First Report of Anther Smut Caused by Microbotryum violaceum on Forked Catchfly (Silene dichotoma) in Turkey

Forked catchfly (Silene dichotoma Ehrh.), family Caryophyllaceae, is a common and native plant in rangelands and pastures in Turkey. It is also an introduced plant that is widely distributed in North America. In May of 2007, approximately 20 forked catchfly plants on the campus of Ondokuz Mayis University in Samsun, Turkey were found diseased with the anther smut fungus Microbotryum violaceum (Pers.:pers.) G. Deml & Oberw. (Basidiomycota, Microbotryomycetes, Microbotryales [3], Microbotryaceae). All anthers in all flowers of diseased plants were smutted. Diseased flowers were collected, air dried, and sent to the quarantine facility of the Foreign Disease-Weed Science Research Unit (FDWSRU), USDA/ARS, Fort Detrick, MD. Teliospores within the flowers were extracted and observed microscopically. Teliospores were globose, 6 to 9 μm (mean 6.5 μm) in diameter, pale violet, with reticulate walls, and matching the description of M. violaceum (4). Nucleotide sequences for the internal transcribed spacers (ITS 1 and 2) and 5.8S ribosomal region (GenBank Accession No. EU122308) were aligned with other sequences in GenBank with the BLAST algorithm. Sequences of this isolate aligned 99% with sequences of other isolates of M. violaceum, M. lychnidis-dioicae (A.P. de Candolle ex J.I. Liro) G. Deml & F. Oberwinkler, and M. silenes-inflatae (A.P. de Candolle ex J.I. Liro) G. Deml & F. Oberwinkler and clustered with other M. violaceum isolates. M. violaceum is an obligate parasite of many plant species in the Caryophyllaceae family, and the fungus has been widely studied as a model for population genetics and evolutionary biology (2). To our knowledge, this is the first report of M. violaceum parasitizing forked catchfly in Turkey, and is the only report of this fungus-plant interaction in Asia Minor (1). The fungus has not been reported from this plant in North America (1). A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI 878235) and living spores are being maintained at FDWSRU. References: (1) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory. Online publication. ARS, USDA, 2007. (2) T. Giraud. Heredity 93:559, 2004. (3) D. S. Hibbett et al. Mycol. Res. 111:509, 2007. (4) K. Vánky. European Smut Fungi. Gustav Fischer Verlag, Stuttgart, Germany, 1994.

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First Report of an Ovary Smut of Italian Thistle Caused by a Microbotryum sp. in Greece

Plant Disease ◽

10.1094/pd-90-0681b ◽

2006 ◽

Vol 90 (5) ◽

pp. 681-681 ◽

Cited By ~ 2

Author(s):

D. K. Berner ◽

M. B. McMahon ◽

J. Kashefi ◽

E. Erbe

Keyword(s):

United States ◽

Biological Control ◽

Biological Control Agent ◽

Science Research ◽

The United States ◽

Internal Transcribed Spacers ◽

Smut Fungi ◽

Invasive Weed ◽

Voucher Specimen ◽

First Report

Italian thistle (Carduus pycnocephalus L.), family Asteraceae, is a common weed in Greece. It is also a problematic invasive weed in the western United States and a target of biological control efforts. In May 2005, smutted capitula of Italian thistle were found in an abandoned field in Halkiades, Greece. A total of 38 smutted plants, representing approximately 20% of those plants present, were found in a portion of the field that was lightly infested with Italian thistle. In most cases, capitula of all diseased flowers were smutted. In one or two cases, capitula on some branches of the plants were smutted, whereas capitula on other branches were healthy. Diseased capitula were noticeably more globose than healthy ovoid capitula, and diseased capitula did not open completely. When diseased capitula were split open, the ovaries in all florets within the capitula were filled with powdery masses of smut teliospores. Diseased capitula were collected, air dried, and sent to the quarantine facility of the Foreign Disease-Weed Science Research Unit (FDWSRU), USDA/ARS, Fort Detrick, MD. Teliospores within the capitula were extracted and observed microscopically. Teliospores of isolate DB05-014 were relatively uniform in shape and size, globose, 12.0 to 17.3 × 12.3 to 18.0 μm (mean 14.5 × 15.1 μm), violet tinted pale to medium yellowish-brown; wall reticulate appearing as coarse, radiate wings on the spore margin, 5 to 7 polyangular meshes per spore diameter, muri, 0.7 to 2.0 μm high in optical median view appearing as gradually narrowing blunt spines, 0.5 to 1 μm wide at their basis; in scanning electron microscopy (SEM), the meshes were subpolygonal, wall and interspaces were finely verruculose. Teliospores were more globose and slightly smaller than the description of Microbotryum cardui (A. A. Fischer Waldh.) Vánky (2), but the mean sizes were within the described range. When compared with teliospores of M. cardui on C. acanthoides, the numbers of polyangular meshes per spore diameter were within the range of the description using SEM, but the muri were about one-half of the height of those described. Nucleotide sequences for the internal transcribed spacers (ITS 1 and 2) and 5.8S ribosomal region (GenBank Accession No. AY280460) were aligned with sequences of other smut fungi using the BLAST algorithm of the National Center for Biotechnology Information. The closest alignment of DB05-014 was with M. scorzonerae (590 of 627 bp identities or 94% with 2% gaps). No sequences of M. cardui were available for comparison, but only M. cardui has been reported on Carduus spp. (1,2). Another smut reported on a Carduus sp. is Thecaphora trailii (1). DB05-014 is a likely variant of M. cardui from a previously unknown host. Italian thistle is an annual plant that reproduces solely by seeds (achenes). Because of the lack of seed production on smutted plants and the systemic nature of the disease, this fungus has great potential as a biological control agent for Italian thistle in the United States. A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI 871812). To our knowledge this is the first report of a Microbotryum sp. parasitizing C. pycnocephalus. References: (1) K. Vánky. European Smut Fungi. Gustav Fischer Verlag, Stuttgart, Germany, 1994. (2) K. Vánky and D. Berner. Mycotaxon 85:307, 2003.

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First Report of Anthracnose of Salsola tragus Caused by Colletotrichum gloeosporioides in Russia

Plant Disease ◽

10.1094/pdis-92-9-1366b ◽

2008 ◽

Vol 92 (9) ◽

pp. 1366-1366 ◽

Cited By ~ 2

Author(s):

T. Kolomiets ◽

O. Skatenok ◽

A. Alexandrova ◽

Z. Mukhina ◽

T. Matveeva ◽

...

Keyword(s):

Colletotrichum Gloeosporioides ◽

Science Research ◽

Research Unit ◽

Internal Transcribed Spacers ◽

Conidial Suspension ◽

Voucher Specimen ◽

First Report ◽

Glucose Agar ◽

Stems And Leaves ◽

C 30

In October of 2006, dying Salsola tragus L. (Russian thistle, tumbleweed), family Chenopodiaceae, plants were found along the Azov Sea at Chushka, Russia. Approximately 40 plants in the area were diseased and almost 80% of these were dying. Plants were approximately 1 m tall × 0.5 m wide. Dying plants had irregular, necrotic lesions along the length of the stems. Leaves of these plants were also necrotic. Lesions on stems and leaves were dark brown and usually coalesced. Diseased stems were cut into 3- to 5-mm pieces, disinfested in 70% ethyl alcohol, and then placed onto the surface of potato glucose agar (PGA). Numerous, waxy, subepidermal acervuli with 110 μm long (mean) black setae were observed in all of the lesions after 2 to 3 days. Conidiophores were simple, short, and erect. Conidia were one-celled, hyaline, ovoid to oblong, falcate to straight, and measured 12.9 to 18.0 × 2.8 to 5.5 μm (mean 15.6 × 4.2 μm). Appressoria formed 24 h after placing conidia on a dialysis membrane over 20% V8 juice agar. Appressoria measured 4.0 to 13.9 × 2.4 to 8.8 μm (mean 7.0 × 5.2 μm). These characters conformed to the description of Colletotrichum gloeosporioides (Penz.) Penz. & Sacc. in Penz. (1). A voucher specimen was deposited with the U.S. National Fungus Collections, Beltsville, MD (BPI 878389). Nucleotide sequences for the internal transcribed spacers (ITS 1 and 2) were deposited in GenBank (Accession No. EU530697) and aligned with ITS sequences of two other isolates from S. tragus. There was 100% similarity to each isolate, one from Greece (Accession No. DQ344621) and one from Hungary (Accession No. EU805538). Axenic cultures on PGA were sent to the Foreign Disease-Weed Science Research Unit, USDA, ARS, Fort Detrick, MD for testing in quarantine. Conidia were harvested from 14-day-old cultures grown on 20% V8 juice agar, and healthy stems and leaves of 30-day-old plants of S. tragus (13 plants) were spray inoculated with an aqueous conidial suspension of 1.0 × 106 conidia/ml plus 0.1% v/v polysorbate 20. Another 13 control plants were sprayed with water and surfactant without conidia. Plants were placed in an environmental chamber at 100% humidity for 16 h in the dark at 25°C. After approximately 24 h, all plants were transferred to a greenhouse at 20 to 25°C, 30 to 50% relative humidity, and natural light augmented by 12-h light periods with 500 W sodium vapor lights. Lesions developed on stems of all inoculated plants after 7 days. After 14 days, nine plants were dead and all inoculated plants were dead after 3 weeks. No symptoms developed on control plants. C. gloeosporioides was reisolated from stem pieces of all inoculated plants, and the morphology of the reisolated pathogen was the same as that of the initially isolated pathogen. To our knowledge, this is the first report of anthracnose caused by C. gloeosporioides on S. tragus in Russia. Reference: (1) B. C. Sutton. Page 15 in: Colletotrichum Biology, Pathology and Control. J. A. Bailey and M. J. Jeger, eds. CAB International, Wallingford, UK, 1992.

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First Report of Leaf Spot Caused by Cercospora bizzozeriana on Hoary Cress in Russia

Plant Disease ◽

10.1094/pdis-92-2-0316c ◽

2008 ◽

Vol 92 (2) ◽

pp. 316-316

Author(s):

Z. M. Mukhina ◽

D. Kassanelly ◽

D. K. Berner ◽

H. J. Dubin

Keyword(s):

Biological Control Agent ◽

Aqueous Suspension ◽

Science Research ◽

Research Unit ◽

Invasive Weed ◽

Voucher Specimen ◽

First Report ◽

Leaf Spots ◽

White Leaf ◽

Hoary Cress

Hoary cress (Lepidium draba (L.) subsp. draba (synonym = Cardaria draba (L.) Desv.) (1), family Brassicaceae, is a common weed in Russia but it is an aggressive invasive weed in the northwestern United States. In the summer of 2006, dying hoary cress plants were found near Kugoyeyskoye in the Krylovskoy area of the Krasnodar Region of Russia. Plants had grayish white leaf spots on most of the leaves. In some cases, the diseased leaf spots dropped out of the leaves producing shot-holes. In most cases, the leaf spots coalesced and the leaves wilted and died. Diseased leaves were collected, air dried, and sent to the quarantine facility of the Foreign Disease-Weed Science Research Unit (FDWSRU), USDA/ARS, Fort Detrick, MD. The air-dried leaves were observed microscopically, and numerous conidiophores and conidia were observed on both sides of leaves within and around the lesions. The fungus isolated (DB06-018) conformed to the description of Cercospora bizzozeriana Saccardo & Berlese (2). Conidiophores were 1 to 5 geniculate, unbranched, pale olive-brown, and uniform in color and width (4 μm). Conidia were multiseptate, hyaline, cylindric, straight to slightly curved, and measured 57 to 171 μm (average 103) long × 3.8 to 6.7 μm (average 4.6) wide. Leaves of rosettes (10 to 15 cm in diameter) of four hoary cress plants were spray inoculated with an aqueous suspension of conidia (1 × 105/ml) and mycelia harvested from 6- to 8-day-old cultures grown on V8 medium. Inoculated plants and two noninoculated plants were placed in a dew chamber at 20°C in darkness and continuous dew. After 96 h, plants were moved from the dew chamber to a greenhouse bench. All plants were watered twice daily. After 12 days, symptoms were observed on all inoculated plants. Symptoms were identical to those observed in the field in Russia. No symptoms were observed on noninoculated plants. C. bizzozeriana was reisolated from the leaves of all symptomatic plants. Nucleotide sequences were obtained for the internal transcribed spacer regions ITS1 and ITS2 and the 5.8S ribosomal RNA gene (GenBank Accession No. EU031780) and aligned with the same sequences obtained from another C. bizzozeriana isolate (GenBank Accession No. DQ370428) collected in Tunisia. There was 100% alignment of the two sequences with no gaps. Both isolates of C. bizzozeriana are destructive pathogens on hoary cress and locally severe epidemics have been observed in both Russia and Tunisia (4). This fungus has also been reported in North America (3) and has the potential as a biological control agent where the weed is a problem. To our knowledge, this is the first report of C. bizzozeriana on L. draba subsp. draba in Russia. A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI 878175). Live cultures are being maintained at FDWSRU. References: (1) I. A. Al-Shehbaz and K. Mummenhoff. Novon 12:5, 2002. (2) C. Chupp. A Monograph of the Fungus Genus Cercospora. C. Chupp, Ithaca, New York, 1953. (3) I. L. Conners. Res. Bra. Can. Dep. Agric. 1251:1, 1967. (4) T. Souissi et al. Plant Dis. 89:206, 2005.

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First Report of a Leaf Spot Caused by Alternaria brassicae on the Invasive Weed Lepidium draba in North America

Plant Disease ◽

10.1094/pdis-93-8-0846a ◽

2009 ◽

Vol 93 (8) ◽

pp. 846-846 ◽

Cited By ~ 1

Author(s):

A. J. Caesar ◽

R. T. Lartey

Keyword(s):

North America ◽

Chinese Cabbage ◽

Leaf Spot ◽

The United States ◽

Alternaria Brassicae ◽

Voucher Specimen ◽

First Report ◽

Leaf Spots ◽

Black Spots ◽

Lepidium Draba

The exotic, rangeland weed Lepidium draba L., a brassicaceous perennial, is widely distributed in the United States. For example, Oregon contains 100,000 ha of land infested with L. draba (2). Because it is capable of aggressive spread and has the potential to reduce the value of wheat-growing land (4), it is the target of biological control research. The application of multiple pathogens has been advocated for control of other brassicaceous weeds, including the simultaneous application of biotrophic and necrotrophic pathogens (3). In pursuit of this approach, in 2007, we discovered the occurrence of leaf spots on approximately 90% of L. draba plants near Shepherd, MT, which were distinct from leaf lesions caused by Cercospora bizzozeriana (1). The lesions were initially tiny, black spots enlarging over time to become circular to irregular and cream-colored around the initial black spots and sometimes with dark brown borders or chlorotic halos. Conidia from the lesions were light brown, elongate and obclavate, produced singly from short conidia, with 8 to 12 transverse septa, and 2 to 6 longitudinal septa. The spore body measured 25 to 35 × 200 to 250 μm with a beak cell 42 to 100 μm long. On the basis of conidial and cultural characteristics, the fungus was identified as Alternaria brassicae (Berk.) Sacc. Leaf tissues bordering lesions were plated on acidified potato dextrose agar. Colonies on V8 and alfalfa seed agar were black with concentric rings, eventually appearing uniformly black after 10 to 14 days. The internal transcribed spacer region of rDNA was amplified using primers ITS1 and ITS4 and sequenced. BLAST analysis of the 575-bp fragment showed a 100% homology with a sequence of A. brassicae Strain B from mustard (GenBank Accession No. DQ156344). The nucleotide sequence has been assigned GenBank Accession No. FJ869872. For pathogenicity tests, aqueous spore suspensions approximately 105/ml were prepared from cultures grown at 20 to 25°C for 10 to 14 days on V8 agar and sprayed on leaves of three L. draba plants. Inoculated plants were enclosed in plastic bags and incubated at 20 to 22°C for 72 to 80 h. In addition, three plants of the following reported hosts of A. brassicae were inoculated: broccoli, canola, Chinese cabbage, collards, broccoli raab, kale, mustard greens, radish, rape kale, and turnip. Within 10 days, leaf spots similar to those described above developed on plants of radish, canola, Chinese cabbage, and turnip and A. brassicae was reisolated and identified. Control plants sprayed with distilled water remained symptomless. These inoculations were repeated and results were the same. To our knowledge, this is the first report of a leaf spot disease caused by A. brassicae on L. draba in North America. A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI No. 878750A). References: (1) A. J. Caesar et al. Plant Dis. 93:108, 2009. (2) G. L. Kiemnec and M. L. McInnis. Weed Technol. 16:231, 2002. (3) A. Maxwell and J. K. Scott. Adv. Bot. Res. 43:143, 2005. (4) G. A. Mulligan and J. N. Findlay. Can. J. Plant Sci. 54:149, 1974.

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First Report of Leaf Spot Caused by Cercospora bizzozeriana on Lepidium draba in the United States

Plant Disease ◽

10.1094/pdis-93-1-0108b ◽

2009 ◽

Vol 93 (1) ◽

pp. 108-108 ◽

Cited By ~ 1

Author(s):

A. J. Caesar ◽

R. T. Lartey ◽

D. K. Berner ◽

T. Souissi

Keyword(s):

United States ◽

North America ◽

Sugar Beet ◽

Leaf Spot ◽

The United States ◽

Initial Report ◽

Voucher Specimen ◽

First Report ◽

Leaf Spots ◽

Lepidium Draba

The herbaceous perennial Lepidium draba L. is an invasive weed of rangelands and riparian areas in North America and Australia. As of 2002, it had infested 40,500 ha of rangeland in Oregon and large areas in Wyoming and Utah. Little is known of plant pathogens occurring on L. draba, especially in the United States, that could be useful for biological control of the weed. Leaf spots were first noted on a stand of L. draba near Shepherd, MT in 1997. The spots were mostly circular but sometimes irregularly shaped and whitish to pale yellow. The pathogen was erroneously assumed to be Cercospora beticola since its morphological traits closely resembled that species and the area had large fields of sugar beet with heavy Cercospora leaf spot incidence. Diseased leaves of L. draba were collected in 1997 and 2007. Conidia, borne singly on dark gray, unbranched conidiophores produced on dark stromata late in the season, were elongate, hyaline, multiseptate, 38 to 120 × 2 to 6 μm (mostly 38 to 50 × 2 to 5 μm) and had bluntly rounded tips and wider, truncate bases. These characteristics were consistent with the description of C. bizzozeriana Saccardo & Berlese (2). To isolate the fungus, spores were picked from fascicles of conidiophores with a fine-tipped glass rod, suspended in sterile water, and spread on plates of water agar. Germinated spores were transferred to potato dextrose agar (PDA). The ITS1, 5.8S, and ITS2 sequences of this fungus (GenBank Accession No. EU887131) were identical to sequences of an isolate of C. bizzozeriana from Tunisia (GenBank Accession No. DQ370428). However, these sequences were also identical to those of a number of Cercospora spp. in GenBank, including C. beticola. We also compared the actin gene sequences of the Montana isolate of C. bizzozeriana (GenBank Accession No. FJ205397) and an isolate of C. beticola from Montana (GenBank Accession No. AF443281); the sequences were 94.6% similar, an appreciable difference. For pathogenicity tests, cultures were grown on carrot leaf decoction agar. Aqueous suspensions of 104 spores per ml from cultures were sprayed on 6-week-old L. draba plants. Plants were covered with plastic bags and placed on the greenhouse bench at 20 to 25°C for 96 h. Koch's postulates were completed by reisolating the fungus from the circular leaf spots that appeared within 10 days, usually on lower leaves. Spores of C. bizzozeriana were also sprayed on seedlings of sugar beet, collard, mustard, radish, cabbage, and kale under conditions identical to those above. No symptoms occurred. After the discovery of the disease in 1997, plants of L. draba in eastern Montana, Wyoming, and Utah were surveyed from 1998 to 2003 for similar symptoms and signs, but none were found. This, to our knowledge, is the first report of C. bizzozeriana in the United States. The initial report of the fungus in North America was from Manitoba in 1938 (1). It has recently been reported as occurring on L. draba in Tunisia (4) and Russia (3) and is reported as common in Europe (2). A voucher specimen has been deposited with the U.S. National Fungus Collections (BPI No. 878750A). References: (1) G. R. Bisby. The Fungi of Manitoba and Saskatchewan. Natl. Res. Council of Canada, Ottawa, 1938. (2) C. Chupp. A Monograph of the Fungus Genus Cercospora. C. Chupp, Ithaca, NY, 1953. (3) Z. Mukhina et al. Plant Dis. 92:316, 2008. (4) T. Souissi et al. Plant Dis. 89:206, 2005.

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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.

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Detection of Tobacco rattle virus (TRV) in Phryma leptostachya L.: A New Native Plant Host in Minnesota

Plant Health Progress ◽

10.1094/php-br-14-0021 ◽

2014 ◽

Vol 15 (4) ◽

pp. 189-190

Author(s):

Sara A. Bratsch ◽

Jennifer S. Flynn ◽

Benham E. Lockhart

Keyword(s):

North America ◽

Tobacco Rattle Virus ◽

Native Plant ◽

Plant Host ◽

First Report ◽

Perennial Plants ◽

Corky Ringspot

To our knowledge, this is the first report of TRV infection in P. leptostachya. The repeated isolation of TRV from plants in isolated, uncultivated habitats suggests that TRV may be endemic to North America. Further studies are needed to determine if infected native perennial plants could serve as a potential TRV reservoir that could cause corky ringspot infection in potato. Accepted for publication 9 October 2014. Published 29 December 2014.

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First Report of Powdery Mildew Podoshaera tridactyla on Prunus hypoleuca in China

Plant Disease ◽

10.1094/pdis-09-14-0914-pdn ◽

2015 ◽

Vol 99 (2) ◽

pp. 289-289 ◽

Cited By ~ 1

Author(s):

L.-C. Bai ◽

Z.-M. Cao ◽

P.-Q. Li ◽

C. Liang

Keyword(s):

Powdery Mildew ◽

Present Report ◽

Phylogenetic Analyses ◽

Its Region ◽

28S Rdna ◽

Width Ratio ◽

Native Plant ◽

Bootstrap Analysis ◽

Voucher Specimen ◽

First Report

Prunus hypoleuca (≡ Maddenia hypoleuca), a native plant in China, grows in the Qinling Mountains that lie at the intersection of several forest regions in north, central, and southwest China. In October 2013, P. hypoleuca suffering from heavy powdery mildew infections was found with approximately 75% of the plants affected. The powdery mildew at first appeared as circular to irregular white patches, which subsequently showed abundant hyphal growth on both sides of leaves, leading to the withering of the leaves. A voucher specimen was maintained in the Mycological Herbarium of Northwest A & F University (Accession No. HMNWAFU-CF 2013166). Hyphal appressoria were nipple-shaped or nearly absent. Conidiophores were cylindrical, measured 83 to 110 × 10 to 12.5 μm, and produced two to five immature conidia in chains with a crenate outline. Foot-cells of conidiophores were straight, cylindrical, and 28 to 62 × 7 to 10 μm. Conidia were hyaline, ellipsoid to ovate, and measured 20 to 32 × 14 to 21 μm (length/width ratio 1.4:1.8). Chasmothecia were scattered or gregarious, depressed globose, and 65 to 112 μm in diameter. Appendages, arising from the upper half of the chasmothecia, usually had two to four dichotomous branches, and were one to three and a half times as long as the chasmothecial diameter. A single ascus in a chasmothecium was subglobose or broadly ellipsoid-ovoid, measured 66 to 86 × 47 to 76 μm and contained six to eight ascospores. The ascospores were ellipsoid-ovoid and 15 to 27 × 12 to 18 μm. The fungus was identified as Podosphaera tridactyla based on its anamorph and teleomorph characteristics (1,2). To confirm the identification, 28S rDNA and the ITS region were amplified. The ITS5/P3 and then PM5/ITS4 primers were used to amplify the ITS region by nested PCR. The primers LSU1/LSU2 were used to amplify the 28S rDNA, and the cloned fragments were sequenced. The 28S rDNA and ITS region sequences were deposited in GenBank (Accession Nos. KJ879240 and KM213121). A GenBank BLAST search of two sequences revealed 99% identity with P. tridactyla infecting Prunus salicina Lindl. in Korea (3). Based on ITS and a 28S rDNA phylogenetic tree, the two sequences retrieved from the Chinese specimen clustered within a strongly supported clade (bootstrap value = 100%) with P. tridactyla (JQ517296 and AB022393, respectively). Cladistic trees were constructed using the neighbor-joining method with the Kimura two-parameter substitution model in MEGA 5.0. Branch robustness was assessed via bootstrap analysis with 1,000 replicates. Phylogenetic analysis data were in agreement with morphological characters (3). To our knowledge, this is the first report of powdery mildew caused by P. tridactyla on P. hypoleuca. While Koch's postulates have not been carried out because of the biotrophic nature of the pathogen, the present report serves as a novel resource in order to improve the understanding of the etiology and epidemiology of the powdery mildew (P. tridactyla) on P. hypoleuca. The occurrence of P. tridactyla, a common powdery mildew on Prunus s. lat., supports recently published results of phylogenetic analyses of the Prunus complex, indicating that Maddenia must be reduced to synonymy with Prunus (4). References: (1) U. Braun. Beih. Nova Hedwigia 89:1, 1987. (2) U. Braun and R. T. A. Cook. Taxonomic Manual of the Erysiphales (Powdery Mildews), CBS Biodiversity Series No. 11. CBS, Utrecht, Netherlands, 2012. (3) S. C. Lee et al. Res. Plant Dis. 18:49, 2012. (4) J. Wen and W. T. Shi. PhytoKeys 17(2):39, 2012.

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First Report of Anthracnose of Mile-a-Minute (Persicaria perfoliata) Caused by Colletotrichum cf. gloeosporioides in Turkey

Plant Disease ◽

10.1094/pdis-03-12-0282-pdn ◽

2012 ◽

Vol 96 (10) ◽

pp. 1578-1578

Author(s):

D. K. Berner ◽

C. A. Cavin ◽

I. Erper ◽

B. Tunali

Keyword(s):

Biological Control ◽

Rating Scale ◽

Biological Control Agent ◽

Aqueous Suspension ◽

Botanical Garden ◽

Control Agent ◽

Internal Transcribed Spacers ◽

Voucher Specimen ◽

First Report ◽

Persicaria Perfoliata

Mile-a-minute (Persicaria perfoliata (L.) H. Gross; family: Polygonaceae) is an exotic annual barbed vine that has invaded the northeastern USA and Oregon (2). In July of 2010, in a search for potential biological control pathogens (3), diseased P. perfoliata plants were found along the Firtina River near Ardesen, Turkey. Symptoms were irregular dark necrotic lesions along leaf margins and smaller irregular reddish lesions on the lamellae of leaves. Symptomatic leaves were sent to the quarantine facility of FDWSRU, USDA, ARS in Ft. Detrick, MD, for pathogen isolation and testing. Symptomatic leaves were excised, surface disinfested in 0.615% NaOCl, and then incubated for 2 to 3 days in sterile moist chambers at 20 to 25°C. Numerous waxy sub-epidermal acervuli with 84-μm-long (mean) black setae were observed in all of the lesions after 2 to 3 days of incubation. Conidiophores within acervuli were simple, short, and erect. Conidia were one-celled, hyaline, guttulate, subcylindrical, straight, 12.3 to 18.9 × 3.0 to 4.6 μm (mean 14.3 × 3.7 μm). Pure cultures were obtained by transferring conidia onto 20% V-8 juice agar. Appressoria, formed 24 h after placing conidia on dialysis membrane over V-8 juice agar, were smooth, clavate, aseptate, regular in outline, and 6.4 to 10.0 × 5.1 to 7.2 μm (mean 7.5 × 6.6 μm). These characters conformed to the description of Colletotrichum gloeosporioides (Penz.) Penz. & Sacc. (1). A voucher specimen was deposited in the U.S. National Fungus Collections (BPI 882461). Nucleotide sequences for the internal transcribed spacers (ITS 1 and 2), directly sequenced from ITS 1 and ITS 4 standard primers (4), were deposited in GenBank (JN887693). A comparison of these sequences with ITS 1 and 2 sequences of the C. gloeosporioides epitype IMI 356878 (GenBank EU 371022) (1) using BLAST found 479 of 482 identities with no gaps. Conidia from 14-day-old cultures, in an aqueous suspension of 1.0 × 106 conidia ml–1, were spray-inoculated onto healthy stems and leaves of twenty 30-day-old P. perfoliata plants. Another 10 plants were not inoculated. All plants were placed in a dew chamber at 25°C for 16 h with no lighting. They were then placed in a 20 to 25°C greenhouse with a 14-h photoperiod. Light was generated using 400W sodium vapor lights. Lesions developed on leaves and stems of all inoculated plants after 7 days, and symptoms were the same as observed in the field. Each plant was rated weekly for disease severity on a 0 to 10 rating scale where 0 = no disease symptoms and 10 = 100% symptomatic tissue. After 28 days, the average disease rating of inoculated plants was 3.95 ± 0.94. No disease developed on noninoculated plants. C. gloeosporioides was reisolated from all inoculated plants. Host range tests will determine the potential of this isolate as a biological control agent for P. perfoliata. To our knowledge, this is the first report of anthracnose caused by C. gloeosporioides on P. perfoliata. References: (1) P. F. Cannon et al. Mycotaxon 104:189, 2008. (2) J. T. Kartesz and C. A. Meacham. Synthesis of the North American Flora, Version 1.0., North Carolina Botanical Garden, Chapel Hill, N.C. 1999. (3) D. L. Price et al. Environ. Entomol. 32:229, 2003. (4) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. Academic Press, Inc., San Diego, CA, 1990.

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First Report of Powdery Mildew on Nandina domestica (Berberidaceae) in North America

Plant Disease ◽

10.1094/pdis.2000.84.6.705c ◽

2000 ◽

Vol 84 (6) ◽

pp. 705-705 ◽

Cited By ~ 1

Author(s):

G. S. Saenz ◽

S. T. Koike ◽

H. J. Scheck

Keyword(s):

North America ◽

Powdery Mildew ◽

Santa Barbara ◽

Voucher Specimen ◽

First Report ◽

The United Kingdom ◽

Humidity Chamber ◽

Powdery Mildew Pathogen ◽

The University ◽

Germ Tubes

Nandina domestica Thunb. (heavenly bamboo) is an ornamental plant that is widely planted in landscapes in California and other states. Since 1996, powdery mildew disease has been seen on outdoor landscape N. domestica in various regions of California (Alameda, Monterey, Riverside, and Santa Barbara counties). Symptoms consist of reddening of leaf and stem tissues colonized by the fungus and curling and twisting of infected leaves. The following observations were the same for all collected isolates. White ectophytic mycelium was observed on leaves and petioles. Mycelium on leaves was amphigenous, mostly epiphyllous, and effused or in patches. Hyphal appressoria were nipple-shaped to lobed and sometimes opposite in orientation. Conidiophores were cylindrical, straight, sometimes slightly flexuous, 22 to 32 × 6 to 8 μm in dimension, and followed by one to two shorter cells. Conidia were cylindrical, produced singly, and 27 to 42 × 11.5 to 14 μm in dimension. Fibrosin bodies were not observed. Conidial germ tubes were approximately twice the length of the spore, originated from the ends of the spore, and terminated in simple appressoria. Cleistothecia were not present. Based on these characteristics, the fungus was identified as Microsphaera berberidis (DC) Lév. (1). Pathogenicity was confirmed by gently pressing diseased leaves on leaves of healthy N. domestica plants. Plants were incubated in a humidity chamber at 22 to 24°C, and after 10 to 14 days, powdery mildew colonies developed. A voucher specimen was deposited in the University of California Herbarium (UC 1738622). Additional inoculation experiments showed that four other N. domestica cultivars were susceptible (Compacta Nana, Gulf Stream, Harbour Dwarf, and Royal Princess). Helfer (2) noted several possible candidates for the Nandina powdery mildew pathogen in the United Kingdom. However, due to the conidial characteristics of that fungus and the paucity of character descriptions for the several species mentioned, no species name was given to the Edinburgh isolate. In contrast, the mitosporic characteristics of our isolates fit the description for M. berberidis. This is the first report of powdery mildew on N. domestica in North America. References: (1) U. Braun. Nova Hedwigia 89:1, 1987. (2) S. Helfer. Plant Dis. 79:424, 1995.

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