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

Plant Disease ◽  
2008 ◽  
Vol 92 (6) ◽  
pp. 982-982
Author(s):  
A. Garibaldi ◽  
P. Pensa ◽  
A. Minuto ◽  
M. L. Gullino

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.

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 ◽  
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 ◽  
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 ◽  
2001 ◽  
Vol 85 (4) ◽  
pp. 446-446
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Pot marigold (Calendula officinalis) has recently become popular as a potted ornamental plant in Italy. During the spring 1999, a sudden wilt of 120 day-old plants was observed in the Albenga region of Northern Italy, an area of intensive floriculture production. 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 resulted, covered with whitish mycelium that produced dark, spherical (2- to 6-mm diameter) sclerotia. Sclerotinia sclerotiorum was consistently recovered from symptomatic stem sections surface disinfested 1 min in 1% NaOCl and plated on potato dextrose agar (PDA), amended with 100 ppm streptomycin sulfate. Pathogenicity of three isolates was confirmed by inoculating 90-day-old pot marigold plants grown in containers. Inoculum that consisted of wheat kernels infested with mycelium and sclerotia was placed on the soil surface around the base of previously wounded or non-wounded plants. Non-inoculated plants served as controls. All plants were kept outdoors where temperatures ranged between 8 and 16°C, under 50% shade and were maintained moist. Inoculated plants developed symptoms of leaf yellowing, followed by wilt within 7 days, while control plants remained symptomless. Sclerotia developed on infected tissues and S. sclerotiorum was reisolated from inoculated plants. This is the first report of stem blight of C. officinalis caused by S. sclerotiorum in Europe. The disease was previously observed in the United States (1). Reference: (1) D. F. Farr et al. 1989. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN.


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 ◽  
2006 ◽  
Vol 90 (9) ◽  
pp. 1260-1260 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
D. Minerdi ◽  
M. L. Gullino

Penstemon barbatus (Cav.) Roth (synonym Chelone barbata), used in parks and gardens and sometimes grown in pots, is a plant belonging to the Scrophulariaceae family. During the summers of 2004 and 2005, symptoms of a root rot were observed in some private gardens located in Biella Province (northern Italy). The first symptoms resulted in stunting, leaf discoloration followed by wilt, root and crown rot, and eventually, plant death. The diseased tissue was disinfested for 1 min in 1% NaOCl and plated on a semiselective medium for Oomycetes (4). The microorganism consistently isolated from infected tissues, grown on V8 agar at 22°C, produced hyphae with a diameter ranging from 4.7 to 5.2 μm. Sporangia were papillate, hyaline, measuring 43.3 to 54.4 × 26.7 to 27.7 μm (average 47.8 × 27.4 μm). The papilla measured from 8.8 to 10.9 μm. These characteristics were indicative of a Phytophthora species. The ITS region (internal transcribed spacer) of rDNA was amplified using primers ITS4/ITS6 (3) and sequenced. BLASTn analysis (1) of the 800 bp obtained showed a 100% homology with Phytophthora citrophthora (R. & E. Sm.) Leonian. The nucleotide sequence has been assigned GenBank Accession No. DQ384611. For pathogenicity tests, the inoculum of P. citrophthora was prepared by growing the pathogen on autoclaved wheat and hemp kernels (2:1) at 25°C for 20 days. Healthy plants of P. barbatus cv. Nano Rondo, 6 months old, were grown in 3-liter pots (one plant per pot) using a steam disinfested substrate (peat/pomix/pine bark/clay 5:2:2:1) in which 200 g of kernels per liter of substrate were mixed. Noninoculated plants served as control treatments. Three replicates were used. Plants were maintained at 15 to 20°C in a glasshouse. The first symptoms, similar to those observed in the gardens, developed 21 days after inoculation, and P. citrophthora was consistently reisolated from infected plants. Noninoculated plants remained healthy. The pathogenicity test was carried out twice with similar results. A nonspecified root and crown rot of Penstemon spp. has been reported in the United States. (2). To our knowledge, this is the first report of P. citrophthora on P. barbatus in Italy as well as in Europe. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997 (2) F. E. Brooks and D. M. Ferrin. Plant Dis. 79:212, 1995. (3) D. E. L. Cooke and J. M. Duncan. Mycol. Res. 101:667, 1997. (4) H. Masago et al. Phytopathology 67:425, 1977.


Plant Disease ◽  
1999 ◽  
Vol 83 (3) ◽  
pp. 302-302 ◽  
Author(s):  
Gy. Bohár ◽  
L. Kiss

Common ragweed (Ambrosia artemisiifolia L.) is reported as a host of Sclerotinia sclerotiorum (Lib.) de Bary in North America (2,4), but not in Europe. A Hungarian survey of fungal diseases of ragweed in 1994 did not find sclerotinia rot of common ragweed (A. artemisiifolia var. elatior (L.) Descourt.) (1). In autumn 1998, mature ragweed plants, 1 to 1.5 m tall, were collected from the borders of four sunflower (Helianthus annuus L.) fields in which sclerotinia rot of sunflower was frequently observed during the season, and also from six other roadside sites in Hungary. Ragweed plants exhibiting symptoms characteristic of sclerotinia rot, i.e., wilting foliage and light brown, dry lesions on the stems, were found only near two sunflower fields. Black, round to irregular or oblong sclerotia were also observed on the infected ragweed plants both externally on the stem lesions and internally, in the pith cavity. Sclerotia measured up to 5 mm in diameter and were 5 to 14 mm long. After isolation on potato dextrose agar, the pathogen produced abundant aerial mycelium and large sclerotia characteristic of S. sclerotiorum. To confirm pathogenicity, potted seedlings and mature plants of ragweed were inoculated in the greenhouse with autoclaved wheat grains colonized with mycelia of S. sclerotiorum placed 0.5 to 1 cm from the collar of the test plants. Seedlings were killed in 2 to 3 days while mature plants wilted after 5 to 6 days. In a field test, six mature plants were inoculated by attaching mycelial disks to their stems with Parafilm. These plants wilted 12 to 14 days after inoculation. The pathogen was reisolated from all diseased plants. This is the first report of S. sclerotiorum on common ragweed in Europe. Nonsclerotial mutants of the fungus (3) are being produced to be tested as potential biocontrol agents of common ragweed, which has become not only the most widespread, but also the most important allergenic plant species in Hungary since the early 1990s. References: (1) Gy. Bohár and L. Vajna. Nōvényvédelem 32:527, 1996. (2) G. J. Boland and R. Hall. Can. J. Plant Pathol. 16:93, 1994. (3) G. J. Boland and E. A. Smith. Phytopathology 81:766, 1991.(4) D. F. Farr et al. 1989. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN.


Plant Disease ◽  
2010 ◽  
Vol 94 (11) ◽  
pp. 1374-1374 ◽  
Author(s):  
G. L. Miller ◽  
D. E. Desjardin ◽  
L. P. Tredway

Seashore paspalum (Paspalum vaginatum Sw.) is a newly cultivated C4 turfgrass that has exceptional salinity tolerance and is highly suited for use on golf courses in coastal areas. In October 2008 and June 2009, circular patches of blighted seashore paspalum ranging from 30 cm to >3 m in diameter were observed in fairways, tees, and roughs established with ‘Supreme’ seashore paspalum at Roco Ki Golf Club in Macao, Dominican Republic. Affected patches were initially chlorotic followed by reddish brown necrosis of leaves and leaf sheaths. Reddish brown-to-gray lesions were also observed on leaf sheaths during the early stages of necrosis. During periods of wet or humid weather from June through October, basidiocarps were produced on necrotic plant tissue and identified as Marasmiellus mesosporus Singer (2). Three isolates were obtained by plating symptomatic leaf sheaths that were surface sterilized with a 0.5% NaOCl solution on potato dextrose agar amended with 50 ppm each of streptomycin, chloramphenicol, and tetracycline (PDA+++). Sequences of the internal transcribed spacer (ITS) region of rDNA, obtained from these three isolates and three stipes of basidiocarps, were identical to each other and 99% similar to a M. mesosporus sequence deposited in the NCBI database (Accession No. AB517375). To confirm pathogenicity, a M. mesosporus isolate obtained from symptomatic plant tissue was inoculated onto 6-week-old P. vaginatum (‘Seaspray’) planted (0.5 mg seed/cm2) in 10-cm-diameter pots containing a mixture of 80% sand and 20% reed sedge peat. Two weeks prior to inoculation, the isolate was grown on a sterilized mixture of 100 cm3 of rye grain, 4.9 ml of CaCO3, and 100 ml of water. Infested grains were placed 0.5 cm below the soil surface for inoculation. Pots were inoculated with five infested grains or five sterilized, uninfested grains with three replications of each treatment. After inoculation, pots were placed in a growth chamber with a 12-h photoperiod set to 30°C during the day and 26°C at night. Approximately 20% of plants in inoculated pots were necrotic 7 days postinoculation and this increased to 75% by 21 days postinoculation. Diseased plants in inoculated pots exhibited symptoms similar to those observed in the field. Leaves were initially chlorotic with brown lesions on lower leaf sheaths and eventually turned necrotic, reddish brown, and collapsed. Pots receiving uninfested grains were healthy and showed no symptoms on all rating dates. At 21 days postinoculation, basidiocarps were observed emerging from three colonized plants at the base of the oldest leaf sheath near the crown. Three reisolations were made on PDA+++ from stem lesions surface sterilized with a 0.5% NaOCl solution. All reisolations were confirmed as M. mesosporus by culture morphology and ITS sequence data. M. mesosporus was previously reported causing disease on American beachgrass (Ammophila breviligulata Fernald) in North Carolina (1) and recently in Japan (3). The pathogen was initially placed in the genus Marasmius and reported as the cause of the disease Marasmius blight (1). Subsequent morphological observation found that the pathogen belonged in the genus Marasmiellus (2). To our knowledge, this is the first report of M. mesosporus causing Marasmiellus blight on seashore paspalum, a high-amenity turfgrass. References: (1) L. Lucas et al. Plant Dis. Rep. 55:582, 1971. (2) R. Singer et al. Mycologia 65:468, 1973. (3) S. Takehashi et al. Mycoscience 48:407, 2007.


Plant Disease ◽  
2011 ◽  
Vol 95 (8) ◽  
pp. 1031-1031
Author(s):  
Y. Gai ◽  
R. Pan ◽  
D. Xu ◽  
C. Ji ◽  
M. Deng ◽  
...  

During October 2009, the occurrence of a disease on soybean (Glycine max) was observed in several fields in Boluo County and Zengcheng City, Guangdong Province. Top leaves of infected plants initially turned yellow and plants eventually were defoliated, while stems and roots became black and rotted. The stem lesions sometimes extended 10 to 15 cm upward from the soil surface. Orange-to-brown spherical fruiting bodies, which were very similar with those of the soybean red crown rot pathogen, scattered or congregated on the stem lesions. Plants with symptoms were sampled from fields. Fruiting bodies were excised from diseased tissues. Microscopic examination revealed that they were perithecia, globose to pyriform, ostiolate with a short neck, and measured 160 to 298 × 151 to 235 μm. Under gentle pressure, asci and ascospores were exuded from these perithecia. Asci were eight spored, narrowly cylindrical to clavate, thin walled, with a short stalk, and measured 58 to 124 μm long and 8 to 15 μm in diameter. Ascospores were uniseriately arranged, globose to ellipsoid, thick walled, one celled, hyaline to pale, and measured 14 to 17 × 8 to 12 μm. Isolation was made from stem tissues at the edge of disease lesions on potato dextrose agar (PDA) amended with streptomycin sulfate and incubated at 25°C. Mycelia were white and floccose. Conidia were cylindrical to oblong-ellipsoidal, hyaline, one celled, and measured 6 to 22 × 2 to 5 μm, aggregating in a slimy mass on the apex of the conidiogenous cell. Abundant orange-to-brown spherical perithecia were produced on the colony. Ascospores had walls with a rugose ornamentation that could be clearly seen under a scanning electron microscope. The fungus was identified as Neocosmospora vasinfecta var. vasinfecta (anamorph Acremonium sp.) (1). The internal transcribed spacer (ITS) region of rDNA of two isolates were amplified with universal primers ITS1/ITS4 and sequenced (GenBank Accession No. JF705861 and JF705862), and comparisons with GenBank accessions showed 99% similarity with N. vasinfecta strain Pec070 (Accession No. FJ940902) and strain NRRL22497 (Accession No. AY381142). Pathogenicity tests were conducted. Five, 3-week-old seedlings of soybean cv. Huaxia No. 3 planted in plastic pots (20 cm in diameter) were wounded with a needle at the base of the stem below the soil line and near the root system, and then inoculated by drenching the soil with a conidial suspension (105 per ml). Control plants were inoculated with sterile water. There were six replicates for each treatment. The treated plants were incubated at 25 ± 2°C in a greenhouse. All inoculated plants exhibited symptoms of leaf yellowing and black rot of stems and roots 3 weeks after inoculation. N. vasinfecta var. vasinfecta was reisolated from the diseased plants. All control plants remained healthy. To our knowledge, this is the first observation of Neocosmospora stem rot of soybean in China. The pathogen could pose a threat to soybean, which is a major crop in China. This disease has been previously reported in the United States though the anamorph of the pathogen has either not been identified or has been identified as a Cylindrocarpon sp. (2,4). This fungus is also associated with human infections (3). References: (1) P. F. Cannon and D. L. Hawksworth. Trans. Br. Mycol. Soc. 82:673, 1984. (2) F. A. Gray et al. Plant Dis. 64:321, 1980. (3) P. Manikandan et al. Med. Mycol. 46:279, 2008. (4) D. V. Phillips. Phytopathology 62:612, 1972.


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