scholarly journals First Report of Powdery Mildew Caused by Erysiphe betae on the Invasive Weed Dysphania ambrosioides in Korea

Plant Disease ◽  
2012 ◽  
Vol 96 (4) ◽  
pp. 592-592
Author(s):  
M. J. Park ◽  
S. E. Cho ◽  
S. Wolcan ◽  
H. D. Shin

Dysphania ambrosioides (L.) Mosyakin & Clemants (formerly Chenopodium ambrosioides L.), commonly known as epazote, is an herb that is native to Central America, South America, and southern Mexico. As well as in its native areas, it is used as an herb, tea, and food commodity in warm temperate to subtropical areas of Europe, the United States, and Asia. In Korea, however, this plant was accidentally introduced around the 1970s and has become widely naturalized by replacing indigenous plants and disrupting native ecosystems (3). Since 2006, powdery mildew infections of epazote have been consistently found in the southern part of Korea, including Jeju Island. Specimens (n = 8) have been deposited in the Korea University Herbarium (KUS). White mycelial and conidial growth was present mostly on leaf surfaces with sparse growth on young stems and inflorescences. Severely infected leaves were malformed. Slight purplish discoloration was present on the leaves contiguous with colony growth. Mycelial colonies were conspicuous, amphigenous, and epiphytic. Appressoria on the mycelia were lobed. Conidiophores were 110 to 200 μm long and produced conidia singly. Conidia were hyaline, oblong-elliptical, measured 30 to 48 × 13 to 18 μm, lacked fibrosin bodies, and produced germ tubes on the subterminal position. Chasmothecia were amphigenous, scattered or partly clustered, dark brown, spherical, 110 to 130 μm in diameter, and contained four to seven asci. Appendages were mycelioid, numbered 50 to 80 per chasmothecium, 0.5 to 1.5 times as long as the chasmothecial diameter, one- to three-septate, and brown at the base while becoming paler toward the tip. Asci were short stalked, 60 to 75 × 30 to 38 μm, and contained three to five spores. Ascospores were ellipsoid-ovoid with dimensions of 20 to 28 × 14 to 18 μm. On the basis of these morphological features, this fungus was identified as Erysiphe betae (Vanha) Weltzien (1). To confirm the identification, the complete internal transcribed spacer (ITS) region of rDNA from KUS-F23213 was amplified with primers ITS5 and P3 and sequenced (4). The resulting sequence of 560 bp was deposited in GenBank (Accession No. JQ041419). A GenBank BLAST search with the current data showed >99% (558 of 560 bp) similarity with the results for E. betae ex Beta vulgaris (sugar beet). Therefore, the sequence analysis verified the pathogen to be E. betae. Previous epazote infections by E. betae have been recorded in Argentina, Mexico, Romania, India, and Japan (1,2). In Taiwan, an epazote powdery mildew associated with Oidium erysiphoides f. sp. chenopodii J.M. Yen, an anamorph of E. betae, was recorded (1,2). To our knowledge, this is the first record of E. betae on epazote in Korea, and the first confirmation of epazote powdery mildew being identified as E. betae on the basis of holomorphic characteristics and ITS rDNA sequences. Our field observation suggests that the powdery mildew is acting as one of several limiting factors to suppress the expansion of this invasive weed in Korea. References: (1) U. Braun. Beih. Nova Hedw. 89:1, 1987. (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/ , November 22, 2011. (3) C. G. Song and Y. H. Yang. The Naturalized Plants in Jeju Island. Nam-Jeju County, Jeju, Korea, 2005. (4) S. Takamatsu et al. Mycol. Res. 113:117, 2009.

Plant Disease ◽  
2014 ◽  
Vol 98 (8) ◽  
pp. 1159-1159 ◽  
Author(s):  
S. E. Cho ◽  
J. H. Park ◽  
S. H. Hong ◽  
B. S. Kim ◽  
H. D. Shin

Verbena brasiliensis Vell., commonly known as Brazilian verbena, is native to South America and has been introduced into North America, coastal Europe, southern Africa, and Australasia. Though partly cultivated for garden use, it is invasive in riverine areas and also on roadsides, forest margins, pastures, and waste areas (4). In Korea, this plant was first reported in 1998 in Jeju Island and has become widely naturalized by replacing indigenous plants and disrupting native ecosystems in most of southern part of Korea (3). Since 2009, powdery mildew on Brazilian verbena has been consistently found in several locations of Busan City, Korea. Symptoms appeared as circular to irregular white patches, which subsequently showed abundant hyphal growth on both sides of the leaves and on stems. High disease severity caused poor growth of the plants, resulting in premature senescence and reduced flowering. Specimens (n = 5) were deposited in the Korea University Herbarium (KUS). Appressoria on the mycelium were nipple-shaped or nearly absent. Conidiophores were 140 to 190 × 11 to 12.5 μm and produced 2 to 7 immature conidia in chains with a crenate outline. Foot-cells in conidiophores were straight, cylindric, relatively short, 50 to 65 μm long, and constricted at the very base of branching point from the hypha. Conidia were hyaline, ellipsoid to ovate, measured 28 to 38 × 18.5 to 22 μm (length/width ratio of 1.2 to 1.8), and contained distinct fibrosin bodies. Germ tubes were produced from the lateral position of conidia. No chasmothecia were observed. These structures are typical of the powdery mildew Euoidium anamorph of the genus Podosphaera. The morphological characteristics and measurements were consistent with those of P. xanthii (Castagne) U. Braun & Shishkoff (1). To confirm the identity, the complete internal transcribed spacer (ITS) region of rDNA of the isolate KUS-F27220 was amplified with primers ITS1/ITS4, and sequenced. The resulting 477-bp sequence was deposited in GenBank (Accession No. KJ472787). A GenBank BLAST search of this sequence revealed 100% identity with Podosphaera sp. on V. bonariensis and V.× hybrida from Japan (AB462804 and AB040347). The Podosphaera sp. isolates listed above are now placed in P. xanthii (1). Pathogenicity was confirmed through inoculation by gently pressing a diseased leaf onto leaves of three healthy, potted 2-month-old Brazilian verbena plants. Three non-inoculated plants served as controls. Inoculated plants developed signs and symptoms after 6 days, whereas the control plants remained symptomless. The fungus present on the inoculated leaves was identical morphologically to that originally observed on diseased plants. Powdery mildew of Verbena spp. associated with Podosphaera sp. (including Sphaerotheca sp.) has been globally reported, but not on V. brasiliensis (1,2). To our knowledge, this is the first report of powdery mildew disease caused by P. xanthii on V. brasiliensis globally. Our field observations suggest that the powdery mildew could limit expansion of V. brasiliensis in Korea. References: (1) U. Braun and R. T. A. Cook. Taxonomic Manual of the Erysiphales (Powdery Mildews), CBS Biodiversity Series No.11. CBS, Utrecht, 2012. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, ARS, USDA, Retrieved February 18, 2014. (3) C. G. Song and Y. H. Yang. The Naturalized Plants in Jeju Island. Nam-Jeju County, Jeju, Korea, 2005. (4) P. F. Yao. Kew Bull. 45:101, 1990.


Plant Disease ◽  
2013 ◽  
Vol 97 (8) ◽  
pp. 1117-1117 ◽  
Author(s):  
S. E. Cho ◽  
J. H. Park ◽  
S. H. Hong ◽  
H. D. Shin

Japanese hop (Humulus japonicus Siebold & Zucc. = H. scandens (Lour.) Merr.), native to East Asia, is an annual, climbing or trailing vine. The vines can spread to cover large areas of open ground or low vegetation, eventually blanketing the land and vegetation. Pollen of H. japonicus is allergenic, and this species is considered as one of the important causes of pollinosis in Korea and China. It is a notorious invasive weed in the United States and also in France, Hungary, and Italy (1). In September 2012, zonate leaf spots were observed on Japanese hops growing in wetlands in Yeongdong County of Korea. A voucher specimen was preserved in the Korea University Herbarium (KUS-F26901). Initial symptoms included grayish-green to grayish-brown spots without border lines. As the lesions enlarged, they coalesced, leading to leaf blight. Sporophores on the leaf lesions were dominantly hypophyllous, rarely epiphyllous, solitary, erect, easily detachable, and as long as 700 μm. The upper portion of the sporophores consisted of a pyramidal head was ventricose, 320 to 520 μm long and 110 to 150 μm wide. The fungus was isolated from leaf lesions and maintained on potato dextrose agar (PDA). Sclerotia were produced on PDA after 4 to 5 weeks at 18°C without light, but conidia were not observed in culture. These morphological and cultural characteristics were consistent with those of Hinomyces moricola (I. Hino) Narumi-Saito & Y. Harada (= Cristulariella moricola (I. Hino) Redhead) (3,4). An isolate was preserved in the Korean Agricultural Culture Collection (Accession No. KACC46955). Genomic DNA was extracted using the DNeasy Plant Mini DNA Extraction Kit (Qiagen Inc., Valencia, CA). The complete internal transcribed spacer (ITS) region of rDNA was amplified with the primers ITS1/ITS4 and sequenced. The resulting sequence of 452 bp was deposited in GenBank (Accession No. KC460209). A BLAST search in GenBank revealed that the sequence showed an exact match with those of C. moricola (JQ036181 ex Acer negundo and JQ036182 ex Glycine max). To determine the pathogenicity of the fungus, according to the procedure of Cho et al. (2), sporophores with the pyramidal head were carefully detached from a lesion on the naturally infected leaf using a needle. Each sporophore was transferred individually onto five places of four detached healthy leaves. The leaves were placed in dew chambers and incubated at 16°C. Symptoms were observed after 2 days on all inoculated leaves. A number of sporophores and immature sclerotia which were morphologically identical to the ones observed in the field were formed on the abaxial surface of the leaf 2 weeks after inoculation. The pathogen was reisolated from lesions on the inoculated leaves, confirming Koch's postulates. No symptoms were observed on the control leaves kept in humid chambers for 2 weeks. H. moricola was known to cause zonate leaf spots and defoliation on a wide range of woody and annual plants (3). To the best of our knowledge, this is the first report of Hinomyces infection on Japanese hops in Korea. References: (1) Anonymous. Humulus japonicus (Cannabaceae): Japanese hop. Eur. Medit. Plant Prot. Org. (EPPO). 2012. (2) S. E. Cho et al. Plant Dis. 96:906, 2012. (3) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, ARS, USDA, Retrieved December 8, 2012. (4) S. A. Redhead. Can. J. Bot. 53:700, 1975.


Plant Disease ◽  
2005 ◽  
Vol 89 (12) ◽  
pp. 1362-1362
Author(s):  
B. Jacobsen ◽  
M. R. Johnston ◽  
H. C. Weltzien

Wide spread powdery mildew infections on sugar beets were observed at the Southern Agricultural Experiment Station in Huntley, MT during September, 2003. Throughout the area, lower leaves were frequently heavily covered by the vegetative stage of the fungus with plants at the edge of the field having clearly visible abundant mature (black) and immature (brown) globose ascocarps on the leaf surfaces and stems. The fruiting structures had mostly branched appendages and were imbedded in the superficial mycelium. Their diameter ranged from 70 to 100 μm. Each ascocarp contained five to eight asci with one to four ascospores (mostly three) per ascus. Elliptical ascospores were hyaline and measured 20 to 25 μm long and 12 to 20 μm wide. On the basis of the descriptions given for isolates from Idaho and Colorado (1) and the usage of Erysiphe polygoni DC for powdery mildew on sugar beet in the United States, this isolate may be classified as E. polygoni DC. However, measurements taken show that ascocarps, asci, and ascospores also fall within the range of E. betae (Vanha) Weltz. as described by Weltzien (2). We strongly suggest that these species be compared by using rDNA analysis of the ITS region to determine whether they are separate species. If survival of the ascocarps and the viability and pathogenicity of the ascospores can be confirmed, epidemics of sugar beet powdery mildew could be understood as local and regional events that are not dependant on long distance dispersal of conidiospores. The occurrence of the perfect stage also could lead to the more frequent appearance of new races through genetic recombination. References: (1) J. J Gallian and L. E. Hanson. Plant Dis. 87:200, 2003. (2) H. C. Weltzien. Phytopathol. Z. 47:123, 1963.


Plant Disease ◽  
2013 ◽  
Vol 97 (6) ◽  
pp. 843-843 ◽  
Author(s):  
Y. J. La ◽  
S. E. Cho ◽  
H. D. Shin

Platanus occidentalis L., called American sycamore or American plane, is native to North America. The trees are commonly planted throughout the world on the sides of roads and in parks. In June 2012, diseased leaves exhibiting signs of powdery mildew from a park in Daegu City of Korea were sent to Plant Clinic of Seoul National University for diagnosis. Our observations in Daegu City during September and October 2012 showed that nearly 99% of the approximately 1,000 trees surveyed were infected with a powdery mildew. Voucher specimens (n = 6) were deposited at the Korea University Herbarium (KUS). Symptoms were characterized by chlorosis, distortion, or cupping of young leaves. White superficial colonies developed amphigenously on leaves. Hyphae were flexuous to straight, branched, septate, 4 to 7 μm wide, and had lobed appressoria. Conidiophores were 120 to 350 × 5 to 7.5 μm and produced conidia singly. Foot-cells of conidiophores were straight, cylindric, and 115 to 200 μm long. Conidia were hyaline, ellipsoid-ovoid, measured 33 to 47.5 × 17.5 to 29 μm with a length/width ratio of 1.5 to 2.0, lacked distinct fibrosin bodies, and showed reticulate wrinkling of the outer walls. Germ tubes were produced on the subterminal position of conidia. No chasmothecia were observed. The structures and measurements were compatible with those of the anamorphic state of Erysiphe platani (Howe) U. Braun & S. Takam. (1). To confirm the identification, the complete internal transcribed spacer (ITS) region of the rDNA from isolate KUS-F26959 was amplified with nested PCR and sequenced. The resulting sequence of 625 bp was deposited in GenBank (Accession No. JX997805). A GenBank BLAST search of this sequence showed only one base substitution with the four sequences (JQ365940 to JQ365943) of E. platani on Platanus spp. Pathogenicity was confirmed through inoculation tests by gently pressing diseased leaves onto young leaves of three 2-year-old disease-free seedlings. Three non-inoculated plants were used as control. Plants were maintained in a greenhouse at 24 to 30°C. Inoculated leaves developed symptoms after 7 days, whereas the control plants remained symptomless. The fungus present on the inoculated leaves was morphologically identical to that observed on the original diseased leaves, fulfilling Koch's postulates. Since E. platani first was recorded in the United States in 1874, it has been regarded as endemic in North America. From the second half of the 20th century, introduction and expansion of the range of this fungus to South America, South Africa, Australia and New Zealand, Europe, and Asia have been reported (1,2). To our knowledge, this is the first report of E. platani infections of P. occidentalis in Korea. This species was recorded on P.× hispanica from Japan in 1999 (4) and on P. orientalis from China in 2006 (3), suggesting invasive spread of the sycamore powdery mildew in East Asia. Since American sycamores are widely planted in Korea, control measures should be made to prevent further spread of the disease. References: (1) U. Braun and R. T. A. Cook. Taxonomic Manual of the Erysiphales (Powdery Mildews), CBS Biodiversity Series No.11. CBS, Utrecht, 2012. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, ARS, USDA, Retrieved October 22, 2012. (3) C. Liang et al. Plant Pathol. 57:375, 2008. (4) S, Tanda. J. Agric. Sci., Tokyo Univ. Agric. 43:253, 1999.


Plant Disease ◽  
2010 ◽  
Vol 94 (1) ◽  
pp. 130-130 ◽  
Author(s):  
M. Troisi ◽  
D. Bertetti ◽  
A. Garibaldi ◽  
M. L. Gullino

Gerbera (Gerbera jamesonii) is one of the top 10 economically important flower crops in Europe as well as the United States. The acreage devoted to this crop continues to increase especially for use in landscape typologies. Abundant flowering from spring until autumn allows the use of this plant to decorate gardens, terraces, and borders. During the summer of 2009, an outbreak of a previously unknown powdery mildew was observed on potted gerbera ‘Mini Yellow’ growing in a private garden in Turin (northern Italy). Adaxial leaf surfaces were covered with white mycelium and conidia, and as the disease progressed, infected leaves turned yellow and died. Conidia were hyaline, ellipsoid, borne in chains (three conidia per chain), and measured 16 to 45 × 10 to 30 μm. Conidiophores measured 109 to 117 × 11 to 13 μm and had a foot cell measuring 72 to 80 × 11 to 12 μm followed by two shorter cells measuring 19 to 29 × 11 to 14 and 20 to 32 × 12 to 14 μm. Fibrosin bodies were absent and chasmothecia were not observed in the collected samples. On the basis of its morphology, the pathogen was identified as Golovinomyces cichoracearum. The internal transcribed spacer (ITS) region of rDNA was amplified with primers ITS1/ITS4 and sequenced. BLASTn analysis of the 548-bp fragment showed an E-value of 0.0 and a percentage homology of 99% with G. cichoracearum isolated from Coreopsis leavenworthii (Accession No. DQ871605) confirming diagnosis inferred by morphological analysis. The nucleotide sequence has been assigned GenBank Accession No. GQ870342. Pathogenicity was confirmed through inoculation by gently pressing diseased leaves onto leaves of three healthy potted plants of Gerbera ‘Mini Yellow’. Three noninoculated plants served as the control. Plants were maintained in a greenhouse at temperatures ranging between 20 and 30°C. Inoculated plants developed signs and symptoms after 8 days, whereas control plants remained healthy. The fungus present on inoculated plants was morphologically identical to that originally observed on diseased plants. To our knowledge, this is the first report of the presence of powdery mildew caused by G. cichoracearum on gerbera in Italy. Specimens are available at the Agroinnova Collection at the University of Torino. Gerbera is also susceptible to different powdery mildews. Powdery mildew of Gerbera jamesonii caused by Sphaerotheca fusca was reported in Italy (4). G. cichoracearum on Gerbera jamesonii was reported in North America (2), Argentina (3), and Switzerland (1). References: (1) A. Bolay. Cryptogam. Helv. 20:1, 2005. (2) M. Daughtrey et al. Page 39 in: Compendium of Flowering Potted Plant Diseases. The American Phytopathological Society, St Paul, MN, 1995. (3) R. Delhey et al. Schlechtendalia 10:79, 2003. (4) F. Zaccaria et al. Ann. Fac. Agrar. Univ. Stud. di Napoli Federico II 34:44, 2000.


Plant Disease ◽  
2012 ◽  
Vol 96 (11) ◽  
pp. 1695-1695 ◽  
Author(s):  
C. Liang ◽  
H. H. Xing ◽  
S. E. Cho ◽  
H. D. Shin

Photinia serrulata Franch. & Sav. (syn. P. serratifolia (Desf.) Kalkman), called Chinese photinia, is native to China, Taiwan, Japan, Indonesia, the Philippines, and India. The plants are evergreen shrubs to small trees belonging in the Rosaceae, and are widely cultivated throughout the world for ornamental purposes. Since 2005, severe powdery mildew infection has been observed on this plant in the Chengyang District of Qingdao City in Shandong Province, China. Powdery mildew colonies were circular to irregular white patches on both sides of the leaves and on young stems. As the disease progressed, white mycelial growth covered the entire shoot portion, causing leaf distortion. Voucher specimens (n= 7) were deposited in the herbarium of Qingdao Agricultural University, China. Hyphae were flexuous to straight, branched, septate, 4 to 6 μm wide, and had nipple-shaped appressoria. Conidiophores arising from the upper part of the hyphae were 110 to 185 × 9 to 12 μm and produced two to six immature conidia in chains with a crenate outline. Foot cells of conidiophores were straight, 30 to 40 μm long, and cylindric to somewhat attenuated toward the base. Conidia were hyaline, ellipsoid-ovoid, 22 to 32 × 13.5 to 20 μm (length/width ratio = 1.5 to 1.9), and had distinct fibrosin bodies. No chasmothecia were observed. The structures and measurements were compatible with those of the anamorphic state of Podosphaera leucotricha (Ellis & Everh.) E.S. Salmon as described by Braun (2). To confirm the identification, the complete internal transcribed spacer (ITS) region of the rDNA was amplified with nested PCR (4) and sequenced. The resulting sequence of 562 bp was deposited in GenBank (Accession No. JQ999954). A GenBank BLAST search of this sequence revealed 100% identity with that of seven isolates of P. leucotricha on rosaceous plants. Pathogenicity was confirmed through inoculation tests by gently pressing diseased leaves onto young leaves of three asymptomatic, potted 3-year-old photinia plants. Three non-inoculated plants were used for a control treatment. Plants were maintained in a greenhouse at 22 ± 2°C. Inoculated leaves developed symptoms after 5 days, whereas the control plants remained symptomless. The fungus present on the inoculated leaves was morphologically identical to that observed on the original diseased leaves, fulfilling Koch's postulates. The powdery mildew infections of P. serrulata associated with P. leucotricha have been recorded in New Zealand, Ukraine, Italy, and the United States (1,3). To our knowledge, P. leucotricha on P. serrulata has not been reported in Asia except for a record of a Podosphaera sp. on P. serratifolia in Japan (3). Since this ornamental shrub is native to China and nearby countries, occurrence of powdery mildew in China poses a potential threat to the health of photinia in other places. References: (1) E. Baldacci. Rev. Appl. Mycol. 16:358, 1937. (2) U. Braun. Beih. Nova Hedw. 89:1, 1987. (3) D. F. Farr and A. Y. Rossman. Fungal Databases, Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrieved from , May 14, 2012. (4) Y. Matsuda et al. Phytopathology 95:1137, 2005.


Plant Disease ◽  
2014 ◽  
Vol 98 (10) ◽  
pp. 1429-1429 ◽  
Author(s):  
Y. Zhang ◽  
F. L. Zhang ◽  
P. Cao ◽  
Y. Liu ◽  
K. Liu ◽  
...  

Swiss chard (Beta vulgaris L. subsp. cicla) is a widely planted vegetable in China. From May to June 2013, an outbreak of powdery mildew on Swiss chard cultivar Fangzheng was observed in the commercial fields in Zhoukou city of Henan Province, located in central China. More than 80% of the plants exhibited symptoms of the disease. At the beginning of infection, circular, white, dust-like colonies of powdery mildew occurred mainly on adaxial surfaces of leaves. As the disease progressed, white mycelia covered the foliar parts of plant. No cleistothecia were found on or in collected samples. Upon microscopic evaluation, conidiophores were unbranched with the length of 63 to 126 and width of 7 to 10 μm (n = 50), produced conidia singly, and composed of a cylindrical foot cell followed by one to three short cells. Conidia were colorless, hyaline, ovoid, measured 29 to 40 × 12 to 18 μm (n = 100), lacked fibrosin bodies, and produced germ tubes on the ends of the conidia. The fungus was identified as Erysiphe betae according to the morphological features (1). To verify the identity, the internal transcribed spacer (ITS) region was amplified with the universal primers ITS1 and ITS4 (2) and sequenced. The ITS sequence obtained was assigned as Accession No. KF268348 in GenBank, which showed 100% homogeneity with two ITS sequences of E. betae isolates from UK (DQ164432 and DQ164436). Koch's postulates were conducted by inoculating 15 healthy 5-week-old plants (cv. Fangzheng) with detached infected leaves, which grew in a growth chamber under 22/16°C (day/night), 50% relative humidity, 120 μmol/m2/s light and a 16-h photoperiod. Fifteen non-inoculated plants grew in another growth chamber with the same conditions as control. Symptoms consistent with the infected field plants were observed on the inoculated plants, while no symptoms were found on the control plants. Microscopic observation revealed that the pathogen growing on the inoculated plants was consistent with the morphology of the original fungus. To our knowledge, this is the first report of E. betae infection on Swiss chard in China (3). References: (1) S. Francis. Mol. Plant Pathol. 3:119, 2002. (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, San Diego, CA, 1990. (3) R. Y. Zheng et al. Page 63 in: Flora Fungorum Sinicorum, Vol. 1, Erysiphales. Science Press, Beijing, 1987.


2018 ◽  
Vol 19 (1) ◽  
pp. 69-70 ◽  
Author(s):  
Michael Bradshaw

Columbine (Aquilegia sp., Ranunculaceae) is a late summer to fall flowering ornamental. Powdery mildew was collected from columbine plants growing outdoors in the botanical garden at the Center for Urban Horticulture, University of Washington (47.65°N; 122.29°W) in October 2016. Morphological characteristics of the fungus were consistent with those of Erysiphe aquilegiae. To confirm species identification, the internal transcribed (ITS) region of rDNA was amplified with the primers ITS4/ITS6. E. aquilegiae (LC009944) was the most similar species with eight nucleotide differences (98.6% similarity). Based on morphological and molecular characteristics, it was concluded that the powdery mildew fungus was E. aquilegiae. To the author’s knowledge, this is the first unequivocal report of E. aquilegiae occurring within the United States. These results are important for the U.S. floral industry, for which Aquilegia is a major crop.


2019 ◽  
Vol 20 (3) ◽  
pp. 179-179 ◽  
Author(s):  
Thies Marten Heick ◽  
Anne Lisbet Hansen ◽  
Annemarie Fejer Justesen ◽  
Lise Nistrup Jørgensen

Powdery mildew caused by Erysiphe betae is one of the major fungal diseases in sugar beet in Denmark and Sweden. Frequent applications of fungicides mitigate the risk of powdery mildew epidemics and, consequently, reduce yield losses conferred by the disease. So far, mixtures of quinone outside inhibitors (QoIs) and triazoles have provided good efficacy against E. betae in field trials and common farming practice. However, development of fungicide resistance is a real risk, because only a limited number of active ingredients are available for the control of powdery mildew in sugar beet, and several other active ingredients are expected to be banned following reevaluation when the most recent European Union legislation is implemented. The G143A mutation associated with QoI resistance has been previously found in the United States. In this brief, its presence in Europe is reported for the first time. The current finding strongly encourages the adoption of anti-resistance strategies that minimize the spread of QoI resistance in sugar beet powdery mildew. Those strategies should be based on integrated pest management measures, including disease monitoring, the use of resistant cultivars, and the use of biological products. A sole reliance on QoI fungicides for sugar beet powdery mildew control should be avoided.


Plant Disease ◽  
2008 ◽  
Vol 92 (2) ◽  
pp. 313-313 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
J. Rossi ◽  
M. L. Gullino

Hedera helix L. (Araliaceae) is a common ornamental species that is able to grow in shaded areas and is often used in parks and gardens. During the fall of 2006, severe outbreaks of a previously unknown powdery mildew were observed in several gardens in Liguria (northern Italy). Both surfaces of young leaves of affected plants were covered with dense, white mycelia and conidia. As the disease progressed, infected leaves turned yellow and dropped. Mycelia and conidia were also observed on young stems. Conidia were hyaline, cylindrical, borne singly, and measured 38 to 51 × 12 to 18 (average 42 × 16) μm. Single germ tubes, moderately long (average 26 μm), developed at the end of conidia. Appressoria of germ tubes and hyphae were lobed (three to four lobes). Conidiophores, 68 to 82 × 7 to 8 (average75 × 8) μm, showed foot cells measuring 39 to 60 × 7 to 8 (average 52 × 8) μm, followed by one shorter cell measuring 19 to 28 × 8 to 9 (average 23 × 9) μm. Fibrosin bodies were absent. Chasmothecia were numerous, spherical, amber-colored then brown at maturity, with diameters ranging from 97 to 140 (average 120) μm, containing four asci shortly stalked, 57 to 72 × 32 to 51 (average 65 × 41 μm). Ascospores were ellipsoid and measured 24 to 34 × 15 to 20 (average 30 × 17) μm. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 613-bp fragment showed an E-value of 0.0 with Erysiphe heraclei. The nucleotide sequence has been assigned GenBank Accession No. EU 010381. In GenBank, our nucleotide sequence shows an E-value of 0.0 also with E. betae. However, the comparison of appressorium shape and germ tube length observed on our microorganism with those described for E. betae by Braun (2) suggests that the causal agent of the powdery mildew reported on ivy is E. heraclei. Furthermore, symptoms described on our host, appressorium shape and the length of conidiophores, are different from those of Oidium araliacearum described by Braun (2) on Araliaceae. Inoculations were made by gently pressing diseased leaves onto leaves of five healthy H. helix plants. Three noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a greenhouse at temperatures between 21 and 25°C. After 15 days, typical powdery mildew colonies developed on inoculated plants. Noninoculated plants did not show symptoms. The pathogenicity test was carried out twice. To our knowledge, this is the first report of the presence of powdery mildew on H. helix caused by E. heraclei in Italy. A powdery mildew caused by E. cichoracearum was previously reported on H. canariensis var. azorica in Italy (3), while a powdery mildew on H. helix caused by O. araliacearum and Golovinomyces orontii, respectively, were observed in the United States (4) and Germany. Herbarium specimens of this disease are available at AGROINNOVA Collection, University of Torino, Italy. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) U. Braun. A Monograph of the Erysiphaceae (Powdery Mildews). Cramer, Berlin, Germany, 1987. (3) C. Nali. Plant Dis. 83:198, 1999. (4) G. S. Saenz and S. T. Koike. Plant Dis. 82:127, 1998.


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