First Report of Choanephora Rot Caused by Choanephora cucurbitarum on Hosta plantaginea in Korea

Hosta plantaginea (Lam.) Asch. is an herbaceous perennial plant with ornamental value. In August 2013, water-soaked spots and wet rot were found on flowers of H. plantaginea in a garden bedded out for landscaping in Hongcheon County, Korea. Symptoms initially appeared as water-soaked spots at the tips of flowers. Dark gray spots on flower petals often coalesced and led to rotting of flowers, with abundant sporulation. However, no symptoms were found on the leaves. Approximately 30% of the flowers were affected in the landscape bed. A fungal isolate was obtained by plating surface-disinfested diseased flower tissue on potato dextrose agar (PDA). Fungal colonies covering the plate (diam. 90 mm) in 48 h were white at first, with abundant aerial mycelia, but later turned pale yellow with abundant sporangiola. Sporangiophores bearing sporangiola were aseptate, hyaline, and usually arose from infected tissue. Sporangiola were ellipsoid to ovoid, indehiscent, brown to dark brown, pediculate, 7 to 12 μm wide and 9 to 20 μm high, and showed longitudinal striations at high magnification. Sporangia were few-spored to multispored, pale brown to brown, and 50 to 150 μm. Sporangiospores from sporangia were broadly ellipsoid, brown to pale brown, with hyaline polar appendages, 8 to 10 μm wide and 15 to 22 μm high. Zygospores were not observed. The morphological and cultural characteristics, especially based on shape and striation of sporangiola, were identical with those of Choanephora cucurbitarum (Berk. & Ravenel) Thaxt. (2,3). A representative specimen was deposited in the Korea University Herbarium (KUS-F27540). Genomic DNA was extracted using a DNeasy Plant Mini Kit (Qiagen Inc., Valencia, CA). The primers ITS1/ITS4 and NL1/LR3 were used to amplify the internal transcribed spacer (ITS) region of rDNA and the D1/D2 region of the large subunit (LSU), respectively (4). The PCR products were purified and directly sequenced. The resulting 594-bp ITS and 680-bp D1/D2 sequences were submitted to GenBank (Accession Nos. KM200034 and KM200035). A GenBank BLAST search of the fungal database showed that the sequences of ITS and D1/D2 regions matched those of C. cucurbitrarum (JN943006 and JN939195) with 100% similarity. A pathogenicity test was conducted by spraying three healthy potted plants (2 months old) with a sporangiola suspension (2 × 104 conidia/ml). Another three potted plants of the same age were treated with sterile water and served as controls. The plants were kept in humid chambers for 2 days and placed in a greenhouse (28°C and 60 to 80% RH). After 4 to 5 days, water-soaked spots were evident on the flowers of inoculated plants. No symptoms were observed on control plants. A pathogenicity test was conducted twice with the same results, fulfilling Koch's postulates. C. cucurbitarum has a wide host range but has not been previously reported to cause disease on H. plantaginea (1). To our knowledge, this is the first report of C. cucurbitarum on H. plantaginea globally as well as in Korea. Choanephora rot of flowers is an issue under high-moisture conditions, so allowing for adequate airflow and a dry plant canopy should aid in disease suppression. References: (1) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab. Online publication, ARS, USDA, retrieved July 11, 2014. (2) P. M. Kirk. Mycol. Pap. 152:1, 1984. (3) A. Saroj et al. Plant Dis. 96:293, 2012. (4) G. Walther et al. Persoonia 30:11, 2013.

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First Report of Leaf Blight on Woodland Sage Caused by Rhizoctonia solani AG 1 in Italy

Plant Disease ◽

10.1094/pdis-94-8-1071c ◽

2010 ◽

Vol 94 (8) ◽

pp. 1071-1071 ◽

Cited By ~ 2

Author(s):

A. Garibaldi ◽

G. Gilardi ◽

D. Bertetti ◽

M. L. Gullino

Keyword(s):

Rhizoctonia Solani ◽

Aqueous Suspension ◽

Its Region ◽

Morphological Characters ◽

Leaf Blight ◽

Pathogenicity Test ◽

First Report ◽

Leaf Petiole ◽

Perennial Plant ◽

Potted Plants

Woodland sage (Salvia nemorosa L.; Lamiaceae) is a hardy herbaceous perennial plant that is easy to grow and propagate and is used in parks and grown as potted plants. During the summer of 2009 in a nursery near Torino in northern Italy, a leaf blight was observed on 30-day-old plants of cv. Blau Koenigin grown in pots under shade. Semicircular, water-soaked lesions developed on leaves just above the soil line at the leaf-petiole junction and later along leaf margins. Lesions expanded along the midvein until the entire leaf was destroyed. Blighted leaves turned brown, withered, and clung to the shoots. No symptoms were observed on the roots. Severely infected plants died. Diseased tissue was disinfested for 10 s in 1% NaOCl, rinsed with sterile water, and plated on potato dextrose agar (PDA) amended with 25 mg/liter of streptomycin sulfate. A fungus with morphological characters of Rhizoctonia solani (3) was consistently recovered. Ten-day-old mycelium grown on PDA at 22 ± 1°C appeared light brown, rather compact, and with radial growth. Sclerotia were irregular and measured between 0.5 and 2 mm. Pairings were made with tester isolates of AG 1, 2, 3, 4, 5, 6, 7, 11, and AG B1. The only successful anastomosis was with tester isolate AG 1 (ATCC 58946). The hyphal diameter at the point of anastomosis was reduced, the anastomosis point was obvious, and cell death of adjacent cells was observed. Results were consistent with other reports on anastomosis reactions (2). The description of sclerotia of the isolate AG1 was typical for subgroup 1A Type 2 (3). The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 688 bp showed a 100% homology with the sequence of R. solani AG-1A and the nucleotide sequence has been assigned (GenBank Accession No. HM044764). For pathogenicity tests, the inoculum of one isolate of R. solani from the nursery was prepared by growing the pathogen on PDA for 7 days. The foliage of 30-day-old potted plants of S. nemorosa cv. Blau Koenigin was artificially inoculated with an aqueous suspension of PDA and mycelium fragments (1 g per mycelium per plant) prepared from cultures with a blender. Plants were covered with plastic bags for 3 days. Plants inoculated with water and PDA fragments alone served as control treatments. Plants were maintained in a glasshouse at 20 to 25°C. The first symptoms, similar to those observed in the nursery, developed 7 days after foliar inoculation. R. solani was consistently reisolated from infected leaves. Control plants remained healthy. The pathogenicity test was carried out twice with similar results. To our knowledge, this is the first report of leaf blight of S. nemorosa caused by R. solani in Italy as well as worldwide. The importance of the disease is still unknown. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) D. E. Carling. Page 35 in: Rhizoctonia Species: Taxonomy, Molecular Biology, Ecology, Pathology and Disease Control. Kluwer Academic Publishers, the Netherlands, 1996. (3) B. Sneh et al. Identification of Rhizoctonia Species. The American Phytopathological Society, St Paul, MN, 1991.

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First Report of Powdery Mildew Caused by Podosphaera xanthii on Calendula officinalis in Italy

Plant Disease ◽

10.1094/pdis-92-1-0174c ◽

2008 ◽

Vol 92 (1) ◽

pp. 174-174 ◽

Cited By ~ 1

Author(s):

A. Garibaldi ◽

G. Gilardi ◽

M. L. Gullino

Keyword(s):

Powdery Mildew ◽

Its Region ◽

Pathogenicity Test ◽

Podosphaera Xanthii ◽

Calendula Officinalis ◽

First Report ◽

Potted Plants ◽

Blastn Analysis ◽

Voucher Specimens ◽

Pot Marigold

Calendula officinalis L. (Asteraceae) (pot marigold or English marigold) is an ornamental species grown in gardens and as potted plants for the production of cut flower. It was also used in ancient Greek, Roman, Arabic, and Indian cultures as a medicinal herb as well as a dye for fabrics, foods, and cosmetics. During the summer of 2007, severe outbreaks of a previously unknown powdery mildew were observed on plants in several gardens near Biella (northern Italy). Both surfaces of leaves of infected plants were covered with dense, white mycelia and conidia. As the disease progressed, infected leaves turned yellow and died. Mycelia and conidia also were observed on stems and flower calyxes. Conidia were hyaline, ellipsoid, born in short chains (four to six conidia per chain), and measured 27.0 to 32.1 (31.4) × 12.9 to 18.4 (18.2) μm. Conidiophores measured 49 to 77.3 (67.2) × 8 to 13.3 (10.8) μm and showed a foot cell measuring 44 to 59 (51.9) × 9.3 to 12.6 (11.3) μm followed by one shorter cell measuring 15.6 to 18.9 (17.6) × 10.4 to 13.6 (12.2) μm. Fibrosin bodies were present. Chasmothecia were spherical, amber colored, with a diameter of 89 to 100 (94.5) μm. Each chasmothecium contained one ascus with eight ascospores. On the basis of its morphology, the causal agent was determined to be a Podosphaera sp. (2). The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 588 bp showed a 100% homology with the sequence of Podosphaera xanthii (2). The nucleotide sequence has been assigned GenBank Accession No. EU100973. Pathogenicity was confirmed through inoculations by gently pressing diseased leaves onto leaves of healthy C. officinalis plants. Five plants were inoculated. Five noninoculated plants served as control. Plants were maintained in a greenhouse at temperatures ranging from 20 to 26°C. Eleven days after inoculation, typical symptoms of powdery mildew developed on inoculated plants. Noninoculated plants did not show symptoms. The pathogenicity test was carried out twice. To our knowledge, this is the first report of powdery mildew on C. officinalis in Italy. C. officinalis was previously described as a host to Sphaerotheca fuliginea (synonym S. fusca) in Great Britain (4) as well as in Romania (3). Voucher specimens are available at the AGROINNOVA Collection, University of Torino. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (3) E. Eliade. Rev. Appl. Mycol. 39:710, 1960. (4) F. J. Moore. Rev. Appl. Mycol. 32:380, 1953.

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First Report of Choanephora Blight Caused by Choanephora infundibulifera on Hibiscus rosa-sinensis in Korea

Plant Disease ◽

10.1094/pdis-02-14-0218-pdn ◽

2014 ◽

Vol 98 (9) ◽

pp. 1275-1275 ◽

Cited By ~ 2

Author(s):

J. H. Park ◽

S. E. Cho ◽

K. S. Han ◽

S. H. Lee ◽

H. D. Shin

Keyword(s):

Large Subunit ◽

Aerial Mycelium ◽

Its Region ◽

The United States ◽

Pathogenicity Test ◽

Potential Threat ◽

First Report ◽

Hibiscus Rosa Sinensis ◽

Initial Symptoms ◽

Chinese Hibiscus

Hibiscus rosa-sinensis L., commonly known as Chinese hibiscus, is an evergreen flowering shrub belonging to the Malvaceae and is widely cultivated throughout Asia including Korea. In August 2013, blight was observed on Chinese hibiscus in a commercial flower nursery in Seoul, Korea. Initial symptoms began as reddish purple spots at the tip of flowers and expanded to encompass entire flowers. Infected lesions appeared water-soaked, reddish brown, and were followed by rapid rotting of infected tissues. Approximately 50% of the plants surveyed were affected. Monosporous sporangiola formed on infected tissue were transferred to potato dextrose agar (PDA). Fungal colonies were obtained that were at first white with abundant aerial mycelium, and then became yellowish with the appearance of sporangiola. Sporangiophores bearing sporangiola were erect to slightly curved, unbranched, and hyaline. Funnel-shaped secondary vesicles formed on the primary vesicles. Sporangiola were indehiscent, ovoid to subglobose, smooth, non-striated, brown to dark brown, 10 to 27.5 × 8.5 to 17 μm, and sometimes germinated in culture. The fungus was identified as Choanephora infundibulifera (Curr.) D.D. Cunn. based on the morphological and cultural characteristics (2). Voucher specimens were housed in the Korea University Herbarium (KUS). An isolate obtained from KUS-F27535 was deposited in the Korean Agricultural Culture Collection (Accession No. KACC47643) and used for a pathogenicity test and molecular analyses. To confirm identity of the fungus, genomic DNA was extracted with DNeasy Plant Mini Kits (Qiagen Inc., Valencia, CA). The internal transcribed spacer (ITS) region of rDNA and the D1/D2 region of the large subunit (LSU) were amplified with the primers ITS1/ITS4 and NL1/LR3, respectively (3), and sequenced. The resulting 635-bp ITS and 680-bp D1/D2 sequences were deposited in GenBank (Accession Nos. KF486539 and KF486538). A GenBank BLAST search revealed that the ITS sequences showed 100% similarity with that of C. infundibulifera (JN943009) and D1/D2 sequences also showed 100% identity with that of C. infundibulifera (JN939193). A sporangiola suspension (2 × 104 cells/ml) was sprayed over three pots of the shrub, kept in a humid chamber for 2 days, and placed in greenhouse (28°C and 80 to 100% RH). Another three potted plants of the same age were sprayed with sterile water and served as controls. After 4 days, typical blossom blight symptoms, identical to the ones observed in the nursery, developed on the inoculated flowers. No symptoms were observed on controls. C. infundibulifera was re-isolated from inoculated plants. Pathogenicity test was conducted twice with the same results, fulfilling Koch's postulates. Choanephora blight caused by C. infundibulifera on H. rosa-sinenesis has been reported in Japan, Myanmar, Nepal, Guinea, and the United States (1). In Korea, there was one record of this fungus on H. syriacus (1). To our knowledge, this is the first report of C. infundibulifera on H. rosa-sinensis in Korea. This pathogen could be a potential threat to the production of this ornamental shrub over a prolonged period of hot and humid weather. References: (1) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, ARS, USDA, Retrieved February 28, 2014. (2) P. M. Kirk. Mycol. Pap. 152:1, 1984. (3) G. Walther et al. Persoonia 30:11, 2013.

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First Report of Puccinia lagenophorae on Common Groundsel (Senecio vulgaris) in Canada

Plant Disease ◽

10.1094/pdis-91-8-1058c ◽

2007 ◽

Vol 91 (8) ◽

pp. 1058-1058 ◽

Cited By ~ 5

Author(s):

W. L. Bruckart ◽

A. S. McClay ◽

S. Hambleton ◽

R. Tropiano ◽

G. Hill-Rackette

Keyword(s):

United States ◽

Its Region ◽

The United States ◽

Representative Specimen ◽

Rust Disease ◽

First Report ◽

Senecio Vulgaris ◽

Pcr Products ◽

Plant Pathol ◽

Common Groundsel

Rust disease on common groundsel was independently collected from two backyard gardens in Alberta, Canada during 2005, the first on September 11 in Sherwood Park (53.542°N, 113.262°W) and the second on September 18 in Edmonton (53.463°N, 113.593°W). Leaves of each specimen had clusters of orange, cup-shaped aecia, bordered by recurved peridia, the principal macroscopic signs of disease. Infected plants had twisted stems and deformed leaves. Spores of isolates from the two locations were (mean diameter [± s.d.; range]) 14.6 (± 1.4; 11.4 to 18.9) × 12.5 (± 1.1; 9.1 to 16.2) μm, orange, oval or angular, and many had refractive granules (3). Genomic DNA was extracted from small leaf pieces with multiple aecia, and the complete internal transcribed spacer (ITS) region of the rust was sequenced from PCR products. The sequences determined for a representative specimen from each location were identical, including two areas of ambiguity in the ITS1 spacer region. At position 7 were two overlapping peaks (A and C), and near position 130, sequencing failed because of a suspected insertion/deletion in some ITS copies. Difficulties of sequencing through this cytosine-rich area were reported by Littlefield et al. (3). Data from cloned PCR products confirmed the presence of two ITS genotypes in each DNA extract, one identical to a sequence published for Puccinia lagenophorae on Senecio vulgaris from the United Kingdom (GenBank Accession No. AY808060 (2), and the other identical to a sequence from the United States (GenBank Accession No. AY852264) (3). They differ by an A/C transversion at position 7 and an indel, an 8/9 base poly-C run beginning at position 130. Telia and teliospores were not observed in any of the 2005 samples (some collected as late as November) or in the 2006 Edmonton site samples. Identification of the pathogen as P. lagenophorae was based on host plant symptoms (3) and molecular characters. The original source of inoculum for these infections is unknown, but on December 5, 2006, diseased specimens with sporulating aecia were found beneath 45 cm of snow at the Edmonton location, in a garden area that had not been weeded during the summer. There is reported evidence that teliospores are not functional and that P. lagenophorae overwinters on infected plants that develop aecia in the spring (1). Specimens have been deposited at the Arthur Herbarium, Purdue University, West Lafayette, IN (Vouchers PUR N5414–N5417) and the National Mycological Herbarium of Canada, Ottawa, ON (Vouchers DAOM 237844, 237845, 237961, 237962, 237982, and 237990). The two cloned variants of the ITS sequence were deposited in GenBank (Accession Nos. EF212446 and EF212447). To our knowledge, this is the first report of groundsel rust caused by P. lagenophorae in Canada (G. Barron, personal communication, has images from Guelph in 2004 but no specimens were examined or preserved). Groundsel rust has been found at several locations in the United States (3) and has been reported on more than 60 species in several genera (4). Questions remain about the amount of damage that P. lagenophorae will cause to groundsel in North America and whether it will affect native Senecio species and their relatives. References: (1) J. Frantzen and H. Müller-Schärer. Plant Pathol. 48:483, 1999. (2) B. Henricot and G. Denton. Plant Pathol. 54:242, 2005. (3) L. Littlefield et al. Ann. Appl. Biol. 147:35, 2005. (4) M. Scholler. J. Plant Dis. Prot. 105:239, 1998.

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First Report of Botrytis Blight Caused by Botrytis cinerea on Gaura lindheimeri in Italy

Plant Disease ◽

10.1094/pdis-93-1-0107c ◽

2009 ◽

Vol 93 (1) ◽

pp. 107-107

Author(s):

A. Garibaldi ◽

D. Bertetti ◽

P. Pensa ◽

M. L. Gullino

Keyword(s):

Botrytis Cinerea ◽

Leaf Tissue ◽

Fluorescent Light ◽

Pathogenicity Test ◽

First Report ◽

Perennial Plant ◽

Potted Plants ◽

Plastic Bags ◽

Pathogenicity Tests ◽

Basal Portion

Gaura lindheimeri (wand flower) is a perennial plant belonging to the Onagraceae family that is used for perennial borders in xeric and mesic landscapes. It produces flowers floating above the plant like small, dancing butterflies. This plant is becoming popular in the Albenga Region (northern Italy) where white and rose varieties are grown as potted plants. In January of 2008, 5-month-old ‘Whirling Butterflies’ plants grown in plastic pots (14 cm in diameter) in the open field started showing symptoms of a previously unknown blight. When the disease developed, temperatures ranged between 3 and 17°C (average 9°C) and average relative humidity was 64%. Small, brown spots appeared on the basal portion of leaves first, eventually spreading to cover entire leaves. Subsequently, the pathogen developed abundant, soft gray mycelium on affected leaf tissue. Severely infected leaves eventually became completely rotten and desiccated. Sixty percent of plants were affected by the disease. Tissues were excised from diseased leaves, immersed in a solution containing 1% sodium hypochlorite for 10 s, and then cultured on potato dextrose agar (PDA) medium. The fungus produced abundant mycelium on PDA medium when incubated under constant fluorescent light at 22 ± 1°C. The conidia were smooth, hyaline, globoid, measuring 11.8 to 9.4 × 8.3 to 6.6 (average 10.7 × 7.4) μm, and are similar to those described for Botrytis cinerea. The identity of the pathogen was also confirmed by the production of numerous sclerotia on PDA plates incubated for 20 days at 8 ± 1°C. Sclerotia were dark, irregular, and measured 3 to 4 × 2 to 3 mm. The fungus was identified as B. cinerea on the basis of these characters (1). Pathogenicity tests were performed by spraying leaves of healthy, potted 8-month-old G. lindheimeri ‘Whirling Butterflies’ plants with a 105 conidia/ml suspension. Plants sprayed with water only served as controls. Five plants per treatment were used. Plants were covered with plastic bags for 6 days after inoculation and maintained in a growth chamber at 20 ± 1°C. The first foliar lesions developed on leaves 5 days after inoculation, whereas control plants remained healthy. B. cinerea was consistently reisolated from these lesions. The pathogenicity test was completed twice. To our knowledge, this is the first report of the presence of B. cinerea on G. lindheimeri in Italy. The economic importance of this disease will increase with the increased cultivation of this species. Reference: (1) H. L. Barnett and B. B. Hunter. Illustrated Genera of Imperfect Fungi. Burgess Publishing Company, Minneapolis, MN, 1972.

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First Report of Gray Mold of Rhizoma paridis Caused by Botrytis cinerea in China

Plant Disease ◽

10.1094/pdis-03-14-0336-pdn ◽

2014 ◽

Vol 98 (10) ◽

pp. 1434-1434 ◽

Cited By ~ 2

Author(s):

J. M. You ◽

Q. H. Wang ◽

X. M. Lin ◽

J. Guo ◽

L. Q. Ai ◽

...

Keyword(s):

Botrytis Cinerea ◽

Leading Edge ◽

Its Region ◽

Gray Mold ◽

Pathogenicity Test ◽

Heat Shock Protein 60 ◽

Chinese Medicinal Herb ◽

First Report ◽

Potted Plants ◽

Plastic Bags

Rhizoma paridis is a perennial, traditional Chinese medicinal herb. In May 2013, a disease was observed in an approximately 10 ha cultivated field in Enshi, Hubei Province, China. Approximately 80% of plants in the field were affected. Symptoms were visible on the basal leaves of affected plants. Chlorosis followed by necrosis started at the leaf tips and margins and gradually spread inward until the entire leaf was necrotic. Thick, gray mycelium and conidia were visible on both sides surface of leaves under wet, humid conditions. The leading edge of the chlorotic leaves was excised from 20 plant samples surface disinfested with 1% NaOCl solution for 1 min, rinsed in sterile water, air dried, and placed on potato dextrose agar (PDA). Plates were incubated at 22°C in the dark. Mycelia were initially hyaline and white, and became dark gray after 72 h. Mycelia were septate with dark branched conidiophores. Conidia were smooth, hyaline, ovoid, aseptate, and ranged from 8 to 14.5 × 7 to 8.5 μm. Numerous hard, small, irregular, and black sclerotia that were 1 to 3 × 2 to 5 mm were visible on PDA plates after 12 days. The fungus was identified as Botrytis cinerea on the basis of these characters (1). The internal transcribed spacer (ITS) region of rDNA was amplified using the ITS1 and ITS4 primer and sequenced (GenBank Accession No. KF265499). BLAST analysis of the PCR product showed 99% identity to Botryotinia fuckeliana (perfect stage of B. cinerea) (EF207415.1, EF207414.1). The pathogen was further identified to the species level as B. cinerea using gene sequences from glyceraldehyde-3-phosphate dehydrogenase (G3PDH), heat-shock protein 60 (HSP60), and DNA-dependent RNA polymerase subunit II (RPB2) (2) (KJ638600, KJ638602, and KJ638601). Pathogenicity was tested by spraying the foliage of 40 two-year-old plants with a suspension of 106 conidia per ml of sterile distilled water. Each plant received 30 ml of the inoculum. Ten healthy potted plants were inoculated with sterilized water as control. All plants were covered with plastic bags for 5 days after inoculation to maintain high relative humidity and were placed in a growth chamber at 22°C. The first foliar lesions developed on leaves 7 days after inoculation and were similar to those observed in the field. No symptoms developed on the control plants. B. cinerea was consistently re-isolated from all artificially inoculated plants. The pathogenicity test was completed twice. To our knowledge, this is the first report of gray mold of R. paridis caused by B. cinerea in China. The root of R. paridis is the most commonly used Chinese herbal medicine to treat viper bites. In recent years, cultivation of this herb has increased in China because of its high value. Consequently, the economic importance of this disease is likely to increase with the greater prevalence of this host species. References: (1) H. L. Barnett and B. B. Hunter. Illustrated Genera of Imperfect Fungi. Burgess Publishing Company, Minneapolis, MN, 1972. (2) M. Staats et al. Mol. Biol. Evol. 22:333, 2005.

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First Report of Gray Mold Caused by Botrytis cinerea on Stevia rebaudiana in Italy

Plant Disease ◽

10.1094/pdis-93-3-0318a ◽

2009 ◽

Vol 93 (3) ◽

pp. 318-318

Author(s):

A. Garibaldi ◽

D. Bertetti ◽

P. Pensa ◽

M. L. Gullino

Keyword(s):

Botrytis Cinerea ◽

Stevia Rebaudiana ◽

Its Region ◽

Morphological Characters ◽

Gray Mold ◽

Fluorescent Light ◽

Pathogenicity Test ◽

Leaf Extracts ◽

First Report ◽

Potted Plants

Stevia rebaudiana (sweetleaf) is a perennial shrub belonging to the Asteraceae family and is widely grown for its sweet leaves. With its extracts having as much as 300 times the sweetness of sugar, this species is used in many countries for the production of sugar substitutes. However, in Italy, as well as in other countries, this species cannot be grown for the use of its leaf extracts. This plant is grown in a few nurseries in the Albenga Region (northern Italy) as potted plants. In February of 2008, 3-month-old plants grown in plastic pots (14-cm diameter) under glasshouse on heated benches started showing symptoms of a previously unknown blight. The temperature in the glasshouse ranged between 16 and 20°C and plants were watered by sprinkle irrigation. Leaves, starting from the basal ones, showed small, brown spots that spread across the entire leaf surface. Subsequently, the crown and stem were infected, and the pathogen developed abundant, soft, gray mycelium on leaves and stems and in the middle of the heads of S. rebaudiana. Flowers were not present when the symptoms appeared. Severely infected leaves dried out and became necrotic. The disease was observed in one nursery in which 5% of the plants were affected. The margins of the lesions were excised from leaves, immersed in a solution containing 1% sodium hypochlorite, and then cultured on potato dextrose agar (PDA) medium. A fungus produced abundant mycelium when incubated under constant fluorescent light at 22 ± 1°C after 10 days. The conidia were smooth, hyaline, ovoid, measuring 15.5 to 8.3 × 11.1 to 7.3 (average 11.6 × 8.6) μm, and were similar to those described for Botrytis cinerea. Conidiophores were slender and branched with enlarged apical cells bearing conidia on short sterigmata. The identity of the fungus was also confirmed by the production of numerous, small, black sclerotia on PDA plates incubated for 20 days at 8 ± 1°C. Sclerotia were dark and irregular with a diameter ranging from 1 to 2 mm. These morphological characters identified the fungus as B. cinerea (2). The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLAST analysis (1) of the 780-bp segment showed a 100% homology with the sequence of Botryotinia fuckeliana (perfect stage of B. cinerea). The nucleotide sequence has been assigned GenBank Accession No. FJ486270. Pathogenicity tests were performed by spraying leaves of six healthy 6-month-old potted S. rebaudiana plants with a 105 conidia/ml suspension. Six plants sprayed with water only served as controls. Plants were covered with plastic bags for 3 days after inoculation to maintain high relative humidity and were placed in a growth chamber at 20 ± 1°C. The first foliar lesions developed on leaves 4 days after inoculation, whereas control plants remained healthy. B. cinerea was consistently reisolated from these lesions. The pathogenicity test was completed twice. To our knowledge, this is the first report of the presence of B. cinerea on S. rebaudiana in Italy. The disease has been reported in Ukraine (3) and more recently in Japan (4). The economic importance of this disease is at the moment limited. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) H. L. Barnett and B. B. Hunter. Illustrated Genera of Imperfect Fungi. Burgess Publishing Company, Minneapolis, MN, 1972. (3) J. Takeuch and H. Horie. Annu. Rep. Kanto-Tosan Plant Prot. Soc. 53:87, 2006. (4) V. F. Zubenko et al. Zash. Rast. 18, 1991.

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First Report of Puccinia pelargonii-zonalis Causing Rust on Pelargonium × hortorum in Xinjiang Province, China

Plant Disease ◽

10.1094/pdis-09-21-1965-pdn ◽

2021 ◽

Author(s):

Jin Sun ◽

Guo Qin Wang ◽

Jia Ge Song ◽

Biao Xu

Keyword(s):

Disease Incidence ◽

Large Subunit ◽

Economic Value ◽

The United States ◽

Concentric Circle ◽

Pathogenicity Test ◽

First Report ◽

Potted Plants ◽

Light Yellow ◽

Initial Symptoms

Geranium (Pelargonium × hortorum) is an ornamental plant cultivated throughout world. In May 2019, typical symptoms of rust with nearly 90% disease incidence were observed on leaves of Pel. × hortorum growing in pots in a scenic spot in the ancient city of Kashgar, Xinjiang province, China. Early symptoms of the disease appeared small lesions with pale-yellow halos on the lower leaf surfaces. Infected tissues subsequently formed a concentric circle of sori on lesion reaching a final diameter of 0.5 to 1.5 cm, which resulted in leaf blighting and premature. Two representative specimens were deposited in the Mycological Herbarium of Tarim University (HMUT 8001 and HMUT 8002). Urediniospores were globose or subglobose to ovoid, light brown, echinulate, thin-walled with two conspicuous subequatorial pores, 19.8 to 27.3 × 17.8 to 23.6 μm (24.3 × 21.7 μm average, n=30). Telia and teliospores were not seen. The sizes and characteristics of urediniospores were similar with those of Puccinia pelargonii-zonalis as described by Doidge (1926). To confirm the identification, genomic DNAs were extracted directly from sori on diseased leaves from isolates HMUT 8001 and HMUT 8002. The part of the nuclear large subunit (LSU, 28S) rDNA was amplified and sequenced following Aime et al. (2006), and deposited in GenBank (Accession Nos. MT648851 and MT648852). An NCBI blast search indicated that 99.6% identity of the LSU (772/775 nucleotides) with Puc. pelargonii-zonalis on Pel. hortorum (KX999887) from Australia (Marin-Felix et al. 2017). The phylogenetic analysis based on the LSU sequences using Maximum-Likelihood and Bayesian methods placed the Xinjiang isolates from Pel. × hortorum in the same clade with the reference sequences of Puc. pelargonii-zonalis. Pathogenicity test was confirmed by Koch’s postulates. Leaves of three healthy potted plants were sprayed with a spore suspension (2 × 105 spores/ml). Sterile water was sprayed on three healthy seedlings as controls. Inoculated and control plants were covered with a plastic bag and placed in a moist chamber with 90% relative humidity at 25°C. Initial symptoms were observed with small light-yellow spots on the upper surface after 15 days, but not in the control plants. Puc. pelargonii-zonalis has been previously reported on Pel. × hortorum in Argentina, Australia, Canada, Georgia, Greece, India, Mexico, New Zealand, Norway, Portugal, South Africa, the United States, and Venezuela (Farr and Rossman 2021). Geranium rust was first found in Yunnan province in southwestern China (Zhou and Zhuang 2005). However, this is the first report of geranium rust in Xinjiang province in northwestern China. The occurrence of the disease seriously affected their ornamental and economic value.

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First Report of Botrytis Blight Caused by Botrytis cinerea on Lavandula stoechas in Italy

Plant Disease ◽

10.1094/pdis-94-3-0380a ◽

2010 ◽

Vol 94 (3) ◽

pp. 380-380 ◽

Cited By ~ 1

Author(s):

A. Garibaldi ◽

D. Bertetti ◽

P. Pensa ◽

M. L. Gullino

Keyword(s):

Botrytis Cinerea ◽

Its Region ◽

Northern Italy ◽

Fluorescent Light ◽

Pathogenicity Test ◽

Commonwealth Mycological Institute ◽

First Report ◽

Potted Plants ◽

Lavandula Stoechas ◽

Plastic Bags

Lavandula stoechas or French lavender (Labiatae) is a perennial shrub that produces pinkish purple flowers and is endemic to the Mediterranean Region. In the Albenga area (northern Italy), this species is grown as a potted plant. In October 2008, symptoms of a previously unknown blight were observed in a commercial glasshouse in the Savona Province (northern Italy) on 10% of 3-month-old ‘Sugarberry Ruffles’ potted plants. Glasshouse temperatures ranged between 11 and 32°C (average of 21°C) and plants were overhead irrigated. Initially, leaves and stems appeared chlorotic. Subsequently, necrotic lesions developed on infected tissues. After 10 days, fluffy, gray mycelium became apparent on symptomatic tissue, especially on the basal parts of the plants. Severely infected plants eventually died. Tissues were excised from diseased leaves, immersed in an aqueous solution of 1% sodium hypochlorite for 10 s, and then cultured on potato dextrose agar (PDA). A fungus developed abundant mycelium when incubated under constant fluorescent light at 22 ± 1°C. Numerous small sclerotia developed on PDA plates incubated for 20 days at 8 ± 1°C. Sclerotia were dark and irregular and measured 2 to 5 × 1 to 2 mm. Conidia were smooth, gray, unicellular, ovoid, measured 9.4 to 13.6 × 6.2 to 7.9 (average 11.4 × 7.2) μm, and similar to those described for Botrytis cinerea (2). The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced. BLAST analysis (1) of the 573-bp segment was 100% similar to the sequence of Botryotinia fuckeliana (perfect stage of B. cinerea). The nucleotide sequence has been assigned GenBank Accession No. GQ375747. Pathogenicity tests were performed by spraying leaves of 9-month-old healthy potted L. stoechas ‘Blue Star’, ‘Madrid Blue’, ‘Madrid Purple’, and ‘Madrid White’ plants with a 7.5 × 104 conidia/ml spore suspension obtained from 7-day-old PDA cultures. Each plant received 5 ml of inoculum. Plants sprayed with water only served as controls. Four plants per treatment and per cultivar were used. Plants were covered with plastic bags for 4 days after inoculation and maintained in a growth chamber at 20 ± 1°C. The first lesions developed on flowers 5 days after inoculation, and 2 days later, lesions developed on leaves and stems. Lesions were similar to those observed in the commercial glasshouse. Control plants remained healthy. B. cinerea was consistently reisolated from these lesions. The pathogenicity test was completed twice. To our knowledge, this is the first report of the presence of B. cinerea on L. stoechas in Italy as well as worldwide. Botrytis blight previously has been described on L. angustifolia in Japan (4) and Poland (3). In Italy, the economic importance of the disease is currently still limited. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) M. B. Ellis. Dematiaceous Hyphomycetes. Commonwealth Mycological Institute, Kew, England, 1971. (3) L. B. Orlikowski and A. Valjiuskaite. Acta Mycol, 42:193, 2007. (4) J. Takeuch and H. Horie. Annu. Rep. Kanto-Tosan Plant Prot. Soc. 53:87, 2006.

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First Report of Botrytis Blight Caused by Botrytis cinerea on Chamelaucium uncinatum in Italy

Plant Disease ◽

10.1094/pdis-93-9-0968b ◽

2009 ◽

Vol 93 (9) ◽

pp. 968-968 ◽

Cited By ~ 1

Author(s):

A. Garibaldi ◽

D. Bertetti ◽

F. Tinivella ◽

M. L. Gullino

Keyword(s):

Botrytis Cinerea ◽

Its Region ◽

Northern Italy ◽

Fluorescent Light ◽

Pathogenicity Test ◽

Commonwealth Mycological Institute ◽

First Report ◽

Potted Plants ◽

Plastic Bags ◽

Chamelaucium Uncinatum

Chamelaucium uncinatum (wax flower), an evergreen shrub belonging to the Myrtaceae family, is suitable for growing in containers. In the Albenga area (northern Italy), this species is grown as a potted plant. In April 2009, symptoms of a previously unknown blight were observed in a commercial glasshouse in the Savona Province (northern Italy) on 80% of 500 potted plants of cv. Snow Flake. Glasshouse temperatures ranged between 16 and 22°C and plants were drip irrigated. Initially, leaves and calyces appeared chlorotic. Subsequently, necrotic lesions developed on flower stalks and occasionally the corollas. After 10 days, soft, gray mycelium became apparent on symptomatic tissue, especially on the foliage. Severely infected leaves and flowers eventually became completely necrotic and abscised. Tissues were excised from diseased leaves, immersed in a solution containing 1% sodium hypochlorite for 10 s, and then cultured on potato dextrose agar (PDA) medium. A fungus developed abundant mycelium when incubated under constant fluorescent light at 23 ± 1°C. Numerous, small sclerotia also developed on PDA plates incubated for 20 days at 8 ± 1°C. Sclerotia were dark, spheroid, and measured 0.5 to 1.8 × 0.5 to 1.5 (average 1.2 × 1.0) mm. Conidia were smooth, gray, unicellular, ovoid, measured 8.5 to 11.1 × 7.1 to 8.6 (average 9.7 × 7.8) μm, and similar to those described for Botrytis cinerea (2). The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLAST analysis (1) of the 495-bp segment showed 100% similarity with the sequence of Botryotinia fuckeliana (perfect stage of B. cinerea). The nucleotide sequence has been assigned the GenBank Accession No. GQ149477. Pathogenicity tests were performed by spraying leaves of healthy potted C. uncinatum with a spore suspension (2 × 104 conidia/ml) obtained from PDA cultures of the pathogen. Each plant received 30 ml of the inoculum. Plants sprayed with water only served as controls. Three plants per treatment were used. Plants were covered with plastic bags for 5 days after inoculation and maintained in a growth chamber at 20 ± 1°C. The first foliar lesions developed on leaves 7 days after inoculation and were similar to those observed in the commercial glasshouse, whereas control plants remained healthy. B. cinerea was consistently reisolated from these lesions. The pathogenicity test was completed twice. To our knowledge, this is the first report of the presence of B. cinerea on C. uncinatum in Italy as well as in Europe. The disease has been reported in California (3) and more recently in South Africa (4). In Italy, the economic importance of the disease is currently still limited. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) M. B. Ellis. Dematiaceous Hyphomycetes. Commonwealth Mycological Institute, Kew, England, 1971. (3) A. M. French. California Plant Disease Host Index. Calif. Dep. Food Agric., Sacramento, 1989. (4) L. Swart and S. Coertze. Plant Dis. 86:440, 2002.

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