Rapid Tentative Identification of Rhizoctonia spp. Associated with Diseased Turfgrasses. Bruce Martin, Assistant Plant Pathologist, Department of Plant Pathology and Ecology, Connecticut Agricultural Experiment Station, 123 Huntington Street, P. O. Box 1106, New Haven 06504. Plant Dis. 71:47-49. Accepted for publication 18 September 1986. Copyright 1987 The American Phytopathological Society. DOI: 10.1094/PD-71-0047.

Fluorescence microscopy using the DNA-binding probe 4',6'-diamidino-2-phenylindole (DAPI) was used successfully to determine number of nuclei per hyphal cell of Rhizoctonia spp. that cause patch diseases of turfgrasses. The procedure included growth of the hyphae from diseased tissue onto agar-coated microscope slides followed by rapid fixation with 3% formaldehyde. Samples were rinsed with distilled water and flooded with a 1-ppm solution of DAPI, then destained by flooding the sample with distilled water. Most of the water was then removed, a drop of glycerin was applied followed by a coverslip, and the sample was viewed using ultraviolet excitation with epiillumination and Neofluar objectives. Nuclei within isolates of R. solani, R. cerealis, R. zeae, and R. oryzae were clearly differentiated by the method. This method combines speed and reliability as a diagnostic tool.