First Report of Powdery Mildew Caused by Podosphaera fusca on Herba eupatorii in China

Herba eupatorii, one of the most important Chinese medicinal herbs, belongs to the Asteraceae family. In June 2012, a previously unknown disease, tentatively identified as powdery mildew, was observed on H. eupatorii growing in Shangqiu, in eastern Henan Province, China. Symptoms began as white mycelium partially covering upper leaf surfaces; as the disease progressed, it spread to cover entire leaf surfaces. The infected leaves became yellow and necrotic at advanced stages of infection. Specimens consisting of infected leaves were maintained at the Plant-Microbe Interaction Laboratory at Shangqiu Normal University. Microscopic observations of the morphology of the fungus revealed oval primary conidia measuring 18 to 27 × 15 to 22 μm. A long unbranched germ tube that germinated laterally from the ends of conidia was observed in some samples. Conidiophores were cylindrical, simple unbranched, and composed of a basal cell with a swollen base and three to six barrel-shaped conidia formed in chains, measuring 112 to 180 × 9 to 12 μm. Mycelial appressoria were nipple-shaped. Chasmothecia were not observed in the collected samples. To verify the identity of the fungus, the internal transcribed spacer (ITS) rDNA was amplified with ITS1 and ITS4 primers (3) and sequenced. The sequences were deposited as GenBank Accession No. JX546297. Comparison with sequences in the GenBank database revealed that the ITS sequence was 100% homologous with the sequence of Podosphaera fusca on Calendula officinalis (AB525914) (2) and Syneilesis palmata (AB040349) (1). The ITS sequence analysis verified that the causal agent was P. fusca, which is reported to be a cosmopolitan powdery mildew fungus, parasitic on numerous plant species in the Asteraceae family. Koch's postulates were completed by inoculating healthy H. eupatorii plants with a conidial suspension (prepared in distilled water) of 105 conidia/ml collected from infected plants. Five plants were sprayed until the suspension ran off the leaves, while five additional plants were sprayed with distilled water as a control. Plants were maintained in a climate cell under the following conditions: day, 24°C, 16 h; night, 20°C, 8 h; 85% humidity. After 10 days, inoculated plants developed symptoms similar to those observed in the field, whereas control plants remained healthy. Further examination showed that the inoculated plants were infected by P. fusca. To our knowledge, this is the first report of P. fusca affecting H. eupatorii in China. Because there are no fungicides labeled for use on this plant, the appearance of powdery mildew caused by P. fusca could result in substantial production loss of H. eupatorii. References: (1) T. Hirata et al. Can. J. Bot. 78:1521, 2000. (2) S. Takamatsu et al. Persoonia 24:38, 2010. (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, San Diego, CA, 1990.

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First Report of Powdery Mildew Caused by Golovinomyces cichoracearum on Sonchus asper in China

Plant Disease ◽

10.1094/pdis-01-12-0033-pdn ◽

2012 ◽

Vol 96 (5) ◽

pp. 766-766 ◽

Cited By ~ 2

Author(s):

D. Pei ◽

X. Xu ◽

Y. Feng ◽

C. Li

Keyword(s):

Powdery Mildew ◽

Antibacterial Properties ◽

Its Sequence ◽

Conidial Suspension ◽

Powdery Mildew Fungus ◽

Sonchus Asper ◽

First Report ◽

Its Sequence Analysis ◽

Golovinomyces Cichoracearum ◽

Asteraceae Family

Sonchus asper is an exotic annual herb belonging to the Asteraceae family. Crude extracts of S. asper leaves have antiphlogistic and antibacterial properties. In May 2011, severe infection of powdery mildew was observed on S. asper in Henan Province, a central area of China. Symptoms began as small, nearly circular white spots that later enlarged and coalesced. As the disease progressed, white mycelia covered the entire plant, including the inflorescence. The voucher specimens are kept at the Key Laboratory of Plant-Microbe Interaction, Shangqiu Normal University. Conidiophores were erect, 108 to 220 × 10 to 12 μm, and composed of a cylindrical foot cell followed by two to three short cells. Nipple-shaped appressoria were formed on ectophytic mycelia. Conidia were hyaline and cylindrical, without distinct fibrosin bodies, and ranging from 29 to 42 × 19 to 24 μm. Long, unbranched germ tubes were formed from the ends of the conidia. These morphological characteristics suggested that the powdery mildew fungus is the anamorph of Golovinomyces cichoracearum (1,2). Chasmothecia were not observed in the collected samples. To confirm the identification, the internal transcribed spacer (ITS) region of the rDNA was amplified with ITS1 and ITS4 primers (4) and sequenced. The ITS sequence obtained was assigned Accession No. JQ010848 in GenBank, and had 99% similarity to two ITS sequences from different G. cichoracearum accessions (HM449077 and AY739111). The ITS sequence analysis further verified that the causal agent of the powdery mildew on S. asper was G. cichoracearum. Pathogenicity was confirmed by inoculating five healthy plants of S. asper with a conidial suspension (105 conidia/ml) from the infected plants, with five noninoculated plants serving as control. Inoculated plants developed the original powdery mildew symptoms after 10 days, whereas control plants remained healthy. G. cichoracearum (synonym Erysiphe cichoracearum) is a cosmopolitan powdery mildew fungus, parasitic on numerous plant species in the Asteraceae family. It was reported to be infecting S. asper in Bulgaria (3). To our knowledge, this is the first report of G. cichoracearum infections on S. asper in China. S. asper is one of the most important Chinese herbal medicines. The sudden appearance of powdery mildew caused by G. cichoracearum on this plant could result in substantial production loss of S. asper unless fungicide applications are employed. References: (1) U. Braun. Beih. Nova Hedwigia 89:1, 1987. (2) R. T. A. Cook and U. Braun. Mycol. Res. 113:616, 2009. (3) G. Negrean and C. M. Denchev. Mycologia Balcanica, 2004, 1:63. (4) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, San Diego, CA, 1990.

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First Report of Powdery Mildew on Pyrus calleryana Caused by Podosphaera leucotricha

Plant Disease ◽

10.1094/pdis-92-1-0176b ◽

2008 ◽

Vol 92 (1) ◽

pp. 176-176 ◽

Cited By ~ 1

Author(s):

L. Vajna ◽

L. Kiss

Keyword(s):

Powdery Mildew ◽

Urban Areas ◽

Its Sequence ◽

Podosphaera Leucotricha ◽

Powdery Mildew Fungus ◽

First Report ◽

Host Genus ◽

Pyrus Calleryana ◽

Single Leaf ◽

Leaf Surfaces

Callery pear (Pyrus calleryana Decne.) is native to Asia and its varieties are planted as ornamentals in urban areas worldwide. It is also used as a source of resistance to fireblight in some breeding programs. In April 2007, symptoms of powdery mildew infection were observed on the foliage of almost every P. calleryana cv. Chanticleer tree planted along a 1.5-km road in Budapest, Hungary. These trees were planted 5 to 6 years ago and were the first callery pears used as ornamentals in Hungary. Powdery mildew infections were also detected on P. calleryana trees planted in other parts of the city. White powdery mildew mycelium appeared on the lower and sometimes upper leaf surfaces, especially on young shoots, and caused chlorotic spots on the upper leaf surfaces and severe distortions of leaves. The spread of the infection was monitored between April and August of 2007 in several sample sites. More than 100 trees that were examined became heavily infected by May 2007. Powdery mildew conidiophores were typical of the genus Oidium subgen. Fibroidium, the anamorph of the teleomorph genus Podosphaera (2). Conidia developed in chains, contained fibrosin bodies, germinated at one of their ends with germ tubes terminating in unlobed appressoria, and measured 16 to 27 × 10 to 15 μm. Hyphal appressoria were nipple shaped or inconspicuous. The teleomorph was not found. To precisely identify the pathogen, DNA was extracted from conidia collected with a sterile brush from a single leaf using a Qiagen DNeasy Plant Kit (Hilden, Germany), and the internal transcribed spacer (ITS) sequence of the ribosomal DNA was amplified and determined as described by Szentiványi et al. (3). The ITS sequence, deposited in GenBank under Accession No. EU148597, was identical to those determined in Podosphaera leucotricha (Ell. & Ev.) Salmon collected from apple in Australia (GenBank Accession No. AF073353) and Canada (GenBank Accession No. AY157844) and also from pear in Canada (GenBank Accession No. AY157845). Thus, the pathogen was identified as Podosphaera leucotricha on the basis of the host genus, morphology of the anamorph, and ITS sequence. Specimens were deposited under Accession No. BPI878262 at the U.S. National Fungus Collection. To our knowledge, Podosphaera leucotricha has not been reported on P. calleryana in any parts of the world so far. An Oidium sp. infecting this plant in Australia was listed by Amano (1), but the exact identity of that fungus is not known. Thus, this is the first report of an identified powdery mildew fungus on P. calleryana. References: (1) K. Amano. Host Range and Geographical Distribution of the Powdery Mildew Fungi. Japan Scientific Societies Press, Tokyo, 1986. (2) U. Braun et al. Pages 13-55 in: The Powdery Mildews: A Comprehensive Treatise. R. R Bélanger et al., eds. American Phytopathological Society, St Paul, MN, 2002. (3) O. Szentiványi et al. Mycol. Res. 109:429, 2005.

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First Report of Colletotrichum acutatum Associated with Stem Blight of Blueberry Plants in China

Plant Disease ◽

10.1094/pdis-08-12-0738-pdn ◽

2013 ◽

Vol 97 (3) ◽

pp. 422-422 ◽

Cited By ~ 3

Author(s):

C.-N. Xu ◽

Z.-S. Zhou ◽

Y.-X. Wu ◽

F.-M. Chi ◽

Z.-R. Ji ◽

...

Keyword(s):

Vaccinium Corymbosum ◽

Colletotrichum Acutatum ◽

Post Inoculation ◽

Pathogenicity Test ◽

Distilled Water ◽

Conidial Suspension ◽

First Report ◽

Rdna Its ◽

Its Sequence Analysis ◽

Species Specific

An anthracnose disease was observed on stems of high-bush blueberry plants (Vaccinium corymbosum L.) in Liaoning Province, China in 2012. The typical symptoms consist of sudden wilting and dieback of stems during the growing season. Dark brown lesions originate from infected buds and kill portions of the stems. Lesions have grayish white centers, with the necrotic areas becoming 6 to 8 cm in length. Disinfected stem pieces were placed on potato dextrose agar (PDA) and incubated at 28°C for 5 to 7 days, after which the emerging colonies were transferred to fresh PDA. All isolates initially produced white growth, but turned pink after 7 days before becoming blackish green. The average colony diameter was 65.5 to 75.0 mm after 7 days. Conidia were aseptate, hyaline, fusiform to ellipsoid, 8.5 to 16.5 × 2.5 to 4.0 μm in size and single celled with two to seven oil globules. Setae were not found on the acervuli. These characteristics matched published descriptions of Colletotrichum acutatum (1) (teleomorph Glomerella acutata). Pathogenicity test was confirmed in 15 2-year-old healthy potted plants of cv. Berkeley. Stems of 10 plants were punctured with flamed needles and sprayed with 5 ml of conidial suspension (106 conidia per ml in sterile distilled water) of isolate LNSW1. Five control plants were inoculated with sterile distilled water. Seven days after inoculation, eight of the 10 blueberry plants exhibited stem lesions, leaf chlorosis, followed by branch dieback 15 days post-inoculation. The symptoms were similar to those observed on diseased plants in the field, and no lesions were observed on control plants. The pathogen was reisolated from the margin of lesions and identified by colony growth characteristics on PDA. PCR amplification of one isolate (LNSW1) was carried out by utilizing the universal rDNA-ITS primer pair ITS1/ITS4. The sequence (557 bp) of isolate LNSW1 (GenBank Accession No. JX392857) showed 99% identity to G. acutata (AB443950) and C. acutatum (AJ749672) in a BLAST search. An approximately 490-bp fragment was amplified from LNSW1 by the species-specific primer pair CaInt2/ITS4 (2). The pathogen was identified as G. acutata (asexual stage: C. acutatum J.H. Simmonds) on the basis of morphological characters, rDNA-ITS sequence analysis, and a PCR product with species-specific primers. To our knowledge, this is the first report of C. acutatum in high-bush blueberry plants in China. References: (1) C. Lei et al. Fungal Diversity 12:183, 2009. (2) S. Sreenivasaprasad et al. Plant Pathol. 45:650, 1996

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First Report of Powdery Mildew Caused by Oidium neolycopersici on Tomato in China

Plant Disease ◽

10.1094/pdis-92-9-1370c ◽

2008 ◽

Vol 92 (9) ◽

pp. 1370-1370 ◽

Cited By ~ 3

Author(s):

C. W. Li ◽

D. L. Pei ◽

W. J. Wang ◽

Y. S. Ma ◽

L. Wang ◽

...

Keyword(s):

Powdery Mildew ◽

Average Length ◽

Pathogenic Fungus ◽

Fruit Size ◽

Morphological Characteristics ◽

Conidial Suspension ◽

Oidium Neolycopersici ◽

First Report ◽

Its Sequence Analysis ◽

Tomato Powdery Mildew

Tomato powdery mildew can cause remarkable reduction in fruit size and quality (4). In March of 2008, powdery mildew appeared as circular, white colonies on leaves, petioles, and stems of tomato plants grown in greenhouses in Shangqiu, Henan Province, China. The pathogenic fungus had unbranched conidiophores with an average length of 58.4 μm and width of 5.1 μm. Conidia were hyaline, elliptical, and were borne singly. Average length and width of conidia were 30.6 and 15.1 μm, respectively. Germ tubes were straight and formed at the ends or very close to the ends of conidia. Chasmothecium was not found in the collected samples. Different tomato cultivars and species, including Lycopersicon esculentum Mill (cvs. Moneymaker, Micro-Tom, Zaofen, Fenguo, and Zhongza series), L. peruvianum cv. LA2172, and L. hirsutum cv. G1.1560, were inoculated with a conidial suspension with a concentration of 5 × 104 conidia/ml. Plants developed powdery mildew symptoms as early as 4 days after inoculation. Susceptible symptoms developed on all L. esculentum cultivars, while L. peruvianum LA2172 and L. hirsutum G1.1560 displayed complete resistance, which is similar to the results of Bai et al 2004 (1) and Lindhout and Pet 1990 (3). Morphological characteristics of the pathogen on susceptible genotypes were similar to those from naturally infected plants. On the basis of the characteristics of the asexual stage, the pathogen was identified as an isolate of Oidium neolycopersici L. Kiss, which was confirmed by internal transcribed spacer (ITS) sequence analysis. PCR amplification and sequencing of the ITS region were performed with primers ITS1 and ITS4. The nucleotide sequence was assigned GenBank Accession No. EU486992, which had a 100% homology with 10 ITS sequences of O. neolycopersici in GenBank (Accession Nos. EU047559 to 047568) (2). In Asia, the spread of this pathogen has been recently reported in Japan (2). To our knowledge, this is the first report of tomato powdery mildew in China. Voucher specimens are available at the Specimen Center in the Department of Life Science, Shangqiu Normal University. References: (1) Y. Bai et al. Mol. Plant-Microbe. Interact. 18:354, 2005. (2) T. Jankovics et al. Phytopathology 98:529, 2008. (3) P. Lindhout and G. Pet. Tomato Gen. Coop. Rep. 40:19, 1990. (4) J. M. Whipps et al. Plant Pathol. 47:36, 1998.

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First Report of Powdery Mildew on Dollar-plant (Crassula ovata) Caused by an Oidium sp.

Plant Disease ◽

10.1094/pdis.1999.83.2.199c ◽

1999 ◽

Vol 83 (2) ◽

pp. 199-199 ◽

Cited By ~ 2

Author(s):

L. Kiss

Keyword(s):

Powdery Mildew ◽

The United States ◽

Diseased Plant ◽

Powdery Mildew Fungus ◽

History Museum ◽

First Report ◽

Powdery Mildews ◽

Leaf Surfaces ◽

Hungarian Natural History Museum ◽

Germ Tubes

Dollar-plant (Crassula ovata) is a perennial, succulent ornamental grown worldwide. In 1998, powdery mildew colonies were observed on the adaxial leaf surfaces of a 4-year-old specimen maintained outdoors. Symptoms included necrosis of the infected tissues and defoliation 2 months after the appearance of the first colonies. Conidia were produced in chains on unbranched conidiophores. Hyphal appressoria were lobed to multi-lobed, mostly opposite or spread. Conidia were ellipsoid to cylindrical, measured 34 to 48 μm × 17 to 26 μm, and contained no fibrosin bodies. On water agar, conidia produced a single germ tube from the end of the conidium. Germ tubes were either very short with lobed appressoria, or were two to three times longer than conidia, and terminated in lobed or unlobed appressoria. Cleistothecia were not produced. The pathogen was identified as an Oidium sp. belonging to the genus Erysiphe sect. Galeopsidis (1). To confirm pathogenicity, small, potted C. ovata plants were placed near the diseased plant in the laboratory. After 2 weeks, powdery mildew appeared on the small plants, and the pathogen was morphologically identical to the original fungus. This is the first report of a powdery mildew fungus on C. ovata, and it is different from both species of the Erysiphaceae identified on other Crassula spp. (1,2). Infected C. ovata leaves were deposited at the Department of Botany of the Hungarian Natural History Museum in Budapest under the accession number BP 91732. References: (1) U. Braun. 1995. The Powdery Mildews (Erysiphales) of Europe. Gustav Fischer Verlag, Jena. (2) D. F. Farr et al. 1989. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN.

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First Report of Powdery Mildew of Tomato Caused by an Erysiphe sp. in Connecticut

Plant Disease ◽

10.1094/pdis.1997.81.2.229a ◽

1997 ◽

Vol 81 (2) ◽

pp. 229-229 ◽

Cited By ~ 9

Author(s):

V. L. Smith ◽

S. M. Douglas ◽

J. A. LaMondia

Keyword(s):

New York ◽

Powdery Mildew ◽

Powdery Mildew Fungus ◽

First Report ◽

Eastern Black Nightshade ◽

Tomato Seedlings ◽

Nicotiana Tabacum L ◽

Leaf Surfaces ◽

Greenhouse Tomatoes ◽

Solanaceous Plants

In 1995 and 1996, powdery mildew was observed on several samples of field-grown tomato foliage (Lycopersicon esculentum Mill.; various cultivars) submitted to the CAES Plant Disease and Information Office. Symptoms included gray superficial mycelium with abundant sporulation on adaxial and abaxial leaf surfaces, followed in the field by dessication of the foliage and rapid defoliation. No cleistothecia were observed, and single-celled, hyaline, ellipsoidal conidia occurred, usually singly, on unbranched conidiophores. Pyriform conidia occurred at a frequency of less than 1%. Conidia ranged in length from 25.6 to 43.2 μm (mean = 33.6, SE = 0.4) and in width from 13.1 to 23.1 μm (mean = 18.2, SE = 0.2; n = 500). Fibrosin bodies were not observed, and vacuoles were present. Based on conidial characteristics, the fungus was identified as an unknown Erysiphe sp. To confirm pathogenicity, 2-week-old tomato seedlings (cv. Rutgers) were inoculated by shaking dry conidia onto the leaves and placed within plastic tents on a greenhouse bench. Control plants were treated identically but not inoculated. The inoculated plants developed foliar powdery mildew symptoms, and sporulation was observed. Susceptible cultivars that were naturally infected included Better Boy, Better Beef, Celebrity, Rutgers, Ultra Magnum, Ultra Sweet, Whopper, Yellow Brandywine; cherry type tomatoes Matts Wild Cherry and Sweet Chelsea; and plum type tomatoes Roma and Super San Marzano. Eastern black nightshade (Solanum ptycanthum Dunal), eggplant (S. melongena L. ‘Black Pride’), and tobacco (Nicotiana tabacum L. ‘C9’) were also naturally infected under greenhouse conditions. However, conidia size and number of conidia per conidiophore differed between hosts. Conidia from tobacco, eggplant, and nightshade averaged 37.8 × 19.1 μm (SE = 0.5 and 0.2, respectively) with a 95% CI of 35.5 to 40.0 × 18.1 to 20.3 μm (n = 300). Conidia from tomato were smaller, averaging 33.6 × 18.2 μm (SE = 0.3 and 0.2, respectively) with a 95% CI of 32.7 to 34.4 × 17.5 to 18.9 μm (n = 300). Factorial inoculation experiments between tomato and other hosts demonstrated cross-infectivity, but isolates originally from tobacco had significantly larger conidia when infecting tomato than isolates originally from tomato infecting tobacco. Powdery mildew isolates on tomato had fewer (P = 0.001) conidia per conidiophore (mean = 1.39, range = 1 to 4) than isolates infecting tobacco inoculated at the same time and held under the same conditions (mean = 2.54, range = 1 to 6). These results demonstrate considerable morphological variation in the powdery mildew fungus, perhaps associated with hosts such as tomato or other solanaceous plants. This is the first report of powdery mildew of tomato and tobacco in Connecticut. Powdery mildew of tomato has been reported to occur in the field in California, and in greenhouse tomatoes in New York (2). Powdery mildew of tobacco has only been reported on artificially inoculated plants in California (1). References: (1) C. R. Arredondo et al. Plant Dis. 80:1303, 1996. (2) D. M. Karasevicz and T. A. Zitter. Plant Dis. 80:709, 1996.

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First report of Podosphaera fusca causing powdery mildew on asparagus bean in Taiwan

Journal of Plant Pathology ◽

10.1007/s42161-021-00862-w ◽

2021 ◽

Author(s):

Yi-Ting Xiao ◽

Chao-Jen Wang ◽

Tung-Chin Huang ◽

Yuan-Min Shen

Keyword(s):

Powdery Mildew ◽

First Report ◽

Asparagus Bean ◽

Podosphaera Fusca

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First Report of Pepper Fruit Rot Caused by Fusarium concentricum in China

Plant Disease ◽

10.1094/pdis-03-13-0325-pdn ◽

2013 ◽

Vol 97 (12) ◽

pp. 1657-1657 ◽

Cited By ~ 6

Author(s):

J. H. Wang ◽

Z. H. Feng ◽

Z. Han ◽

S. Q. Song ◽

S. H. Lin ◽

...

Keyword(s):

Fusarium Species ◽

Fruit Rot ◽

Post Inoculation ◽

Distilled Water ◽

Conidial Suspension ◽

Average Growth ◽

First Report ◽

Control Fruit ◽

Pepper Fruit ◽

Fruit Samples

Pepper (Capsicum annuum L.) is an important vegetable crop worldwide. Some Fusarium species can cause pepper fruit rot, leading to significant yield losses of pepper production and, for some Fusarium species, potential risk of mycotoxin contamination. A total of 106 diseased pepper fruit samples were collected from various pepper cultivars from seven provinces (Gansu, Hainan, Heilongjiang, Hunan, Shandong, Shanghai, and Zhejiang) in China during the 2012 growing season, where pepper production occurs on approximately 25,000 ha. Pepper fruit rot symptom incidence ranged from 5 to 20% in individual fields. Symptomatic fruit tissue was surface-sterilized in 0.1% HgCl2 for 1 min, dipped in 70% ethanol for 30 s, then rinsed in sterilized distilled water three times, dried, and plated in 90 mm diameter petri dishes containing potato dextrose agar (PDA). After incubation for 5 days at 28°C in the dark, putative Fusarium colonies were purified by single-sporing. Forty-three Fusarium strains were isolated and identified to species as described previously (1,2). Morphological characteristics of one strain were identical to those of F. concentricum. Aerial mycelium was reddish-white with an average growth rate of 4.2 to 4.3 mm/day at 25°C in the dark on PDA. Pigments in the agar were formed in alternating red and orange concentric rings. Microconidia were 0- to 1-septate, mostly 0-septate, and oval, obovoid to allantoid. Macroconidia were relatively slender with no significant curvature, 3- to 5-septate, with a beaked apical cell and a foot-shaped basal cell. To confirm the species identity, the partial TEF gene sequence (646 bp) was amplified and sequenced (GenBank Accession No. KC816735). A BLASTn search with TEF gene sequences in NCBI and the Fusarium ID databases revealed 99.7 and 100% sequence identity, respectively, to known TEF sequences of F. concentricum. Thus, both morphological and molecular criteria supported identification of the strain as F. concentricum. This strain was deposited as Accession MUCL 54697 (http://bccm.belspo.be/about/mucl.php). Pathogenicity of the strain was confirmed by inoculating 10 wounded, mature pepper fruits that had been harvested 70 days after planting the cultivar Zhongjiao-5 with a conidial suspension (1 × 106 spores/ml), as described previously (3). A control treatment consisted of inoculating 10 pepper fruits of the same cultivar with sterilized distilled water. The fruit were incubated at 25°C in a moist chamber, and the experiment was repeated independently in triplicate. Initially, green to dark brown lesions were observed on the outer surface of inoculated fruit. Typical soft-rot symptoms and lesions were observed on the inner wall when the fruit were cut open 10 days post-inoculation. Some infected seeds in the fruits were grayish-black and covered by mycelium, similar to the original fruit symptoms observed at the sampling sites. The control fruit remained healthy after 10 days of incubation. The same fungus was isolated from the inoculated infected fruit using the method described above, but no fungal growth was observed from the control fruit. To our knowledge, this is the first report of F. concentricum causing a pepper fruit rot. References: (1) J. F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual. Blackwell Publishing, Ames, IA, 2006. (2) K. O'Donnell et al. Proc. Nat. Acad. Sci. USA 95:2044, 1998. (3) Y. Yang et al. 2011. Int. J. Food Microbiol. 151:150, 2011.

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First Report of Leaf Spot of Rudbeckia hirta var. pulcherrima Caused by Septoria rudbeckiae in Korea

Plant Disease ◽

10.1094/pdis-02-12-0172-pdn ◽

2012 ◽

Vol 96 (6) ◽

pp. 911-911 ◽

Cited By ~ 1

Author(s):

J. H. Park ◽

S. E. Cho ◽

K. S. Han ◽

H. D. Shin

Keyword(s):

Leaf Spot ◽

The United States ◽

Flowering Plant ◽

Leaf Spot Disease ◽

Morphological Identification ◽

Its Sequence ◽

Conidial Suspension ◽

First Report ◽

Rudbeckia Hirta ◽

Close Phylogenetic Relationship

Rudbeckia hirta L. var. pulcherrima Farw. (synonym R. bicolor Nutt.), known as the black-eyed Susan, is a flowering plant belonging to the family Asteraceae. The plant is native to North America and was introduced to Korea for ornamental purposes in the 1950s. In July 2011, a previously unknown leaf spot was first observed on the plants in a public garden in Namyangju, Korea. Leaf spot symptoms developed from lower leaves as small, blackish brown lesions, which enlarged to 6 mm in diameter. In the later stages of disease development, each lesion was usually surrounded with a yellow halo, detracting from the beauty of the green leaves of the plant. A number of black pycnidia were present in diseased leaf tissue. Later, the disease was observed in several locations in Korea, including Pyeongchang, Hoengseong, and Yangpyeong. Voucher specimens were deposited at the Korea University Herbarium (KUS-F25894 and KUS-F26180). An isolate was obtained from KUS-F26180 and deposited at the Korean Agricultural Culture Collection (Accession No. KACC46694). Pycnidia were amphigenous, but mostly hypogenous, scattered, dark brown-to-rusty brown, globose, embedded in host tissue or partly erumpent, 50 to 80 μm in diameter, with ostioles 15 to 25 μm in diameter. Conidia were substraight to mildly curved, guttulate, hyaline, 25 to 50 × 1.5 to 2.5 μm, and one- to three-septate. Based on the morphological characteristics, the fungus was consistent with Septoria rudbeckiae Ellis & Halst. (1,3,4). Morphological identification of the fungus was confirmed by molecular data. Genomic DNA was extracted using the DNeasy Plant Mini DNA Extraction Kit (Qiagen Inc., Valencia, CA.). The internal transcribed spacer (ITS) region of rDNA was amplified using the ITS1/ITS4 primers and sequenced. The resulting sequence of 528 bp was deposited in GenBank (Accession No. JQ677043). A BLAST search showed that there was no matching sequence of S. rudbeckiae; therefore, this is the first ITS sequence of the species submitted to GenBank. The ITS sequence showed >99% similarity with those of many Septoria species, indicating their close phylogenetic relationship. Pathogenicity was tested by spraying leaves of three potted young plants with a conidial suspension (2 × 105 conidia/ml), which was harvested from a 4-week-old culture on potato dextrose agar. Control leaves were sprayed with sterile water. The plants were covered with plastic bags to maintain 100% relative humidity (RH) for the first 24 h. Plants were then maintained in a greenhouse (22 to 28°C and 70 to 80% RH). After 5 days, leaf spot symptoms identical to those observed in the field started to develop on the leaves inoculated with the fungus. No symptoms were observed on control plants. S. rudbeckiae was reisolated from the lesions of inoculated plants, confirming Koch's postulates. A leaf spot disease associated with S. rudbeckiae has been reported on several species of Rudbeckia in the United States, Romania, and Bulgaria (1–4). To our knowledge, this is the first report of leaf spot on R. hirta var. pulcherrima caused by S. rudbeckiae in Korea. References: (1) J. B. Ellis and B. D. Halsted. J. Mycol. 6:33, 1890. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ February 2, 2012. (3) E. Radulescu et al. Septoriozele din Romania. Ed. Acad. Rep. Soc. Romania, Bucuresti, Romania, 1973. (4) S. G. Vanev et al. Fungi Bulgaricae 3:1, 1997.

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First Report of Fusarium solani Causing Root Rot on Coptis chinensis in Southwestern China

Plant Disease ◽

10.1094/pdis-02-14-0164-pdn ◽

2014 ◽

Vol 98 (9) ◽

pp. 1273-1273 ◽

Cited By ~ 2

Author(s):

X.-M. Luo ◽

J.-L. Li ◽

J.-Y. Dong ◽

A.-P. Sui ◽

M.-L. Sheng ◽

...

Keyword(s):

Fusarium Solani ◽

Root Rot ◽

Southwestern China ◽

Molecular Characteristics ◽

Distilled Water ◽

Conidial Suspension ◽

Storage Roots ◽

Coptis Chinensis ◽

Causal Organism ◽

First Report

China is the world's largest producer country of coptis (Coptis chinensis), the rhizomes of which are used in traditional Chinese medicine. Since 2008, however, root rot symptoms, including severe necrosis and wilting, have been observed on coptis plants in Chongqing, southwestern China. Of the plants examined from March 2011 to May 2013 in 27 fields, 15 to 30% were covered with black necrotic lesions. The leaves of infected plants showed wilt, necrotic lesions, drying, and death. The fibrous roots, storage roots, and rhizomes exhibited brown discoloration and progressive necrosis that caused mortality of the infected plants. Infected plants were analyzed to identify the causal organism. Discoloration of the internal vascular and cortical tissues of the rhizomes and taproots was also evident. Symptomatic taproots of the diseased coptis were surface sterilized in 1% sodium hypochlorite for 2 min, rinsed in sterile distilled water for 2 min, and then air-dried in sterilized atmosphere/laminar flow. Small pieces of disinfested tissue (0.3 cm in length) were transferred to petri dishes containing potato dextrose agar (PDA) supplemented with 125 μg ml–1 streptomycin sulfate and 100 μg ml–1 ampicillin, and incubated for 5 days at 25°C with a 12-h photoperiod. Four distinct species of fungal isolates (HL1 to 4) derived from single spores were isolated from 30 plants with root rot symptoms collected from the study sites. To verify the pathogenicity of individual isolates, healthy coptis plants were inoculated by dipping roots into a conidial suspension (106 conidia/ml) for 30 min (15 plants per isolate), as described previously (1). Inoculated plants were potted in a mixture of sterilized quartz sand-vermiculite-perlite (4:2:1, v/v) and incubated at 25/18°C and 85 to 90% relative humidity (day/night) in a growth chamber with a daily 16-h photoperiod of fluorescent light. Plants dipped in sterile distilled water were used as controls. After 15 days, symptoms similar to those observed in the field were observed on all plants (n = 15) that were inoculated with HL1, but symptoms were not observed on plants inoculated with HL2, HL3, and HL4, nor on control plants. HL1 was re-isolated from symptomatic plants but not from any other plants. Morphological characterization of HL1 was performed by microscopic examination. The septate hyphae, blunt microconidia (2 to 3 septa) in the foot cell and slightly curved microconidia in the apical cell, and chlamydospores were consistent with descriptions of Fusarium solani (2). The pathogen was confirmed to be F. solani by amplification and sequencing of the ribosomal DNA internal transcribed spacer (rDNA-ITS) using the universal primer pair ITS4 and ITS5. Sequencing of the PCR product revealed a 99 to 100% similarity with the ITS sequences of F. solani in GenBank (JQ724444.1 and EU273504.1). Phylogenetic analysis (MEGA 5.1) using the neighbor-joining algorithm placed the HL1 isolate in a well-supported cluster (97% bootstrap value based on 1,000 replicates) with JQ724444.1 and EU273504.1. The pathogen was thus identified as F. solani based on its morphological and molecular characteristics. To our knowledge, this is the first report of root rot of coptis caused by F. solani in the world. References: (1) K. Dobinson et al. Can. J. Plant Pathol. 18:55, 1996. (2) J. F. Leslie and B. A. Summerell. The Fusarium Laboratory Manual. Blackwell Publishing, Oxford, 2006.

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