• Korean Journal of Environmental Agriculture
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• v.17 no.4
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• pp.306-311
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• 1998

Effects of soluble silicon and surfactants on the development of powdery mildew of cucumber were tested for environmentally safe powdery mildew control. Tested soluble silicon was potassium silicate$(K_2SiO_3)$ and tested commercial surfactants were Jeonchakje, Silhouette, Kaba, and Tween 20. Tested concentrations were 2, 4, 8, 16mM for the soluble silicon, 0.5 and 1.0% for Tween 20, 0.05 and 0.1% for both Jeonchakje and Kaba, and 0.03 and 0.07% for Silhouette. Water dilutions of tested materials were sprayed on cucumber (Cucumis sativus) leaves once a week for 4 weeks. From 3 days after the second spray, the diseased area and the numbers of fungal colony were measured from the treated leaves for 6 times at 3-4 days interval. Powdery mildew was less severe on treated cucumber compared to distilled water-treated cucumber (check). In all treatments, diseased area index was proportional to the number of the fungal colony. At the end of investigation, there was severe powdery mildew on check cucumbers. Average 30% of a leaf was colonized by powdery mildew fungus and the average number of the fungal colony per leaf reached to more than 70. On the other hand, none of the treated cucumber suffered severe powdery mildew. The treatments including 8 and 16mM of soluble silicon, doubled concentration of Kaba, and 0.5 and 1.0% of Tween 20 showed more than 80% of control effect compared to water-treated cucumber. In addition, no phytotoxicity was found. Potassium silicate and Tween 20 showed the possibility to replace chemical pesticides for the control of powdery mildew.

• Research in Plant Disease
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• v.7 no.1
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• pp.1-7
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• 2001

An isolate of Cucumber mosaic cucumovirus(CMV) was isolated from Hydrangea macrophylla for. otaksa(Sieb. et Zucc. ) Wils. showing mosaic symptoms, and designated as Hm-CMV. Hm-CMV was characterized by the tests of host range, physical properties, serological properties, RNA and coat protein compositions, and reverse transcription and polymerase chain reaction (RT-PCR) analysis. Twelve species in 4 families were used in the host range test of Hm-CMV and could be differentiated from Y-CMV used as a control CMV by the ringspot and line pattern on inoculated leaves of several tobacco plants. Thevirus produced local lesions on inoculated leaves of Chenopodium amarticolor, C. quinoa and Vigna unguiculata. The physical properties of the virus were as follows; thermal inactivation point(TIP) was 60$\^{C}$, dilution end point (DEP) was 10$\^$-3/, and longevity in vitro (LIP) was 3∼4 days. Hm-CMV was serologically identical to Y-CMV. SDS-polyaciylamide gel electrophoresis(SDS-PAGE) showed one major protein band of about 28 kDa. In RNA or dsRNA analysis, Hm-CMV consisted of four RNA or dsRNA species, but satellite RNA was not detected. In RT-PCR using CMV-common primer and CMV subgroup I-specific primer, bothe amplified expected size of about 490 bp and 200 bp DNA fragments from Hm-CMV, respectively. Restriction enzyme analysis of the 490 bp RT-PCR products using EcoR I and Msp I showed that Hm-CMV belonged to CMV subgroup I. However, Hm-CMV could be differentiated from other CMV subgroup I isolates by RNA fingerprinting by arbitrarily primed polymerase chain reaction (RAP-PCR).