Fusarium head blight (FHB) and contamination with deoxynivalenol (DON) prod
uced by the primary pathogen Fusarium graminearum Schwabe [teleomorph Gibbe
rella zeae (Schwein.)] have caused devastating losses to wheat (Triticum ae
stivum L.), durum (Triticum turgidum L. ssp. durum Desf.Husr.), and barley
(Hordeum vulgare L.) growers across the USA since the early 1990s. Evaluati
on of barley, wheat, and related germplasm yielded only a few accessions wi
th partial resistance. This resistance appears, in most cases, to be under
polygenic control, making the development of resistant cultivars with suita
ble agronomic and quality traits a challenge. The insertion of individual a
ntifungal and antitoxin genes via genetic transformation has the potential
to aid in development of resistant wheat and barley cultivars. Although whe
at and barley transformation has been achieved in several laboratories, the
development of a high throughput wheat and barley transformation systems h
as been slowed by genotype effects on plant regeneration, low transformatio
n efficiencies, somaclonal variation, and problems with transgene inheritan
ce and stability of expression. Among the antifungal genes targeted to comb
at FHB are coding sequences for proteins that degrade fungal cell walls, di
sorganize fungal membranes, bolster the host defense response systems, and
interfere with fungal protein synthesis, pathogenesis, and/or accumulation
of DON. Promoter sequences have been selected that confer high levels of ex
pression to the antifungal constructs, particularly in the spike tissues wh
ich are susceptible to FHB. As more antifungal genes are inserted into whea
t and barley, field and greenhouse evaluation will show whether transgenes
achieve their potential in the fight against FHB.