scholarly journals First Report of Powdery Mildew Caused by Oidium Subgenus Pseudoidium on Salvia scabra in Italy

Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Salvia scabra Thunb. is grown and used on the Italian Riviera as a potted plant and used in gardens. During the spring of 2003, severe outbreaks of a previously unknown powdery mildew were observed in a collection of Salvia spp. maintained at an experimental station at Albenga (northern Italy). Powdery mildew was observed only on S. scabra. Leaves were covered with white exophytic mycelia on both surfaces. As the disease progressed, infected leaves turned yellow and died. Conidia were single, hyaline, cylindric, and measured 21.3 to 35.5 × 12.5 to 22.5 μm (average 28.2 × 18.4 μm). Observations made with a light microscope revealed that foot cells were cylindric and appressoria lobed. Cleistothecia were not observed. The pathogen was identified as Oidium subgenus Pseudoidium (1,2), and pathogenicity was confirmed by gently pressing diseased leaves onto mature leaves of healthy, 40-day-old S. scabra plants. Five plants of S. scabra were used as replicates. Noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a growth chamber at 20°C. After 5 days, typical symptoms of powdery mildew 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 S. scabra in Italy as well as in the world. Erysiphe polygoni DC. (Oidium subgenus Pseudoidium) and E. cichoracearum DC. (Oidium subgen us Reticuloidium) were previously reported as causal agents of powdery mildew on other species of Salvia (S. officinalis and S. sclarea) (3,4). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) R. Belanger et al., eds. The Powdery Mildew A Comprehensive Treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia. 89:700, 1987. (3) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (4) A. Pisi and M. G. Bellardi. Inf. Fitopatol. 48(10):57, 1998.

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 ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Mandevilla splendens (Hook.) Woodson is a tropical plant belonging to the Apocynaceae family and grown in Italy as an ornamental. It is generally potted and used to create small barriers on terraces and gardens. During February 2003, severe outbreaks of a previously unknown powdery mildew were observed in a commercial glasshouse located at Albenga (northern Italy) where 30% of the plants were affected by the disease. Infected young leaves were covered on both sides with white mycelia. Mycelia were more evident on the lower surface of older leaves. As the disease progressed, infected leaves turned reddish and eventually became yellow and died. Powdery mildew infections sometimes cause leaves to distort and have reduced growth. Conidia were hyaline, ellipsoid or cylindrical, sometimes appeared to adhere in chains, measured 9 to 15 × 14 to 28 μm (average 12 × 21 μm), and did not show fibrosin bodies. Foot cell was cylindric and appressorium lobed. Cleistothecia were not observed. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1,2,3). Pathogenicity was confirmed by gently pressing diseased leaves onto young leaves of healthy, 1-year-old M. splendens plants grown in 3.5 liter pots. Three plants were inoculated, while three noninoculated plants served as controls. After inoculation, plants were maintained in a growth chamber at 18°C (12-h light, relative humidity >75%). After 60 days, powdery mildew symptoms were observed on inoculated plants. Noninoculated plants remained healthy. The pathogenicity test was carried out twice. To our knowledge, this is the first report of powdery mildew on M. splendens in Italy, as well as in the world. Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) R. Belanger et al., eds. The powdery mildew A comprehensive treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia, 89:700, 1987. (3) R. T. A. Cook et al. Mycol. Res. 101:975, 1997.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Iceland poppy (Papaver nudicaule L.) is grown on the Italian Riviera for export as a cut flower and its importance in the industry is increasing. During the spring of 2003, severe outbreaks of powdery mildew that had not been reported previously, occurred in several commercial plantings grown outdoors in containers near Imperia in northern Italy. Mycelium was observed on all green organs of the plant (leaves, stems, and petioles). Both surfaces on the leaves were affected, and heavily colonized leaves were distorted. As the disease progressed, diseased leaves turned yellow and died. The disease did not affect the flowers. Conidia were hyaline, cylindric, and measured 10.8 to 29.8 × 16.8 to 48.0 μm (average 13.7 × 37.3 μm). Foot cells were cylindric and appressoria unlobed. Fibrosin bodies were not present, and cleistothecia were not observed. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1,2). Pathogenicity was confirmed by gently pressing leaves with visible sporulation onto the leaves of five 90-day-old P. nudicaule plants that were healthy and free of symptoms. Five noninoculated healthy plants served as controls. Inoculated and noninoculated plants were maintained in a growth chamber at 15°C with a 12-h photoperiod. After 7 to 10 days, typical symptoms of powdery mildew developed on inoculated plants but not on noninoculated plants. Previously, Erysiphe cruciferarum Opiz ex L. Junell has been reported on P. nudicaule in all continents, and E. cichoracearum DC. and E. polygoni DC. have been reported in several countries, including Italy, as a causal agent of powdery mildew on other species of Papaver including P. rhoeas and P. strigosum. To our knowledge, this is the first report of powdery mildew caused by an Oidium sp. on P. nudicaule in Italy. The voucher specimen is kept in the department collection at the University of Torino. References: (1) R. Belanger et al., eds. The Powdery Mildew A Comprehensive Treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia. 89:700, 1987.


Plant Disease ◽  
2005 ◽  
Vol 89 (12) ◽  
pp. 1362-1362
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Potentilla fruticosa L. (bush cinquefoil), belonging to the family Rosaceae, is an ornamental plant used in parks and gardens. During the spring and summer of 2005, severe outbreaks of a previously unknown powdery mildew were observed in several private gardens located near Biella (northern Italy). The adaxial and abaxial surfaces of leaves as well as the stems were covered with white mycelium. Buds and flowers also were affected. As disease progressed, infected leaves turned yellow and dehisced. Conidia formed in chains and were hyaline, ovoid, and measured 24.0 to 36.0 × 15.8 to 24.0 μm (average 30.1 × 20.0 μm). Fibrosin bodies were present. Chasmothecia were numerous, sphaerical, amber colored, and diameters ranged from 84.0 to 98.4 μm (average 90.4 μm). Each chasmothecium contained one ascus with eight ascospores. Ascospores measured 26.5 to 27.2 × 13.2 to 15.6 μm (average 26.8 × 14.0 μm). On the basis of its morphology, the causal agent was determined to be Podosphaera aphanis (Wallr.) U. Braun & S. Takamatsu var. aphanis U. Braun (1). Pathogenicity was confirmed through inoculations by gently pressing diseased leaves onto leaves of healthy P. fruticosa plants. Three plants were inoculated. Three noninoculated plants served as a control. Plants were maintained at temperatures ranging from 12 to 23°C. Ten days after inoculation, typical symptoms of powdery mildew 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 powdery mildew on P. fruticosa in Italy. Erysiphe polygoni D.C. and Sphaerotheca macularis (Wallr.:Fr.) Lind were observed in the United States on P. fruticosa (2), while in Japan, the presence of S. aphanis var aphanis was reported (3). Voucher specimens are available at the AGROINNOVA Collection, University of Torino. References: (1) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000 (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) S. Tanda et al. J. Agric. Sci. 39:258, 1995.


Plant Disease ◽  
1998 ◽  
Vol 82 (1) ◽  
pp. 128-128 ◽  
Author(s):  
S. T. Koike ◽  
G. S. Saenz

In December 1996 and January 1997, powdery mildew was observed on potted poinsettia (Euphorbia pulcherrima Willd. ex Klotzsch) plants in Monterey County, CA. Mycelia were observed on stems, petioles, mature and immature leaves, and bracts. Severely diseased leaves became twisted and bent and senesced prematurely. The white mycelia were conspicuous, epiphytic, and amphigenous; hyphae measured 4.6 to 6.9 μm in diameter. Growth initially was in patches but eventually became effused. Appressoria were slightly lobed to lobed and sometimes opposite. Conidiophore foot cells were cylindrical, sometimes bent at the base, and slightly flexuous to flexuous. Foot cells measured 30.0 to 46.2 μm × 5.8 to 6.9 μm and were followed by one to two shorter cells. Conidia were cylindrical to slightly doliform and measured 25.4 to 32.3 μm × 11.6 to 18.5 μm. The length-to-width ratios of conidia generally were greater than 2.0. Conidia were produced singly, placing the fungus in the Pseudoidium-type powdery mildew group. Conidia germinated at the ends, and no fibrosin bodies were observed. Cleistothecia were not found. The fungus was identified as an Oidium species. Pathogenicity was demonstrated by gently pressing infected leaves having abundant sporulation onto leaves of potted poinsettia plants (cvs. Freedom Red, Peter Star Marble, and Nutcracker White), incubating the plants in a moist chamber for 48 h, and then maintaining plants in a greenhouse. After 12 to 14 days, powdery mildew colonies developed on the inoculated plants, and the pathogen was morphologically identical to the original isolates. Uninoculated control plants did not develop powdery mildew. This is the first report of powdery mildew on poinsettia in California. This fungus appears similar to Microsphaera euphorbiae but has longer, slightly flexuous foot cells that do not match the description for M. euphorbiae (1,2). An alternative identification would be Erysiphe euphorbiae; however, there are no available mitosporic descriptions for morphological comparisons (1,2). In the United States, powdery mildew of poinsettia previously has been reported in various states in the Pacific Northwest, Midwest, and Northeast. References: (1) U. Braun. Beih. Nova Hedwigia 89:1, 1987. (2) D. F. Farr et al. 1989. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN.


Plant Disease ◽  
2014 ◽  
Vol 98 (7) ◽  
pp. 1004-1004 ◽  
Author(s):  
M. D. Bolton ◽  
O. T. Neher

The $2.1 billion United States sugar beet (Beta vulgaris L.) industry is the primary provider of domestic sucrose. Sugar beet powdery mildew is caused by Erysiphe polygoni DC and occurs principally in sugar beet growing regions in the western United States. In these regions, the quinone outside inhibitor (QOI) fungicides pyraclostrobin (Headline, BASF, NC) and trifloxystrobin (Gem, Bayer Crop Science, NC) have been important tools to manage powdery mildew since registration in 2002 and 2005, respectively. However, researchers in Idaho reported poor disease management despite QOI application starting in 2011. In 2013, a research plot near Parma, ID, containing natural powdery mildew infection received treatments of pyraclostrobin, trifloxystrobin, or was untreated (control). Since there was no significant reduction in disease levels between QOI-treated blocks and untreated control blocks, experiments were conducted to clone a partial fragment of the E. polygoni cytochrome b (cytb) gene to gain insight into the molecular basis of QOI resistance in this pathosystem. The primers MDB-920 (5′-CACATCGGAAGAGGTTTATA-3′) and MDB-922 (5′-GGTATAGATCTTAATATAGCATAG-3′) were designed based on consensus sequences of several fungal cytb genes obtained from GenBank (data not presented) and used to amplify a 575-bp fragment of the E. polygoni cytb gene using DNA isolated from 12 infected leaf samples collected in September 2013 from the Parma research plot. Each sample consisted of three leaves harvested from three plants (one leaf per plant) in an experimental block. All DNA extraction, PCR, and sequencing procedures were as described previously (1). PCR products derived from six QOI-treated samples and six untreated samples were sequenced directly. Without exception, all QOI-treated samples harbored a point mutation at nucleotide position 143 that encoded a G143A mutation compared with cytb sequence from untreated samples. The two identified cytb haplotypes have been deposited in GenBank under accession numbers KF925325 and KF925326. This is the first report of QOI resistance and the associated cytb G143A mutation in E. polygoni. The G143A mutation has been reported in most QOI-resistant pathogens to date (2). When the G143A mutation dominates in a pathogen population, there is a consistent association with a loss of disease management despite QOI application (3). Careful monitoring and judicious use of QOI fungicides will be necessary to ensure QOI fungicides remain efficacious for sugar beet powdery mildew management in the United States. References: (1) M. D. Bolton et al. Pest Manag. Sci. 69:35, 2013. (2) N. Fisher and B. Meunier. FEMS Yeast Res. 8:183, 2008. (3) U. Gisi et al. Pest Manag. Sci. 58:859, 2002.


Plant Disease ◽  
2004 ◽  
Vol 88 (10) ◽  
pp. 1163-1163 ◽  
Author(s):  
S. Gaetán ◽  
M. Madia

Canola (Brassica napus) is a developing oleaginous crop grown commercially in the Buenos Aires and Santa Fe provinces of Argentina. During the autumn of 2003, typical signs of powdery mildew were observed on canola plants in experimental field plots in Buenos Aires. Average disease incidence was 42% on 3- to 6-month-old canola cultivars developed in the following countries: Argentina (Eclipse, Impulse Master, Mistral, and Nolza); Australia (Oscar and Rainbow); Canada (Sentry); France (Cadillac, Camberra, and Capitol); and Sweden (Maskot, Sponsor, and Wildcat). The range of incidence on these cultivars was 35 to 93%. Other cultivars exhibited an apparent high level of resistance or escaped disease. These included: Charlton (Argentina); 46CO3, Dunkeld, Insignia, Mystic, Monty, Outback, Rivette, and Surpass 400 (Australia), and Caviar (France). Climatic conditions in Buenos Aires, especially rainfall, from March to May 2003 were apparently favorable for powdery mildew development. On susceptible cultivars, fungal growth was observed on leaves, stems, and pods that resulted in premature senescence of the tissues. The mycelium, with multilobed hausthoria, was white to gray, dense or fine, and in patches or covering the entire adaxial leaf surfaces. Appressoria were lobed and conidiophores were straight. Foot cells were cylindrical, straight, measured 35 to 42 × 7 to 10 μm, and were followed by two cells. Conidia were produced singly, cylindrical to ovoid, and measured 36 to 40 × 18 to 20 μm. The conidial length-to-width ratio was 2.0. No fibrosin bodies were observed in the conidia and conidia germinated at the ends. Cleistothecia were not observed. On the basis of mycelial, conidial, and hausthoria characteristics observed on six leaves for each affected cultivar, the fungus was identified as Erysiphe polygoni DC (1). Pathogenicity was confirmed on 5-week-old canola plants of cvs. Eclipse, Impulse, Master, Mistral, and Maskot by gently pressing (1 min) one adaxial infected leaf with abundant sporulation onto one adaxial healthy leaf. The experiment, which included five inoculated plants and three noninoculated control plants for each cultivar, was conducted in a greenhouse at 22 to 24°C and maintained at 75% relative humidity with no supplemental light. Inoculated and control plants were covered with polyethylene bags for 48 h after inoculation. Powdery mildew developed on all inoculated plants of all cultivars after 12 to14 days. The control plants did not develop disease. The experiment was repeated with similar results. E. polygoni has a worldwide distribution (2); however, the results suggest that this fungus may be a threat to the main cultivars being grown in Argentina (Eclipse, Impulse, Master, Mistral, and Nolza), since high levels of disease incidence, as much as 70%, were observed. Under propitious environments, this pathogen could cause severe yield losses in commercially grown canola in Argentina. To our knowledge, this is the first report of canola powdery mildew caused by E. polygoni in Argentina. References: (1) H. J. Boesewinkel. Rev. Mycol. Tome 41:493, 1977. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St.Paul, MN, 1989.


Plant Disease ◽  
2004 ◽  
Vol 88 (9) ◽  
pp. 1045-1045
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Honeysuckle (Lonicera caprifolium L., family Caprifoliaceae) is a climbing shrub used in gardens to cover walls and supports. During the summer of 2003, severe outbreaks of a previously unknown powdery mildew were observed on this species in some gardens near Biella (northern Italy). The first symptoms included extensive chlorosis on leaves, followed by the appearance of white mycelium on the adaxial and abaxial leaf surfaces. As the disease progressed, infected leaves turned yellow and died. Conidia were hyaline, ellipsoidal, and measured 27.6 to 43.2 × 12.2 to 21.6 μm (average 35.7 × 17.6 μm). Foot cells were cylindric and appressoria lobed. Fibrosin bodies were not present. Cleistothecia were not observed during the growing season. The pathogen was identified as Oidium subgenus Pseudoidium (2). The inoculation procedure involved gently pressing diseased leaves onto leaves of healthy L. caprifolium plants. Three plants of L. caprifolium were used as replicates. Noninoculated plants served as control. Inoculated and noninoculated plants were maintained in a garden at temperatures ranging from 15 to 25°C. After 10 days, typical symptoms of powdery mildew developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of powdery mildew on L. caprifolium in Italy. The presence of powdery mildew on different species of Lonicera has been reported in several countries, particularly, Microsphaera miurae U. Braun on L. morowii A. Gray in Germany (1), M. lonicerae (DC.) Winter on L. peryclimenum L. in England (3), and M. lonicerae-ramosissimae on L. ramosissima Fr. & Sav. in Japan (4). The conidia of M. lonicerae are smaller than those of the Oidium sp. reported on L. caprifolium. Voucher specimens are available at DIVAPRA Collection at the University of Torino. References: (1) U. Braun. Mycotaxon 16:417, 1983. (2) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (3) J. Robbins. Cecidology 15:15, 2000. (4) S. Tanda. Mycoscience 41:155, 2000.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Akebia quinata Decne., an ornamental species belonging to the family Lardizabalaceae, is used as a climbing species in gardens to cover walls as well as supports and is very much appreciated because of its dark red flowers. During the summer of 2003, severe outbreaks of a previously unknown powdery mildew were observed on established plantings in several gardens near Biella (northern Italy). The upper surfaces of leaves were covered with white mycelium, and the corresponding abaxial surface of infected leaves were chlorotic. Young, green stems also affected showed extended chlorosis. As the disease progressed, infected leaves turned yellow and died. Foot cell was cylindric and appressorium lobed. Conidia formed singly were hyaline, ellipsoid, and measured 26.4 to 45.6 × 10.6 to 15.6 μm (average 35.1 × 12.7 μm). Fibrosin bodies were not present. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1) partially because cleistothecia were not observed. Conidial measurements are close to those reported for Microsphaera akebiae Sawada. Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of healthy A. quinata plants. Three plants of A. quinata were used as replicates. Noninoculated plants served as controls. Plants were maintained between 20 and 30°C in a garden located 5 km from where the disease was originally found. After 10 days, typical symptoms of powdery mildew 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 A. quinata in Italy. The disease is currently restricted to the area of Biella. The presence of M. akebiae was recently reported in the Netherlands (2). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) U. Braun and S. Takamatsu. Schlechtendalia, 4:1, 2000. (2) M. Scholler and W. Gams. Nova Hedwigia, 67:101, 1998.


Plant Disease ◽  
2019 ◽  
Vol 103 (5) ◽  
pp. 1043-1043
Author(s):  
S. H. Hong ◽  
Y. H. Lee ◽  
Y. J. Choi ◽  
H. D. Shin

Sign in / Sign up

Export Citation Format

Share Document