Authors
M. Mrazkova,
K. Cerny, and
S. Gabrielova, Department of Phytopathology, Silva Tarouca Research Institute for Landscape and Ornamental Gardening, Pruhonice 25243, Czech Republic; and
M. Tomsovsky, Mendel University of Agriculture and Forestry, Brno, 61300, Czech Republic
During the summer and autumn of 2006, a disease of rhododendron plants (Ericaceae) was found in nurseries and public gardens in several areas of the Czech Republic. Leaves of damaged plants showed dark brown-to-black lesions extending along the mid-rib and commonly spreading to petioles and shoots. The infected shoots turned black and died. The cankers on branches, stems, and collars were characterized by reddish, brownish, or blackish discoloration. The disease was identified on Rhododendron catawbiense, R. repens, and other Rhododendron spp. After plating pieces of symptomatic tissue on PARPNH medium (2), several isolates of a homothallic Phytophthora sp. were acquired. Ten representative isolates of the pathogen were cultivated on V8A plates and examined for cultural and morphological characteristics. Colonies had a stellate pattern of growth with sparse aerial mycelium at 20°C; optimum temperature for growth was 25 to 28°C, minimum was 4°C, and maximum was 33°C. Radial growth was 14 mm per day at 20°C on V8A. The isolates produced terminal, spherical, smooth-walled oogonia, which were 19 to 37 μm in diameter. Oospores were plerotic (17 to 32 μm) with walls 2 to 4 μm thick; antheridia were paragynous. Single, terminal, noncaducous, semipapillate sporangia were formed on simple (occasionally sympodial) sporangiophores in nonsterile soil filtrate. The sporangia (28 to 61 × 24 to 35 μm, L:B ratio 1.5) were mostly obpyriform, rarely obovoid, or ovoid-ellipsoid. Morphological and cultural characters resembled those described for Phytophthora citricola Sawada (1). The ITS sequences of the rDNA of the two representative isolates (GenBank Accession Nos. EF194772 and EF194773) showed 100% homology to P. citricola sequences obtained from GenBank, thus the identity was confirmed as P. citricola. Both specimens were deposited in CCF (Culture Collection of Fungi, Charles University, Prague, Czech Republic). To confirm the pathogenicity of isolates, Koch's postulates were tested using 40 3-year-old potted rhododendron (R. catawbiense and R. repens) plants and the two P. citricola strains deposited in CCF. Surfaces of attached healthy leaves were disinfected with 95% ethanol and gently abraded with a sterile scalpel near the mid-rib. Agar plugs from the margin of a 5-day-old colony grown on carrot agar were placed on leaf surfaces and also inserted under flaps of stem tissues made with a sterile scalpel. The leaves and stems were then sealed with Parafilm. Control plants were treated in the same manner with sterile agar plugs. All plants were watered with deionized water, covered with a plastic bag, and maintained in a greenhouse at 21°C for 6 weeks. All inoculated plants exhibited necrotic lesions on leaves and stems around the points of inoculation after 4 days, whereas the control plants remained healthy. The pathogen was consistently reisolated from symptomatic plants. P. citricola is well known as a pathogen of rhododendron (1), but to our knowledge, this is the first report of P. citricola on Rhododendron sp. in the Czech Republic. P. citricola has been found at five different locations and in the most frequently isolated Phytophthora spp. from rhododendron in the Czech Republic.
References: (1) D. C. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society. St. Paul, MN, 1996. (2) T. Jung et al. Eur. J. For. Pathol. 26:253, 1996.
