First Report of Sclerotinia sclerotiorum on Argyranthemum frutescens in Italy

Paris daisy (Argyranthemum frutescens (L.) Sch. Bip.) is an economically important crop on the Riviera Ligure (northern Italy), where approximately 10 million plants per year are produced for export. In the winter of 2007, extensive wilting was observed on 5-month-old potted plants of A. frutescens grown in a commercial greenhouse near Albenga. First symptoms included stem necrosis, darkening and withering of leaves, and wilting of young buds. As stem and foliar necrosis progressed, infected plants wilted and died. Wilt occurred a few days after the appearance of the first symptoms. Infected plants were characterized by the presence of soft, watery tissues. Lesions became covered with a whitish mycelium and dark sclerotia were produced on the mycelium. Diseased stem tissue was surface sterilized for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 mg/l streptomycin sulfate. Sclerotinia sclerotiorum (Lib.) de Bary (2) was consistently recovered from infected stem pieces. Sclerotia produced on PDA measured 1.4 to 5.2 × 2.3 to 6.7 (average 3.3 to 4.2) mm. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and then sequenced. BLAST analysis (1) of the 531-bp segment showed a 100% homology with the sequence of S. sclerotiorum. The nucleotide sequence has been assigned GenBank Accession No. EU 556701. Pathogenicity of two isolates obtained from infected plants was confirmed by inoculating 10 90-day-old plants for each isolate. Plants were grown singly in 18-cm-diameter pots maintained in a greenhouse under shade and were regularly irrigated and fertilized. Mycelium plugs 1 cm2 were excised from a 10-day-old PDA culture of both isolates and placed on the soil surface around the base of each plant. Ten noninoculated plants served as controls. Plants were maintained in a greenhouse under shade at temperatures ranging between 6 and 22°C (average 18°C) and relative humidity at >90%. The inoculation trial was carried out twice. All inoculated plants developed leaf yellowing by 22 days after inoculation. White, cottony mycelium and black sclerotia developed on stems and at the base of all inoculated plants. Eventually, infected plants wilted. Control plants remained symptomless. S. sclerotiorum was reisolated from the stems of inoculated plants. To our knowledge, this is the first report of S. sclerotiorum causing white mold on A. frutescens in Italy as well as worldwide. The economic importance of this disease can be considered limited at the moment. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997 (2) N. F. Buchwald. Kongl. Veterisk Landb. Aarssk. 75, 1949.

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First Report of White Mold Caused by Sclerotinia sclerotiorum on Iberis sempervirens in Italy

Plant Disease ◽

10.1094/pdis-91-4-0464c ◽

2007 ◽

Vol 91 (4) ◽

pp. 464-464

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Disease Incidence ◽

Soil Surface ◽

Northern Italy ◽

White Mold ◽

First Report ◽

Potted Plants ◽

Inoculation Trial ◽

Initial Symptoms ◽

The Moment

Iberis sempervirens (candytuft) is an ornamental plant that thrives in cool conditions, and its growth as a potted plant has been increasing in Liguria (northern Italy). In the spring of 2004, extensive chlorosis was observed on 10-month-old potted plants of I. sempervirens grown in a plastichouse on a commercial farm near Albenga in northern Italy. Initial symptoms included stem necrosis at the soil level and darkening of leaves. As stem and foliar necrosis progressed, infected plants wilted and died. Wilt occurred within a few days on young plants, characterized by the presence of soft, watery tissues, particularly on affected leaves. Symptomatic plants were found on many farms, with an average disease incidence of 5 to 10%. Necrotic tissues became covered with a whitish mycelium that produced dark sclerotia. The diseased stem tissue was surface sterilized for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm of streptomycin sulfate. Sclerotinia sclerotiorum (Lib.) de Bary (1) was consistently recovered from infected stem pieces. Sclerotia observed on infected plants measured 1.4 to 3.2 × 2.1 to 4.1 mm (average 2.1 to 2.7 mm). Sclerotia produced on PDA measured 1.2 to 4.2 × 1.4 to 6.1 mm (average 2.5 to 3.1 mm). Pathogenicity of three isolates obtained from infected plants and used in a mixture was confirmed by inoculating 10 single-potted 120-day-old plants grown in 18-cm diameter pots maintained outside under shade. Inoculum that consisted of 1 cm2 of mycelium excised from a 10-day-old PDA culture plate of each isolate was placed on the soil surface around the base of each plant. Ten noninoculated plants served as control. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 8 and 17°C (average 12.5°C) and watered as needed. All inoculated plants developed symptoms of leaf yellowing within 18 days, soon followed by the appearance of white mycelium and sclerotia, and then eventual wilt. Control plants remained symptomless. S. sclerotiorum was reisolated from the stems of inoculated plants. S. sclerotiorum has been previously reported only on I. umbellata (2). To our knowledge, this is the first report of white mold on I. sempervirens in Italy as well as worldwide. The economic importance of this disease can be considered low at the moment in the case of field-grown plants. References: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift 75, 1949. (2) J. M. Waterston. Report of the Plant Pathologist, 1946. Dep. Agric. Bermuda, 1947.

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First Report of White Mold Caused by Sclerotinia sclerotiorum on Thymus × citriodorus in Italy

Plant Disease ◽

10.1094/pdis.2004.88.9.1044a ◽

2004 ◽

Vol 88 (9) ◽

pp. 1044-1044

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

White Mold ◽

First Report ◽

Potted Plants ◽

Inoculation Trial ◽

Initial Symptoms ◽

Commercial Farms ◽

Stem Necrosis ◽

White Mycelium

Thymus × citriodorus is well known for the citrus aroma released by its leaves and is grown as a potted plant in northern Italy. This species is widely used in gardens and landscapes and for culinary purposes. In the Liguria Region alone, 1.5 million plants are grown. In the winter of 2002, extensive chlorosis was observed on potted plants of Thymus × citriodorus cv. Silver Queen grown outdoors on commercial farms near Albenga. Initial symptoms included stem necrosis at the soil level and darkening of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt, characterized by the presence of soft and watery tissues, occurred within a few days on young plants. Necrotic tissues became covered with whitish mycelium that produced dark sclerotia. Sclerotinia sclerotiorum (Lib.) de Bary (1) was consistently recovered from infected stem pieces of Thymus × citriodorus. The diseased stem tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm of streptomycin sulfate. Sclerotia produced on PDA were ellipsoid and measured 5.2 to 4.4 × 2.1 to 1.5 mm (average 3.5 × 3.0 mm). Pathogenicity of three isolates obtained from infected plants was confirmed by inoculating 30-day-old plants grown in 14-cm-diameter pots in a screenhouse. Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate was placed on the soil surface around the base of each of 10 plants. Noninoculated plants served as controls. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 5 and 26°C and watered as needed. Inoculated plants developed symptoms of leaf yellowing within 13 days, soon followed by the appearance of white mycelium, and eventually wilted. Control plants remained symptomless. White mycelium and sclerotia developed on infected tissues and S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of white mold of Thymus × citriodorus caused by S. sclerotiorum. The economic importance of this disease for the crop can be considered low. Reference: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 1949.

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First Report of White Mold Caused by Sclerotinia sclerotiorum on Persian Buttercup (Ranunculus asiaticus) in Italy

Plant Disease ◽

10.1094/pdis.2003.87.9.1151a ◽

2003 ◽

Vol 87 (9) ◽

pp. 1151-1151 ◽

Cited By ~ 1

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

United States ◽

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

The United States ◽

First Report ◽

Inoculation Trial ◽

Initial Symptoms ◽

Leaf Yellowing ◽

Ranunculus Asiaticus ◽

Stem Necrosis

Persian buttercup (Ranunculus asiaticus L.) is grown in the Albenga Region of northern Italy for cut flower production and exportation to central and northern Europe. During the winter of 2003, sudden wilt was observed in commercial plantings of R. asiaticus. Initial symptoms included stem necrosis at the soil level and yellowing and tan discoloration of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt occurred within a few days on young plants and was characterized by the presence of soft and watery tissues. Necrotic tissues became covered with whitish mycelium that produced dark, spherical sclerotia (1 to 4 mm in diameter). Sclerotinia sclerotiorum (Lib.) de Bary (1) was consistently recovered from infected stem pieces of R. asiaticus that were disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm of streptomycin sulfate. Pathogenicity of three isolates obtained from infected plants of persian buttercup was confirmed by inoculating 30-day-old plants grown in containers. Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate was placed on the soil surface around the base of each of five plants. Noninoculated plants served as controls. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 8 and 22°C and watered as needed. Inoculated plants developed symptoms of leaf yellowing followed by wilt within 15 days, while control plants remained symptomless. White mycelium and sclerotia developed on infected tissues, and S. sclerotiorum was reisolated from inoculated plants. S. sclerotiorum has been previously reported on R. asiaticus in the United States (2) and Japan (3). To our knowledge, this is the first report of wilt of R. asiaticus caused by S. sclerotiorum in Italy and Europe. References: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 1949. (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) T. Urushibara et al. Annu. Rep. Kanto-Tosan Plant Prot. Serv. 46:61, 1999.

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First Report of Sclerotinia Blight Caused by Sclerotinia sclerotiorum on Fan Columbine (Aquilegia flabellata) in Italy

Plant Disease ◽

10.1094/pdis-07-11-0542 ◽

2011 ◽

Vol 95 (11) ◽

pp. 1481-1481

Author(s):

A. Garibaldi ◽

D. Bertetti ◽

A. Poli ◽

M. L. Gullino

Keyword(s):

Relative Humidity ◽

Sclerotinia Sclerotiorum ◽

Its Region ◽

The United States ◽

First Report ◽

Potted Plants ◽

Sclerotinia Blight ◽

Inoculation Trial ◽

Soil Infestation ◽

Stem Necrosis

Fan columbine is a perennial garden species belonging to the family Ranunculaceae. During the spring of 2011, extensive wilting was observed on 5-month-old potted plants of Aquilegia flabellata grown in an experimental glasshouse belonging to the Center AGROINNOVA at Grugliasco (northern Italy). First symptoms included stem necrosis and darkening and withering of leaves. Plant wilt occurred a few days after the appearance of the first symptoms. Infected plants were characterized by the presence of soft, watery tissues. In the presence of high relative humidity, lesions became covered with a whitish mycelium and irregular, dark gray sclerotia (1.5 to 4.0 × 1.0 to 2.8, average 2.8 × 2.1 mm) were produced on the mycelium. Diseased tissue was surface sterilized for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 mg/l of streptomycin sulfate. Sclerotinia sclerotiorum (Lib.) de Bary (2) was consistently recovered from infected stem pieces. Sclerotia produced on PDA measured 2.0 to 7.0 × 2.0 to 5.0 (average 4.2 × 2.9) mm. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS1F/ITS4 and sequenced. BLAST analysis (1) of the 575-bp segment showed a 100% homology with the sequence of S. sclerotiorum (EF091809). The nucleotide sequence has been assigned the GenBank Accession No. JN013184. Pathogenicity of one isolate obtained from sclerotia of infected plants was confirmed by inoculating three 6-month-old plants transplanted in 16-cm-diameter pots in a glasshouse in a sphagnum peat/pomix/pine bark/clay (50:20:20:10) mix. Inoculum that consisted of 3 g/l of substrate of sterile wheat kernels infested with mycelium and sclerotia was placed in the soil and around the base of each plant. Three noninoculated plants served as controls. Plants were maintained in a growth chamber at 21 ± 1°C and relative humidity >90%. The inoculation trial was carried out twice. All inoculated plants developed leaf yellowing within 15 days of soil infestation. White, cottony mycelium and dark sclerotia developed on stems and at the base of all inoculated plants. Eventually, infected plants wilted. Control plants remained symptomless. S. sclerotiorum was reisolated from the stems of inoculated plants. To our knowledge, this is the first report of S. sclerotiorum on A. flabellata in Italy. The disease has been previously reported on A. vulgaris in the United States (3) and A. glandulosa in Russia (4). The economic importance of this disease in Italy is currently limited. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) N. F. Buchwald. Kgl. Veterisk Landb. Aarssk. 75, 1949. (3) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrived from http://nt.ars-grin.gov/fungaldatabases/ , July 7, 2011. (4) P. M. Zhiboedov et al. Mikol. Fitopatol, 36:48, 2002.

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First Report of Sclerotinia sclerotiorum on Campanula carpatica and Schizanthus × wisetonensis in Italy

Plant Disease ◽

10.1094/pdis.2002.86.1.71a ◽

2002 ◽

Vol 86 (1) ◽

pp. 71-71

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

United States ◽

Sclerotinia Sclerotiorum ◽

Ornamental Plants ◽

Soil Surface ◽

The United States ◽

First Report ◽

Potted Plants ◽

Initial Symptoms ◽

Stem Necrosis ◽

Campanula Carpatica

The production of potted ornamental plants is very important in the Albenga Region of northern Italy, where plants are grown for export to central and northern Europe. During fall 2000 and spring 2001, sudden wilt of tussock bellflower (Campanula carpatica Jacq.) and butterfly flower (Schizanthus × wisetonensis Hort.) was observed on potted plants in a commercial greenhouse. Initial symptoms included stem necrosis at the soil line and yellowing and tan discoloration of the lower leaves. As stem necrosis progressed, infected plants growing in a peat, bark compost, and clay mixture (70-20-10) wilted and died. Necrotic tissues were covered with whitish mycelia that produced dark, spherical (2 to 6 mm diameter) sclerotia. Sclerotinia sclerotiorum was consistently recovered from symptomatic stem pieces of both plants disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar amended with streptomycin sulphate at 100 ppm. Pathogenicity of three isolates obtained from each crop was confirmed by inoculating 45- to 60-day-old C. carpatica and Schizanthus × wisetonensis plants grown in containers (14 cm diameter). Inoculum that consisted of wheat kernels infested with mycelia and sclerotia of each isolate was placed on the soil surface around the base of previously artificially wounded or nonwounded plants. Noninoculated plants served as controls. All plants were maintained outdoors where temperatures ranged between 8 and 15°C. Inoculated plants developed symptoms of leaf yellowing, followed by wilt, within 7 to 10 days, while control plants remained symptomless. White mycelia and sclerotia developed on infected tissues and S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of stem blight of C. carpatica and Schizanthus × wisetonensis caused by S. sclerotiorum in Italy. The disease was previously observed on C. carpatica in Great Britain (2) and on Schizanthus sp. in the United States (1). 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) J. Rees. Welsh J. Agric. 1:188, 1925.

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First Report of Sclerotinia sclerotiorum on Gazania sp. Hybrid in Italy

Plant Disease ◽

10.1094/pdis.2001.85.11.1207d ◽

2001 ◽

Vol 85 (11) ◽

pp. 1207-1207

Author(s):

A. Garibaldi ◽

A. Minuto ◽

G. Gilardi ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

Soft Rot ◽

The United States ◽

Crown Rot ◽

First Report ◽

Initial Symptoms ◽

Leaf Yellowing ◽

Stem Necrosis ◽

Wheat Kernels

Gazania sp. hybrid is produced in pots in the Albenga Region of northern Italy for export to central and northern Europe. During fall 2000 to spring 2001, sudden wilt was observed in commercial plantings of this ornamental. Initial symptoms included stem necrosis at the soil level and yellowing and tan discoloration of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt followed by soft rot occurred within a few days on young plants after the first leaf symptoms. Necrotic tissues became covered with white mycelia that produced dark, spherical (2 to 6 mm diameter) sclerotia. Sclerotinia sclerotiorum was consistently recovered from infected stem pieces of Gazania disinfested for 1 min in 1% NaOCl, plated on potato dextrose agar amended with streptomycin sulfate at 100 mg/liter. Pathogenicity of three fungal isolates was confirmed by inoculating 45- to 60-day-old plants grown in containers (14 cm diameter). Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate was placed on the soil surface around the base of each plant. Noninoculated plants served as controls. All plants were maintained outdoors where temperatures ranged between 8 and 15°C. Inoculated plants developed symptoms of leaf yellowing, followed by wilt, within 7 to 10 days, while control plants remained symptomless. White mycelia and sclerotia developed on infected tissues, and S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of wilt of Gazania sp. hybrid caused by S. sclerotiorum in Italy. A crown rot of Gazania caused by S. sclerotiorum has been reported from California in the United States(1). Reference: (1) V. M. Muir and A. H. McCain. Calif. Plant Pathol. 16:1, 1973.

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First Report of White Mold Caused by Sclerotinia sclerotiorum on Rosmarinus officinalis ‘Prostratus’ in Italy

Plant Disease ◽

10.1094/pd-89-1016a ◽

2005 ◽

Vol 89 (9) ◽

pp. 1016-1016

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

The United States ◽

Rosmarinus Officinalis ◽

White Mold ◽

First Report ◽

Potted Plants ◽

Initial Symptoms ◽

Stem Necrosis ◽

Rosmarinus Officinalis L

Rosmarinus officinalis L. ‘Prostratus’ is an evergreen shrub that is native to the Mediterranean Region in southern Europe and grown as a potted plant in Italy. This cultivar is widely used in gardens and landscapes. During the winter of 2002, extensive chlorosis was observed on 8-month-old potted plants of R. officinalis L. ‘Prostratus’ grown outdoors in commercial farms near Albenga in northern Italy. Initial symptoms included stem necrosis at the soil level and darkening of leaves. As stem necrosis progressed, infected plants wilted and died. Wilt, characterized by the presence of soft and watery tissues, occurred within a few days on young plants. The disease infected 15% of the plants. Necrotic tissues became covered with a whitish mycelium that produced dark sclerotia. The diseased stem tissue was surface sterilized for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm of streptomycin sulfate. Sclerotinia sclerotiorum (1) was consistently recovered from infected stem pieces. Sclerotia observed on infected plants measured 0.30 to 3.33 × 1.00 to 4.23 mm (average 1.31 × 1.88 mm). Sclerotia produced on PDA measured 0.09 to 3.08 × 0.38 to 4.05 mm (average 1.94 × 2.43 mm). Pathogenicity of three isolates obtained from infected plants and used in mixture was confirmed by inoculating 60-day-old plants grown in 14-cm-diameter pots in a glasshouse. Inoculum (wheat kernels infested with mycelium and sclerotia) for each isolate was placed on the soil surface around the base of each plant. Pathogenicity tests included three inoculated plants grown in separate pots per isolate. Three noninoculated plants grown in three pots served as controls. The inoculation trial was conducted twice. All plants were kept at temperatures ranging between 8 and 34°C (average 18°C) and watered as needed. Plants were covered with plastic for 96 h after inoculation to increase the moisture level. All inoculated plants developed symptoms of leaf yellowing within 30 days, soon followed by the appearance of white mycelium and sclerotia, and eventual wilt. Control plants remained symptomless. S. sclerotiorum was reisolated from the stems of inoculated plants. To our knowledge, this is the first report of white mold of R. officinalis L. ‘Prostratus’ in Italy and in Europe. S. sclerotiorum has been previously reported on R. officinalis in India (2) and the United States (3). The economic importance of this disease for the crop in Italy can be considered low at the moment. References: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 32:75, 1949. (2) L. Mohan. Indian Phytopathol. 47:443, 1994. (3) M. L. Putnam. Plant Pathol. 53:252, 2004.

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First Report of White Mold Caused by Sclerotinia sclerotiorum on Hutchinsia alpina in Italy

Plant Disease ◽

10.1094/pdis.2004.88.9.1045a ◽

2004 ◽

Vol 88 (9) ◽

pp. 1045-1045

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

Planting Density ◽

White Mold ◽

First Report ◽

Inoculation Trial ◽

Leaf Yellowing ◽

Commercial Farms ◽

White Mycelium ◽

Wheat Kernels

Hutchinsia alpina (Chamois cress), a plant belonging to the Brassicaceae family, is cultivated as a potted ornamental plant in Italy. In the winter of 2002, leaves and stems of plants grown in pots (14-cm diameter) in commercial farms near Albenga (northern Italy) developed soft and watery tissues covered with whitish mycelium at the soil line. As necrosis progressed, infected plants wilted and died. Dark sclerotia developed on infected tissues. Because of high planting density, the infection spread very rapidly. Sclerotinia sclerotiorum was consistently recovered from infected stem pieces of H. alpina disinfested 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm of streptomycin sulfate. Sclerotia produced on PDA were ellipsoid and measured 1.3 to 9.3 × 1.3 to 4.5 mm (average 3.9 × 2.8 mm) (1). Pathogenicity of three isolates obtained from infected plants grown in a single greenhouse was confirmed by inoculating 90-day-old plants grown in pots (14 cm). Inoculum that consisted of wheat kernels infested with mycelium and sclerotia of each isolate were placed on the soil surface around the base of each of 10 plants. Plants treated with plain wheat kernels served as controls. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 5 and 26°C and watered as needed. Inoculated plants developed symptoms of leaf yellowing, followed by the appearance of white mycelium within 15 days, and eventually wilted while control plants remained symptomless. White mycelium and sclerotia developed on infected tissues, and S. sclerotiorum was reisolated only from inoculated plants. To our knowledge, this is the first report of white mold on Hutchinsia alpina caused by S. sclerotiorum. Reference: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 1949.

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First Report of Sclerotinia sclerotiorum on African Daisy (Osteospermum sp.) in Italy

Plant Disease ◽

10.1094/pdis-92-6-0982c ◽

2008 ◽

Vol 92 (6) ◽

pp. 982-982

Author(s):

A. Garibaldi ◽

P. Pensa ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

Its Region ◽

The United States ◽

First Report ◽

Leaf Yellowing ◽

Affected Tissue ◽

Blastn Analysis ◽

Plant Grown ◽

Stem Lesions

African daisy (Osteospermum sp.) is an ornamental plant grown in the winter as a potted plant in Liguria (northern Italy) and is generally marketed in early-to-late spring in Italy and central and northern Europe. In the winter of 2006, stem lesions, general chlorosis, wilt, and plant death occurred in a greenhouse nursery. Affected plants were characterized by the presence of soft, watery tissues. Necrotic tissues were covered with a white, cottony mycelium. During periods of high humidity, black sclerotia differentiated within the mycelium. To recover the pathogen, diseased stem tissue was surface sterilized for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 mg/l of streptomycin sulfate. Sclerotinia sclerotiorum (Lib.) de Bary (2) was consistently isolated from affected tissue. Sclerotia produced on PDA measured 1.3 to 3.1 × 1.5 to 3.5 mm in diameter. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and then sequenced. BLASTn analysis (1) of the 633 bp showed a 100% identity with S. sclerotiorum. The nucleotide sequence was assigned GenBank Accession No. EU 556701. Pathogenicity of two isolates obtained from infected plants was confirmed by inoculating 10 80-day-old plants grown in 14-cm-diameter pots. Inoculum consisted of 1 cm2 of mycelium excised from a 10-day-old PDA culture of each isolate and placed on the soil surface around the base of each plant. Ten plants were inoculated with each isolate and 10 noninoculated plants served as controls. Plants were maintained in a greenhouse under shade at temperatures of 10 to 22°C (average 19°C), in high relative humidity (>90%), and were watered as needed. The trial was conducted twice. All inoculated plants developed leaf yellowing within 12 days of inoculation. White, cottony mycelium and black sclerotia developed on stems and at the base of all inoculated plants, which eventually wilted. Control plants remained symptomless. S. sclerotiorum was reisolated from the stems of inoculated plants. This disease has been reported on an Osteospermum sp. in the United States (3) and Argentina (4). To our knowledge, this is the first report of white mold on an Osteospermum sp. in Italy as well as in Europe. Currently, the economic importance of this disease is limited. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift. 75, 1949. (3) H. S. Gill. Plant Dis. Rep. 59:82, 1975. (4) E. R. Wright et al. Plant Dis. 89:1014, 2005.

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First Report of Sclerotinia sclerotiorum on Calceolaria integrifolia in Italy

Plant Disease ◽

10.1094/pdis-92-7-1133c ◽

2008 ◽

Vol 92 (7) ◽

pp. 1133-1133

Author(s):

A. Garibaldi ◽

A. Minuto ◽

M. L. Gullino

Keyword(s):

Sclerotinia Sclerotiorum ◽

Soil Surface ◽

Its Region ◽

The United States ◽

First Report ◽

Potted Plants ◽

Initial Symptoms ◽

Mycelial Plug ◽

Blastn Analysis ◽

White Mycelium

Calceolaria integrifolia L. is an ornamental species grown as a potted plant in Liguria, northern Italy. In the winter of 2006, extensive chlorosis was observed on approximately 10% of the 10-month-old potted plants in a commercial greenhouse. Initial symptoms included stem necrosis and darkening of leaves. As stem and foliar necrosis progressed, infected plants wilted and died. Wilt occurred on young plants within a few days after the initial appearance of symptoms. Infected plants were characterized by the presence of soft, watery tissues that became covered with white mycelium and dark sclerotia. The diseased stem tissue was surface sterilized for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 mg/liter of streptomycin sulfate. Sclerotinia sclerotiorum (Lib.) de Bary (3) was consistently recovered from infected stem pieces. Sclerotia observed on infected plants measured 0.7 to 1.0 × 2.8 to 4.4 mm (average 1.6 to 2.1 mm). Sclerotia produced on PDA measured 1.0 to 1.1 × 3.0 to 4.2 mm (average 1.7 to 2.3 mm). The internal transcribed spacer (ITS) region of rDNA was amplified with primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 522-bp amplicon resulted in 100% homology with the sequence of S. sclerotiorum. The nucleotide sequence has been assigned GenBank Accession No. EU 627004. Pathogenicity of two isolates obtained from infected plants was confirmed by inoculating 10 120-day-old plants grown in individual 14-cm-diameter pots maintained in a greenhouse under partial shade. Inoculum consisted of 1 cm2 of mycelial plugs excised from a 10-day-old PDA culture of each isolate. Plants were inoculated by placing a mycelial plug on the soil surface around the base of each plant. Ten plants were inoculated per isolate and an equal number of noninoculated plants served as controls. The trial was repeated once. All plants were kept at temperatures ranging between 8 and 17°C (average 12.5°C) and watered as needed. All inoculated plants developed leaf yellowing within 8 days after inoculation, soon followed by the appearance of white mycelium and sclerotia, and then by wilt. Control plants remained symptomless. S. sclerotiorum was reisolated from the stems of inoculated plants. S. sclerotiorum was reported previously on a Calceolaria sp. in the United States (2). To our knowledge, this is the first report of white mold on C. integrifolia in Italy. The economic importance of this disease is currently limited. References (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) Anonymous. USDA Agric. Handb. 165:441, 1960. (3) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift 75, 1949.

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