, were regularly detected in Italy and Hungary. Fusarium culmorum was rarely detected except in Ireland. Log-linear models were used to determine whether there is the independence of the six FEB pathogens at each sampling site. Significant two-pathogen interactions were frequently observed, particularly in harvest samples; all these significant two-pathogen interactions were of the synergistic type, except between F. poae and F. culmorum, and were generally consistent over the 2 years and four countries. Fusarium graminearum and F. poae were least frequently involved in two pathogen interactions but were involved in most of the nine significant three-pathogen interactions. However, only the interaction between F. graminearum, F. avenaceum and F. poae was significant in both years. Potential implications of the present results in FEB management are discussed.
Diverse isolates of the soilborne wilt fungi Verticillium dahliae and V. albo-atrum were studied to understand the nature and origins of those infecting cruciferous hosts. All isolates from cruciferous crops produced microsclerotia, and the majority produced long conidia with a high nuclear DNA content; these isolates were divided into two groups by amplified fragment length polymorphism (AFLP) analysis. One group could be subdivided by other criteria such as rRNA sequences and mitochondrial DNA restriction fragment length polymorphism (RFLP) analysis. Two crucifer isolates were short spored and had a low nuclear DNA content. The results are consistent with the crucifer isolates being interspecific hybrids. The long-spored isolates are best regarded as amphihaploids (or allodiploids) with the AFLP groups probably each representing separate interspecific hybridization events. The short-spored crucifer isolates appear to be derived from interspecific hybrids and are here called 'secondary haploids'. Molecular evidence suggests that one parent in the crosses was similar to V. dahliae. The other parent of the amphihaploids seems to have been more similar to V. albo-atrum than to V. dahliae, but was distinct from all isolates of either species so far studied. The implications for the taxonomy of crucifer isolates are discussed and the use of the name V. longisporum, proposed elsewhere for just some of these isolates, is discouraged.
Polymerase chain reaction (PCR) assays for the detection of various Fusarium species and Microdochium nivale subspecies were compared with conventional visual disease assessment using a field plot of wheat in which the central subplot was inoculated with F. culmorum. Visual disease assessment was performed on a range of samples taken from each of 15 subplots at growth stage 80. At harvest, each sample was divided into its component parts, i.e. grain, glume and rachis, and species-specific PCR analysis was used to detect the presence of F. culmorum, F. poae, F. avenaceum, F. graminearum, M. nivale var. majus and M. nivale var. nivale. Within the inoculated subplot there was good correlation between visual disease assessment and PCR analysis, both techniques indicating a high incidence of F. culmorum in this region. According to the visual disease assessment results, there was also a relatively high incidence of F. culmorum in most other regions of the field plot. However, according to PCR analysis the incidence of F. culmorum in many of the other subplots was relatively low and F. poae, M. nivale var. majus and var. nivale, and F. avenaceum were detected within the grain, glume and rachis tissues of many of the ear samples from these subplots. F. poae predominated in the glume component of ears and M. nivale var. majus and var. nivale in the rachis component. M. nivale PCR results revealed that 64% of infected samples involved var. majus, and 36% var. nivale. PCR analysis has highlighted some difficulties that may arise when using visual assessment for studying disease complexes.
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