scholarly journals First Report of Powdery Mildew Caused by Oidium araliacearum on Ivy in California

Plant Disease ◽  
1998 ◽  
Vol 82 (1) ◽  
pp. 127-127 ◽  
Author(s):  
G. S. Saenz ◽  
S. T. Koike

Powdery mildew was observed on English ivy (Hedera helix L.) in Berkeley, CA, in the spring of 1997. Fungal growth was ectophytic and amphigenous on leaves and petioles and caused slight reddening and buckling of leaves. The mycelium was white, effuse to dense, and had hyphal diameters of 3.5 to 6.9 μm. Appressoria were nipple-shaped to lobed, and sometimes were opposite. The foot cells of the conidiophores were cylindric, sometimes slightly flexuous, and were 18.5 to 30.0 × 6.9 to 9.2 μm in diameter. The foot cells were followed by 1 or 2 cells. When only one cell followed the foot cell, this cell was longer and slightly wider than the foot cell and measured 20.8 to 46.2 × 6.9 to 9.2 μm. When two cells followed the foot cell, these cells were of similar length to the foot cell, with the second cell usually shorter. Conidia were formed singly, were cylindric to slightly doliiform, and measured 32.0 to 44.0 × 11.5 to 19.0 μm. Fibrosin bodies were not observed. Conidia germinated at the ends and germ tubes terminated in lobed appressoria, placing this fungus in the Polygoni-type germination category (2). Cleistothecia were not observed. Based on these characters, the fungus was identified as Oidium araliacearum U. Braun & E. Oehrens B. A specimen was deposited with the University of California at Berkeley herbarium (accession number UC1713247). Pathogenicity was confirmed by gently pressing infected leaves onto leaves of various stages of maturity on ivy vines (3 to 4 vines per plant; 4 plants). Inoculated plants were kept in a moist chamber for 48 h, and then maintained in a greenhouse. Powdery mildew developed on inoculated plants, primarily on leaves of intermediate maturity, after 14 days, while uninoculated plants did not develop disease. Phyllactinia guttata is the only other powdery mildew recorded on English ivy (2). O. araliacearum differs from P. guttata in conidial shape (cylindric vs clavate), germination habit (end vs side of conidia), and asexual genus (Oidium vs Ovulariopsis) (2). Previous to this report, O. araliacearum was described only on Pseudopanax valdiviensis, another Araliaceae plant, in Chile (1). This is the first report of a powdery mildew disease of ivy in California, and the first report of Hedera helix as a host of O. araliacearum. References: (1) U. Braun. Mycotaxon 25:259, 1986. (2) U. Braun. Nova Hedwigia 89:1, 1987.

Plant Disease ◽  
1999 ◽  
Vol 83 (2) ◽  
pp. 198-198
Author(s):  
C. Nali

A powdery mildew disease of variegated ivy (Hedera canariensis L. var. azorica) was observed on the Tyrrhenian coast in Tuscany (Italy) in spring 1998. Symptoms began as small, nearly circular reddish spots that later enlarged and coalesced. The hyaline mycelium produced abundant, ellipsoid conidia in long chains that ranged from 20 to 40 μm in length and from 12 to 25 μm in width. Cleistothecia were globose (100 to 120 μm diameter), dark brown (when mature) with a basal ring of mycelioid appendages, and contained several (up to 20) ovate asci, each generally containing two ascospores. Ascospores were hyaline, one-celled, ellipsoid (20 to 35 μm in length and 10 to 20 μm in width). The morphological characteristics of this fungus were those given for Erysiphe cichoracearum DC. Infection also was found on English ivy (Hedera helix L.). It is reported that this species is, occasionally, subject to powdery mildew caused by E. cichoracearum (1). Conidia from infected leaves were shaken onto leaves of melon (Cucumis melo L.), cucumber (Cucumis sativus L.), watermelon (Citrullus lanatus [Thunb.] Matsum. & Nakai), lettuce (Lactuca sativa L.), tomato (Lycopersicon esculentum Mill.), tobacco (Nicotiana tabacum L.) and variegated and English ivy. After 7 days, the disease was observed on cucumber, melon, watermelon, tobacco, and variegated ivy. Examination confirmed that test plants were infected with E. cichoracearum. This is the first report of E. cichoracearum on variegated ivy in Italy. Reference: (1) P. P. Pirone. 1970. Diseases and Pests of Ornamental Plants. The Ronald Press, New York.


Plant Disease ◽  
1998 ◽  
Vol 82 (6) ◽  
pp. 711-711 ◽  
Author(s):  
S. T. Koike ◽  
R. F. Smith

Tomatillo or husk tomato (Physalis ixocarpa Brot.) is an annual Solanaceous bush grown for its fruit, which are harvested when the fruit fill the enlarged calyx and are used primarily in Hispanic cooking. In the summer of 1997, commercial field-grown tomatillo in the Salinas Valley (Monterey County) was severely affected by a powdery mildew disease. Fungal growth was found on leaves, petioles, and calyces and resulted in twisting, desiccation, and premature senescence of the tissues. The mycelium was white to gray, ectophytic, amphigenous, and effuse. Mycelial appressoria were indistinct. Conidiophore foot cells were straight, cylindric, measured 36.1 to 61.1 µm (mean 47.0) × 11.1 to 13.9 µm (mean 11.7), and were followed by 1 to 3 shorter cells. Doliform conidia were formed in chains and measured 25.0 to 50.0 µm (mean 32.5) × 11.1 to 22.2 µm (mean 17.7). The length-to-width ratios of conidia generally were less than 2.0, and fibrosin bodies were present. Germ tubes usually were laterally inserted, lacked conspicuous appressoria, and were of the pannosa-type. Cleistothecia were not observed. Based on these characters, the fungus was identified as Sphaerotheca fusca (Fr.) Blumer, Beitr. Krypt.-Fl. Schweiz (1). Pathogenicity was confirmed by gently pressing infected leaves onto leaves of potted tomatillo. Inoculated plants were kept in a chamber at 100% humidity for 48 h, and then maintained in a greenhouse. Powdery mildew developed on inoculated plants after 12 to 14 days, while uninoculated plants did not develop disease. The experiment was conducted a second time and the results were the same. This is the first report of a powdery mildew disease of tomatillo in California. Reference: (1) U. Braun. Nova Hedwigia 89:1, 1987.


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.


Plant Disease ◽  
1999 ◽  
Vol 83 (4) ◽  
pp. 399-399 ◽  
Author(s):  
S. T. Koike ◽  
G. S. Saenz

In 1997 and 1998, the white fungal growth of a powdery mildew was observed on leaves and stems of both nursery and landscape spearmint (Mentha spicata) growing in coastal California (Monterey County). Mycelia were conspicuous, amphigenous, and epiphytic with indistinct to nipple-shaped appressoria. Conidiophore foot cells were cylindrical, straight, nonconstricted at the base, 61 to 92 μm × 11 to 14 μm in size, and were followed by 1 to 3 cells. Doliiform conidia, which were borne in chains of at least 3 to 5 conidia, measured 28 to 33 μm × 17 to 22 μm. Catenate conidia had sinuate edge lines. Conidia lacked fibrosin bodies. Upon germination, conidia produced germ tubes that were mostly apically inserted and ended in club-shaped appressoria, which fit Braun's Cichoracearum-type of conidial germination (1). Cleistothecia were not observed. Based on these features, the pathogen was identified as Erysiphe orontii Cast. (1). Pathogenicity was demonstrated by gently pressing diseased leaves onto leaves of potted spearmint, incubating plants in a humidity chamber for 48 h, then maintaining plants in a greenhouse. The powdery mildew that later developed was morphologically identical to the original isolates. While powdery mildew on spearmint has been observed previously in the state, this is the first report of the disease and first characterization of the pathogen for California. Reference: (1) U. Braun. Beih. Nova Hedwigia 89:1, 1987.


Plant Disease ◽  
2000 ◽  
Vol 84 (6) ◽  
pp. 705-705 ◽  
Author(s):  
G. S. Saenz ◽  
S. T. Koike ◽  
H. J. Scheck

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.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 681-681
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Aquilegia flabellata Sieb. and Zucc. (columbine) is a perennial garden species belonging to the family Ranunculaceae. During the summer of 2003, a severe outbreak of a previously unknown powdery mildew was observed in several gardens near Biella (northern Italy). Upper surfaces of leaves were covered with a white mycelium and conidia, and as the disease progressed infected leaves turned yellow and died. Foot cell was cylindric and appressorium lobed. Conidia were hyaline, ellipsoid, and measured 31.2 to 47.5 × 14.4 to 33 μm (average 38.6 × 21.6 μm). Fibrosin bodies were not present. Cleistothecia were globose, brown, had simple appendages, ranged from 82 to 127 (average 105) μm in diameter, and contained one to two asci. Ascocarp appendages measured five to eight times the ascocarp diameter. Asci were cylindrical (ovoidal) and measured 45.3 to 58.2 × 30.4 to 40.2 μm. Ascospores (three to four per ascus) were ellipsoid or cylindrical and measured 28.3 to 31.0 × 14.0 to 15.0 μ;m. On the basis of its morphology, the pathogen was identified as Erysiphe aquilegiae var. aquilegiae (1). Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of five, healthy A. flabellata plants. Five noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a garden where temperatures ranged between 20 and 30°C. After 10 days, typical powdery mildew symptoms developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of the presence of powdery mildew on Aquilegia flabellata in Italy. E. communis (Wallr.) Link and E. polygoni DC. were reported on several species of Aquilegia in the United States (2), while E. aquilegiae var. aquilegiae was previously observed on A. flabellata in Japan and the former Union of Soviet Socialist Republics (3). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) U. Braun. Nova Hedwigia, 89:700, 1987. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (3) K. Hirata. Host Range and Geographical Distribution of the Powdery Mildews. Faculty of Agriculture, Niigata University, 1966.


Plant Disease ◽  
2021 ◽  
Author(s):  
Alma Rosa Solano-Báez ◽  
Santos Gerardo Leyva-Mir ◽  
Moises Camacho-Tapia ◽  
Alfonso Arellano Victoria ◽  
Geremias Rodríguez-Bautista ◽  
...  

Wild blackberry species (Rubus spp. L.; Rosaceae) represents an invaluable source of genes for the generation of new varieties, but also serve as a primary source of disease inoculum. During April of 2020, symptoms of powdery mildew were observed on four populations of wild blackberry species located in the states of Chiapas (16°59'11"N, 92°59'07"W; 16°47'08"N, 92°31'05"W) and Michoacán (19°37'17"N, 100°08'59"W; 19°29'25"N, 101°32'54"W), Mexico. Signs of the pathogen were white powdery masses mainly on the top of new shoots. Symptoms included yellowing, necrosis, and early defoliation of the plants. Hyphae were tin-walled, hyaline, smooth, and 4.0–9.0 mm wide. Appressoria were indistinct -to- nipple-shaped. Conidiophores (n=30, 75–225 × 10.5–13.5 μm) were straight, and unbranched with cylindrical foot cells (n=30, 31.5–158 × 8–13.5 μm), straight, somewhat widening upwards, followed by 1–3 shorter cells. Conidia (n=100; 25.5–38.5 × 9.5–22.5 μm) were catenulate, ellipsoid-ovoid -to- doliiform, containing fibrosin bodies (in 3% KOH). Germ tubes (n=30, 13.5–40.5 × 4.5 μm) emerged laterally, and were unbranched with slightly swollen tips. Chasmothecia were not found. Morphological characters of the fungus in all samples corresponded to the previous descriptions of Podosphaera aphanis by Braun and Cook (2012) and Stevanovi´c et al. (2020). Voucher specimens were deposited in the Department of Agricultural Parasitology Herbarium at the Chapingo Autonomous University under accessions UACH421, UACH423, UACH425, UACH426. To confirm the species identification, the internal transcribed spacer (ITS) of one sample was amplified using the primers ITS5 (White et al. 1990) and P3 (Kusaba and Tsuge, 1995) and sequenced. The sequence was deposited in GenBank (accession number MW988591). A phylogenetic analysis using Bayesian inference and maximum likelihood was performed (Hernández-Restrepo et al. 2018) and included other Podosphaera species (Takamatsu et al. 2010). The sequence from the isolate UACH426 clustered with the strain MUMH1871 of P. aphanis forming a definite clade and remained as a sister taxon of P. pannosa. Pathogenicity was verified through inoculation by gently dusting conidia from one powdery mildew patch onto leaves of five healthy blackberry plants of each specie. The same number of noninoculated plants served as controls. All plants were maintained in a greenhouse at 25–30°C with 75% relative humidity. All inoculated plants developed powdery mildew symptoms after 12 days, whereas no symptoms were observed on noninoculated plants. The fungus recovered from the inoculated plants was morphologically identical to that originally observed on diseased blackberry plants, demonstrating the pathogenicity of the fungus. Based on morphological data and phylogenetic analysis, the fungus was identified as P. aphanis. This fungus has been reported to cause powdery mildew on blackberry plants in Serbia (Stevanovi´c et al. 2020). This is the first report of P. aphanis causing powdery mildew on wild backberry species in Mexico according to Farr and Rossman (2021). The primary source of inoculum of powdery mildew for commercial plantings is wild blackberry plants from noncultivated areas and may warrant control of wild populations.


Plant Disease ◽  
2016 ◽  
Vol 100 (4) ◽  
pp. 859-859
Author(s):  
J. M. Tovar-Pedraza ◽  
S. G. Leyva-Mir ◽  
M. Camacho-Tapia ◽  
E. H. Nieto-López ◽  
V. Ayala-Escobar ◽  
...  

Plant Disease ◽  
2010 ◽  
Vol 94 (2) ◽  
pp. 276-276 ◽  
Author(s):  
D. B. Marcum ◽  
K. Perez ◽  
R. M. Davis

In August of 2009, powdery mildew was observed on peppermint (Mentha piperita L.) in several commercial fields in the Fall River Valley of eastern Shasta County, California. Plant growth was apparently reduced by the disease, but its impact on yield was unknown. White fungal growth was restricted to the adaxial surfaces, where colonies were thin and effused. Heavily infected leaves developed a reddish tint as growth prematurely ceased. Doliform conidia ([26.6-] 29.2 [-31.7] × [13.2-] 15.6 [-16.8] μm) were produced in chains of approximately six conidia. Foot cells were cylindrical ([41.3-] 55.2 [-75.0] × [11.2-] 12.0 [-12.8] μm). Immature chasmothecia were yellowish brown and approximately 100.0 μm in diameter with flexuous, mycelium-like appendages up to 200 μm long. All these features were consistent with those of Golovinomyces biocellatus. Asci were not observed. To confirm the identity of the fungus, nuclear rDNA internal transcribed spacer (ITS) regions were amplified by PCR with universal primers ITS4 and ITS5. The sequence (537 bp) was an exact match for several submissions of G. biocellatus in GenBank (e.g., Accession No. EU035602, a sequence of the fungus from mint in Australia [1]). Pathogenicity was confirmed by brushing spores from naturally infected leaves onto three rooted cuttings of M. piperita ‘Black Mitchum’. After the plants were covered with a plastic bag for 36 h to maintain high humidity, they were kept on a greenhouse bench at 23 to 28°C. Three noninoculated plants, which served as controls, were placed in another greenhouse in similar conditions. The experiment was repeated once. All inoculated plants developed signs of powdery mildew within 7 days of inoculation whereas noninoculated plants remained disease free. The fungus on inoculated leaves was morphologically indistinguishable from the one used to inoculate the plants. To our knowledge, this is the first report of G. biocellatus on peppermint in California. References: (1) J. R. Liberato and J. H. Cunnington. Australas, Plant Dis. Notes 2:38, 2007.


Plant Disease ◽  
2007 ◽  
Vol 91 (4) ◽  
pp. 461-461 ◽  
Author(s):  
R. Raid ◽  
C. Miller ◽  
K. Pernezny

Parsley (Petroselinum crispum (Mill.) Nym. ex A.W. Hill) is an important leaf crop in the Everglades Agricultural Area of southern Florida. During the spring of 2005 and 2006, disease signs and symptoms resembling those incited by powdery mildew were observed on parsley at a commercial vegetable farm located 15 km east of Belle Glade. Symptoms consisted of leaf chlorosis, particularly in the dense lower canopy, and desiccation of affected tissue. A dense, white-to-light gray fungal growth was visible macroscopically on the surface of affected leaf tissue. Microscopic examinations revealed ectophytic hyphae with lobed appressoria and hyaline, straight conidiophores bearing single conidia. Conidia were short-cylindrical to cylindrical, measured 33 to 44 μm long and 13 to 16 μm wide, and lacked fibrosin bodies. Conidiophore foot cells were also cylindrical, straight, and measured 27 to 37 × 9 to 10 μm. Ascocarps of the teleomorph were not observed. The fungus closely matched the description of Erysiphe heraclei DC, a pathogen previously reported as attacking parsley on the U.S. West Coast (1,2). Pathogenicity was verified by inoculating adaxial leaf surfaces of 12 plants (cv. Dark Green Italian) with conidia collected from infected tissue by using a small brush. Inoculated plants and 12 noninoculated plants were lightly misted, held in a moist chamber for 48 h (22°C), and then incubated in a growth chamber for 4 weeks at 22°C with a photoperiod of 16 h. Symptoms that developed on inoculated plants were similar to those observed in the field, with no symptoms evident on the controls treated in a similar manner. To our knowledge, this is the first report of powdery mildew on parsley in Florida, even though parsley has been grown in the area for at least six decades. Noted as being somewhat unique among fungal pathogens because it favors dry rather than moist climatic conditions, it is probably no coincidence that powdery mildew was observed both years during the month of April, the height of Florida's dry season. The fact that monthly rainfall totals of 22 and 35 mm were recorded during April of 2004 and 2005, respectfully, well below the historical average of 72 mm, may have been a contributing influence. Glawe et al. (1), in issuing a first report of E. heraclei on carrots and parsley in the state of Washington and observing ascocarps on carrot tissue, mentioned the prospect of contaminated seed serving as a potential source of dissemination. Although they did not observe the teleomorph on parsley, prospects for its occurrence seem likely. With the bulk of parsley seed planted in Florida being produced in Washington, Oregon, or California, the observations reported herein may provide credence to such a hypothesis. References: (1) D. A. Glawe et al. Online publication. doi:10.1094/PHP-2005-0114-01-HN. Plant Health Progress, 2005. (2) S. T. Koike and G. S. Saenz. Plant Dis. 78:1219, 1994.


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