First Report of Powdery Mildew of Omphalodes cappadocica Caused by Golovinomyces cynoglossi (Erysiphe cynoglossi) in North America

2006 ◽  
Vol 7 (1) ◽  
pp. 47
Author(s):  
Dean A. Glawe ◽  
Joseph F. Ammirati

Omphalodes cappadocica DC (Boraginaceae) is grown as an ornamental plant in the USA. Powdery mildew was observed on specimen plants of O. cappadocica growing in a private garden in Seattle, WA in August 2006. This report describes and illustrates powdery mildew of O. cappadocica as well as taxonomically-important features of the causal organism. Accepted for publication 6 October 2006. Published 27 November 2006.

2010 ◽  
Vol 11 (1) ◽  
pp. 53
Author(s):  
Dean A. Glawe ◽  
Tess Barlow ◽  
Michael E. Matheron

Tecoma capensis (Thunb.) Lindl. (Bignoniaceae, common name: Cape honeysuckle), native to southern Africa, is grown as an ornamental plant in warm regions of the USA. The powdery mildew reported previously from T. capensis in North America was an undetermined Oidium species in Florida. The present report documents the occurrence of the powdery mildew fungus Erysiphe peruviana (Syd.) U. Braun & S. Takam. on T. capensis in Arizona. Accepted for publication 4 January 2010. Published 15 March 2010.


2007 ◽  
Vol 8 (1) ◽  
pp. 36 ◽  
Author(s):  
Dean A. Glawe ◽  
Steven T. Koike

During the summer of 2007 the authors encountered a previously unrecorded powdery mildew disease on several plants of the perennial ornamental plant Stachys byzantina K. Koch ex Scheele (common names: woolly hedgenettle, woolly betony, and lamb's ear) growing in a plant bed near a commercial building in Salinas (Monterey Co.), California. This report documents the occurrence of Neoerysiphe galeopsidis on this host in North America. Accepted for publication 11 October 2007. Published 17 December 2007.


2004 ◽  
Vol 5 (1) ◽  
pp. 16
Author(s):  
Dean A. Glawe

Chinese matrimony-vine (Lycium chinense Mill.) is a traditional medicinal plant grown in China and used as a perennial landscape plant in North America. This report documents the presence of powdery mildew on L. chinense in the Pacific Northwest and describes and illustrates morphological features of the causal agent. It appears to be the first report of a powdery mildew caused by Arthrocladiella in the Pacific Northwest. Accepted for publication 10 November 2004. Published 8 December 2004.


2003 ◽  
Vol 4 (1) ◽  
pp. 33 ◽  
Author(s):  
Dean A. Glawe

American sycamore (Platanus occidentalis L.) is a common native species in eastern North America and is planted widely as a landscape tree in other regions. During a survey of powdery mildew diseases in Washington State, the fungus Microsphaera platani Howe was found on American sycamore trees in Madison Park, Seattle. This report documents the presence of M. platani in Washington State and presents information on the fungus. Accepted for publication 30 July 2003. Published 18 August 2003.


2006 ◽  
Vol 7 (1) ◽  
pp. 54
Author(s):  
Frank M. Dugan ◽  
Dean A. Glawe

Common teasel (Dipsacus sylvestris) is a European species introduced into North America, and is now widely established and regarded as a noxious weed. In October 2005, a powdery mildew was observed on D. sylvestris in two locations in Pullman, Whitman Co., WA. Examination of diseased material confirmed that the causal agent was S. dipsacearum. This report provides the first documentation of S. dipsacearum on D. sylvestris in North America. Accepted for publication 20 April 2006. Published 7 June 2006.


2003 ◽  
Vol 4 (1) ◽  
pp. 41
Author(s):  
Dean A. Glawe

Mahonia aquifolium is a widely-grown plant in the coastal Pacific Northwest. This report documents for the first time a powdery mildew on M. aquifolium in North America caused by a fungus fitting the description of Microsphaera berberidis. Accepted for publication 14 January 2003. Published 6 February 2003.


Plant Disease ◽  
2020 ◽  
Author(s):  
Mo Zhu ◽  
Jie Ji ◽  
Xiao Duan ◽  
Wenqi Shi ◽  
YongFang Li

Bromus catharticus, rescuegrass, is a brome grass that has been cultivated for herbage production, and been widely naturalized in many provinces of China, including Henan province. During April and May 2020, powdery mildew was found on leaves of Br. catharticus on the campus of Henan Normal University, Xinxiang city (35.3°N; 113.9°E), Henan Province, China. Abundant white or grayish irregular or coalesced circular powdery colonies were scattered on the adaxial surface of leaves and 70% of the leaf areas were affected. Some of the infected leaves either were chlorotic or senescent. About 60% of the observed plants showed powdery mildew symptoms. Conidiophores (n = 25) were 32 to 45 μm × 7 to 15 μm and composed of foot cells and conidia (mostly 6 conidia) in chains. Conidia (n = 50) were 25 to 35 μm × 10 to 15 μm, on average 30 × 13 μm, with a length/width ratio of 2.3. Chasmothecia were not found. Based on these morphologic characteristics, the pathogen was initially identified as Blumeria graminis f. sp. bromi (Braun and Cook 2012; Troch et al. 2014). B. graminis mycelia and conidia were collected, and total genomic DNA was extracted (Zhu et al. 2019). The rDNA internal transcribed spacer (ITS) region was amplified with primer pairs ITS1/ITS4. The amplicon was cloned and sequenced. The sequence (574 bp) was deposited into GenBank under Accession No. MT892940. BLASTn analysis revealed that MT892940 was 100% identical to B. graminis f. sp. bromi on Br. catharticus (AB000935, 550 of 550 nucleotides) (Takamatsu et al. 1998). Phylogenetic analysis of MT892940 and ITS of other B. graminis ff. spp. clearly indicated least two phylogenetically distinct clades of B. graminis f. sp. bromi and that MT892940 clustered with the Takamatsu vouchers. Leaf surfaces of five healthy plants were fixed at the base of a settling tower and then inoculated by blowing conidia from diseased leaves using pressurized air. Five non-inoculated plants served as controls. The inoculated and non-inoculated plants were maintained separately in two growth chambers (humidity, 60%; light/dark, 16 h/8 h; temperature, 18℃). Thirteen- to fifteen-days after inoculation, B. graminis signs and symptoms were visible on inoculated leaves, whereas control plants remained asymptomatic. The pathogenicity assays were repeated twice with the same results. The observed signs and symptoms were morphologically identical to those of the originally infected leaves. Accordingly, the causal organism of the powdery mildew was confirmed as B. graminis f. sp. bromi by morphological characteristics and ITS sequence data. B. graminis has been reported on Br. catharticus in the United States (Klingeman et al. 2018), Japan (Inuma et al. 2007) and Argentina (Delhey et al. 2003). To our best knowledge, this is the first report of B. graminis on Br. catharticus in China. Since hybridization of B. graminis ff. spp. is a mechanism of adaptation to new hosts, Br. catharticus may serve as a primary inoculum reservoir of B. graminis to infect other species (Menardo et al. 2016). This report provides fundamental information for the powdery mildew that can be used to develop control management of the disease in Br. catharticus herbage production.


Plant Disease ◽  
2021 ◽  
Author(s):  
Zong-ming Sheu ◽  
Ming-hsueh Chiu ◽  
Lawrence Kenyon

Mungbean (Vigna radiata L.) is routinely grown in the experimental fields at the headquarters of the World Vegetable Center (23°6'30.88"N, 120°17'51.31"E) for breeding, research and germplasm multiplication. In a spring 2016 mungbean trial, about 50% of the plants were affected with powdery mildew. The white, powdery-like patches first appeared on the upper leaf surfaces, and soon developed to grey patches on both sides of the leaves. Purple to brown discoloration appeared on the underside of the infected leaf. Microscopy examination revealed that the causal organism was not Erysiphe polygoni, which had previously been documented as the powdery mildew pathogen on mungbean in Taiwan (Hartman et al. 1993). The fungus produced typical structures of the powdery mildew Euoidium, anamorph of the genus Podosphaera. The mycelium consisted of septate, flexuous hyphae with indistinct appressoria. The erect conidiophores arising from superficial hyphae varied from straight or slightly curved to curled. Three to ten conidia were borne in long chains with crenate edges. Foot-cells were straight, cylindrical and measured 30 to 52 µm long. Conidia were hyaline, ellipsoid-ovoid to barrel-shaped, with fibrosin bodies, and measured 27 to 33 (mean = 30.4) × 15 to 20 (mean = 16.6) µm. Germ tubes were clavate and occasionally forked, and were produced from the lateral sites of the conidia. No chasmothecia were found in the samples. The morphological characteristics were consistent with P. xanthii (Castagne) U. Braun & Shishkoff (Braun & Cook 2012). To confirm the identity, the internal transcribed spacer (ITS) region of rDNA and partialβ-tubulin gene (TUB2) for the isolate MG3 were amplified with the primers ITS4/ITS5 (White et al. 1990) and BtuF5/BtuR7a (Ellingham et al. 2019), respectively. BLASTn analysis revealed the ITS sequence (MN833717) was 100% identical to many records of P. xanthii whereas the TUB2 sequence (MW363957) was 100% identical to a record of P. fusca (syn. P. xanthii; KC333362) in NCBI GenBank. A pathogenicity test was conducted by dusting conidia from an infected leaf onto six healthy four-week-old mungbean plants (cv ‘Tainan No. 3’). Another three plants were not inoculated and were used as control. All the plants were maintained in a greenhouse at 25 to 28°C. All inoculated plants developed powdery mildew symptoms after 10 days, whereas the control plants remained symptomless. To our knowledge, this is the first report of P. xanthii causing disease on mungbean in Taiwan. P. xanthii also has been reported on mungbean in Thailand (Meeboon et al. 2016), while other records referring to E. polygoni infecting Vigna spp. are from Brazil and Fiji (Farr & Rossman 2020). Although both P. xanthii and E. polygoni have now been reported as causing powdery mildew on mungbean in Taiwan, which species predominates or is more important remains unclear. A comprehensive survey with accurate species identification is required to develop effective management of the disease, particularly for resistance breeding.


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 ◽  
2003 ◽  
Vol 87 (4) ◽  
pp. 451-451 ◽  
Author(s):  
C. Nischwitz ◽  
G. Newcombe

Caragana arborescens Lam. is an exotic ornamental that can also be somewhat invasive. In July 2002, powdery mildew was observed on C. arborescens along the Idaho-Washington border in Moscow and Pullman, respectively. Leaves were colonized as soon as they emerged, and entire plants were affected. The fungus covered both leaf surfaces, but cleistothecia were more abundant on abaxial surfaces. The mean diameter of the cleistothecia was 91 (± 9.8) μm. Short-stalked asci averaged 67 (± 7.1) μm × 37 (± 5.2) μm, and the ascospores were 21 (± 2.0) μm × 13 (± 0.8) μm. There are records of four species of Microsphaera on C. arborescens in Europe and Asia. The measurements fit the description of Microsphaera palczewskii Jacz. (1), and the identification was confirmed by comparison with specimens of this fungus on C. arborescens from Sweden (U.S. National Fungus Collections: BPI 749057 and 749058). Specimens of M. grossulariae (Wallr. ex Fr.) Lev. on Ribes divaricatum Dougl. from California (BPI 558266) were also examined, but the cleistothecial appendages were distinctly different from those of the Idaho specimens. To our knowledge, this is the first reported occurrence in North America of powdery mildew on C. arborescens and the first report of M. palczewskii. The latter may have been introduced recently into North America because there are areas in southern Canada and the northern United States in which C. arborescens is unaffected by powdery mildew. Interestingly, it is only in recent decades that M. palczewskii has spread from Asia into Europe (2). Now, host and parasite have been reunited in North America as well. Specimens have been deposited in the U.S. National Fungus Collections (BPI). References: (1) U. Braun. A monograph of the Erysiphales (powdery mildews) J. Cramer, Berlin-Stuttgarg, 1987. (2) S. Huhtinen et al. Karstenia 41:31, 2001.


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