First Report of Plectosporium Blight on Pumpkin and Squash Caused by Plectosporium tabacinum in New York

In early August 2004, pumpkin and zucchini squash (Cucurbita pepo) plants grown in conventional and organic commercial operations in Orange and Dutchess counties, respectively, showed spindle-shaped lesions on vegetative tissues and silver russeting and spots on fruit, typical of Plectosporium blight. Approximately 20% of pumpkin fruit were affected at this early time in yield development, while the zucchini planting had been abandoned due to disease. Symptomatic pieces of stem, petioles, and main leaf veins were excised, surface disinfected with 0.5% sodium hypochlorite, placed on one-quarter-strength potato dextrose agar, and incubated at 21°C with a 12-h photoperiod. Pale pink colonies with pinkish, hyaline, aerial mycelium developed from the tissues. When examined microscopically, simple and branched conidiophores with apical phialides were observed, as well as non- and one-septate ellipsoidal to slightly curved conidia that measured 7.5 to 13.0 × 2.5 to 3.3 μm. The fungus fits the description of Plectosporium tabacinum (van Beyma) M.E. Palm, W. Gams, & H.I. Nirenberg (synonyms Microdochium tabacinum (von Arx, 1984) and Fusarium tabacinum (Gams & Gerlagh, 1968) (1). Pathogenicity was tested on 10 seedlings each of pumpkin, zucchini, gourd (C. pepo), winter squash (C. moschata), and cucumber (Cucumis sativa). Plants were spray inoculated at the three true-leaf stage with a spore suspension at 104 conidia/ml in water with 1% gelatin. Plants were held overnight in a moist chamber and then transplanted into 12-cm-diameter pots and kept in the greenhouse for the rest of the experiment. P. tabacinum was reisolated from all inoculated plants which completes Koch's postulates. Symptoms were noted 3 days after inoculation on pumpkin, zucchini, and gourd, with typical spindle-shaped lesions on the main stem, petioles, and main leaf veins (2). Symptoms developed after 1 week on winter squash, and lesions were mostly concentrated on the older portion of the stem with occasional lesions on the petiole and main leaf veins. Symptoms on cucumber, however, did not develop until 2 weeks after inoculation and appeared as an inconspicuous line of coalesced lesions on the ridges of the main stem only. These symptoms could easily be misidentified as physical abrasions from handling or from wind scarring. These results confirm the high susceptibility of C. pepo species, and indicate that other cucurbits are susceptible, albeit at a lower level. To our knowledge, this is the first report of P. tabacinum in New York. A voucher specimen has been deposited in the Cornell Plant Pathology Herbarium (Accession No. CUP 67504). References: (1) M. E. Palm et al. Mycologia 87:397, 1995; (2) T. A. Zitter. Microdochium blight. Page 28 in: Compendium of Cucurbit Diseases. T. A. Zitter, D. L. Hopkins, and C. E. Thomas, eds. The American Phytopathological Society, St. Paul, MN, 1996.

Download Full-text

First Report of Leaf Spot Caused by Periconia igniaria on Yellow Starthistle in Russia

Plant Disease ◽

10.1094/pdis-92-6-0983a ◽

2008 ◽

Vol 92 (6) ◽

pp. 983-983 ◽

Cited By ~ 4

Author(s):

T. Kolomiets ◽

L. Pankratova ◽

Z. Mukhina ◽

D. Kassanelly ◽

T. Matveeva ◽

...

Keyword(s):

Aqueous Suspension ◽

Soil Fungus ◽

Aerial Mycelium ◽

Its Sequences ◽

Yellow Starthistle ◽

Invasive Weed ◽

Voucher Specimen ◽

First Report ◽

Russian State ◽

Nutrition Medium

Yellow starthistle (YST), Centaurea solstitialis L., is a weedy plant that is widely distributed in the Krasnodar Region of Russia. It is also an aggressive invasive weed in the western United States and a target of biological control efforts. In the summer of 2006, several hundred diseased plants were found near Taman, Russia. Symptoms of the disease were yellow, water-soaked leaf spots. Diseased leaves were collected, air dried, and sent to the Russian State Collection of Phytopathogenic Organisms at the All Russia Institute of Phytopathology (ARIP). The fungus isolated from the diseased leaves conformed to Periconia igniaria E.W. Mason & M.B. Ellis (teleomorph Didymosphaeria igniaria C. Booth) (1). Colonies of the fungus grew rapidly on potato glucose nutrition medium with aerial mycelium from fluffy to pressed and colorless at the beginning and darkening to black with age. The medium side of the colonies gradually became violet purple to wine colored. Conidiophores had aerial mycelia as much as 550 μm long and 9 to 13 μm wide tapering to 6 to 10 μm. Conidiophores were dark with short, swollen branched stipes. Conidia, formed in short twisted chains, were spherical, dark brown, 7 to 9 μm in diameter, and covered by 1 μm long spines. Yellow starthistle plants were grown in growth chambers with day/night air temperatures of 26 to 28/20 to 22°C, 60 to 70% relative air humidity, and 10,000 lx light for 16 h. Fifteen plants in the rosette stage were spray inoculated with an aqueous suspension of P. igniaria conidia at 5 × 106 conidia/ml and 5 ml per plant. Disease on leaves was observed on all plants 3 to 4 weeks after inoculation when the plants started to bolt. When the plants reached flowering stage, diffused yellow spots were observed on stems and inflorescences and all flowers died. Diseased leaves were surface disinfested and put on potato saccharose nutrition medium. P. igniaria was reisolated from 3 to 5 leaves of each plant and from flowers and stems that developed from 10 inoculated rosettes. Flowers of 10 YST plants were also inoculated with P. igniaria isolated from the previously inoculated plants. Disease developed in the flowers of all inoculated plants, and the symptoms were identical to those observed when rosettes were inoculated and disease followed bolting and flowering. No symptoms developed on four noninoculated plants included in each test. Internal transcribed spacer (ITS) sequences of the fungus were obtained and compared with sequences from GenBank. An uncultured soil fungus and three isolates of P. macrospinosa Lefebvre & Aar.G. Johnson produced the best homology (96%). No sequences for P. igniaria were available for comparison, but the description of P. macrospinosa (conidia 18 to 32 μm in diameter with 2.5 to 6 μm long spines) is clearly different than our isolate. ITS sequences for our isolate have been deposited in GenBank (Accession No. EU367468) and a voucher specimen has been deposited with the U.S. National Fungus Collection (BPI 878355). To our knowledge, this is the first report of P. igniaria causing disease on YST. Live cultures are being maintained at the Russian State Collection of Phytopathogenic Organisms in ARIP. Reference: (1) M. B. Ellis. Dematiaceous Hyphomycetes. CMI, Kew, UK, 1971.

Download Full-text

First Report of Stem Canker Disease of Pitaya (Hylocereus undatus and H. polyrhizus) Caused by Neoscytalidium dimidiatum in Taiwan

Plant Disease ◽

10.1094/pdis-08-11-0689-pdn ◽

2012 ◽

Vol 96 (6) ◽

pp. 906-906 ◽

Cited By ~ 18

Author(s):

M. F. Chuang ◽

H. F. Ni ◽

H. R. Yang ◽

S. L. Shu ◽

S. Y. Lai ◽

...

Keyword(s):

New York ◽

Aerial Mycelium ◽

Its Region ◽

Stem Canker ◽

Canker Disease ◽

First Report ◽

Neoscytalidium Dimidiatum ◽

Succulent Plant ◽

Sterile Medium ◽

Hylocereus Undatus

Pitaya (Hylocereus undatus and H. polyrhizus Britt. & Rose), a perennial succulent plant grown in the tropics, is becoming an emerging and important fruit plant in Taiwan. In September of 2009 and 2010, a number of pitaya plants were found to have a distinctive canker on stems. The disease expanded quickly to most commercial planting areas in Taiwan (e.g., Pintung, Chiayi, and Chunghua). Symptoms on the stem were small, circular, sunken, orange spots that developed into cankers. Pycnidia were erumpent from the surface of the cankers and the stems subsequently rotted. After surface disinfestation with 0.1% sodium hypochloride, tissues adjacent to cankers were placed on acidified potato dextrose agar (PDA) and incubated at room temperature for 1 week, after which colonies with dark gray-to-black aerial mycelium grew. Hyphae were branched, septate, and brown and disarticulated into 0- to 1-septate arthrospores. Sporulation was induced by culturing on sterile horsetail tree (Casuarina equisetifolia) leaves. Conidia (12.79 ± 0.72 × 5.14 ± 0.30 μm) from pycnidia were one-celled, hyaline, and ovate. The internal transcribed spacer (ITS) region of ribosomal DNA was PCR amplified with primers ITS1 and ITS4 (2) and sequenced. The sequence (GenBank Accession No. HQ439174) showed 99% identity to Neoscytalidium dimidiatum (Penz.) Crous & Slippers (GenBank Accession No. GQ330903). On the basis of morphology and nucleotide-sequence identity, the isolates were identified as N. dimidiatum (1). Pathogenicity tests were conducted in two replicates by inoculating six surface-sterilized detached stems of pitaya with either mycelium or conidia. Mycelial plugs from 2-day-old cultures (incubated at 25°C under near UV) were inoculated to the detached stems after wounding with a sterile needle. Conidial suspensions (103 conidia/ml in 200 μl) were inoculated to nonwounded stems. Noninoculated controls were treated with sterile medium or water. Stems were then incubated in a plastic box at 100% relative humidity and darkness at 30°C for 2 days. The symptoms described above were observed on inoculated stems at 6 to 14 days postinoculation, whereas control stems did not develop any symptoms. N. dimidiatum was reisolated from symptomatic tissues. To our knowledge, this is the first report of N. dimidiatum causing stem canker of pitaya. References: (1) P. W. Crous et al. Stud. Mycol. 55:235, 2006. (2) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, New York, 1990.

Download Full-text

First Report of Sclerotinia sclerotiorum on Common Ragweed (Ambrosia artemisiifolia) in Europe

Plant Disease ◽

10.1094/pdis.1999.83.3.302c ◽

1999 ◽

Vol 83 (3) ◽

pp. 302-302 ◽

Cited By ~ 1

Author(s):

Gy. Bohár ◽

L. Kiss

Keyword(s):

Sclerotinia Sclerotiorum ◽

Aerial Mycelium ◽

The United States ◽

Ambrosia Artemisiifolia ◽

American Phytopathological Society ◽

Common Ragweed ◽

First Report ◽

Sclerotinia Rot ◽

Stem Lesions ◽

Test Plants

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.

Download Full-text

First Report of Diaporthe phaseolorum on Sunflower (Helianthus annuus) in Croatia

Plant Disease ◽

10.1094/pdis-93-10-1074c ◽

2009 ◽

Vol 93 (10) ◽

pp. 1074-1074 ◽

Cited By ~ 2

Author(s):

K. Vrandecic ◽

J. Cosic ◽

D. Jurkovic ◽

T. Duvnjak ◽

L. Riccioni

Keyword(s):

New York ◽

Helianthus Annuus ◽

Morphological Characteristics ◽

Aerial Mycelium ◽

Petri Dish ◽

Aluminum Foil ◽

Pathogenic Fungi ◽

Fungal Species ◽

Universal Primers ◽

First Report

Sunflower (Helianthus annuus L.) is a crop that is grown worldwide for the production of edible oil. In Croatia, it has considerable economic significance. From 2004 to 2007, sunflower stems showed light-to-dark brown lesions of different sizes and shapes. The lesions were observed for the presence of pycnidia in affected areas. Isolations from infected tissue on potato dextrose agar (PDA) yielded in two fungal species. One, which was isolated in most cases, was the well known sunflower pathogen Diaporthe helianthi Munt. Cvet. Morphological characteristics, stromata pattern, formation of alpha and beta conidia, and ascostromata characteristic of the other isolated fungus matched the description of D. phaseolorum (Cooke & Ellis) Sacc. (2). D. phaseolorum frequency was 5%. On PDA, the fungus formed white, floccose, aerial mycelium that filled a petri dish (9 cm) in 6 days. D. phaseolorum produces conidiomata in black stromatic structures, which consist of pycnidia with alpha and beta conidia. The alpha conidia were unicellular, hyaline, ellipsoidal to fusiform, and 5.6 to 10.0 × 1.9 to 4.8 μm. The beta conidia were hyaline, elongated, filiform, straight, curved at one or both ends, and 11.7 to 27.6 × 0.7 to 2.0 μm. After 50 days, perithecia were formed. Asci were clavate and 27.64 to 40.1 × 5.70 to 8.2 μm. Eight ascospores formed within asci. Ascospores were two-celled, elliptic, hyaline, and slightly constricted at the septa, and 8.93 to 13.5 × 2.1 to 4.0 μm. Amplification and sequencing of the internal transcribed spacer (ITS) rDNA region were performed with ITS4 and ITS5 universal primers (3) on two isolates (Su9 and Su10) and data were deposited in GenBank (Accession Nos. GQ149763 and GQ149764). Comparison of sequences available in GenBank revealed that the ITS sequence was identical to D. phaseolorum found on Stokesia laevis Hill (Greene) (U11323/U11373) and identical to the strain CBS 116020 isolated from Aster exilis Elliot. (AY745018). On the basis of the obtained results of morphological characteristics and molecular approaches, the pathogen was identified as D. phaseolorum. Pathogenicity evaluation consisted of artificial infections on field-grown sunflower plants at the full button stage as described by Bertrand and Tourvielle (1). A leaf test was done by placing a mycelial plug of 5 × 5 mm from a cork borer of two isolates (Su9 and Su10) on the tip of the main vein. The inoculation site was covered with moistened, cotton wool and wrapped in aluminum foil to prevent the inoculum from drying out. Ten plants of each of the four replications were inoculated. Control plants were inoculated with pure PDA plugs. Lesions of 12 to 40 mm long were observed on the sunflower leaf 10 days after inoculation. Control plants did not develop symptoms. The pathogen was reisolated from the infected plants. To our knowledge, this is the first report of the finding of D. phaseolorum on sunflower in Croatia and we have no literature data about the occurrence of this fungus on sunflower in the world. References: (1) F. Bertrand and D. Tourvielle. Inf. Tech. CETIOM 98:12,1972. (2) E. Punithalingma and P. Holliday. No. 336 in: Descriptions of Pathogenic Fungi and Bacteria. CMI/CAB, Kew, Surrey, England, 1972. (3) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, Inc., New York, 1990.

Download Full-text

First Report of Powdery Mildew Caused by Podosphaera (Sphaerotheca) fusca on Euryops pectinatus in North America

Plant Disease ◽

10.1094/pdis.2000.84.9.1048a ◽

2000 ◽

Vol 84 (9) ◽

pp. 1048-1048 ◽

Cited By ~ 1

Author(s):

G. S. Saenz ◽

S. T. Koike ◽

N. Shishkoff

Keyword(s):

United States ◽

New York ◽

North America ◽

Powdery Mildew ◽

Fungal Growth ◽

The United States ◽

Voucher Specimen ◽

First Report ◽

Humidity Chamber ◽

Powdery Mildew Pathogen

Gray-leaved Euryops (Euryops pectinatus Cass., Asteraceae) is an evergreen shrub that is widely planted in landscapes in the United States. In the fall of 1999, powdery mildew was observed on E. pectinatus planted in landscapes in Redlands (San Bernardino County), CA. Symptoms consisted only of slight cupping of leaves. Fungal growth was observed on stems, leaves, petioles, and pedicels and was ectophytic and amphigenous. The white mycelium was patchy to effuse. Hyphal appressoria were indistinct (1). Conidiophore foot cells were cylindric and sometimes were tapered toward or constricted at the base. Foot cells measured 30 to 50 by 10 to 12 μm and were followed by one to two shorter cells. Conidia were cylindric to slightly doliform, borne in chains of two to three, and measured 26 to 38 by 14 to 18 μm. Conidial length to width ratios ranged from 1.7 to 2.4. Catenate conidia had crenate edge lines (3). Conidia possessed conspicuous fibrosin bodies and from their sides produced short germ tubes without appressoria. Cleistothecia were not observed. Based on these characters, the fungus was identified as Podosphaera fusca (Fr.) U. Braun & N. Shishkoff (Podosphaera sect. Sphaerotheca) (1,2). Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of healthy E. pectinatus plants. Plants were incubated in a humidity chamber at 22 to 24°C and after 12 to 14 days powdery mildew colonies developed. E. pectinatus cv. Viridis, a cultivar that lacks the extensive pubescence of E. pectinatus, also developed disease when inoculated. This appears to be the first report of powdery mildew on E. pectinatus in North America. A voucher specimen has been deposited into the University of California Herbarium (accession # UC1738635). P. fusca was also observed on cv. Viridis in a nursery in New York in 1999. It is unclear where this pathogen originated. P. fusca parasitizes a large number of asteraceous species including dandelion (Taraxacum officinalis) and sowthistle (Sonchus spp.) weeds, which occur in the area and sometimes are infected with powdery mildew. The Euryops powdery mildew pathogen may be a race that is different than those found on other composites in the United States. The fungus was observed on plants in shaded areas but not on plants in full sun. References: (1) U. Braun. Nova Hedwigia 89:1, 1987. (2) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (3) H. D. Shin and Y. J. La. Mycotaxon 46:445, 1993.

Download Full-text

First Report of Puccinia polysora on Corn in Argentina

Plant Disease ◽

10.1094/pdis.2002.86.2.187b ◽

2002 ◽

Vol 86 (2) ◽

pp. 187-187 ◽

Cited By ~ 1

Author(s):

J. R. Hernández ◽

M. Yasem de Romero ◽

C. G. Díaz ◽

J. C. Ramallo

Keyword(s):

New York ◽

Zea Mays L ◽

Rust Fungus ◽

Growing Season ◽

Rust Fungi ◽

Yield Losses ◽

American Phytopathological Society ◽

First Report ◽

Northwest Argentina ◽

Puccinia Polysora

Corn (Zea mays L.) is an important crop in northwest Argentina but acreage has declined over the last several years due to disease problems. During the 2000 to 2001 growing season, leaf diseases were observed on corn growing in northeastern Tucumán Province (Departamiento Leales), which resulted in yield losses. One of the most prevalent diseases was caused by a rust fungus that produced both uredinial and telial stages. At the time of flowering 32% of the leaf area was infected, and 3 weeks later 69% was infected. Three rust fungi are known from corn (2), and this fungus was identified as Puccinia polysora Underw. based on the morphology of the two types of sori and spores (1). Although known from most tropical and subtropical regions, to our knowledge, this is the first report of P. polysora in Argentina (voucher BPI 841342). Tucumán Province, where the disease was observed, is a subtropical region with temperatures during the growing season >24°C and a relative humidity >90%. P. polysora has not been observed in the Pampas Humedas, the corn belt of Argentina, possibly because the area is more temperate than northwest Argentina and therefore the environment is not conducive to disease development or perhaps P. polysora has not been introduced into the region. References: (1) G. B. Cummins. The Rust Fungi of Cereals, Grasses and Bamboos. Springer-Verlag, New York, 1971. (2) J. K. Pataky. Rusts. Pages 35–38 in: Compendium of Corn Diseases, 3rd ed. The American Phytopathological Society, St. Paul, MN, 1999.

Download Full-text

First Report of Root Rot on Asparagus Caused by Phytophthora megasperma in Canada

Plant Disease ◽

10.1094/pdis.2003.87.4.447a ◽

2003 ◽

Vol 87 (4) ◽

pp. 447-447 ◽

Cited By ~ 1

Author(s):

V. Vujanovic ◽

C. Hamel ◽

S. Jabaji-Hare ◽

M. St-Arnaud

Keyword(s):

New York ◽

Root Rot ◽

Yield Loss ◽

Crown Rot ◽

Asparagus Officinalis ◽

American Phytopathological Society ◽

Phytophthora Megasperma ◽

First Report ◽

Rainy Period ◽

Crown Tissue

In August 2002, Phytophthora megasperma Drechs. was isolated from wilted plants of Asparagus officinalis L. cv. Guelph Millenium displaying spear and crown rot. Six affected plants were sampled in a commercial asparagus field located in the Saguenay-Lac-Saint-Jean Region (300 km northeast of Montreal, Quebec, Canada). The fungus was isolated from asparagus fern stalks, crown tissue, and spears after a rainy period and identified using morphological and cultural characteristics (2). In pinkish 4-week-old cultures, unbranched stalks bore abundant sporangia, which were ovoid to obpyriform in shape, 15 to 45 m long, and 10 to 30 m in diameter. Characteristic circular oospores >30 m in diameter were produced on V8 juice agar at 25°C in darkness after 1 month. Pathogenicity was tested on asparagus cvs. Guelph Millenium and Jersey Knight. A mycelium suspension (3 ml at 106 CFU/ml) prepared from 1-week-old shaken potato dextrose (PD) broth was sprayed on 30 1-week-old seedlings grown in petri plates filled with sterilized, moist, sandy soil and held at 20°C (day/night). Controls received sterile PD broth. Within 3 weeks of incubation in the dark, inoculated seedlings exhibited necrotic symptoms similar to those observed initially, while controls remained healthy. The pathogen was isolated from 75% of the ‘Guelph Millenium’ and 98% of the ‘Jersey Knight’ symptomatic seedlings, but not isolated from the control seedlings. In North America, disease caused by P. megasperma resulting in yield loss has been reported in California and New York (1,3). In Canada, the etiology of asparagus diseases is not well characterized. To our knowledge, this is the first report of P. megasperma on asparagus plants in Canada. References: (1) P. A. Ark and J. T. Barrett. Phytopathology 28:754, 1938. (2) D. C. Erwin et al. Phytophthora: Its Biology, Taxonomy, Ecology, and Pathology. The American Phytopathological Society, St Paul, MN, 1983. (3) T-L. Kuan and D. C. Erwin. Phytopathology 70:333, 1980.

Download Full-text

First Report of Powdery Mildew Caused by an Oidium sp. on Papaver nudicaule in Italy

Plant Disease ◽

10.1094/pdis.2004.88.6.682b ◽

2004 ◽

Vol 88 (6) ◽

pp. 682-682

Author(s):

A. Garibaldi ◽

A. Minuto ◽

D. Bertetti ◽

M. L. Gullino

Keyword(s):

Powdery Mildew ◽

Northern Italy ◽

Cut Flower ◽

Plant Leaves ◽

American Phytopathological Society ◽

Voucher Specimen ◽

First Report ◽

Erysiphe Cruciferarum ◽

Comprehensive Treatise ◽

The University

Iceland poppy (Papaver nudicaule L.) is grown on the Italian Riviera for export as a cut flower and its importance in the industry is increasing. During the spring of 2003, severe outbreaks of powdery mildew that had not been reported previously, occurred in several commercial plantings grown outdoors in containers near Imperia in northern Italy. Mycelium was observed on all green organs of the plant (leaves, stems, and petioles). Both surfaces on the leaves were affected, and heavily colonized leaves were distorted. As the disease progressed, diseased leaves turned yellow and died. The disease did not affect the flowers. Conidia were hyaline, cylindric, and measured 10.8 to 29.8 × 16.8 to 48.0 μm (average 13.7 × 37.3 μm). Foot cells were cylindric and appressoria unlobed. Fibrosin bodies were not present, and cleistothecia were not observed. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1,2). Pathogenicity was confirmed by gently pressing leaves with visible sporulation onto the leaves of five 90-day-old P. nudicaule plants that were healthy and free of symptoms. Five noninoculated healthy plants served as controls. Inoculated and noninoculated plants were maintained in a growth chamber at 15°C with a 12-h photoperiod. After 7 to 10 days, typical symptoms of powdery mildew developed on inoculated plants but not on noninoculated plants. Previously, Erysiphe cruciferarum Opiz ex L. Junell has been reported on P. nudicaule in all continents, and E. cichoracearum DC. and E. polygoni DC. have been reported in several countries, including Italy, as a causal agent of powdery mildew on other species of Papaver including P. rhoeas and P. strigosum. To our knowledge, this is the first report of powdery mildew caused by an Oidium sp. on P. nudicaule in Italy. The voucher specimen is kept in the department collection at the University of Torino. References: (1) R. Belanger et al., eds. The Powdery Mildew A Comprehensive Treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia. 89:700, 1987.

Download Full-text

First Report of Anthracnose Caused by Colletotrichum sansevieriae on Sansevieria in Korea

Plant Disease ◽

10.1094/pdis-04-13-0402-pdn ◽

2013 ◽

Vol 97 (11) ◽

pp. 1510-1510 ◽

Cited By ~ 2

Author(s):

J. H. Park ◽

K. S. Han ◽

J. Y. Kim ◽

H. D. Shin

Keyword(s):

United States ◽

Agricultural Research ◽

Aerial Mycelium ◽

Its Region ◽

The United States ◽

Culture Collection ◽

Infected Leaf ◽

Conidial Suspension ◽

Voucher Specimen ◽

First Report

Sansevieria, Sansevieria trifasciata Prain, is cultivated in greenhouses and is used as a potted interior foliage plant in Korea. In April 2012, several plants (cv. Moonshine) exhibiting typical anthracnose symptoms from a local nursery were sent to the plant clinic of Gyeonggi-Do Agricultural Research and Extension Services for diagnosis. The leaf lesions began as round, partly water-soaked, pale greenish to grayish spots, which enlarged and ultimately coalesced, resulting in severe leaf blight. Concentric rings of blackish acervuli were formed in the expanding lesions of mostly 2 to 4 cm in diameter. Acervuli were mostly epiphyllous, circular to ellipsoid. Setae were aseptate to 3-septate, dark brown at the base, paler upwards, acicular, and up to 180 μm long. Conidia (n = 30) were oblong-elliptical to obovate, sometimes fusiform-elliptical, guttulate, hyaline, and 14 to 24 × 5 to 7.5 μm (mean 18.6 × 6.4 μm). Hyphopodial appressoria were dark brown to blackish, globose to clavate in outline, and 5 to 12 × 4 to 8 μm. Colonies on potato dextrose agar (PDA) were grayish-white, felted with cottony-white aerial mycelium on a gray to olivaceous gray background in culture. Gelatinous salmon- to orange-colored conidial masses were produced abundantly after one week's incubation. The morphological and cultural characteristics of the fungus were consistent with the description of Colletotrichum sansevieriae M. Nakamura & M. Ohzono (2,3). A voucher specimen was deposited in the Korea University herbarium (KUS-F26637). An isolate was deposited in the Korean Agricultural Culture Collection (Accession No. KACC46835). Fungal DNA was extracted with DNeasy Plant Mini DNA Extraction Kits (Qiagen Inc., Valencia, CA). The complete internal transcribed spacer (ITS) region of rDNA was amplified with the primers ITS1/ITS4 and sequenced. The resulting 569-bp sequences were deposited in GenBank (Accession No. KC847065). A BLAST search in GenBank exhibited 100% nucleotide identity with sequence of C. sansevieriae (JF911349) from the United States and >99% similarity with that of HQ433226 from Australia. To confirm pathogenicity, inoculum was prepared by harvesting conidia from 3-week-old cultures on PDA. A conidial suspension (2 × 106 conidia/ml) was sprayed over the five leaves of sansevieria ‘Moonshine’ wounded with a fine needle. Five leaves sprayed with sterile water served as controls. Plants were covered with plastic bags to maintain 100% relative humidity for 48 h and then kept in a greenhouse (22 to 28°C and 70 to 80% RH). Within 12 days, symptoms identical to those observed in originally infected leaf developed on all inoculated leaves. No symptoms were observed on control plants. C. sansevieriae was reisolated from the lesions of inoculated plants, fulfilling Koch's postulates. Sansevieria anthracnose associated with C. sansevieriae has been reported in Japan (2), Australia (1), and the United States (3). To our knowledge, this is the first report of sansevieria anthracnose in Korea. Our observations in sansevieria nurseries suggest that preventing wound infection as well as maintaining good plant hygiene in greenhouses might be main strategies for this disease. References: (1) R. Aldaoud et al. Australas. Plant Dis. Notes 6:60, 2011. (2) M. Nakamura et al. J. Gen. Plant Pathol. 72:253, 2006. (3) A. J. Palmateer et al. Plant Dis. 96:293, 2012.

Download Full-text