scholarly journals First Report of Sclerotinia Blight Caused by Sclerotinia sclerotiorum on Spearmint in Northern Italy

Plant Disease ◽  
2013 ◽  
Vol 97 (10) ◽  
pp. 1384-1384 ◽  
Author(s):  
A. Garibaldi ◽  
P. Pensa ◽  
D. Bertetti ◽  
A. Poli ◽  
M. L. Gullino

Spearmint (Mentha spicata L.) is an aromatic plant belonging to the family Lamiaceae, grown as well as an ornamental potted plant. During the beginning of 2013, extensive wilting was observed on 4-month-old potted plants of M. spicata ‘Moroccan’ grown in a commercial, unheated, plastic house located near Albenga (Savona, northern Italy). Initial symptoms included stem necrosis and darkening and withering of leaves. Wilting of the plant occurred 2 to 4 days after the appearance of the initial symptoms. Infected plants were characterized by the presence of cottony soft rot. In the presence of high relative humidity, lesions became covered with a whitish mycelium and irregular, dark gray sclerotia (2.0 to 9.0 × 1.8 to 4.0, average 4.0 × 2.6 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 streptomycin sulfate. White colonies developed from infected stem pieces and produced sclerotia, mainly at the peripheries of the plates, measuring 2.0 to 8.0 × 2.0 to 6.0 (average 4.4 × 3.1) mm. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS1F/ITS4 and sequenced. BLAST analysis (1) of the 514-bp segment showed a 99% homology with the sequence of Sclerotinia sclerotiorum (JN012605). The nucleotide sequence has been assigned the GenBank Accession KC848769. The morphological and molecular identification permitted to identify as S. sclerotiorum (Lib.) de Bary (2) the causal agent of the disease observed on M. spicata. Pathogenicity of one isolate obtained from infected plants was confirmed by inoculating three 7-month-old plants cv. Moroccan transplanted in 1 liter pots in a glasshouse in a sphagnum peat/pomix/pine bark/clay (50:20:20:10) mix. Each plant was inoculated by placing 4 g of sterile wheat kernels infested with mycelium and sclerotia in the soil and around the collar. Three non-inoculated plants served as controls. Plants were maintained in a growth chamber at 24 ± 1°C and relative humidity >90%. The inoculation trial was carried out twice. All inoculated plants developed the symptoms, consisting of stem necrosis, 5 days after soil infestation, followed by leaf yellowing. 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 M. spicata in Italy as well as worldwide. The disease has been previously reported on M. piperita in the United States (4) and on M. arvensis in India (3). The economic importance of this disease in Italy is at present limited. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) N. F. Buchwald. Kongl. Veterisk Landb. Aarssk. 75, 1949. (3) K. Perveen et al. Indian Phytopathol. 62:310, 2009. (4) C. B. Skotland and J. D. Menzies. Plant Dis. Rep. 41:493, 1957.

Plant Disease ◽  
2005 ◽  
Vol 89 (11) ◽  
pp. 1241-1241 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Several species of Diplotaxis (D. tenuifolia, D. erucoides, and D. muralis), known as wild or sand rocket, are widely cultivated in Italy. Rocket is used in Mediterranean cuisine as salad, a component of packaged salad products, and as a garnish for food. In winter 2003, a severe disease was observed on D. tenuifolia grown in unheated glasshouses on 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 was extremely severe in the presence of high relative humidity and mild temperature (15°C). Necrotic tissues became covered with white mycelium that produced dark sclerotia. Diseased stem tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar (PDA) amended with 100 ppm streptomycin sulfate. Sclerotinia sclerotiorum (1) was consistently recovered from infected stem pieces. Sclerotia observed on infected plants measured 1.23 to 3.00 × 1.40 to 5.38 mm (average 2.10 × 2.85 mm). Sclerotia produced on PDA measured 1.00 to 4.28 × 1.00 to 6.01 mm (average 2.38 × 3.23 mm). Pathogenicity of three isolates obtained from infected plants was confirmed by inoculating 30-day-old plants of D. tenuifolia grown in 18-cm-diameter pots in a glasshouse. Inoculum, 2 g per pot of wheat kernels infested with mycelium and sclerotia of each isolate, was placed on the soil surface around the base of each plant. Three replicates of five pots each were used per isolate. Noninoculated plants served as controls. The inoculation trial was repeated once. All plants were kept at temperatures ranging between 10 and 26°C (average 15°C) with an average relative humidity of 80% and were watered as needed. Inoculated plants developed symptoms of leaf yellowing within 12 days, soon followed by the appearance of white mycelium and sclerotia, and eventually wilted. Control plants remained symptomless. S. sclerotiorum was reisolated from inoculated plants. To our knowledge, this is the first report of infection of D. tenuifolia by S. sclerotiorum in Italy as well as worldwide. The disease currently has been observed in the Liguria Region but not yet in other areas where sand rocket is cultivated. The economic importance of this disease for the crop can be considered medium at the moment, but is expected to increase in the future. Reference: (1) N. F. Buchwald. Den. Kgl. Veterin.er-og Landbohojskoles Aarsskrift, 75, 1949.


Plant Disease ◽  
2001 ◽  
Vol 85 (11) ◽  
pp. 1207-1207
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
G. Gilardi ◽  
M. L. Gullino

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.


Plant Disease ◽  
2011 ◽  
Vol 95 (11) ◽  
pp. 1481-1481
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
A. Poli ◽  
M. L. Gullino

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.


Plant Disease ◽  
2002 ◽  
Vol 86 (1) ◽  
pp. 71-71
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

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.


Plant Disease ◽  
2005 ◽  
Vol 89 (9) ◽  
pp. 1016-1016
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

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.


Plant Disease ◽  
2000 ◽  
Vol 84 (9) ◽  
pp. 1048-1048
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

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.


Plant Disease ◽  
2008 ◽  
Vol 92 (7) ◽  
pp. 1133-1133
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

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.


Plant Disease ◽  
2003 ◽  
Vol 87 (9) ◽  
pp. 1151-1151 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

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.


Plant Disease ◽  
2008 ◽  
Vol 92 (8) ◽  
pp. 1250-1250 ◽  
Author(s):  
A. Garibaldi ◽  
P. Pensa ◽  
M. L. Gullino

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.


Plant Disease ◽  
2009 ◽  
Vol 93 (12) ◽  
pp. 1353-1353 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
P. Pensa ◽  
M. L. Gullino

Petunia × hybrida (Solanaceae) includes several hybrids that are grown as ornamental plants and are very much appreciated for their long-lasting flowering period. During the spring of 2009, extensive wilting was observed on 2-month-old potted plants of Petunia × hybrida cv. Sanguna Lilac Vein grown in a commercial glasshouse near Albenga (northern Italy). First symptoms included stem necrosis and darkening and withering of leaves. 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 (3.0 to 6.5 × 2.0 to 5.0 mm, average 4.8 × 3.3 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 (3) was consistently recovered from infected stem pieces. Sclerotia produced on PDA measured 2.0 to 6.0 × 1.5 to 5.0 mm (average 3.9 × 3.1) mm. The internal transcribed spacer (ITS) region of rDNA was amplified with primers ITS4/ITS6 and sequenced. BLAST analysis (1) of the 548-bp segment showed a 100% homology with the sequence of S. sclerotiorum. The nucleotide sequence has been assigned GenBank Accession No. GQ375746. Pathogenicity of one isolate obtained from sclerotia of infected plants was confirmed by inoculating three 90-day-old plants belonging to cv. Sanguna Lilac Vein transplanted in 22-cm-diameter pots in a glasshouse in a sphagnum peat/pomix/pine bark/clay (50:20:20:10) mix. Inoculum that consisted of 2 g/liter of substrate of 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 greenhouse at temperatures ranging between 22 and 26°C and relative humidity >90%. The inoculation trial was carried out twice. All inoculated plants developed leaf yellowing by 20 days after 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 Petunia × hybrida in Italy. The disease has been previously reported on Petunia × hybrida in Bermuda (2) and the United States (4). References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997 (2) R. M. Brien. N.Z. J. Sci. Tech., A, 24, 62, 1942. (3) N. F. Buchwald. Kongl. Veterisk Landb. Aarssk. 75, 1949. (4) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989.


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