A comparative assessment of potential components of partial disease resistance to Fusarium head blight using a detached leaf assay of wheat, barley and oats

2005 ◽  
Vol 112 (3) ◽  
pp. 247-258 ◽  
Author(s):  
R.A. Browne ◽  
B.M. Cooke
Author(s):  
Juho Hautsalo ◽  
Satu Latvala ◽  
Outi Manninen ◽  
Minna Haapalainen ◽  
Asko Hannukkala ◽  
...  

Abstract Cultivar resistance is essential for the management of Fusarium head blight (FHB) disease in oat production. However, the breeders lack methods suitable for phenotyping disease resistance and resistance sources. In this paper we compared two oat genotypes, a rejected variety BOR31 and a landrace VIR7766, with four different traits that could reflect resistance to FHB in a greenhouse environment. Spray and point inoculations were used to inoculate Fusarium graminearum into flowering oat plants. When spray-inoculated, VIR7766 was significantly more resistant against the initial infection than BOR31, measured by the number of Fusarium-infected kernels and by DON accumulation. In the point-inoculated oats, the loss of fresh weight in the inoculated spikelet correlated well with the increasing F. graminearum biomass in the spikelet, measured six days after inoculation. However, no difference in the growth of the fungus was observed between the tested oat genotypes by point inoculation. We speculate that once the infection is established, the ability of the oat plant to resist the spread of the infection within a spikelet is low in the genotypes studied, although oat, in general, due to its panicle structure, is considered to have a high resistance against Fusarium infection.


2014 ◽  
Vol 94 (2) ◽  
pp. 371-381 ◽  
Author(s):  
Gary Martens ◽  
Lakhdar Lamari ◽  
Ardelle Grieger ◽  
Robert H. Gulden ◽  
Brent McCallum

Martens, G., Lamari, L., Grieger, A., Gulden, R. H. and McCallum, B. 2014. Comparative yield, disease resistance and response to fungicide for forty-five historic Canadian wheat cultivars. Can. J. Plant Sci. 94: 371–381. Forty-five historic Canadian spring wheat cultivars, ranging from Red Fife (1870) to modern cultivars, were compared for yield and disease resistance in field trials from 2007 to 2010. A split-plot design was used to test yield, leaf rust and Fusarium head blight resistance, with or without a fungicide application. Older cultivars were generally lower yielding and more leaf rust susceptible than modern cultivars; this difference was greatest in 2007 and 2010 under heavier leaf rust. Response to fungicide application was highest in 2007 and 2010. In 2008, leaf rust was very low, and fungicide application had a slightly negative effect on yield overall. Cultivars that have good leaf rust resistance, such as Pasqua, AC Minto, and 5600 HR, had a negligible response to fungicide, whereas older, susceptible cultivars had a larger response. Fusarium head blight levels were too low to compare the cultivars. The highest-yielding cultivars in the untreated plots were AC Domain, 5500HR, AC Cora, Roblin and Barrie, whereas AC Cora, AC Domain, McKenzie, Roblin and AC Intrepid were the highest yielding in the fungicide-treated plots. AC Domain, AC Barrie and Roblin were among the most popular wheat cultivars in Manitoba, in terms of seeded area from the early 1990s to 2009.


2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Jyotirmoy Halder ◽  
Jinfeng Zhang ◽  
Shaukat Ali ◽  
Jagdeep S. Sidhu ◽  
Harsimardeep S. Gill ◽  
...  

Abstract Background In the late 1920s, A. E. Watkins collected about 7000 landrace cultivars (LCs) of bread wheat (Triticum aestivum L.) from 32 different countries around the world. Among which 826 LCs remain viable and could be a valuable source of superior/favorable alleles to enhance disease resistance in wheat. In the present study, a core set of 121 LCs, which captures the majority of the genetic diversity of Watkins collection, was evaluated for identifying novel sources of resistance against tan spot, Stagonospora nodorum blotch (SNB), and Fusarium Head Blight (FHB). Results A diverse response was observed in 121 LCs for all three diseases. The majority of LCs were moderately susceptible to susceptible to tan spot Ptr race 1 (84%) and FHB (96%) whereas a large number of LCs were resistant or moderately resistant against tan spot Ptr race 5 (95%) and SNB (54%). Thirteen LCs were identified in this study could be a valuable source for multiple resistance to tan spot Ptr races 1 and 5, and SNB, and another five LCs could be a potential source for FHB resistance. GWAS analysis was carried out using disease phenotyping score and 8807 SNPs data of 118 LCs, which identified 30 significant marker-trait associations (MTAs) with -log10 (p-value) > 3.0. Ten, five, and five genomic regions were found to be associated with resistance to tan spot Ptr race 1, race 5, and SNB, respectively in this study. In addition to Tsn1, several novel genomic regions Q.Ts1.sdsu-4BS and Q.Ts1.sdsu-5BS (tan spot Ptr race 1) and Q.Ts5.sdsu-1BL, Q.Ts5.sdsu-2DL, Q.Ts5.sdsu-3AL, and Q.Ts5.sdsu-6BL (tan spot Ptr race 5) were also identified. Our results indicate that these putative genomic regions contain several genes that play an important role in plant defense mechanisms. Conclusion Our results suggest the existence of valuable resistant alleles against leaf spot diseases in Watkins LCs. The single-nucleotide polymorphism (SNP) markers linked to the quantitative trait loci (QTLs) for tan spot and SNB resistance along with LCs harboring multiple disease resistance could be useful for future wheat breeding.


2021 ◽  
pp. 9-18
Author(s):  
Oleh Hrytsev ◽  
Oleg Liudvinovskyi ◽  
Julia Shevchenko ◽  
Veronika Dzhagan ◽  
 Larysa Skivka

Fusarium species infect cereal spikes during anthesis and cause Fusarium head blight (FHB), a destructive disease of cereal crops with worldwide economic relevance. The necessity for these phytopathogenic fungi effective control becomes increasingly important for the production of both cultivated plants and those plants seeds. Fungicide application is a key methodology for controlling the disease development and mycotoxin contamination in cereals. Polymerase chain reaction (PCR) is currently the most commonly admitted DNA-based technology for specific, rapid and precise Fusarium detection. We have developed and patented the method for detection and quantitative determination of phytopathogenic fungi F. avenaceum and F. graminearum in plant seeds using Real-Time PCR with a pair of primers, designed to amplify sequences of the internal transcribed spacer at the ribosomal RNA gene cluster of those phytopathogenic fungi. This study was aimed to perform a comparative assessment of the efficacy of different spray nozzles for antifungal treatment to control F. avenaceum and F. graminearum infection of barley grains using a developed qPCR diagnostic system. A single application of a fungicide (active ingredient's content: 250 g/l propiconazole, 80 g/l cyproconazole) at BBCH 65 (middle of flowering) was carried out. For this purpose, four spray nozzles with different technical characteristics were used: Flat Fan 030, Amistar 030, Defy 3D 030 and Vegetable 060 (Pentair, USA). DNA-based fungi detection and identification was performed using conventional PCR and developed qPCR. The level of mycotoxins in barley grain was determined using enzyme-linked immunosorbent assay (ELISA). Grain count in the ear of barley and thousand seed weight (TSW) were also examined. A single application of the fungicide inhibited the development of FHB and is accompanied by the slight increase of TSW values in treated plants. It was found, that the most effective fungicide was against F. avenaceum and F. graminearum. The inhibitory effect depended on sprayer type. According to qPCR results, the best performance was achieved when using Amistar 030 and Flat Fan (FF) 030 sprayers. The average concentration of deoxynivalenol (DON) content in all barley grain samples were up to 4 times higher than the permissible level. Overall, because of the high contamination levels, found in tested samples, it is possible to state that a single application of the fungicide at the flowering phase was not able to effectively reduce DON contamination in barley samples. The developed test-system for qPCR provides new important information in the study of the effectiveness of fungicides and development of strategies to control FHB in cereals, not achievable with conventional PCR.


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