scholarly journals First Report of Southern Blight Incited by Sclerotium rolfsii on Potato (Solanum tuberosum) in Northern Italy

Plant Disease ◽  
2006 ◽  
Vol 90 (8) ◽  
pp. 1114-1114 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
M. L. Gullino
Keyword(s):  
Solanum Tuberosum ◽  
Solanum Tuberosum L ◽  
Sclerotium Rolfsii ◽  
Soil Surface ◽  
The United States ◽  
Northern Italy ◽  
Strong Increase ◽  
Southern Blight ◽  
White Mycelium ◽  
The Moment

During the summer of 2005, plants of potato (Solanum tuberosum L.) showing severe basal rot symptoms were observed in a commercial field near Alessandria (northern Italy). The first symptoms were detected during early July in correspondence with a strong increase of air temperature (as much as 38°C, with an average monthly increase of 10°C) and relative humidity. Infected plants showed dry collar rots and extensive necrosis of cortical tissues. Leaves of infected plants were chlorotic. As the disease progressed, tubers rotted and plants wilted. Infected plants appeared in patches, encompassing 10 to 15% of the cultivated area. In the presence of abundant moisture, a white mycelium occurred on infected tissues. On their surface, infected tubers showed a fan-like mycelial growth. Later, white or light-to-dark brown sclerotia (2 to 4 mm in diameter) developed from mycelium. Clamp connections were present. The diseased tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 mg/liter of streptomycin sulfate. Sclerotium rolfsii was consistently isolated from infected plants. Pathogenicity of one isolate obtained from infected plants was confirmed by inoculating healthy S. tuberosum plants (cv. Hermes) grown in 2:l volume pots (1 plant per pot, seven replicates). Inoculum that consisted of 1 g/pot of wheat kernels infested with mycelium and sclerotia was placed on the soil surface. Seven noninoculated plants served as controls. The inoculation trial was repeated once. Plants were kept at temperatures ranging between 25 and 32°C and watered as needed. Inoculated plants developed symptoms of leaf yellowing within 10 days, soon followed by the appearance of white mycelium and sclerotia and then eventually wilted. Control plants remained symptomless. Sclerotium rolfsii was reisolated from inoculated plants.Possible attacks of Sclerotium rolfsii on S. tuberosum were described as rarely occurring in southern Italy (3). The disease, detected at the moment in very few farms and on cvs. Hermes and Monalisa, was particularly severe on the last variety, causing 5 to 15% yield losses because of premature plant death and rotting of tubers. This disease has been reported in several countries such as India (1), Israel (2), and the United States of America (4). References: (1) N. S. Bisht. Indian Phytopathol. 35:148, 1982. (2) Y. Elad et al. Soil Biol. Biochem. 16:381, 1984. (3) R. Gigante. Ital. Agric. 87:263, 1946. (4) G. F. Weber. Phytopathology, 33:615, 1943.

scholarly journals First Report of Southern blight Incited by Sclerotium rolfsii on Dichondra repens in Italy

Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 203-203 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino
Keyword(s):  
Sclerotium Rolfsii ◽  
Soil Surface ◽  
The United States ◽  
First Report ◽  
Southern Blight ◽  
Inoculation Trial ◽  
Leaf Yellowing ◽  
White Mycelium ◽  
Wheat Kernels ◽  
Reddish Brown Color

Kidney weed (Dichondra repens) is increasingly used for low maintenance turf in Italy, particularly for gardens and parks in areas characterized by mild climate. During September 2003, on the D. repens turf of a private garden located near Imperia (northern Italy), yellow, circular areas as much as 60 cm in diameter appeared with the grass becoming chlorotic and thin. A ring of the patch at its periphery exhibited a reddish brown color and eventually died. An area of green grass remained in the center of the patch. Rings of dead grass enlarged rapidly during hot, humid weather. In the presence of abundant moisture, a white mycelium occurred on the dying grass at the periphery of the ring. White or light-to-dark brown sclerotia (1 to 3 mm in diameter) developed from mycelium on the dead grass. The diseased tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar amended with 100 mg/l of streptomycin sulphate. Sclerotium rolfsii was consistently isolated from infected plants. Pathogenicity of three isolates obtained from infected plants was confirmed by inoculating healthy D. repens turf (1 m2 plots and three replicates). Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate was placed on the soil surface. Noninoculated plots served as controls. The inoculation trial was repeated once. Turf was covered with a plastic film for 7 days, kept at temperatures ranging between 22 and 25°C, and watered as needed. Inoculated plants developed symptoms of leaf yellowing within 11 days, soon followed by the appearance of white mycelium and sclerotia, and then eventually wilted. Control plants remained symptomless. Sclerotium rolfsii was re-isolated from inoculated plants. To our knowledge, this is the first report of S. rolfsii on D. repens in Italy. This disease has been reported on kidney weed in several countries such as the United States (3), Brazil (1), and India (2). References: (1) M. Menezes and J. A. A. Lima. Fitossanidade 1:18, 1974. (2) K. Ranganathan and N. Shanmugam. Indian Phytopathol, 27:113, 1974. (3) J. D. Smith et al. Fungal Diseases of Amenity Turf Grasses. E & F.N. Spon, London, 1989.

scholarly journals Blight of English Ivy (Hedera helix) Caused by Sclerotium rolfsii in Sicily

Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 635-635 ◽  
Author(s):  
A. Pane ◽  
F. Raudino ◽  
S. Adornetto ◽  
G. Proietto Russo ◽  
S. O. Cacciola
Keyword(s):  
Irrigation System ◽  
Sclerotium Rolfsii ◽  
Soil Surface ◽  
Pathogenic Fungi ◽  
Plant Diseases ◽  
Hedera Helix ◽  
Southern Blight ◽  
White Mycelium ◽  
Foliage Plant ◽  
English Ivy

English ivy, Hedera helix L. (Araliaceae), an evergreen climbing vine is widely cultivated as an ornamental and foliage plant. In the summer of 2005, a severe blight of ivy plants trained as topiaries and grown in an open field was observed in a nursery near Giarre (eastern Sicily). Foliage of infected plants appeared lighter green and progressively turned bronze and withered. Eventually, the entire plant collapsed. Foliar symptoms were associated with basal stem and root rot. White, cottony mycelium and numerous sclerotia developed externally on the lower stem and on the soil around the affected plants. The disease was randomly distributed, affecting approximately 5% of plants in a stock of 1,500 English ivy plants. Sclerotium rolfsii Sacc. (teleomorph Athelia rolfsii (Curzi) Tu & Kimbrough) was consistently isolated from symptomatic basal stem tissues by disinfecting in 1% NaOCl and plating on potato dextrose agar (PDA) amended with 100 mg/liter of streptomycin sulfate. The isolated fungus was identified on the basis of morphological and cultural characteristics (2). On PDA, it produced a densely, floccose, white mycelium. Mycelium was septate with clamp connections at hyphal septa. Optimum growth temperature was 30 ± 2°C. Numerous small (0.5 to 1.9 mm in diameter) sclerotia developed on the colony surface; they were spherical, occasionally slightly ellipsoidal, quite uniform in size (modal value of the diameter 1.4 mm), with a smooth surface. The surface color of the sclerotia was initially white, turned to pinkish buff, then to olive-brown, and eventually to clove brown as sclerotia matured. Sclerotia were most numerous in the center as well as close to the edge of petri dishes. Pathogenicity of one isolate obtained from infected plants was confirmed by inoculating 10 1-year-old potted English ivy plants by placing mycelium-infested wheat kernels and sclerotia on the soil surface around the collar of each plant. Ten noninoculated plants served as control. Plants were held in a dew chamber for 48 h at 28°C and subsequently placed in a greenhouse where the temperature ranged between 25 and 31°C. Plants showed wilting within 3 weeks after inoculation. Fans of white mycelium and numerous sclerotia were produced on the basal stem of inoculated test plants. Noninoculated controls remained healthy. S. rolfsii was reisolated from infected plants to fulfill Koch's postulates. English ivy has been already reported as a host of S. rolfsii, the causative agent of southern blight in nurseries of ornamentals (1). However, to our knowledge, this is the first report of southern blight on English ivy in Italy. The disease may have been favored by warm summer temperatures and overwatering with a drip irrigation system. References: (1) A. R. Chase. Compendium of Ornamental Foliage Plant Diseases. The American Phytopathological Society, St. Paul, MN, 1992. (2) J. E. M. Mordue. Corticium rolfsii. No. 410 in: Description of Pathogenic Fungi and Bacteria. CMI. Kew, Surrey, UK, 1974.

scholarly journals First Report of Sclerotium rolfsii on Jerusalem Cherry (Solanum pseudocapsicum) in Europe

Plant Disease ◽  
2000 ◽  
Vol 84 (9) ◽  
pp. 1048-1048
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino
Keyword(s):  
United States ◽  
Sclerotium Rolfsii ◽  
Soil Surface ◽  
The United States ◽  
Northern Italy ◽  
Ornamental Plant ◽  
Potato Dextrose Agar ◽  
First Report ◽  
Initial Symptoms ◽  
Stem Necrosis

Jerusalem cherry (Solanum pseudocapsicum) has recently become popular as a potted ornamental plant in Italy. During the summer of 1999, a sudden wilt of 60-day-old plants was observed in the Albenga region (Northern Italy), an area of intensive floriculture. Initial symptoms included stem necrosis at the soil line and yellowing and tan discoloration of leaves. As stem necrosis progressed, infected plants wilted and died. Necrotic tissues were covered with whitish mycelium that differentiated into reddish brown, spherical (1 to 2 mm diameter) sclerotia. Sclerotium rolfsii was consistently recovered from the surface of symptomatic stem sections that were disinfected for 1 min in 1% NaOCl and then plated on potato-dextrose agar (PDA) amended with 100 ppm streptomycin sulfate. Pathogenicity of three S. rolfsii isolates was confirmed by inoculating 90-day-old S. pseudocapsicum plants grown in pots. Inoculum consisted of mycelium and sclerotia of the pathogen placed on the soil surface around the base of each plant. Noninoculated plants served as controls. All plants were kept in a growth chamber at 18 to 28°C and RH > 85%. Inoculated plants developed symptoms within 7 days, while control plants remained symptomless. Sclerotia developed on infected tissues and S. rolfsii was reisolated from symptomatic tissues. The disease has been observed in the United States (1), but this is the first report of stem blight of S. pseudocapsicum caused by S. rolfsii in Europe. Reference: (1) S. A. Alfieri, Jr., K. R. Langdon, C. Wehlburg, and J. W. Kimbrough, J. W. Index Plant Dis. Florida Bull. 11:215, 1984.

scholarly journals First Report of Southern Blight Caused by Sclerotium rolfsii on St.-John's-Wort

Plant Disease ◽  
1999 ◽  
Vol 83 (7) ◽  
pp. 696-696 ◽  
Author(s):  
A. P. Keinath ◽  
J. W. Rushing ◽  
R. J. Dufault
Keyword(s):  
Sclerotium Rolfsii ◽  
Soil Surface ◽  
The United States ◽  
Pathogenicity Test ◽  
First Report ◽  
Southern Blight ◽  
St John’S Wort ◽  
St John's Wort ◽  
Pathogenicity Tests ◽  
Hypericum Perforatum L

Interest in commercial production of common St.-John's-wort (Hypericum perforatum L.), an herb that is dried, processed, and used as an anti-depressant medication, is increasing. In August 1998, St.-John's-wort growing in the field at Charleston, SC, showed blight symptoms. Leaves on prostrate branches turned reddish-yellow, then brown, and then abscised. As the disease progressed, branches and approximately 10% of the plants were killed. Coarse, white mycelia were present on the bases of dead branches. Segments cut from symptomatic branches were disinfested in 0.5% sodium hypochlorite and placed on potato dextrose agar (PDA) at 25°C. Sclerotium rolfsii Sacc. was isolated from one of 12 branches with discolored leaves and six of six dead branches. For pathogenicity tests, sclerotia were harvested from 6-week-old cultures on PDA. Ten-week-old St.-John's-wort plants, growing in potting mix in 10-cm pots, were inoculated by placing four sclerotia on the soil surface 1 to 1.5 cm from the main stem of each plant. Plants were grown in a greenhouse at 90% relative humidity and 25 to 35°C. Single blighted branches were observed on three plants 12 days after inoculation and all plants were blighted 28 days after inoculation. S. rolfsii was recovered from 10 and 9 of 10 plants inoculated with isolates of S. rolfsii from St.-John's-wort and tomato, respectively. All 10 noninoculated plants remained symptomless. The pathogenicity test was repeated and the results were similar. This is the first report of S. rolfsii causing Southern blight on St.-John's-wort in the United States.

scholarly journals First Report of Powdery Mildew Caused by Erysiphe aquilegiae var. aquilegiae on Aquilegia flabellata in Italy

Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 681-681
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino
Keyword(s):  
United States ◽  
Powdery Mildew ◽  
The United States ◽  
Northern Italy ◽  
American Phytopathological Society ◽  
First Report ◽  
Powdery Mildews ◽  
The Family ◽  
White Mycelium ◽  
The University

Aquilegia flabellata Sieb. and Zucc. (columbine) is a perennial garden species belonging to the family Ranunculaceae. During the summer of 2003, a severe outbreak of a previously unknown powdery mildew was observed in several gardens near Biella (northern Italy). Upper surfaces of leaves were covered with a white mycelium and conidia, and as the disease progressed infected leaves turned yellow and died. Foot cell was cylindric and appressorium lobed. Conidia were hyaline, ellipsoid, and measured 31.2 to 47.5 × 14.4 to 33 μm (average 38.6 × 21.6 μm). Fibrosin bodies were not present. Cleistothecia were globose, brown, had simple appendages, ranged from 82 to 127 (average 105) μm in diameter, and contained one to two asci. Ascocarp appendages measured five to eight times the ascocarp diameter. Asci were cylindrical (ovoidal) and measured 45.3 to 58.2 × 30.4 to 40.2 μm. Ascospores (three to four per ascus) were ellipsoid or cylindrical and measured 28.3 to 31.0 × 14.0 to 15.0 μ;m. On the basis of its morphology, the pathogen was identified as Erysiphe aquilegiae var. aquilegiae (1). Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of five, healthy A. flabellata plants. Five noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a garden where temperatures ranged between 20 and 30°C. After 10 days, typical powdery mildew symptoms developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of the presence of powdery mildew on Aquilegia flabellata in Italy. E. communis (Wallr.) Link and E. polygoni DC. were reported on several species of Aquilegia in the United States (2), while E. aquilegiae var. aquilegiae was previously observed on A. flabellata in Japan and the former Union of Soviet Socialist Republics (3). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) U. Braun. Nova Hedwigia, 89:700, 1987. (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) K. Hirata. Host Range and Geographical Distribution of the Powdery Mildews. Faculty of Agriculture, Niigata University, 1966.

scholarly journals First Report of Stem and Crown Rot of Garbanzo Caused by Sclerotinia minor in the United States and by Sclerotinia sclerotiorum in Arizona

Plant Disease ◽  
2000 ◽  
Vol 84 (11) ◽  
pp. 1250-1250 ◽  
Author(s):  
M. E. Matheron ◽  
M. Porchas
Keyword(s):  
United States ◽  
Cicer Arietinum ◽  
Soil Surface ◽  
The United States ◽  
Crown Rot ◽  
Sclerotinia Minor ◽  
First Report ◽  
Initial Symptoms ◽  
Stem Necrosis ◽  
White Mycelium

In March 2000, plants began to die within two garbanzo (Cicer arietinum L.) fields about 48 km apart in southwestern Arizona. Initial symptoms included wilting of leaves and stem necrosis on individual branches, followed by entire plant necrosis and death. White mycelium was present on plant stems near the soil surface. In one field, small black irregularly shaped sclerotia (1 mm in diameter) were present on the infected stem surface along with the white mycelia, whereas in the other field the associated sclerotia were of similar shape but larger (5 to 6 mm in diameter). Isolation from diseased garbanzo stem tissue from the respective fields yielded Sclerotinia minor, which produced small sclerotia when cultured on potato-dextrose agar and S. sclerotiorum, which produced the typical larger sclerotia of this species. To fulfill Koch's postulates, healthy plants and associated soil from a garbanzo field with no evidence of infection by Sclerotinia were removed with a shovel and transferred into a series of 8-liter plastic pots. After transporting back to the laboratory, some of the plants were inoculated by wounding stems with a 5-mm-diameter cork borer, placing an agar disk containing either S. minor or S. sclerotiorum onto each wound, securing the agar disk to the stem with plastic tape, then incubating the plants at 25°C for 7 days. Control plants were treated similarly except that agar disks did not contain Sclerotinia. Stems inoculated with S. minor or S. sclerotiorum developed symptoms of wilt and necrosis, including the appearance of white mycelium and sclerotia on the stem surface, whereas control plants remained healthy. S. minor or S. sclerotiorum were recovered from garbanzo stems inoculated with the respective species of the pathogen. Sclerotinia leaf drop, which can be caused by S. minor or S. sclerotiorum on lettuce in Arizona, had been observed in both fields previously. Garbanzo fields in Arizona usually are watered by furrow irrigation. Disease was most severe in areas of the garbanzo fields that were heavily irrigated with resultant wetting of tops of plant beds. Proper management of irrigation water and avoidance of establishing a garbanzo planting in fields following lettuce could help reduce future losses from these pathogens. S. minor previously had been reported as a pathogen on Cicer arietinum from the island of Sardinia (2); however, this is apparently the first report of the pathogen on garbanzo other than in Sardinia. S. sclerotiorum has been reported as a pathogen on this host in several countries including the United States (California) (1) but not previously in the state of Arizona. References: (1) I. W. Buddenhagen, F. Workneh, and N. A. Bosque-Perez. Int. Chickpea Newsl. 19:9–10, 1988. (2) F. Marras. Rev. Appl. Mycol. 43:112, 1964.

scholarly journals Southern Blight of Jerusalem Artichoke Caused by Sclerotium rolfsii in California

Plant Disease ◽  
2004 ◽  
Vol 88 (7) ◽  
pp. 769-769 ◽  
Author(s):  
S. T. Koike
Keyword(s):  
Sclerotium Rolfsii ◽  
Jerusalem Artichoke ◽  
The United States ◽  
Peat Moss ◽  
Stem Tissue ◽  
Disease Symptoms ◽  
Southern Blight ◽  
Potted Plants ◽  
Initial Symptoms ◽  
Advanced Stages

Jerusalem artichoke or sunchoke (Helianthus tuberosus) is a specialty vegetable that is grown commercially in California. The fleshy tubers are harvested and used as a fresh salad ingredient or cooked vegetable. During 2003, field plantings of Jerusalem artichoke in coastal California (Santa Cruz County) showed symptoms of an unfamiliar disease. Initial symptoms consisted of wilting of new shoots and leaves followed by browning and collapse of all foliage. Crown and lower stem tissues turned tan to brown. In advanced stages of the disease, crown and stem tissues were colonized internally and externally by white, cottony mycelium. Tan, spherical sclerotia that measured approximately 1 mm in diameter formed on the surfaces of the affected crowns and stems. Mycelia and sclerotia also grew on the soil adjacent to infected plants. Isolations from symptomatic crowns, mycelia, and sclerotia produced colonies that were identified as Sclerotium rolfsii. Pathogenicity was tested using two methods that included sclerotial inocula collected from five isolates grown on potato dextrose agar plates. With the first method, sclerotia of each isolate were applied to sets of tubers (10 tubers per isolate) prior to planting tubers into a soilless, peat moss-based medium in pots. With the second method, 3-week-old potted plants were inoculated by placing sclerotia of each isolate adjacent to stem tissue that was 3 cm below the surface of the soilless medium. Noninoculated controls were included for both methods. All plants were incubated in a greenhouse at 21 to 24°C. For the first method, by the third week after planting, 10 to 40% of plants did not emerge because the tubers were rotted and decayed. For the plants that did emerge, wilting of foliage and browning of crown and stem tissue occurred approximately 6 weeks after planting and by 10 weeks, all plants were diseased. S. rolfsii was reisolated from all necrotic tuber, crown, and stem tissues. For the second method, disease symptoms and signs of the pathogen occurred 5 weeks after inoculation and by week 10, 75% of test plants were symptomatic. S. rolfsii was again reisolated from all necrotic tuber, crown, and stem tissues. Symptoms were not observed on any of the noninoculated plants. To my knowledge, this is the first report of southern blight of Jerusalem artichoke in California. This disease has been reported on Jerusalem artichoke in several southern U.S. states (1,2). The two inoculation methods demonstrated that the pathogen could infect propagation organs (tubers) and also emergent stems of this host. References: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989. (2) S. M. McCarter and S. J. Kays. Plant Dis. 68:299, 1984.

scholarly journals Occurrence of Black Dot of Potato Caused by Colletotrichum coccodes in Central Italy

Plant Disease ◽  
2002 ◽  
Vol 86 (5) ◽  
pp. 562-562 ◽  
Author(s):  
R. Buonaurio ◽  
G. Natalini ◽  
L. Covarelli ◽  
C. Cappelli
Keyword(s):  
Solanum Tuberosum L ◽  
Disease Incidence ◽  
Central Italy ◽  
Morphological Characteristics ◽  
Fungal Growth ◽  
Soil Surface ◽  
The United States ◽  
Colletotrichum Coccodes ◽  
Tuber Quality ◽  
Black Dot

Between 1997 and 2000, black dot of potato (Solanum tuberosum L.), caused by the polyphagous soilborne fungus Colletotrichum coccodes (Wallr.) Hughes, was observed each summer in fields located in Umbria (central Italy). Disease incidence ranged from 50 to 100%, and early potato cultivars were generally more susceptible than late-maturing ones. Disease symptoms were first observed during August as a yellowing and wilting of foliage in the tops of plants, followed by rotting of the roots and stems, which led to the premature death of 50 to 70% of plants. Setose1 sclerotia (300 to 500 mm in diameter) and acervuli of the fungus were found on roots and stems of infected plants. Acervuli produced hyaline, aseptate, cylindrical conidia (16 to 22 × 2.5 to 4.5 μm) formed on unicellular cylindrical phialidic conidiophores. The fungus was isolated from diseased stems and roots on potato dextrose agar (PDA) at pH 6.5. Pathogenicity of the fungus was confirmed by fulfilling Koch's postulates using 3- to 4-week-old potato plants of a local cultivar. A superficial 5-mm vertical cut was made with a scalpel into the base of potato stems (2 cm beneath the soil surface), and 5-mm-diameter plugs of PDA alone (control plants) or PDA plus fungal growth were placed over the cuts. The wounds were sealed with wet cotton swabs that were held in place with Parafilm. Symptoms that resembled those in the field were observed on inoculated plants 6 to 8 weeks postinoculation. Symptoms did not appear on the control plants. The same fungus was reisolated from the diseased plants. Based on morphological characteristics of sclerotia, acervuli, and conidia, as well as pathogenicity tests, the fungus was identified as C. coccodes. To our knowledge, this is the first report of C. coccodes as the causal agent of black dot of potato in central Italy. We did not observe foliar outbreaks of the disease, which were reported from the United States (2). In both 1921 (1) and 1951 (3), the fungus was reported to cause severe outbreaks of the disease in northern Italy. Since then, its presence in Italy has been rarely recorded in potato (4). The occurrence of extremely dry and hot weather conditions during the summers of 1997 to 2000, which are favorable for disease development, made the disease particularly severe. We cannot exclude the possibility that the disease may have been present in central Italy before our observations, as it can be misdiagnosed and its symptoms can be masked by the symptoms of other diseases. The significance of black dot in central Italy needs to be reappraised in terms of both yield loss and tuber quality. References: (1) C. Arnaudi. Atti Ist. Bot. Univ. Pavia. Ser. 3, 1:71, 1924. (2) A. W. Barkdoll and J. R. Davis. Plant Dis. 76:131, 1992. (3) G. Goidanich. Inf. Fitopatol. 1:5, 1951. (4) S. Vitale et al. J. Plant Pathol. 80:265, 1998.

scholarly journals Occurrence of Blight Caused by Sclerotium rolfsii on Lolium perenne in Argentina

Plant Disease ◽  
2007 ◽  
Vol 91 (7) ◽  
pp. 910-910
Author(s):  
L. Goldring ◽  
M. Lacasa ◽  
E. R. Wright ◽  
B. A. Pérez ◽  
M. C. Rivera
Keyword(s):  
United States ◽  
Lolium Perenne ◽  
Perennial Ryegrass ◽  
Tap Water ◽  
Sclerotium Rolfsii ◽  
Soil Surface ◽  
Pathogenic Fungi ◽  
The United States ◽  
Buenos Aires Province ◽  
Pathogenicity Test

A perennial ryegrass (Lolium perenne L.) lawn located at Castelar (Buenos Aires Province) showed disease symptoms during the summer of 2003. Chlorotic patches as much as 15 cm in diameter appeared on the lawn. Later, dead plants with white mycelia developing on the crown and surrounding soil occurred at the periphery of the rings. Plants showed leaf chlorosis and crown and root rot. No sclerotia developed on plant organs. Diseased plants were collected, washed with running tap water for 4 h, and disinfested in 5% NaOCl for 2 min. Pieces, 3 to 5 mm long from symptomatic leaves, crowns, and roots, were incubated on 2% potato dextrose agar (PDA) at 22 to 25°C with a 12-h light/dark cycle. Mycelia growing on the soil surface was transferred to PDA and incubated under the same conditions. After 3 to 4 days, white, conspicuous mycelia that produced sclerotia grew from diseased tissue pieces and soil mycelial samples. Sclerotia were nearly spherical, 1 to 2 mm in diameter, white but turning brown with age, and produced in large numbers over the entire colony surface. Primary hyphae showed clamp connections at the septa. A pathogenicity test was performed with 20 1-month-old plants of L. perenne grown in a 1:1 (v/v) mixture of sand and soil contained in 24- × 17- × 4-cm plastic trays. Seven-day-old fungal cultures grown on PDA were cut into 1- cm2 pieces and placed among the plants on the substrate. Each tray was inoculated with seven inoculum pieces. Five trays of plants were inoculated with the fungus, and plants in five trays that served as controls had only sterile pieces of PDA placed on the substrate. All plants were maintained at 25°C and watered frequently. First symptoms, consisting of chlorosis, were observed 4 days after inoculation. Of the plants, 34, 59, 60, 65, and 70% developed symptoms 6, 9, 14, 17, and 21 days after inoculation, respectively. Control plants remained healthy. The fungus was reisolated from diseased plants and identified as Sclerotium rolfsii Sacc. (teleomorph Athelia rolfsii (Curzi) C.C. Tu & Kimbr.) on the basis of morphological and cultural characteristics (3,4). The disease has been observed causing stalk rot on perennial ryegrass in the United States (1) and Australia (2). To our knowledge, this is the first report of S. rolfsii causing disease on L. perenne in Argentina. References: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society. St. Paul, MN. 1989. (2) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory. Online publication. ARS, USDA, 2007. (3) J. E. M. Mordue. No. 410 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, UK, 1974. (4) Z. K. Punja and A. Damiani. Mycologia 88:694, 1996.

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