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Fusarium head blight (scab) is a devastating disease of wheat and barley throughout the world. The disease has been reported worldwide wherever cereals are grown, cutting across diverse ecological and geographical distribution. In addition to being pathogenic to plants, which may cause severe crop yield reduction, many Fusarium species are also capable of producing mycotoxins deleterious to human health as secondary metabolites. Fusarium toxins are commonly detected in wheat, barley, maize, rice and beer. Traditionally malted barley (Hordeum vulgare L.) is the principal ingredient in clear beer and Fusarium toxins incidences are of major concern. Moreover, the spent grain from the brewing industry is used as feed and presence of mycotoxins can lead to harmful effects on domestic animals and also find a way into the human food chain. Studies carried out in Kenya have revealed presence of various Fusarium species with ability to produce mycotoxins and presence of Fusarium toxins in wheat and maize and beer. Based on the ubiquitous nature of Fusarium mold and the fact that barley production takes place in maize and wheat growing areas, this study set out to investigate the occurrence of Fusarium molds in Equatorial barley grown in Kenya and the ability of the isolates to produce selected mycotoxins. Grain samples were obtained from newly delivered barley lots originating from two regions and stored grain awaiting malting after break of dormancy from Kenya Maltings Ltd., Nairobi. The Fusarium isolates were identified to species level based on cultural and morphological characteristics. Additionally, they were screened in-vitro on rice cultures for their ability to produce Type A trichothecenes (T-2 toxin, HT-2 toxin, Diacetoxyscirpenol), Type B trichothecenes (deoxynivalenol and nivalenol) and Zearalenone. Samples from all sources were contaminated with Fusarium, but at varying magnitudes - 50%, 33.3% and 25% for barley kernels originating from Timau, Olchoro and in-storage grain with no common history of origin, respectively. The distribution of the species showed some regional specificity. F. graminearum and F. poae predominated in kernels sourced from Olchoro region. All strains of F. graminearum produced both deoxynivalenol and zearalenone. F. poae strains and F. chlamydosporum did not produce detectable amounts of the screened mycotoxins. However, two inconclusively identified isolates of Fusarium spp. isolated from Timau samples produced deoxynivalenol only. The study revealed that a number of toxigenic Fusarium spp. do occur in Equatorial barley grown in Kenya. Key words: Barley, Fusarium, trichothecenes, zearalenone, Kenya., INTRODUCTION Most genera of cultivated plants are susceptible to diseases caused by Fusarium species including all members of the Gramineae family [1]. Fusarium head blight (scab) is a devastating disease [...]

Control of Fusarium head blight (FHB), incited primarily by Fusarium graminearum Schwabe [telomorph Gibberella zea (Schwein)], has been a challenge for barley (Hordeum vulgare L.) producers in the upper midwestern United States for more than a decade. This disease manifests primarily in the form of food safety issues and quality discounts due to the presence of deoxynivalenol (DON), a mycotoxin produced by the pathogen. Cultural practices and fungicides only provide partial control; genetic resistance to FHB and DON accumulation may add to control of the disease. Field studies in North Dakota and China were conducted in FHB disease nurseries using 118 double-haploid lines from the cross C93-3230-24/'Foster'. Foster is susceptible to FHB, and C93-3230-24 is moderately resistant. The quantitative trait locus (QTL) analysis revealed five putative QTL for Type I FHB resistance; however, only the one in bins 7 and 8 of chromosome 2H was detected in more than 70% of the environments. In addition, QTL associated with late days to heading and maturity and tall plant height also were located in the same region. Three putative QTL for increased DON accumulation were detected; however, none were detected in more than three of the eight environments where data were collected. On the basis of these results, it is unlikely that C93-3230-24 has a novel QTL for FHB resistance different from those identified in other resistant accessions. However, C93-3230-24 is unique in that it provides QTL for improved FHB resistance but not reduced DON accumulation. This is an atypical response compared with other sources of FHB resistance and provides evidence that FHB resistance and DON accumulation are under separate genetic control.

Molecular marker technology shows potential to select and combine favorable alleles via genotypic selection and can be used to develop improved crop cultivars with considerable resource savings. In the present investigation, the utility of molecular markers for net blotch resistance identified in Australian breeding material was investigated for Canadian breeding material. Screening 42 Canadian, Australian, and international barley (Hordeum vulgare L.) lines with 10 Canadian Pyrenophora teres Drechs. isolates identified three lines resistant to all isolates evaluated. Net-form net blotch isolates were more virulent than spot-form net blotch isolates. The strong agreement between seedling and adult-plant reactions indicated that seedling screening could be useful for selection for adult-plant resistance. Evaluation of the inheritance of resistance in four Australian populations against Canadian P. teres isolates revealed one to three resistance genes, depending on the isolate used. The majority of Australian barley mapping population parents were susceptible to Canadian P. teres isolates, suggesting markers linked to their resistance may not be useful for Canadian breeding; however, some molecular markers identified by Australian workers could be used for Canadian barley breeding. This study demonstrates that the differences in germplasm and fungal pathogen strains used in different countries result in molecular markers that may not be applicable in all breeding programs for that crop.

Breeding for resistance to Fusarium head blight {FHB; caused by Fusarium graminearum Schwabe [teleomorph Gibberella zeae (Schwein) Petch]} is complicated because there is no accurate method for quantifying the disease organism. Most breeders rely on visual scoring for FHB and deoxynivalenol (DON) analysis to assess disease severity, but both DON and visual scoring are subject to error. The objective of this study was to compare a Fusarium-specific quantifiable enzyme-linked immunosorbent assay (ELISA) to DON and visual assessment of FHB. A doubled-haploid mapping population was grown in two environments and breeding lines in the North American Barley Scab Evaluation Nursery (NABSEN) were grown at four locations. Both experiments used a randomized complete block design and were analyzed for Fusarium by ELISA, DON, and visually scored for FHB. ELISA values for the doubled-haploid lines were consistent over years, and lines that were low in ELISA were also Iow in DON. Broad sense heritability was greater for ELISA (0.48) than DON (0.19) or visual scores of disease (0.29) in the NABSEN study. Numbers of locations and replications necessary to screen for disease were calculated for ELISA, DON, ancl FHB. ELISA required one-third to one-fourth as many replications and locations as did DON or FHB. Temperature and osmotic potential had little effect on mycelial antigen used for ELISA in vitro, but both affected DON. ELISA is a practical alternative to combined visual scores and DON analysis for breeders interested in improving FHB resistance.

Inheritance studies on the nonhost resistance of plants would normally require interspecific crosses that suffer from sterility and abnormal segregation. Therefore, we developed the barley-Puccinia rust model system to study, using forward genetics, the specificity, number, and diversity of genes involved in nonhost resistance. We developed two mapping populations by crossing the line SusPtrit, with exceptional susceptibility to heterologous rust species, with the immune barley cultivars Vada and Cebada Capa. These two mapping populations along with the Oregon Wolfe Barley population, which showed unexpected segregation for resistance to heterologous rusts, were phenotyped with four heterologous rust fungal species. Positions of QTL conferring nonhost resistance in the three mapping populations were compared using an integrated consensus map. The results confirmed that nonhost resistance in barley to heterologous rust species is controlled by QTL with different and overlapping specificities and by an occasional contribution of an R-gene for hypersensitivity. In each population, different sets of loci were implicated in resistance. Few genes were common between the populations, suggesting a high diversity of genes conferring nonhost resistance to heterologous pathogens. These loci were significantly associated with QTL for partial resistance to the pathogen Puccinia hordei and with defense-related genes.

A trichothecene biosynthesis gene (TRI)-based PCR assay is employed to analyze a collection of 336 isolates from Gibberella zeae from barley, wheat, potatoes, and sugar beets and determine the toxigenic potential of G. zeae. The findings from the studies might be applied to monitor mycotoxin contamination and to formulate Fusarium head blight (FHB) management strategies for these crops.

PAV, one of the luteoviruses inducing the barley yellow dwarf disease, greatly reduces yield of cereal crops and has been reported to cause reddening in several varieties of maize (Zea mays L.). However, there have been no reports that the virus causes significant reductions in size or yield of irrigated maize. Trials to assess the effect of PAV on maize yields were conducted for 3 yr with two hybrids (`Dea' and `Nobilis') and two isolates of PAV (2t and L14). These two isolates differed in geographic origin and virulence on barley (Hordeum vulgare L.), but they multiplied similarly to wild isolates in leaves of maize hybrids. The virus was detected in maize leaves during the same period after inoculation in two out of three years. The reason for low levels of virus in leaves in the 1996 season may have been high temperatures ([is greater than] 30 ° C) following inoculation. Under these conditions, the virus was restricted to the roots for long periods. This blocking of virus migration and/or foliar multiplication was accompanied by less reddening, and there was almost no decrease in grain yield. High early leaf infection of the virus had little effect on the vegetative development of the hybrids ([is less than] 10% reduction in plant height), but grain yield was between 15 and 20% lower for a production of 10 to 12 t [ha.sup.-1]. This drop in yield was due to fewer kernels of maize per ear, while the 1000 kernel mass was unaffected. The loss in yield was not affected by either the virus isolate or the maize hybrid, although the intensity of symptoms differed between hybrids. The data show that there are potential losses incurred by PAV on maize yield. Therefore, these findings justify the establishment of a breeding program., BARLEY YELLOW DWARF VIRUSES (BYDVs) are frequently encountered in maize crops in temperate areas. Those viruses of similar biology designated GPV, MAV, PAV, RMV, RPV, and SGV have been detected [...]

When Russian wheat aphids dine on tender young barley plants, they leave a trail of microscopic puncture marks on the leaves. Scientists are finding that the more of these tracks [...]