cercosporin has been researched along with Disease-Resistance* in 2 studies
2 other study(ies) available for cercosporin and Disease-Resistance
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Engineering Cercospora disease resistance via expression of Cercospora nicotianae cercosporin-resistance genes and silencing of cercosporin production in tobacco.
Fungi in the genus Cercospora cause crop losses world-wide on many crop species. The wide host range and success of these pathogens has been attributed to the production of a photoactivated toxin, cercosporin. We engineered tobacco for resistance to Cercospora nicotianae utilizing two strategies: 1) transformation with cercosporin autoresistance genes isolated from the fungus, and 2) transformation with constructs to silence the production of cercosporin during disease development. Three C. nicotianae cercosporin autoresistance genes were tested: ATR1 and CFP, encoding an ABC and an MFS transporter, respectively, and 71cR, which encodes a hypothetical protein. Resistance to the pathogen was identified in transgenic lines expressing ATR1 and 71cR, but not in lines transformed with CFP. Silencing of the CTB1 polyketide synthase and to a lesser extent the CTB8 pathway regulator in the cercosporin biosynthetic pathway also led to the recovery of resistant lines. All lines tested expressed the transgenes, and a direct correlation between the level of transgene expression and disease resistance was not identified in any line. Resistance was also not correlated with the degree of silencing in the CTB1 and CTB8 silenced lines. We conclude that expression of fungal cercosporin autoresistance genes as well as silencing of the cercosporin pathway are both effective strategies for engineering resistance to Cercospora diseases where cercosporin plays a critical role. Topics: Ascomycota; Disease Resistance; Drug Resistance, Fungal; Gene Expression Regulation, Fungal; Gene Silencing; Genes, Fungal; Genetic Engineering; Nicotiana; Perylene; Plants, Genetically Modified; Transformation, Genetic; Transgenes | 2020 |
In vitro screening of calli of mungbean to cercosporin, a photoactivated toxin.
Mungbean or Green gram [Vigna radiata (L.) R. Wilczek] is an arid/semiarid pulse crop, native to India, grown mostly as a rotational crop with cereals like wheat, rice, maize, sorghum, etc. It is an affordable source of protein, carbohydrate, vitamins and minerals preferred for its nutrient digestibility, food processing properties and bioavailability. India accounts for 65% of mungbean’s world acreage and 54% of its world production. Various pests, diseases and environmental stresses have kept mungbean yield quite unstable over decades and researcher’s worldover are looking for resistant varieties to overcome these challenges. Cercospora leaf spot (CLS) caused by Cercospora canescens is one of the most destructive diseases of mungbean and the key polyketide toxin cercosporin plays an important role in pathogenesis. Such toxins as selective agents in the tissue culture medium can help in selecting genotype with suitable levels of resistance to the toxin and/or to the pathogen among the available germplasm. Here, we standardized the dose of cercosporin for in vitro selection of resistant mungbean genotypes and variable expression of peroxidase, catalase and superoxide dismutase. Murashige and Skoog (MS) medium supplemented with 1.0 mg L-1 NAA and 1.0 mg L-1 BAP was standardized for the development of callus from mungbean using hypocotyls as an explant. The calli from six cultivars of mungbean were tested in medium amended with cercosporin (0-40 µg mL-1) and calli survived up to 20 µg mL-1 of cercosporin. The calli from resistant cultivars survived 83.33-93.00%, and showed lower reduction in fresh weight (25.97-28.83%). Calli from the susceptible cultivars survived 50-60% and showed higher reduction in fresh weight. Callus showed browning, exposure to cercosporin (5-20 µg mL-1). Enzymes assay from survived calli of different cultivars showed higher peroxidase activity (7.90-8.91 ∆OD min-1 mg‑1 callus), superoxide dismutase (0.96-1.03 ∆OD min-1 mg-1 callus) and a lower catalase (0.35-0.43 µ moles of H2O2 utilized min-1 mg‑1 callus) in resistant, followed by moderately resistance and susceptible cultivars. The necrosis in leaves was recorded with 200 µg mL-1 of cercosporin, and no visible necrosis was observed below this concentration. Enzyme assayed from the controlled and cercosporin-treated (100-200 µg mL-1) leaves of mungbean genotypes showed variable activity of peroxidase, catalase and superoxide dismutase. Topics: Disease Resistance; Genotype; Oxidoreductases; Perylene; Plant Leaves; Plant Proteins; Vigna | 2017 |