scholarly journals First Report of Bremia lactucae Causing Downy Mildew on Helichrysum bracteatum in Italy

Plant Disease ◽  
2003 ◽  
Vol 87 (3) ◽  
pp. 315-315 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
G. Gilardi ◽  
M. L. Gullino

Helichrysum bracteatum, also known as strawflower, is commonly grown for the production of dried flowers and, more recently, as a potted plant. This latter cultivation system is becoming increasingly important on the Liguria Coast in northern Italy. During the spring of 2002, severe oubreaks of a previously unknown disease were observed in commercial farms in the area of Albenga (northern Italy) on several cultivars of H. bracteatum. Leaves of infected plants appeared curled and blistered; the infected portions of leaves turned chlorotic. On the lower leaf surface of chlorotic areas, a dense, whitish growth was evident. Infected leaves eventually wilted without dropping. Basal leaves with poor air circulation were the most severely affected. Certain cultivars of H. bracteatum (such as ‘Florabella Pink’) were most seriously affected, while others (‘Florabella Gold’ and ‘Florabella White’) had less disease. Microscopic observations revealed sporangiophores emerging from the stomata that were dichotomically branched, ending with 4 to 7 sterigmata. The sporangia were globose and measured 15.5 to 16.8 μm in diameter. The pathogen was identified as Bremia lactucae based on the morphological characteristics. Pathogenicity was confirmed by inoculating healthy H. bracteatum (100-day-old ‘Florabella Gold’) as well as Lactuca sativa (25-day-old ‘Salad bowl’) plants with a sporangial suspension (1 × 105 sporangia/ml). Five plants of H. bracteatum and 10 of lettuce were used as replicates. Noninoculated plants served as controls. Inoculated and uninoculated plants were maintained in a growth chamber at 20°C and 90 to 95% relative humidity. After 7 to 10 days, typical symptoms of downy mildew developed on H. bracteatum and lettuce plants artificially inoculated. Bremia lactucae was observed on infected leaves. Uninoculated plants did not show symptoms. To our knowledge, this is the first report of Bremia lactucae on H. bracteatum in Italy. B lactucae was previously reported as the causal agent of downy mildew on H. bracteatum in several countries including the United Kingdom (3), the United States (1), and Egypt (2). References: (1) S. A. Alfieri et al. Index of plant diseases in Florida. Bull No. 11, 1984. (2) H. Elarosi and M. W. Assawah. Rev. Plant Prot. Res., 39:583, 1959. (3) W. C. Moore. British Parasitic Fungi. Cambridge University Press, Cambridge, 1959.

Plant Disease ◽  
2006 ◽  
Vol 90 (9) ◽  
pp. 1261-1261
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Iberis sempervirens (evergreen candytuft) is a garden species belonging to the Brassicaceae family. During June 2004, a damaging foliar disease was observed in several commercial farms near Albenga (northern Italy) on I. sempervirens plants grown outdoors in containers. More than 30% of the plants were affected. Symptoms appeared on both sides of leaves, buds, flowers, and fruits. Initially, leaves were slightly chlorotic, but within 5 to 7 days a characteristic whitish furry growth developed on the lower and upper leaf surfaces. The efflorescence was particularly evident on the lower surfaces of leaves and consisted of sporangiophores and sporangia. The appearance and severity of the disease increased because of overhead sprinkler irrigation. Microscopic observations revealed dichotomously branched sporangiophores with slender curved tips. Sporangiophores with a length of 115 to 410 μm (average 295 μm) ended with sterigmata bearing single sporangia. Sporangia were ovoid and measured 18 to 28 × 25 to 45 μm (average 22 × 35 μm). The pathogen was identified as Peronospora parasitica on the basis of its morphological characteristics (3). Pathogenicity was confirmed by inoculating leaves of 10 45-day-old healthy plants grown in 14-cm-diameter pots with a sporangial suspension (1 × 103 conidia/ml). Ten noninoculated plants served as controls. Plants were maintained outdoors at 50% light intensity with temperatures ranging between 16 and 25°C (average 18°C) and 85 to 100% relative humidity. The pathogenicity test was carried out twice. After 18 days, typical symptoms of downy mildew developed on the inoculated plants and P. parasitica was observed on the leaves. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of P. parasitica on evergreen candytuft in Italy. P. parasitica was previously reported on I. sempervirens in the United Kingdom (1) and on I. amara in California (2). Voucher specimens are available at the AGROINNOVA Collection, University of Torino, Italy. References: (1) S. Francis and G. Waterhouse. Trans. Br. Mycol. Soc. 91:1, 1988. (2) P. R. Muller et al. Index of Plant Diseases in the United States. USDA Handbook No. 165, 1960. (3) D. M. Spencer. The Downy Mildews. Academic Press, New York, 1981.


Plant Disease ◽  
2007 ◽  
Vol 91 (3) ◽  
pp. 324-324 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
M. L. Gullino

Camellia cultivation has a long history in the Lake Maggiore area of northern Italy where a wide selection of varieties is present. Camellias are appreciated for their large, colorful flowers that bloom from late fall through early spring. In July 2005, a previously unknown foliar disease was observed on a collection of 2- to 12-month-old camellia cultivars (Camellia japonica) grown in several nurseries located in the Verbania Province (northern Italy). The disease was observed on plants grown in pots (10 to 24 cm in diameter) that were maintained either in the open or in a greenhouse and was present for the entire growing season. However, symptoms were more severe during the summer with temperatures ranging between 25 and 30°C with high relative humidity values. During the months of June and July of 2005, severe attacks involving as much as 70% of plants were observed on C. japonica cvs. Mrs. Tingley, Burnside, Hagoromo (synonym Magnoliaeflora), and Giuseppe Traverso. The disease was again observed in 2006. On the upper side of the younger leaves, small necrotic spots (3 to 8 mm in diameter) initially developed mainly at the margin of the leaves and near the petioles. Necrotic areas were surrounded by a chlorotic halo that turned progressively black. The necrotic areas often coalesced, generating larger spots with a diameter ranging from 15 to 30 mm. Severely affected plants were defoliated. Infected plants sometimes died. The presence of lesions on mature plants decreased aesthetic quality and market value. Leaf spots contained dark brown, multicellular, pyriform conidia. Conidia, generally in short chains, were 20.5 to 34.8 μm (average 29.3 μm) long, 6.9 to 12.2 μm (average 9.9 μm) wide, with 3 to 4 longitudinal cross walls, and an average of 5.7 single cells. From 15 samples of infected leaves, several isolates of a fungus identified on the basis of its morphological characteristics as belonging to the Alternaria alternata complex (2) were consistently isolated on potato dextrose agar containing 25 mg/l of streptomycin sulfate. Pathogenicity tests were performed by spraying leaves of healthy 6-month-old potted C. japonica cv. Burnside plants with a spore and mycelial suspension (1 × 105 CFU/ml) prepared by using a mixture of three isolates obtained in 2005 grown on PDA for 30 days at 23 ± 2°C in a growth chamber (12 h of light per day). Plants without inoculation served as a control. Five plants were used for each treatment. Plants were covered with plastic bags for 3 days after inoculation and maintained at 25°C in growth chambers. The first lesions developed on leaves 3 days after inoculation, while control plants remained healthy. Sixty days after artificial inoculation, 25% of the inoculated plants were dead, while the control plants remained healthy. From lesions of infected plants, a fungus belonging to the A. alternata complex was consistently reisolated. The pathogenicity test was carried out twice. The presence of A. alternata on C. sinensis, the commercial tea plant, was reported in India (1). Previously, a flower blight caused by A. tenuis was reported in the United States (3). This is, to our knowledge, the first report of A. alternata on C. japonica in Italy and probably in the world. The disease was present in 2005 and 2006 in several commercial nurseries affecting 50% of plants of susceptible cultivars. References: (1) B. N. Chakraborty et al. Plant Pathol. 55:303, 2006. (2) E. G. Simmons. Pages 1–35 in: Alternaria Biology, Plant Diseases and Metabolites. J. Chelchowski and A. Visconti, eds. Elsevier, Amsterdam, 1992. (3) A. J. Watson. Plant Dis. Rep. 34:186, 1950.


Plant Disease ◽  
2004 ◽  
Vol 88 (8) ◽  
pp. 909-909 ◽  
Author(s):  
S. N. Wegulo ◽  
S. T. Koike ◽  
M. Vilchez ◽  
P. Santos

During February 2004, diseased double impatiens (Impatiens walleriana) plants were received from a commercial grower in southern California. The upper surfaces of symptomatic leaves were pale yellow with no distinct lesions. Diseased leaves later wilted, and severely affected leaves abscised from the stem. At the nursery, only double impatiens plants in the Fiesta series were infected, and some cultivars were more heavily infected than others. Disease incidence in cv. Sparkler Hot pink was nearly 100%. The interior of infected leaves was colonized by coenocytic mycelium. A conspicuous white growth was observed only on the underside of leaves. Sporangiophores were hyaline, thin walled, emergent from stomata, and had slightly swollen bases. Sporangiophore branching was distinctly monopodial. Smaller sporangiophore branches were arranged at right angles to the supporting branches, and tips of branches measured 8 to 14 μm long. Sporangia were ovoid and hyaline with a single pore on the distal ends. Distal ends of sporangia were predominantly flat but occasionally had a slight papilla. Short pedicels were present on the attached ends. Sporangia measured 19.4 to 22.2 (-25.0) μm × 13.9 to 16.7 (-19.4) μm. Oospores were not observed in leaf tissue. On the basis of symptoms and morphology of the organism, the pathogen was identified as Plasmopara obducens J. Schröt. Pathogenicity tests were done on double type cvs. Fiesta, Tioga Red, and Tioga Cherry Red and on single type cvs. Cajun Watermelon and Accent Lilac. Plants were spray inoculated with sporangiospore suspensions (1 × 104 sporangiospores per milliliter), incubated for 24 h in a dew chamber (18 to 20°C), and then maintained in a greenhouse (22 to 24°C). Symptoms and signs of downy mildew developed after 12 days only on inoculated cv. Fiesta plants, and the pathogen morphology matched that of the originally observed pathogen. Nontreated control plants did not develop downy mildew. To our knowledge, this is the first report of downy mildew on impatiens in California. P. obducens is one of two causal agents of downy mildew of impatiens (2,4). The other pathogen, Bremiella sphaerosperma, has dichotomous sporangiophore branching and causes lesions with well-defined margins (2,4). In the United States, the disease has been recorded in the eastern and northeastern states and in Indiana, Minnesota, Mississippi, Montana, and Wisconsin (3). In Canada, the disease has been recorded in Manitoba and Quebec (1). References: (1) I. L. Conners. An Annotated Index of Plant Diseases in Canada and Fungi Recorded on Plants in Alaska, Canada, and Greenland. Research Branch, Canada Department of Agriculture, Publication 1251, 1967. (2) O. Constantinescu. Mycologia 83:473, 1991. (3) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, 1989. (4) G. W. Wilson. Bull. Torrey Bot. Club 34:387, 1907.


Plant Disease ◽  
2008 ◽  
Vol 92 (1) ◽  
pp. 173-173 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Hydrangea anomala subsp. petiolaris (synonym H. petiolaris and H. scandens), also known as climbing hydrangea, is cultivated as an ornamental for landscaping in parks and gardens. This species, belonging to the Hydrangeaceae and native to the woodlands of Japan and coastal China, is widely appreciated for its abundant, creamy white flowers with a sweet aroma, particularly in shade gardens. During the summer of 2006, extensive necroses were observed on leaves and young stems of 3-year-old plants grown outdoors in several gardens of Piedmont of northern Italy. In many cases, on the upper side of the leaves, necrotic spots (4 to 10 mm in diameter) turned progressively black. Lesions often coalesced, generating larger (2 to 6 cm in diameter) necrotic areas. Necroses initially developed mainly at leaf margins and near petioles, and severely affected plants were defoliated. Infected plants rarely died, but the presence of lesions reduced the aesthetic quality and subsequently the commercial value. The disease occurred on 50 of 100 plants. A fungus was consistently isolated from infected leaves on potato dextrose agar (PDA) and identified on the basis of its morphological characteristics as an Alternaria sp. Conidia were dark gray, multicellular, clavate to pear shaped, measuring 23 to 54 × 10 to 13 μm (average 38 × 12 μm), with five longitudinal crosswalls and a relatively short apical beak. DNA was extracted with a Nucleospin Plant Kit (Macherey Nagel, Brockville, ON, Canada) and PCR was carried out with ITS 6/ITS 4 primer (2). A 557-bp PCR product was sequenced, and a BLASTn search (1) confirmed that the sequence corresponded to Alternaria compacta (99% homology). The nucleotide sequence has been assigned GenBank Accession No. EU 128529. Pathogenicity tests were performed by spraying leaves of healthy 1-year-old potted H. anomala plants with an aqueous 105 CFU/ml spore suspension. The inoculum was obtained from cultures of the fungus grown on sterilized host leaves placed on PDA for 20 days in light/dark at 23 ± 1°C. Plants sprayed only with water served as controls. Five plants were used for each treatment. Plants were covered with plastic bags for 3 days after inoculation and maintained between 12 and 22°C. Lesions developed on leaves 8 days after inoculation with the spore suspension, whereas control plants remained healthy. A. compacta was consistently reisolated from these lesions. The pathogenicity test was repeated twice. The presence of an Alternaria sp. on H. macrophylla was reported in the United States (3), whereas A. hortensiae was observed in Spain on H. hortensis. Recently, A. alternata belonging to the alternata group was reported on H. macrophylla in Italy (4). This is, to our knowledge, the first report of A. compacta on H anomala subsp. petiolaris in Italy. References: (1) S. F. Altschud et al. Nucleic Acids Res. 25:3389, 1997. (2) D. E. L. Cooke and J. M. Duncan. Mycol. Res. 101:667, 1997. (3) M. L. Daughtrey et al. Page 9 in: Compendium of Flowering Potted Plant Diseases. American Phytopathological Society. St. Paul, MN, 1995. (4) A. Garibaldi et al. Plant Dis. 91:767, 2007.


Plant Disease ◽  
2003 ◽  
Vol 87 (6) ◽  
pp. 751-751 ◽  
Author(s):  
G. E. Holcomb

A blight (wet rot) of petunia (Petunia ×hybrida Hort. Vilm.-Andr.) was observed in a wholesale propagation nursery in Baton Rouge, LA in September 2002. The grower reported that plants wilted and then completely rotted. The disease occurred during a period of hot, humid, and cloudy weather. Approximately 100 flats of flowering-age plants of cvs. Rose and White Madness were destroyed. No fungal sporulation was noticed on dead plants, but occasional strands of white mycelium were observed. The grower's use of azoxystrobin, iprodione, and thiophanate methyl plus mancozeb fungicides during current and past outbreaks of this disease did not prevent disease spread, but disease activity stopped after temperature and humidity dropped in early October. A fungus that produced white aerial mycelia that later developed light yellow areas and also black aerial spore masses was consistently isolated from diseased tissue placed on acidified potato dextrose agar (APDA). The fungus was identified as Choanephora cucurbitarum (Berk. & Ravenel) Thaxt. on the basis of cultural and morphological characteristics (3). Sporangiola were ellipsoid, pale brown to reddish brown with distinct longitudinal striations and measured 15 to 20 × 9 to 14 μm. Sporangiospores were broadly ellipsoid, pale brown to reddish brown, indistinctly striate with fine, hyaline polar appendages, and measured 16 to 34 × 7 to 12 μm. Spore measurements were within the range previously given for C.cucurbitarum (3). Pathogenicity tests were performed by misting a mixture of sporangiola and sporangiospores (25,000 to 70,000 per ml of water taken from 7- to 10-day-old cultures grown on APDA) on flowering-age petunia plants (cvs. Rose Madness, White Madness, and Dreams Pink). Tests were repeated twice. Inoculated plants and uninoculated control plants (2 to 4 of each treatment in each test) were held in a dew chamber at 28°C for 48 h and then moved to a greenhouse. Within 48 h after inoculation, plants developed water-soaked lesions on flowers, leaves, and stems, then wilted and rotted. Uninoculated plants remained disease free except for several that developed disease symptoms in the first test, apparently from the presence of natural inoculum on healthy-appearing plants that were obtained from the nursery where the disease was found. Koch's postulates were completed by reisolation of the pathogen from diseased inoculated plants. C. cucurbitarum (1) and C. infundibulifera (Curr.) Sacc. (2) have been reported to cause flower blight of petunia in the United States and whole plant blight (wet rot) of petunia in Japan (4). To our knowledge, this is the first report of C. cucurbitarum causing whole plant blight of petunia in the United States. References: (1) M. L. Daughtrey et al. Choanephora wet rot of poinsettia. Page 15 in: Compendium of Flowering Potted Plant Diseases. The American Phytopathological Society, St. Paul, MN, 1995. (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) P. M. Kirk. Mycological Paper 152:1, 1984. (4) J. Takeuchi and H. Horie. Jpn. J. Phytopathol. 66:72, 2000.


Plant Disease ◽  
2007 ◽  
Vol 91 (6) ◽  
pp. 767-767 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
S. Frati ◽  
M. L. Gullino

Hydrangea macrophylla is cultivated as an ornamental and also used in the landscape. During the fall of 2005, leaves and young stems on 12-month-old plants (cvs. Hanabi, Nigra, and Zaffiro) grown in pots in several gardens and commercial nurseries in the Piedmont (northern Italy) had extensive necrosis. In many cases, 4-mm-diameter spots on the upper side of the leaves were surrounded by a chlorotic halo, which turned progressively black. Lesions often coalesced into 3- to 8-cm-diameter necrotic areas. Initial necrosis developed mainly on the leaf margins and near the petioles. Severely affected plants were defoliated. Infected plants rarely died, but the presence of lesions reduced the aesthetic quality and subsequently the commercial value. The disease occurred on 30 to 50% of the plants. Leaf spots contained dark brown, multicellular, pear-shaped conidia. Conidia were 19.2 to 36.5 μm (average 26.3 μm) long and 7.7 to 11.5 μm (average 8.9 μm) wide, with 3 to 4 longitudinal cross walls and an average of 4.4 single cells. A fungus identified on the basis of its morphological characteristics as an Alternaria sp. was consistently isolated from symptomatic leaves onto potato dextrose agar. DNA was extracted from mycelium (Nucleospin Plant Kit, Macherey Nagel, Brockville, ON, Canada) and PCR was completed using Alt-for/Alt-rev primers (3), which amplified a part of the gene that encodes for the protein Alt a 1, the major allergen produced by the genus Alternaria. A 305-bp fragment was amplified, sequenced, and the sequence was subjected to BLASTn analysis (1), which confirmed that the isolate belonged to the genus Alternaria and to the alternata group (3). The nucleotide sequence has been deposited in GenBank (Accession No. EF446670). Pathogenicity tests were performed by spraying leaves of healthy potted H. macrophylla plants, cvs. Zaffiro (6-month-old) and Hanabi (12-month-old) with a spore suspension (105 conidia/ml). Plants sprayed with water only served as a control. Ten plants per cultivar were used for each treatment. Plants were covered with plastic bags for 5 days after inoculation and maintained at 20°C for an additional 7 days. Plants were transferred outdoors and kept at temperatures ranging from 19 to 25°C. The first foliar lesions developed on leaves 15 days after inoculation, whereas control plants remained healthy. Alternaria sp. was consistently reisolated from these lesions. The pathogenicity test was completed twice. The presence of Alternaria sp. on Hydrangea spp. was reported in the United States (2), whereas A. hortensiae was observed in Spain (4). To our knowledge, this is the first report of Alternaria sp. belonging to the alternata group infecting H. macrophylla in Italy. The disease is currently spreading in other Italian areas. References: (1) S. F. Altschud et al. Nucleic Acids Res. 25:3389, 1997. (2) M. L. Daughtrey et al. Page 9 in: Compendium of Flowering Potted Plant Diseases. The American Phytopathological Society, St. Paul, MN, 1995. (3) S. Gyu Hong et al. Fungal Genet. Biol. 42:119, 2005. (4) L. M. Unamuno. An. Jard. Bot. Madr. 4:145, 1944.


Plant Disease ◽  
2013 ◽  
Vol 97 (10) ◽  
pp. 1382-1382
Author(s):  
L. L. Duarte ◽  
Y. J. Choi ◽  
R. W. Barreto

African daisy (Gerbera jamesonii Bolus ex Hook. f.) is an important species for both the cut flower and potted plant industries worldwide (4). Since the winter of 2009, plants showing severe downy mildew symptoms have been observed in a greenhouse located in an experimental area of the Universidade Federal de Viçosa (state of Minas Gerais, Brazil). The disease appeared as ill-delimited adaxial chlorosis of lamina; tissues became yellow and then brown with age with intense blighting of leaves of entire plants, leading to their death, when untreated. Dense, whitish sporulation was observed on the lower surfaces since early stages. A representative sample was dried in a plant press and deposited in the local herbarium under accession number VIC 32070. Slides were prepared with fungal structures mounted in lactofuchsin and observed under a light microscope (Olympus BX 51). Fungus morphology: Sporangiophores hypophyllous, emerging through stomata, cylindrical, up to 650 μm long and 5 to 10 μm wide, with slightly swollen base from 6.5 to 13 μm, hyaline, aseptate, straight, with up to 6 monopodial ramifications occurring mainly at right angles, the final branch ending in 3 or 4 ultimate branchlets; sporangia globose to ovoid, from 20 to 28 μm long and 13 to 18 μm wide, hyaline, smooth. Oospores were not observed. In order to further clarify the identity of the fungus on G. jamesonii, genomic DNA was extracted directly from the plant tissue and part of cytochrome c oxidase subunit 2 was amplified with the primers COX2 (3). The generated sequence was submitted to GenBank (Accession No. KC690148) and when compared with other entries revealed a high sequence similarity (99%) with Plasmopara halstedii (Farl.) Berl. & De Toni (EU743813) from Helianthus annuus L. This was also supported by the morphological data as compared with published descriptions (2) and it was then concluded that the chromistan fungus involved in downy mildew of African daisy was P. halstedii. Two different downy mildew genera, Bremia and Plasmopara, cause downy mildew disease on G. jamesoni. Bremia lactucae has been recorded in Argentina, Brazil, Germany, and Poland (4). There is only one record of a Plasmopara on this host in the United States (1), but this is an obscure report with no identification at the species level. Although P. halstedii has been commonly recorded on numerous hosts belonging to the Asteraceae worldwide, it has never been reported on G. jamesoni. To our knowledge, this is the first report of P. halstedii on G. jamesoni in Brazil. This disease has the potential to become important and cause significant losses because of a combination of the high severity to untreated plants and the increasing importance of African daisy in the flower market in Brazil. References: (1) S. A. Alfieri, Jr. et al. Bull. 11. Index of Plant Diseases in Florida (Revised). Florida Dep. Agric. Consumer Serv., Div. Plant Ind., 1984. (2) G. Hall. Plasmopara halstedii. CMI Descriptions of Pathogenic Fungi and Bacteria No 979. Mycopathologia 106:205, 1989. (3) D. S. S. Hudspeth et al. Mycologia 92:674, 2000. (4) S. M. Wolcan, Australas. Plant Dis. Notes 5:98, 2010.


Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 205-205 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
M. L. Gullino

Lamb's lettuce (Valerianella olitoria) is increasingly grown in Italy and used in the preparation of processed salad. In the fall of 2003, plants of lamb's lettuce cvs. Trophy and Palmares showing symptoms of severe stunting were observed in several commercial plastic greenhouses near Bergamo in northern Italy. The distribution of the disease was generally uniform in the greenhouses and 10 to 30% of the plants were affected. The first symptoms, consisting of reduced growth of the plants and extensive chlorosis, developed in October at temperatures ranging between 10 and 20°C on 30-day-old plants. The roots of diseased plants showed extensive necrosis that extended to the crown of the plants. The diseased tissue was disinfested for 1 min in 1% NaOCl and plated on potato dextrose agar amended with 100 µg/l streptomycin sulfate. A fungus with the morphological characteristics of Thielaviopsis basicola was consistently and readily isolated from symptomatic tissues (1). Catenulate, cylindrical, hyaline endoconidia and catenulate, subrectangular, thick-walled chlamydospores (aleuriospores) were observed. Ten-day-old plants of cvs. Trophy and Palmares were artificially inoculated by dipping three isolates of T. basicola obtained from infected plants for 15 min in a spore suspension (1 × 106 CFU/ml). Noninoculated plants served as control treatments. Each treatment consisted of 30 plants. Plants were maintained at 20°C in a growth chamber, with 12 h of light/day. Symptoms developed 25 days after the artificial inoculation on both cultivars, and T. basicola was consistently reisolated from diseased plants. The noninoculated plants remained healthy. The pathogenicity test was carried out twice. To our knowledge, this is the first report of T. basicola on lamb's lettuce in Italy as well as in the world. The same disease was described on corn salad (Valerianella locusta) in the United States (2). References: (1) D. E. Mathre and A.V. Ravenscroft. Phytopathology 56:337, 1966. (2) M. E. Stanghellini et al. Plant Dis. 74:81, 1990.


Plant Disease ◽  
2003 ◽  
Vol 87 (10) ◽  
pp. 1265-1265 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Iceland poppy (Papaver nudicaule L.) is increasingly grown on the Italian Riviera for export as a cut flower. During the spring of 2003, leaves with irregular, brown, angular spots were collected from a commercial crop grown outdoors near Ventimiglia (northern Italy) with temperatures ranging from 3 to 14°C. Leaves of infected plants appeared curled and blistered; the infected portions of the leaves turned chlorotic. On both surfaces of infected leaves, a characteristic gray, furry growth was evident, particularly at the center of the necrotic areas. Infected leaves eventually died without dropping. Basal leaves with poor air circulation were the most severely affected by the disease. Microscopic observations revealed conidiophores branching dichotomically at least five times. Conidiophores ended with sterigmata bearing single conidia. Conidia measured 19 to 24 × 16 to 18 μm and were elliptical to near spherical and hyaline. Oospores were not present. The pathogen was identified as Peronospora arborescens based on the morphological characteristics (2). Pathogenicity was confirmed by inoculating 60-day-old healthy P. nudicaule plants with a conidial suspension (1 × 105 conidia per ml). Five plants were used as replicates. Inoculated and noninoculated plants were maintained in a growth chamber at 15°C and 90 to 95% relative humidity. After 7 to 10 days, typical symptoms of downy mildew developed oninoculated plants. Peronospora arborescens was observed on infected leaves. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of Peronospora arborescens on P. nudicaule in Italy. Peronospora arborescens was previously reported on P. nudicaule and on many other species of Papaver (P. somniferum, P. dubium, P. caucasicum, P. rhoeas, P. setigerum, and P. argemone) in everal countries (1,2). References: (1) P. J. Cotteril and I. G. Pascoe. Australas. Plant Pathol. 27:263, 1998. (2) S. M. Francis. No. 686 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, U.K., 1981.


Plant Disease ◽  
2014 ◽  
Vol 98 (5) ◽  
pp. 696-696 ◽  
Author(s):  
J. A. Crouch ◽  
M. P. Ko ◽  
J. M. McKemy

Downy mildew of impatiens (Impatiens walleriana Hook.f.) was first reported from the continental United States in 2004. In 2011 to 2012, severe and widespread outbreaks were documented across the United States mainland, resulting in considerable economic losses. On May 5, 2013, downy mildew disease symptoms were observed from I. walleriana ‘Super Elfin’ at a retail nursery in Mililani, on the Hawai'ian island of Oahu. Throughout May and June 2013, additional sightings of the disease were documented from the islands of Oahu, Kauai, Maui, and Hawai'i from nurseries, home gardens, and botanical park and landscape plantings. Symptoms of infected plants initially showed downward leaf curl, followed by a stippled chlorotic appearance on the adaxial leaf surfaces. Abaxial leaf surfaces were covered with a layer of white mycelia. Affected plants exhibited defoliation, flower drop, and stem rot as the disease progressed. Based on morphological and molecular data, the organism was identified as Plasmopara obducens (J. Schröt.) J. Schröt. Microscopic observation disclosed coenocytic mycelium and hyaline, thin-walled, tree-like (monopodial branches), straight, 94.0 to 300.0 × 3.2 to 10.8 μm sporangiophores. Ovoid, hyaline sporangia measuring 11.0 to 14.6 × 12.2 to 16.2 (average 13.2 × 14.7) μm were borne on sterigma tips of rigid branchlets (8.0 to 15.0 μm) at right angle to the main axis of the sporangiophores (1,3). Molecular identification of the pathogen was conducted by removing hyphae from the surface of three heavily infected leaves using sterile tweezers, then extracting DNA using the QIAGEN Plant DNA kit (QIAGEN, Gaithersburg, MD). The nuclear rDNA internal transcribed spacer was sequenced from each of the three samples bidirectionally from Illustra EXOStar (GE Healthcare, Piscataway, NJ) purified amplicon generated from primers ITS1-O and LR-0R (4). Resultant sequences (GenBank KF366378 to 80) shared 99 to 100% nucleotide identity with P. obducens accession DQ665666 (4). A voucher specimen (BPI892676) was deposited in the U.S. National Fungus Collections, Beltsville, MD. Pathogenicity tests were performed by spraying 6-week-old impatiens plants (I. walleriana var. Super Elfin) grown singly in 4-inch pots with a suspension of 1 × 104 P. obducens sporangia/ml until runoff using a handheld atomizer. Control plants were sprayed with distilled water. The plants were kept in high humidity by covering with black plastic bags for 48 h at 20°C, and then maintained in the greenhouse (night/day temperature of 20/24°C). The first symptoms (downward curling and chlorotic stippling of leaves) and sporulation of the pathogen on under-leaf surfaces of the inoculated plants appeared at 10 days and 21 days after inoculation, respectively. Control plants remained healthy. Morphological features and measurements matched those of the original inoculum, thus fulfilling Koch's postulates. To our knowledge, this is the first report of downy mildew on I. walleriana in Hawai'i (2). The disease appears to be widespread throughout the islands and is likely to cause considerable losses in Hawai'ian landscapes and production settings. References: (1) O. Constantinescu. Mycologia 83:473, 1991. (2) D. F. Farr and A. Y. Rossman. Systematic Mycology and Microbiology Laboratory, ARS, USDA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ July 16, 2013. (3) P. A. Saccardo. Syllogue Fungorum 7:242, 1888. (4) M. Thines. Fungal Genet Biol 44:199, 2007.


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