In the spring and summer of 2002, bermudagrass (Cynodon dactylon × C. transvaalensis) turf in two golf courses located in Sardinia and Apulia (central and southern Italy, respectively) exhibited circular patches that were 10 to 70 cm in diameter. Patches developed in the spring on cv. Santa Ana in Sardinia and cv. Tifway 419 in Apulia, after the turf broke winter dormancy. Although the turf partially recovered during the summer, damage was evident throughout the year in greens, tees, and fairways. Patches coalesced to form large areas of straw-colored, blighted turfgrass. The symptoms observed on single plants resembled those of spring dead spot (SDS), including the presence of root rotting. The upper leaf blades, upper leaf sheaths, and upper culms of the diseased bermudagrass plants were bleached and dessicated, or dead. Infected roots, stolons, and rhizomes were covered with black ectotrophic mycelium. Isolation from infected roots on potato dextrose agar (PDA), supplemented with 100 mg/liter of streptomycin sulfate, consistently yielded a fungus with gray, fluffy, aerial mycelium that was at first light gray and later becoming darker. The maximum daily growth rates of all isolates on PDA ranged from 3 to 4.5 mm at 25°C. The cultural characteristics and growth rates of the isolates corresponded to those described for Ophiosphaerella korrae (4). Pathogenicity tests were performed on 8-week-old C. dactylon × C. transvaalensis (cvs. Santa Ana and Tifway 419) grown in plastic pots (15 × 15 cm). The substrate (sandy soil/sphagnum peat/perlite, 50:35:15) was infested separately with three isolates of O. korrae grown on autoclaved oat kernels, using 10 infested kernels per pot. Three replicates were used. Blight symptoms developed on inoculated plants after 8 weeks. Noninoculated plants remained healthy. The pathogen was consistently reisolated from inoculated plants. The pathogenicity test was carried out twice. SDS incited by O. korrae was reported in Australia (4) and the United States (1,2). To our knowledge, this is the first report of SDS on warm-season turfgrass in Italy, as well as in Europe. SDS continued to be observed in the following years after its first detection (3). In 2006, the disease was observed in Apulia (southern Italy). References: (1) J. N. Crayhay et al. Plant Dis. 72:945, 1988. (2) R. M. Endo et al. Plant Dis. 69:235, 1985 (3) P. Titone et al. Acta Hortic. 661:491, 2004. (4) J. Walker and A. M. Smith. Trans. Br. Mycol. Soc. 58:459, 1972.
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http://dx.doi.org/10.1094/PDIS-91-9-1200C | DOI Listing |
J Org Chem
May 2022
Organic Chemistry Laboratory, University Bayreuth, Universitaetsstraße 30, 95440 Bayreuth, Germany.
Ophiofuranones A and B, metabolites of the fungus , were synthesized in 16 steps and 12%/22% yield. The stereogenic centers were established by Sharpless dihydroxylations and epoxidation, the 1,3-dienes via Wittig or HWE olefinations. The rings were closed through Knoevenagel-type condensation and lactonization.
View Article and Find Full Text PDFPlant Dis
June 2021
Nanjing Agricultural University, 70578, Agro-grassland Science, Nanjing, Jiangsu, China;
Hybrid bermudagrass (Cynodon dactylon×C. transvaalensis) is widely used as turf in transition zone of China. Spring dead spot (SDS) is one of the most damaging diseases of hybrid bermudagrass.
View Article and Find Full Text PDFRSC Adv
January 2019
Department of Natural Product Chemistry, Key Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University Jinan 250012 People's Republic of China +86-531-88382019 +86-531-88382012.
The isolation of the cytotoxic fractions from the endolichenic fungus yielded six new metabolites, including five polyketides (ophiofuranones A (1) and B (2), with unusual furopyran-3,4-dione-fused heterocyclic skeletons, ophiochromanone (3), ophiolactone (4), and ophioisocoumarin (5)), one sesquiterpenoid ophiokorrin (10), and nine known compounds. Their structures were established on the basis of the analysis of HRESIMS and NMR spectroscopic data. ECD calculations, GIAO NMR shift calculations and single-crystal X-ray diffraction were employed for the stereo-structure determination.
View Article and Find Full Text PDFData Brief
October 2018
Department of Plant Pathology, University of Wisconsin-Madison, 1630 Linden Drive, Madison, WI, USA.
Loop-mediated isothermal amplification (LAMP) and recombinase polymerase amplification (RPA) are two rapid isothermal amplification methods for detecting three common fungal root pathogens of cool-season turfgrass: , and Detection of root-infecting fungi on cool-season turfgrasses using loop-mediated isothermal amplification and recombinase polymerase amplification (Karakkat et al., 2018) [1]. The data provided here describe the information for designing primers and probes for LAMP and RPA, how specific they are for each of the three fungi, and the evaluation of RPA on field samples.
View Article and Find Full Text PDFACS Omega
January 2018
Department of Natural Products Chemistry, Key Lab of Chemical Biology (MOE), School of Pharmaceutical Sciences, Shandong University, No. 44 West Wenhua Road, Jinan 250012, People's Republic of China.
Ophiosphaerellins A-I (-), the first example of bicyclo[4.1.0]heptenones, as well as their biosynthetic relatives ophiosphaerekorrins A-B (-) were isolated from the endolichenic fungus .
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