scholarly journals First Report of Powdery Mildew Caused by Golovinomyces cichoracearum on English Daisy (Bellis perennis) in Italy

Plant Disease ◽  
2008 ◽  
Vol 92 (3) ◽  
pp. 484-484 ◽  
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Bellis perennis (English daisy) is a flowering plant belonging to the Asteraceae and is increasingly grown as a potted plant in Liguria (northern Italy). In February 2007, severe outbreaks of a previously unknown powdery mildew were observed on plants in commercial farms at Albenga (northern Italy). Both surfaces of leaves of affected plants were covered with white mycelia and conidia. As the disease progressed, infected leaves turned yellow. Mycelia and conidia also were observed on stems and flower calyxes. Conidia were hyaline, ellipsoid, borne in chains (as many as three conidia per chain), and measured 27.7 × 16.9 (15.0 to 45.0 × 10.0 to 30.0) μm. Conidiophores measured 114.0 × 12.0 (109.0 to 117.0 × 11.0 to 13.0) μm and showed a foot cell measuring 78.0 × 11.0 (72.0 to 80.0 × 11.0 to 12.0) μm followed by two shorter cells. Fibrosin bodies were absent. Chasmothecia were not observed in the collected samples. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 415 bp obtained showed an E-value of 7e–155 with Golovinomyces cichoracearum (3). The nucleotide sequence has been assigned the GenBank Accession No. AB077627.1 Pathogenicity was confirmed through inoculations by gently pressing diseased leaves onto leaves of healthy B. perennis plants. Twenty plants were inoculated. Fifteen noninoculated plants served as a control. Plants were maintained in a greenhouse at temperatures ranging from 10 to 30°C. Seven days after inoculation, typical symptoms of powdery mildew developed on inoculated plants. The fungus observed on inoculated plants was morphologically identical to that originally observed. 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 B. perennis in Italy. The disease was already reported in other European countries (2). Voucher specimens are available at the AGROINNOVA Collection, University of Torino. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) U. Braun The Powdery Mildews (Erysiphales) of Europe. Gustav Fischer Verlag, Jena, Germany, 1995. (3) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000.

Plant Disease ◽  
2008 ◽  
Vol 92 (6) ◽  
pp. 975-975 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
S. Frati ◽  
M. L. Gullino

Rudbeckia fulgida (orange coneflower), a flowering plant belonging to the Asteraceae, is increasingly used as a border in parks and gardens. In September 2007, severe outbreaks of a previously unknown powdery mildew were observed on plants in a public park in Torino (northern Italy). More than 90% of the plants were affected by the disease. Both surfaces of leaves of affected plants were covered with white mycelia and conidia. As the disease progressed, infected leaves turned yellow and wilted. Mycelia and conidia also were observed on stems and flower calyxes. Conidia were hyaline, ellipsoid, borne in chains (as many as three to four conidia per chain) and measured 34 × 23 (30 to 39 × 21 to 25) μm. Conidiophores measured 129 × 12 (89 to 181 × 11 to 13) μm and showed a foot cell measuring 88 × 12 (48 to 129 × 11 to 13) μm followed by two shorter cells. Fibrosin bodies were absent. Chasmothecia were not observed in the collected samples. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 619 bp showed a 100% homology with the sequence of Golovinomyces cichoracearum (3). The nucleotide sequence has been assigned GenBank Accession No. EU 233820. Pathogenicity was confirmed through inoculations by gently pressing diseased leaves onto leaves of healthy R. fulgida plants. Twenty plants were inoculated. Fifteen noninoculated plants served as the control. Plants were maintained in a greenhouse at temperatures ranging from 18 to 22°C. Eight days after inoculation, typical symptoms of powdery mildew developed on inoculated plants. The fungus observed on inoculated plants was morphologically identical to that originally observed. 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 R. fulgida in Italy. Powdery mildew on Rudbeckia spp. was previously reported in the United States (4), Poland, and more recently, India and Switzerland. Particularly, in Switzerland the disease has been observed on R. laciniata and R. nitida (2). The economic importance of this disease is currently limited. Voucher specimens are available at the AGROINNOVA Collection, University of Torino. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) A. Bolay. Cryptogam. Helv. 20:1, 2005. (3) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (4) D. F. Farr et al. Page 82 in: Fungi on Plants and Plants Products in the United States. The American Phytopathological Society, St Paul, MN, 1989.


Plant Disease ◽  
2008 ◽  
Vol 92 (7) ◽  
pp. 1135-1135
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
S. Frati ◽  
A. Minuto ◽  
M. L. Gullino

Paris daisy (Argyranthemum frutescens), also known as Marguerite daisy, is an economically important crop in the Riviera Ligure (northern Italy) where approximately 18 million potted plants per year are produced for export. During the fall and winter of 2007, Paris daisy ‘Bright Carmen’ plants, started in a greenhouse and growing outside in a commercial nursery at Albenga, showed a previously unknown powdery mildew. Young stems, particularly in the interior portions of the plant, were covered with a white mycelium. As the disease progressed, leaves became covered with the mycelium, resulting in smaller, chlorotic leaves. Conidia were hyaline, cylindrical, borne in chains (two to three conidia per chain) and measured 30 × 12 μm (20 to 34 × 10 to 15 μm). Conidia were generated by conidiophores represented by a foot cell measuring 55 to 101 × 11 to 12 μm followed by two shorter cells measuring 19 to 29 × 11 to 14 and 24 to 33 × 12 to 14 μm. Fibrosin bodies were absent. Chasmothecia were not observed in the collected samples. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 441 bp showed a 100% homology with the sequence of Golovinomyces cichoracearum (= Erysiphe cichoracearum) (3). The nucleotide sequence has been assigned GenBank Accession No. EU486992. Pathogenicity was confirmed through inoculation by gently pressing diseased leaves onto leaves of healthy Paris daisy plants of cvs. Blazer Rose, Bright Carmine, Cherry Harmony, Crowned Rose, Fulvia, Sole Mio, Stella 2000, Summit Pink, and Sun Light. Three plants per cultivar were inoculated, while the same number served as noninoculated controls. The pathogenicity test was carried out twice. Plants were maintained in a greenhouse at temperatures ranging from 15 to 21°C. Fifteen days after inoculation, typical symptoms of powdery mildew developed on inoculated plants of all cultivars, with the exception of Stella 2000. The fungus observed on inoculated plants was morphologically identical to that originally observed. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of powdery mildew on A. frutescens in Italy. G. cichoracearum has been reported on Chrysanthemum frutescens in Switzerland (2). The economic impact of this disease is limited but can easily increase because of the intensive cultivation of this crop. The availability of resistant or partially resistant cultivars will help reduce the impact of this new disease. Voucher specimens are available at the AGROINNOVA Collection, University of Torino. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) A. Bolay, Cryptogam. Helv. 20:1, 2005. (3) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000.


Plant Disease ◽  
2008 ◽  
Vol 92 (1) ◽  
pp. 174-174 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
M. L. Gullino

Calendula officinalis L. (Asteraceae) (pot marigold or English marigold) is an ornamental species grown in gardens and as potted plants for the production of cut flower. It was also used in ancient Greek, Roman, Arabic, and Indian cultures as a medicinal herb as well as a dye for fabrics, foods, and cosmetics. During the summer of 2007, severe outbreaks of a previously unknown powdery mildew were observed on plants in several gardens near Biella (northern Italy). Both surfaces of leaves of infected plants were covered with dense, white mycelia and conidia. As the disease progressed, infected leaves turned yellow and died. Mycelia and conidia also were observed on stems and flower calyxes. Conidia were hyaline, ellipsoid, born in short chains (four to six conidia per chain), and measured 27.0 to 32.1 (31.4) × 12.9 to 18.4 (18.2) μm. Conidiophores measured 49 to 77.3 (67.2) × 8 to 13.3 (10.8) μm and showed a foot cell measuring 44 to 59 (51.9) × 9.3 to 12.6 (11.3) μm followed by one shorter cell measuring 15.6 to 18.9 (17.6) × 10.4 to 13.6 (12.2) μm. Fibrosin bodies were present. Chasmothecia were spherical, amber colored, with a diameter of 89 to 100 (94.5) μm. Each chasmothecium contained one ascus with eight ascospores. On the basis of its morphology, the causal agent was determined to be a Podosphaera sp. (2). The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 588 bp showed a 100% homology with the sequence of Podosphaera xanthii (2). The nucleotide sequence has been assigned GenBank Accession No. EU100973. Pathogenicity was confirmed through inoculations by gently pressing diseased leaves onto leaves of healthy C. officinalis plants. Five plants were inoculated. Five noninoculated plants served as control. Plants were maintained in a greenhouse at temperatures ranging from 20 to 26°C. Eleven 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 C. officinalis in Italy. C. officinalis was previously described as a host to Sphaerotheca fuliginea (synonym S. fusca) in Great Britain (4) as well as in Romania (3). Voucher specimens are available at the AGROINNOVA Collection, University of Torino. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (3) E. Eliade. Rev. Appl. Mycol. 39:710, 1960. (4) F. J. Moore. Rev. Appl. Mycol. 32:380, 1953.


Plant Disease ◽  
2007 ◽  
Vol 91 (9) ◽  
pp. 1203-1203 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Coreopsis lanceolata L. (Asteraceae) is an ornamental species grown in parks and gardens and very much appreciated for its long-lasting flowering period. During the summer and fall of 2006, severe outbreaks of a previously unknown powdery mildew were observed on plants in several gardens near Biella (northern Italy). Both surfaces of leaves of the affected plants were covered with dense white mycelia and conidia. As the disease progressed, infected leaves turned yellow and died. Mycelia and conidia also were observed on stems and flower calyxes. Conidia were hyaline, ellipsoid, borne in short chains (5 to 6 conidia per chain) and measured 33 × 20 (27 to 35 × 17 to 22) μm. Conidiophores, 68 × 11 (62 to 76 × 10 to 12) μm, showed the foot cell measuring 50 × 11 (38 to 58 × 10 to 12) μm, followed by one shorter cell measuring 18 × 12 (13 to 19 × 12 to 13) μm. Fibrosin bodies were present. Chasmothecia were spherical and amber with a diameter of 99 (93 to 105) μm. Each chasmothecium contained one ascus with eight ascospores. On the basis of its morphology, the causal agent was determined to be a Podosphaera sp. (1). The ITS region (internal transcribed spacer) of rDNA was amplified using primers ITS4/ITS6 and sequenced. BLASTn analysis (1) of the 531 bp obtained showed an E-value of 0.0 with Podosphaera fusca (3). The nucleotide sequence has been assigned GenBank Accession No. EF 442023. Pathogenicity was confirmed through inoculations by gently pressing diseased leaves onto leaves of healthy C. lanceolata plants. Three plants were inoculated. Three noninoculated plants served as the control. Plants were maintained in a greenhouse at temperatures ranging from 20 to 28°C. Twelve 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 C. lanceolata in Italy. Species of Coreopsis were previously described as host to Erysiphe cichoracearum, Sphaerotheca macularis and Leveillula taurica and S. fusca (2,4). Voucher specimens are available at the AGROINNOVA Collection, University of Torino. 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, GDR, 1987. (3) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000 (4) 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 ◽  
2010 ◽  
Vol 94 (1) ◽  
pp. 130-130 ◽  
Author(s):  
M. Troisi ◽  
D. Bertetti ◽  
A. Garibaldi ◽  
M. L. Gullino

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


Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 632-632
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Petunia × hybrida (Solanaceae) includes several hybrids that are grown as ornamental plants and are very much appreciated for their long-lasting flowering period. Among those, the variety pendula is often selected because of its hanging growth habit that is favorable for balcony decoration. During the summer of 2005, severe outbreaks of a previously unknown powdery mildew were observed on all petunia plants in several gardens near Biella and Torino (northern Italy). Both surfaces of the leaves of affected plants were covered with white, dense mycelia and conidia. As the disease progressed, infected leaves turned yellow and died. Mycelia also were observed on stems and flowers. Conidia were hyaline, ellipsoid, borne in short chains (with a maximum of four conidia per chain), and measured 27 to 36 × 17 to 21 μm (average 31 × 19 μm). Conidiophores, 130 to 154 μm (average 140 μm) long, showed the foot cell (measuring 42 to 65 × 10 to 12 μm, average 52 × 11 μm) followed by three shorter cells measuring 27 to 30 × 13 to 17 μm (average 29 to 14 μm). Fibrosin bodies were absent. Chasmothecia were not observed in the collected samples. The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS4/ITS6 (3) and sequenced. BLASTn analysis (1) of the 588 bp obtained showed an E-value of 0.0 with Golovinomyces orontii (Erysiphe orontii) (2). The nucleotide sequence has been assigned GenBank Accession No. DQ 987491. Inoculations were made by gently pressing diseased leaves onto leaves of five healthy Petunia × hybrida var. pendula plants, belonging to cv. Surfinia. Five noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a greenhouse at temperatures between 14 and 30°C. After 10 days, typical powdery mildew symptoms 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 P. × hybrida caused by G. orontii in Italy. A powdery mildew of P. × hybrida reported in 1966 in Romania has been attributed to E. cichoracearum (4), while Braun (2) reported P. × hybrida as a possible host of E. orontii. 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, GDR, 1987. (3) D. E. L. Cooke and J. M. Duncan. Mycol. Res. 101:667, 1997. (4) E. Eliade. Reprium nov. Spec. Regni veg.73:43, 1966.


Plant Disease ◽  
2021 ◽  
Author(s):  
Yuan Yuan Xu ◽  
Jia Tong Zhang ◽  
Man Xu ◽  
Dong Mei Liu ◽  
Jinping Ding ◽  
...  

Scarlet Beebalm (Monarda didyma) is a perennial ornamental flowering plant in the mint family, Labiatae. Due to low-maintenance, and a long blooming period, it is commonly cultivated in gardens as an ornamental plant in China. In May 2021, a disease was observed on the leaves of a capitals beebalm plant in a Ten Mile Flower Sea in Xiayi county (116°13′8″E, 34°14′45″N), Henan province of China. Symptoms first appeared as nearly circular, small, white, powdery mildew-like spots on the leaves which gradually expand, covering the entire leaves. The lesions spread from the lower leaves to the upper canopy, and the stems were also covered by white mycelia. In severe cases, early defoliation occured. About 30% plants were affected. Representative voucher specimens (SQNUMd04, SQNUDn4) were deposited in the herbarium of Shangqiu Normal University (SQNU), Shangqiu, China. Conidiophores (n = 30) were cylindrical, 92.0 to 142.2 µm long and 10.8 to 14.2 µm wide, and produced 5 to 7 immature conidia in a chain. Foot-cells of conidiophores were mostly curved at the base. Conidia (n = 30) were hyaline, ellipsoid, 23.3 to 29.8 μm (avg. 26.6 μm) long, and 11.2 to 16.9 μm (avg. 14.5μm) width, a length/width ratio of 1.5 to 2.1, and germ tubes were produced at the perihilar position. No chasmothecia were observed. Based on morphological comparison using the description by Scholler et al. (2016) description the fungus was tentatively identified as Golovinomyces monardae (G.S. Nagy) M. Scholler, U. Braun & Anke Schmidt. For molecular identification, DNA was extracted from mycelia and conidia, which were collected by scraping symptomatic leaves.The ITS regions and LSU were amplified using primers ITS1/ITS4 (White et al. 1990) and NL1/NL4 (Horisawa et al. 2013). BLASTn analysis of the (MZ303741) and LSU (MZ305434) sequences showed 100% identity with those of G. monardae (AB307667, LC076800, LC076802, LC076808, and AB077691) reported on Monarda species (Matsuda et al. 2003; Takamatsu et al. 2013; Scholler et al. 2016). Pathogenicity tests were carried out by gently dusting conidia from infected leaves onto healthy leaves of five M. didyma plants and five non-inoculated plants used as controls. After 9 days, typical powdery mildew colonies started to appear on the inoculated leaves while control plants remained disease free. All plants were placed in a greenhouse without temperature and humidity control. Based on morphology, fungus was identified as the same as that used for inoculum, fulfilling Koch's postulates. Although G. monardae has been reported on various genera in the Labiatae and Verbenaceae (Farr and Rossman 2021), to our knowledge, this is the first report of G. monardae causing powdery mildew of Scarlet Beebalm(M. didyma) in China.


Plant Disease ◽  
2011 ◽  
Vol 95 (2) ◽  
pp. 225-225 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. T. Amatulli ◽  
M. L. Gullino

Moth mullein (Verbascum blattaria) is an herbaceous plant belonging to the Scrophulariaceae family. It has alternate, simple leaves on stiffly, erect, green stems. Flowers are yellow or white, borne in summer through fall, and is increasingly used in gardens in low-maintenance borders. During the fall of 2009, 4-month-old plants grown in a greenhouse near Torino (northern Italy) showed signs and symptoms of an unknown powdery mildew. The adaxial leaf surfaces were covered with white mycelia and conidia, while the abaxial surfaces were less infected. As the disease progressed, infected leaves turned yellow and wilted. Mycelia were also observed on stems, petioles, and flower calyxes of inflorescences. Powdery mildew was observed on moth mullein naturally diffused in Italian flora and on V. blattaria var albiflorum cv. White Blush. The same symptoms and signs were observed in summer 2010 on V. blattaria plants grown in a garden near Biella. Conidia were hyaline, elliptical, borne in short chains (as many as five conidia per chain), and measured 35 × 22 (29 to 42 × 19 to 24) μm. Conidiophores were erect with a cylindrical foot cell measuring 147 × 11 (93 to 177 × 10 to 12) μm, followed by one to two shorter cells measuring 23 × 11 (15 to 33 × 10 to 12) μm. Fibrosin bodies were absent. Chasmothecia were not observed in the collected samples. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced (1) (GenBank Accession No. HQ316555). The 542-bp amplicon had 99% homology with the sequence of Golovinomyces cichoracearum (GenBank Accession No. EU819552. Pathogenicity was confirmed through inoculation by gently pressing diseased leaves onto leaves of healthy V. blattaria plants. Five plants were inoculated, while the same number of noninoculated plants served as a control. Plants were maintained at temperatures from 19 to 25°C. Fifteen days after inoculation, symptoms and signs of powdery mildew developed on inoculated plants. The conidial morphology of the powdery mildew fungus that developed on inoculated plants was identical to the conidial morphology observed in the original fungus. Noninoculated plants remained healthy. The pathogenicity test was carried out twice. G. cichoracearum, formerly Erysiphe verbasci (synonym E. cichoracearum), has been reported on V. blattaria in Hungary, Romania, and the former USSR (2,3). In conclusion, to our knowledge, it is the first report of G. cichoracearum affecting moth mullein in northern Italy. The economic importance of this disease is at present limited in Italy because of limited planting of this host. However, the ecological characteristics and flowering of V. blattaria make it interesting for low-maintenance gardens. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) K. Amano. Host Range and Geographical Distribution of the Powdery Mildew Fungi. Japan Scientific Societies Press. Tokyo, 1986. (3) U. Braun. The Powdery Mildews (Erysiphales) of Europe. Gustav Fischer Verlag, Stuttgart, Germany, 1995.


Plant Disease ◽  
2006 ◽  
Vol 90 (6) ◽  
pp. 831-831
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
D. Minerdi ◽  
M. L. Gullino

Veronica spicata (spike speedwell) is a perennial garden species belonging to the family Scrophulariaceae. During the summer through fall of 2004 and 2005, severe outbreaks of a previously unknown powdery mildew were 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. Very rarely was the mycelium observed on the lower surface of leaves or on petioles and flowers. Foot cell was cylindric and measured 19.2 to 25.7 × 10.8 to 14.3 μm (average 21.9 × 12.0 μm). Conidia were hyaline, ellipsoid, brought in short chains (three conidia per chain), and measured 22.2 to 40.8 × 13.6 to 21.6 μm (average 30.1 × 17.0 μm). Conidiophores measured 45.5 to 74.0 × 10.4 to 11.0 μm (average 59.4 × 10.6 μm). Fibrosin bodies were absent. Cleistothecia were never observed on the samples collected. The ITS region (internal transcribed spacer) of rDNA was amplified using the primers ITS4/ITS6 (3) and sequenced. BLASTn analysis (1) of the 504 bp obtained showed an E-value of 0.0 with Erysiphe (Golovinomyces) orontii (2). The nucleotide sequence has been assigned GenBank Accession No. DQ386696. Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of five healthy Veronica spicata plants. Five noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a greenhouse where temperatures ranged between 15 and 28°C. After 15 days, typical powdery mildew symptoms 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 V. spicata in Italy. Sphaerotheca fuliginea has been reported as the causal agent of powdery mildew on V. spicata (4). Specimens of this disease are available at DIVAPRA Collection, University of Torino. References: (1) S. F. Altschul et al. Nucleic Acids Res. 25:3389, 1997. (2) U. Braun. Nova Hedwigia 89:166, 1987. (3) D. E. L. Cooke and J. M. Duncan. Mycol. Res. 101:667, 1997. (4) B. Ing. Mycologist 4:125, 1990.


Plant Disease ◽  
2007 ◽  
Vol 91 (11) ◽  
pp. 1515-1515 ◽  
Author(s):  
A. Garibaldi ◽  
G. Gilardi ◽  
D. Bertetti ◽  
M. L. Gullino

In the winter of 2007 in Piedmont (northern Italy), symptoms of a previously unknown disease were observed on beet (Beta vulgaris L. subsp. vulgaris) (garden beet group) grown under a tunnel on several commercial farms near Cuneo. First symptoms appeared on 1-month-old plants, occurring as brown, round-to-oval spots as much as 2 cm in diameter with dark concentric rings near the perimeter. Small, dark pycnidia were present throughout the spots in concentric rings. Generally, older, lower leaves were affected more than the younger ones. Ten to fifteen percent of the plants were affected. Symptoms on the roots began near the crown as small, dark, sunken spots that became soft and water soaked. Eventually, spots on the roots turned dark brown to black and black lines separated diseased and healthy tissues. Older infected tissues were black, dry, shrunken, and spongy. Pycnidia were not observed on affected roots. From infected leaves and roots, a fungus was consistently isolated on potato dextrose agar (PDA) amended with 25 mg/l of streptomycin. The fungus was grown on PDA and maintained at 22°C (12 h of light, 12 h of dark). After 10 days, black pycnidia (130 to 328 [204] μm in diameter) developed, releasing abundant hyaline, elliptical, nonseptate conidia measuring 3.9 to 6.7 (5.1) × 2.4 to 5.9 (3.6) μm. On the basis of its morphological characteristics, the fungus was identified as a Phoma sp. (1). The internal transcribed spacer (ITS) region was amplified using primers ITS4/ITS6 (2) and sequenced. BLASTn analysis of the 557 bp obtained showed an E-value of 0.0 with Phoma betae. The nucleotide sequence has been assigned GenBank Accession No. EU003450. Pathogenicity tests were performed by spraying leaves of healthy 20-day-old potted B. vulgaris plants with a spore and mycelial suspension (1 × 106 spores or mycelial fragments per ml). Noninoculated plants sprayed only with water served as controls. Fifteen plants (three per pot) were used for each treatment. Plants were covered with plastic bags for 5 days after inoculation and kept in a growth chamber at 20°C. Symptoms previously described developed on leaves of all inoculated plants 5 days after inoculation, while control plants remained healthy. Later, pycnidia and conidia, with the same dimensions and characteristics previously described, were observed on the infected leaves. The fungus was consistently reisolated from the lesions of the inoculated plants. The pathogenicity test was carried out twice. P. betae on B. vulgaris var. cycla has been reported in Canada (3) as well as in other countries. The same pathogen was reported in Italy on sugar beet (2). References: (1) G. H. Boerema and G. J. Bollen. Persoonia 8:111, 1975. (2) A. Canova. Inf. Fitopatol. 16:207, 1966. (3) D. E L. Cooke and J. M. Duncan. Mycol. Res. 101:667, 1997. (4) J. R. Howard et al. Diseases of Vegetable Crops in Canada. Canadian Phytopathological Society, 1994.


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