Plant Diseases: Their Biology and Social Impact. 1991. By Gail L. Schumann. American Phytopathological Society, St. Paul, Minnesota. 397 pp. $45.00, hardbound.

1991 ◽  
Vol 6 (4) ◽  
pp. 188-189
Author(s):  
Robert D. Lumsden
Mycologia ◽  
1992 ◽  
Vol 84 (2) ◽  
pp. 267
Author(s):  
Edward E. Butler ◽  
Gail L. Schumann
Keyword(s):  

Plant Disease ◽  
2005 ◽  
Vol 89 (8) ◽  
pp. 909-909 ◽  
Author(s):  
S. O. Cacciola ◽  
A. Chimento ◽  
A. Pane ◽  
D. E. L. Cooke ◽  
G. Magnano di San Lio

Lantana (Lantana camara L.) is an evergreen shrub in the Verbenaceae. In some countries, this plant has been declared a noxious weed. However, a number of sterile or near-sterile forms are cultivated as attractive flowered potted and garden plants. In early spring 2004, ≈4,000 potted, small trees of lantana grown in a screenhouse in a commercial nursery of ornamentals near Giarre, Sicily, showed symptoms of chlorosis, defoliation, and sudden collapse of the entire plant. These aboveground symptoms were associated with a reduced root system, rot of feeder roots, and brown discoloration of the base of the stem. A Phytophthora sp. was isolated consistently from roots and basal stems of symptomatic plants using the selective medium of Masago et al. (3). Cardinal temperatures for radial growth of pure cultures obtained by single hypha transfer were 2°C minimum, 25°C optimum, and 30 to 35°C maximum. Sporangia produced in the saline solution of Chen and Zentmyer (3) were obpyriform, persistent, and nonpapillate. All isolates were A1 mating type and differentiated oospores with amphigynous antheridia in dual cultures with A2 reference isolates of P. cryptogea Pethybr. & Laff. and P. drechsleri Tucker (3). Electrophoretic patterns of total mycelial proteins (3) of the isolates from lantana were very similar to those of reference isolates of P. cryptogea from different hosts, but clearly distinct from those of reference isolates of other species included in Waterhouse's taxonomic group VI (3). Indeed, isolates from lantana were identified as P. cryptogea on the basis of morphological and cultural characters as well as the electrophoretic phenotype. Sequences of internal transcribed spacer (ITS) regions of rDNA (1) confirmed the identification as P. cryptogea. Pathogenicity of a representative isolate from lantana (IMI 392045) was tested in a screenhouse by transplanting 20 6-month-old rooted cuttings of lantana in pots (12 cm in diameter) filled with infested soil; the soil was prepared by mixing steam-sterilized sandy loam soil at a concentration of 4% (vol/vol) with inoculum produced on a mixture of vermiculite and autoclaved oat seeds. Twenty control plants were transplanted in pots containing noninfested soil. The soil was saturated with water by plugging the pots' drainage holes for 48 h and watering. After 40 days, all plants except the controls showed symptoms of root and foot rot, and P. cryptogea was reisolated from infected tissues. To our knowledge, this is the first report of P. cryptogea on lantana. On this host and other species in the verbena family, only P. nicotianae van Breda de Haan (= P. parasitica Dastur) has been previously reported (2,3,4). A possible cause of the high incidence of this disease in the nursery was waterlogging due to heavy rain and excessive irrigation. References: (1) S. O. Cacciola et al. For. Snow Landsc. Res. 76:387, 2001. (2) M. L. Daughtrey et al. Compendium of Flowering Potted Plant Diseases. The American Phytopathological Society, St. Paul, MN, 1995. (3) D. C Erwin and O. K. Ribeiro. Pages 39–41, 84–95, 138–139 in: Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN, 1996. (4) K. H. Lamour et al. Plant Dis. 87:854, 2003.


Plant Disease ◽  
2003 ◽  
Vol 87 (6) ◽  
pp. 751-751 ◽  
Author(s):  
G. E. Holcomb

A blight (wet rot) of petunia (Petunia ×hybrida Hort. Vilm.-Andr.) was observed in a wholesale propagation nursery in Baton Rouge, LA in September 2002. The grower reported that plants wilted and then completely rotted. The disease occurred during a period of hot, humid, and cloudy weather. Approximately 100 flats of flowering-age plants of cvs. Rose and White Madness were destroyed. No fungal sporulation was noticed on dead plants, but occasional strands of white mycelium were observed. The grower's use of azoxystrobin, iprodione, and thiophanate methyl plus mancozeb fungicides during current and past outbreaks of this disease did not prevent disease spread, but disease activity stopped after temperature and humidity dropped in early October. A fungus that produced white aerial mycelia that later developed light yellow areas and also black aerial spore masses was consistently isolated from diseased tissue placed on acidified potato dextrose agar (APDA). The fungus was identified as Choanephora cucurbitarum (Berk. & Ravenel) Thaxt. on the basis of cultural and morphological characteristics (3). Sporangiola were ellipsoid, pale brown to reddish brown with distinct longitudinal striations and measured 15 to 20 × 9 to 14 μm. Sporangiospores were broadly ellipsoid, pale brown to reddish brown, indistinctly striate with fine, hyaline polar appendages, and measured 16 to 34 × 7 to 12 μm. Spore measurements were within the range previously given for C.cucurbitarum (3). Pathogenicity tests were performed by misting a mixture of sporangiola and sporangiospores (25,000 to 70,000 per ml of water taken from 7- to 10-day-old cultures grown on APDA) on flowering-age petunia plants (cvs. Rose Madness, White Madness, and Dreams Pink). Tests were repeated twice. Inoculated plants and uninoculated control plants (2 to 4 of each treatment in each test) were held in a dew chamber at 28°C for 48 h and then moved to a greenhouse. Within 48 h after inoculation, plants developed water-soaked lesions on flowers, leaves, and stems, then wilted and rotted. Uninoculated plants remained disease free except for several that developed disease symptoms in the first test, apparently from the presence of natural inoculum on healthy-appearing plants that were obtained from the nursery where the disease was found. Koch's postulates were completed by reisolation of the pathogen from diseased inoculated plants. C. cucurbitarum (1) and C. infundibulifera (Curr.) Sacc. (2) have been reported to cause flower blight of petunia in the United States and whole plant blight (wet rot) of petunia in Japan (4). To our knowledge, this is the first report of C. cucurbitarum causing whole plant blight of petunia in the United States. References: (1) M. L. Daughtrey et al. Choanephora wet rot of poinsettia. Page 15 in: Compendium of Flowering Potted Plant Diseases. The American Phytopathological Society, St. Paul, MN, 1995. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989. (3) P. M. Kirk. Mycological Paper 152:1, 1984. (4) J. Takeuchi and H. Horie. Jpn. J. Phytopathol. 66:72, 2000.


Plant Disease ◽  
2000 ◽  
Vol 84 (1) ◽  
pp. 100-100 ◽  
Author(s):  
M. C. Rush ◽  
A. K. M. Shahjahan ◽  
J. P. Jones ◽  
D. E. Groth

False smut, caused by Ustilaginoidea virens (Cooke) Takah., has been occurring in Louisiana rice since at least 1906 (4). A color plate (no. 69) of the disease was published in the Compendium of Rice Diseases published by the American Phytopathological Society (3). The slide for this plate was taken by M. C. Rush in 1976 of rice grown at the Rice Research Station at Crowley, LA. Since that time, the disease has been sporadic and light in Louisiana. In 1997, however, incidence was high. False smut was present on many germ plasms at the Rice Research Station in Crowley and was observed on commercial cultivars in several growers' fields in southwestern Louisiana. Incidence ranged from 1 to 15% of tillers infected with at least two to three spore balls per infected panicle. The disease occurred on both long- and medium-grain cultivars. False smut of rice occurs in the field at the hard dough to mature stages of the crop. A few spikelets in a panicle transform into globose, yellowish green, velvety spore balls that are 2 to 5 cm in diameter and covered by a thin orange membrane. The membrane bursts open and releases powdery dark green spores. The chlamydospores formed in the spore balls are spherical to elliptical, warty, olivaceous, and 3 to 5 × 4 to 6 μm in dimension. Some of the spore balls develop one or more sclerotia, which are the overwintering structure, in the center. False smut has been considered a minor disease of rice that occurs sporadically in Louisiana. The recent discovery of ustilotoxin, a phytotoxin and mycotoxin, produced by this pathogen on diseased tissues suggests that the fungus may be of concern as a contaminant on rice products consumed by livestock and humans (1,2). This increases the need to monitor the incidence of this disease. References: (1) Koiso et al. Ustiloxin: A phytotoxin and a mycotoxin from false smut balls on rice panicles. Tetrahedron Lett. 33:4157, 1992. (2) Koiso et al. Ustiloxins, antimitotic cyclic peptides from false smut balls on rice panicles caused by Ustilaginoidea virens. J. Antibiot. 47:765, 1994. (3) F. N. Lee and P. S. Gunnel. 1992. Compendium of Rice Diseases. The American Phytopathological Society, St. Paul, MN. p. 28. (4) W. A. Orton. 1907. Plant diseases of 1906. Yearbook U.S. Department of Agriculture. U.S. Government Printing Office, Washington, DC, pp. 499–508.


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