Evidence that wheat cultivars differ in their ability to build up inoculum of the take-all fungus, Gaeumannomyces graminis var. tritici, under a first wheat crop

2010 ◽  
Vol 60 (2) ◽  
pp. 200-206 ◽  
Author(s):  
V. E. McMillan ◽  
K. E. Hammond-Kosack ◽  
R. J. Gutteridge
1987 ◽  
Vol 38 (6) ◽  
pp. 1011 ◽  
Author(s):  
GC MacNish ◽  
DA Nicholas

The relationship between grass production in subterranean clover pastures with two different rotation histories and take-all in a subsequent wheat crop following barley was studied. Grass production in the pastures ranged from 0 to 1700 kg ha-1. The incidence of take-all in the wheat crop ranged from 10 to l00%, while the take-all severity percentage ranged from 4 to 99.In one rotation series (pasture 9 years; barley, barley, pasture, wheat), each kilogram increase in grass production in the last pasture year caused a 0.087% increase in the take-all severity rating. In the second series (pasture 7 years; oats, pasture 3 years; barley, wheat), each kilogram increase in grass production caused a 0.040% increase in severity. These figures are significantly different (P < 0.05). Thus the field history ranging back at least four seasons influenced the effects that grass level in the last pasture year had on take-all severity. Reductions in wheat yields ranged from 8.6 to 10.5 kg ha-1 for each 1% increase in take-all severity rating.


1979 ◽  
Vol 93 (2) ◽  
pp. 377-389 ◽  
Author(s):  
D. B. Slope ◽  
R. D. Prew ◽  
R. J. Gutteridge ◽  
Judith Etheridge

SUMMARYThe Rothamsted ley–arable experiments were on two fields with similar soils but with contrasting previous cropping: old grass on Highfield, old arable on Fosters field. Damage by take-all (Qaeumannomyces graminis var. tritici) occurred sooner in successive wheat crops grown after a lucerne ley and arable sequence (LU) than after a grass-clover ley and arable sequence (LC). On Highfield the difference was consistent and large, it occurred as soon as a second wheat crop was grown and resulted in wheat yielding 1 t/ha less after the LU than after the LC sequence. This difference did not persist in the next wheat crop where take-all was prevalent after both sequences. On Fosters field take-all developed more slowly and differences between sequences were mostly smaller.Wheat seedling bio-assay of soil cores from the LU and LC sequences showed that little take-all fungus persisted through the leys and that soils were much infested after a first wheat crop in the LU sequence on Highfield, but not in the LC sequence on Highfield or in either sequence on Fosters field. Microscopic examination of roots from assay seedlings and from field plants showed that Phialophora radicicola var. graminicola (PRG) was most common in soils where take-all developed slowly, but our results did not show if this was a causal relationship. The occurrence of much PRG in the LU sequence on Fosters conflicts with previous reports which associate large populations of this fungus only with grassland soils.


1991 ◽  
Vol 31 (4) ◽  
pp. 509 ◽  
Author(s):  
DK Roget ◽  
AD Rovira

. This paper describes results obtained from an 8-year field trial on a calcareous sandy loam in South Australia. Different crop rotations resulted in varying percentages of plants with take-all [caused by Gaeumannomyces graminis var. tritici (Ggt)]. The results demonstrated that in a wheat-grass/medic pasture rotation, take-all caused an average annual yield loss in wheat of 29%. These yield losses were strongly correlated with disease incidence and rainfall in September (r2 = 0.91, P = 0.07) but only moderately correlated to disease incidence alone (r2 = 0.44, P = 0.09). The level of early infection (at 10 weeks) by Ggt was influenced by spring rainfall in the previous season. A regression model was developed to predict the incidence of take-all in a wheat crop from the incidence of take-all and the August-September rainfall the previous season (r2 = 0.96, P = 0.007) for a wheat-grass/medic pasture rotation (successive host plants).


2010 ◽  
Vol 100 (5) ◽  
pp. 404-414 ◽  
Author(s):  
Youn-Sig Kwak ◽  
Peter A. H. M. Bakker ◽  
Debora C. M. Glandorf ◽  
Jennifer T. Rice ◽  
Timothy C. Paulitz ◽  
...  

Dark pigmented fungi of the Gaeumannomyces–Phialophora complex were isolated from the roots of wheat grown in fields in eastern Washington State. These fungi were identified as Phialophora spp. on the basis of morphological and genetic characteristics. The isolates produced lobed hyphopodia on wheat coleoptiles, phialides, and hyaline phialospores. Sequence comparison of internal transcribed spacer regions indicated that the Phialophora isolates were clearly separated from other Gaeumannomyces spp. Primers AV1 and AV3 amplified 1.3-kb portions of an avenacinase-like gene in the Phialophora isolates. Phylogenetic trees of the avenacinase-like gene in the Phialophora spp. also clearly separated them from other Gaeumannomyces spp. The Phialophora isolates were moderately virulent on wheat and barley and produced confined black lesions on the roots of wild oat and two oat cultivars. Among isolates tested for their sensitivity to 2,4-diacetylphloroglucinol (2,4-DAPG), the 90% effective dose values were 11.9 to 48.2 μg ml–1. A representative Phialophora isolate reduced the severity of take-all on wheat caused by two different isolates of Gaeumannomyces graminis var. tritici. To our knowledge, this study provides the first report of an avenacinase-like gene in Phialophora spp. and demonstrated that the fungus is significantly less sensitive to 2,4-DAPG than G. graminis var. tritici.


Author(s):  
J. Walker

Abstract A description is provided for Gaeumannomyces graminis var. tritici. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Gramineae, especially Triticum, Hordeum, Secale, Agropyron and several other grass genera and, more rarely, Sorghum and Zea; also recorded from the roots of plants in other families. DISEASE: Take-all of cereals and grasses (also referred to as deadheads or whiteheads, pietin and pied noir (France), Schwarzbeinigkeit and Ophiobolus Fusskrankheit (Germany), Ophiobolusvoetziekt (Netherlands) and others). Root infection is favoured by soil temperature from 12-20°C (Butler, 1961). Ascospore germ tubes penetrate root hairs and the epidermis in the meristematic region (Weste, 1972) leading to plugging of xylem and root death. GEOGRAPHICAL DISTRIBUTION: (CMI Map 334, ed. 3, 1972). Widespread, especially in temperate zones. Africa; Asia (India, Iran, Japan, USSR): Australasia and Oceania; Europe; North America (Canada, USA); South America (Argentina, Brazil, Chile, Colombia, Uruguay). TRANSMISSION: In soil on infected organic fragments, as runner hyphae on roots of cereals and grasses and, under special conditions, by ascospores. Seed transmission very doubtful (47, 3058).


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