Phylogeny and taxonomy of Golovinomyces orontii revisited

2019 ◽  
Vol 18 (3) ◽  
pp. 335-357 ◽  
Author(s):  
U. Braun ◽  
H.D. Shin ◽  
S. Takamatsu ◽  
J. Meeboon ◽  
L. Kiss ◽  
...  
Plant Disease ◽  
2017 ◽  
Vol 101 (1) ◽  
pp. 251-251 ◽  
Author(s):  
D. L. Pei ◽  
X. Q. Zhu ◽  
Y. Y. Xu ◽  
C. W. Li

Data in Brief ◽  
2018 ◽  
Vol 17 ◽  
pp. 210-217
Author(s):  
Mulpuri Sujatha ◽  
Kandasamy Ulaganathan ◽  
Bhupatipalli Divya Bhanu ◽  
Prashant Kumar Soni

2008 ◽  
Vol 9 (1) ◽  
pp. 37 ◽  
Author(s):  
Dean A. Glawe ◽  
Steven T. Koike

Periwinkle is a trailing, spreading evergreen plant used in landscapes as a groundcover. Beginning in 2005, a powdery mildew was observed on periwinkle in coastal (Monterey Co.) California. As reported herein, the causal agent was determined to be Golovinomyces orontii (Castagne) V.P. Heluta. This appears to be the first record of a powdery mildew species on Vinca spp. in North America. Accepted for publication 16 October 2008. Published 12 December 2008.


Plant Disease ◽  
2012 ◽  
Vol 96 (2) ◽  
pp. 291-291 ◽  
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
A. Poli ◽  
M. L. Gullino

Creeping (June) bellflower (Campanula rapunculoides) is an herbaceous plant belonging to the Campunalaceae family. It has showy flowers, which is very much appreciated for gardens and landscaping. During the summer of 2011, 6- to 9-month-old plants grown in a garden near Biella (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. Seventy percent of plants were diseased. Conidia were hyaline, elliptical to ovoid (sometimes doliform), borne in short chains (up to three conidia per chain), and measured 27 to 42 (34) × 16 to 24 (19) μm. Conidiophores were erect with a cylindrical foot cell measuring 64 to 105 (80) × 11 to 12 (11) μm and followed by two shorter cells measuring 17 to 24 (20) × 11 to 15 (13) 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 ITS1F/ITS4 and sequenced (3) (GenBank Accession No. JN639855). The 405-bp amplicon had 98% homology with the sequence of Golovinomyces orontii GQ183948. Pathogenicity was confirmed through inoculation by gently pressing diseased leaves onto leaves of healthy C. rapunculoides plants. Three plants were inoculated while the same number of noninoculated plants served as a control. Plants were maintained outside at temperatures from 10 to 26°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. orontiii has been reported on C. rapunculoides in several eastern European countries as well as in Switzerland and Germany (1,2). To our knowledge, this is the first report of the disease in Italy. The economic importance of this disease is currently limited in Italy because of limited planting of this host. References: (1) A. Bolay. Cryptogam. Helv. 20:1, 2005. (2) U. Braun. The Powdery Mildews (Erysiphales) of Europe. Gustav Fischer Verlag, Stuttgart, Germany, 1995. (3) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. M. A. Innis et al., eds. Academic Press, San Diego, 1990.


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 ◽  
2018 ◽  
Vol 102 (10) ◽  
pp. 2041-2041
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
S. Matić ◽  
M. L. Gullino

Plant Disease ◽  
2021 ◽  
Author(s):  
Taijun Fang ◽  
Wenjun Shang ◽  
luchao bai ◽  
Nuyi Ya ◽  
Jiezhuoma Duo ◽  
...  

Hydrangea macrophylla (Thunb.) Ser. (Hydrangeaceae) is the most popular hydrangea species grown in home gardens and landscapes in China. Plants of H. macrophylla with symptoms of powdery mildew were found in a commercial wholesale nursery in Huzhu, Haidong (36°49'11.87" N, 101°57′03.36″E, alt. 2490 m), in May 2020, with disease incidence reaching 80%. Symptoms included yellowing and necrosis of leaves. Upon microscopic observation, masses of conidia and mycelium were observed covering the symptomatic tissues. Fungal isolates displayed nipple-shaped hyphal appressoria, often poorly developed, conidiophores erect, arising laterally or from the upper surface of hyphal mother cells, and positioned almost centrally or towards one end of the cells, up to about 160 μm long (n = 30), with foot cells straight or flexuous, 32 to 86 × 8 to 13 μm (n = 50), followed by one to three shorter cells about 11 to 24 × 10 to 15 μm (n = 50), forming catenescent conidia in usually predominantly chains, conidia doliiform to limoniform, hyaline, 24 to 35 × 13 to 25μm (n = 50). Conidial germination was of the Euoidium type. Chasmothecia were not observed. To confirm fungal classification, single spores were isolated and cultured on detached leaf bioassay following the protocol described in Farinas et al. (2019). Total DNA was extracted directly from single-spore cultures using a Chelex extraction method (Walsh et al. 1991). The rDNA internal transcribed spacer (ITS) regions were amplified by polymerase chain reaction (PCR) utilizing the universal primer pairs ITS1/ITS4 (White et al. 1990). The sequences (726-727 bp) were deposited in GenBank (accessions no. MT568633, MT757924 and MT757925). The ITS sequences showed 99.9-100% identity with a sequence of Golovinomyces orontii reported on Papaver rhoeas (AB769466) in Switzerland. Based on the ITS rDNA phylogenetic tree, the sequences retrieved from the specimen clustered within a strongly supported clade with G. orontii (AB769466), confirming the identity of the pathogen (Takamatsu 2013). Cladistic trees were constructed using the neighbor-joining method with the Kimura 2-parameter substitution model in MEGA 6.0. Branch robustness was assessed via bootstrap analysis with 1,000 replicates. To confirm pathogenicity, eight H. macrophylla plants were sprayed until run-off with a suspension containing 1 × 105 conidia/ml. Four plants were used for fulfilling Koch’s postulates and four plants were used as mock-inoculated controls sprayed only with sterile distilled water. Inoculated and non-inoculated plants were covered with plastic bags separately and maintained overnight in a greenhouse at 25 ± 2°C and 50 to 60% relative humidity. Typical powdery mildew colonies developed on inoculated plants 10 to 15 days after inoculation, which were morphologically identical to those originally observed on the diseased plats, whereas the control plants remained symptomless. To our knowledge, this is the first report of powdery mildew caused by G. orontii on H. macrophylla in Qinghai-Tibet Plateau, China (Braun and Cook 2012).


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