scholarly journals First report of Erysiphe corylacearum, agent of powdery mildew, on hazelnut (Corylus avellana) in Romania

Plant Disease ◽  
2021 ◽  
Author(s):  
Marco Rosati ◽  
Marian Bogoescu ◽  
Davide Spadaro

Romania has an area dedicated to hazelnut (Corylus avellana L.), covering 890 hectares as of 2019. During October 2020, powdery mildew symptoms were observed on the upper side of leaves of hazelnut ‘Tonda di Giffoni’ in two commercial orchards in Dudeștii Vechi, Romania (Fig. 1). The disease was present on 70% of the trees in planting, with at least 5 leaves per tree having powdery mildew. Micromorphological examination revealed amphigenous, hyaline, branched, septate mycelial patches of 2.3 to 3.6 μm in diameter. Conidiophores measured 24-60 × 5-6 (average: 45 × 6) μm and consisted of erect, cylindrical to flexuous foot cells, followed by 1-2 shorter cells. Ellipsoid, ovoid to doliform conidia were produced singly and they measured 19-35 × 16-24 (average: 28 × 19) μm. Chasmothecia were spherical, 75 to 107 (average: 88) μm in diameter. Nine to thirteen straight, sometimes flexuous, appendages measured 54 to 92 (average: 66) μm in length and they had five times dichotomous branched apices with curved tips (Fig. 2). Each chasmothecium contained three to five ellipsoid, ovoid to subglobose asci measuring 41-58 × 29-55 μm (average 52 × 43) μm. The asci contained four to eight ascospores measuring 13-24 × 11-15 (average 18 × 14) μm. Morphological identification was confirmed by sequencing the ITS-region of rDNA using two isolates from leaves, stored as frozen mycelium at -20°C. PCR was performed with Erysiphales-specific primer pair PMITS1/PMITS2 (Cunnington et al. 2003). The obtained sequences were deposited in GenBank (Accession n° MW423075, MW423076). Blast analysis of both sequences had 100% identity to ITS rDNA sequences of Erysiphe corylacearum from Azerbaijan (Abasova et al. 2018; Accession n° LC270863), Turkey (Sezer et al. 2017; KY082910), Switzerland (Beenken et al. 2020; MN82272), Iran (Arzanlou et al. 2018; MH047243), Italy (Mezzalama et al. 2020; MW045425) and 99% identity from Georgia (Meparishvili et al. 2019; MK157199). The sequences had a lower percent identity (83%) to Phyllactinia guttata (Accession n° AB080558) (Fig. 3). Pathogenicity was verified on one-year-old plants of C. avellana ‘Tonda di Giffoni’, which were artificially inoculated with a conidial suspension from infected leaves (n = 25). Inoculated plants were incubated at 20 to 28°C with 70 to 80% relative humidity. White mycelium appeared on the upper surface of the leaves at 8 to 10 days after inoculation. No symptoms were found on control plants sprayed with sterile water. The fungus present on inoculated leaves was morphologically identical to the original isolates from diseased trees from the field. E. corylacearum is native to East Asia and was previously reported in Japan on wild species of Corylus (Takamatsu et al. 2015; Accession n° LC009928). The pathogen most likely spread into Europe from east to west of Europe (Heluta et al. 2019), through the Caucasus, starting from Turkey, Azerbaijan, Georgia, and Iran. P. guttata was considered the only causal agent of powdery mildew on hazelnut in most countries, including Romania (Brown 1995). Compared to P. guttata, which generally develops a mycelium on the underside of leaves, E. corylacearum grows with a white mycelium on the upper side of the leaves. Recently, E. corylacearum on C. avellana was reported also in Ukraine (Heluta et al. 2019), from which it could have moved to Romania. Crop protection strategies for hazelnut should be revised according to the new pathogen occurrence.

Plant Disease ◽  
2020 ◽  
Author(s):  
Monica Mezzalama ◽  
Vladimiro Guarnaccia ◽  
Guido Martano ◽  
Davide Spadaro

Hazelnut (Corylus avellana) is widely grown in Italy, which is the second largest producer worldwide with 132,700 tonnes harvested from 78,593 hectares (FAOSTAT, 2018 ). Powdery mildew caused by Phyllactinia guttata has been reported in Italy and in other European countries, but recently in Austria, Switzerland and in central Europe a new species was discovered (Voglmayr et al., 2020; Beenken, 2020). During summer 2020, in Villar Fioccardo (Torino province, Piedmont, Italy) on hazelnut (cv. ‘Tonda Gentile’) growing on the edges of private gardens and parks, an extensive colonization of the adaxial side of the leaves with white powdery mycelium covering more than 80% of the surface was observed. Also, the abaxial side of the leaves showed the scattered presence of powdery, white, and thin mycelium. The powdery fungal pathogen collected from leaves had amphigenous, hyaline, branched, septate 1.5 to 3.7 μm wide mycelium; lobed, solitary hyphal appressoria; vertically elevated above the mycelium 53 to 82 μm long and 5 to 12 μm wide conidiophores (n = 30); hyaline, ellipsoid, ovoid to doliform conidia, solitary on conidiophores, 21 to 36 μm long, 15 to 21 μm wide (average 28 to 18 μm) (n = 50). Chasmothecia appeared in late September 2020 and they were spherical, single or in groups, 83 to 138 (average 100) μm in diameter (n = 50); 7 to 15 aseptate appendages were straight, sometimes flexuous, 55 to 111 (average 73) μm long (n = 50), with four to five times dichotomous branched apexes and recurved tips. In each chasmothecium, there were three to five ellipsoid, ovoid to subglobose asci with a length of 41 to 60 μm and a width of 28 to 56 μm (average 52 to 44 μm) (n = 30). Asci contained four to eight ascospores, 15 to 26 μm long and 10 to 17 μm wide (average 19 to 12 μm) (n =50). Mycelia were carefully scraped from the leaves with a scalpel and DNA was extracted by using the E.Z.N.A. Fungal DNA Mini Kit (Omega Bio-Tek, Darmstadt, Germany). Partial rDNA internal transcribed spacer region (ITS) of two isolates (DB20SET01, DB20SET01) was amplified using specific primers PMITS1/PMITS2 (Cunnington et al. 2003) and sequenced. Obtained sequences were deposited in GenBank (Accession Nos. MW045425, MW045426). BLAST analysis of the obtained 749-bp fragments showed 100% identity to ITS rDNA sequences of Erysiphe corylacearum from Switzerland (MN822721) and Azerbaijan (LC270863). One-year-old plants of C. avellane cv. Tonda Gentile were artificially inocuated by dusting conidia from infected leaves. Inoculated plants were incubated under controlled conditions at 23°C ± 1 and 70 to 80% relative humidity. Typical symptoms (white bloom) appeared on the upper surface of the leaves at 8 to 10 days after inoculation. No symptoms were found on control plants treated with sterile water. The fungus isolated from inoculated leaves was morphologically identical to the original isolates from diseased plants collected from Villar Fioccardo. Erysiphe corylacearum causes a new and aggressive form of powdery mildew. Since the first observation in north-eastern Turkey in 2013, it has spread rapidly throughout the Black Sea region, causing significant economic losses (Sezer et al., 2017). It has also been reported in Iran, Azerbaijan, and Ukraine (Arzanlou et al. 2018; Heluta et al., 2018). The disease has been observed sporadically in Piedmont, Italy, during summer 2020 (Regione Piemonte & Agrion, 2020) in some hazelnut growing areas, but presently, doesn’t appear to impact yield. This is the first report of E. corylacearum, causing an aggressive powdery mildew on hazelnut in Italy, and as such, may more severely affect hazelnut groves in Italy and cause considerable yield losses. Literature cited Arzanlou M et al. 2018. Forest Pathology, 48:e12450. https://doi.org/10.1111/efp.12450. Beenken L et al. 2020. New Disease Reports 41, 11. http://dx.doi.org/10.5197/j.2044-0588.2020.041.011. Cunnington JH et al. 2003. Australasian Plant Pathology, 32, 421-428. Food and Agriculture Organization (FAO). 2018. http://www.fao.org/faostat/en/#home Heluta V.P. et al.2019. Ukrainian Botanical Journal, 2019, 76(3), 252-259. Regione Piemonte SFR & Agrion. 2020. https://www.regione.piemonte.it/web/sites/default/files/media/documenti/2020-10/mal_bianco_nocciolo_da_erysiphe_corylacearum.pdf Sezer AD et al. 2017. Phytoparasitica, 45, 577-581. Voglmayr H et al. 2020. New Disease Reports, 42, 14 http://dx.doi.org/10.5197/j.2044-0588.2020.042.014


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 ◽  
2002 ◽  
Vol 86 (9) ◽  
pp. 1049-1049 ◽  
Author(s):  
B. de los Santos ◽  
C. Blanco ◽  
M. Porras ◽  
C. Barrau ◽  
F. Romero

In February 2001, in seven small tunnel production fields in southwestern Spain, symptoms and signs of powdery mildew were detected on strawberry (Fragaria × ananassa) cvs. Camarosa, Andana, and Carisma. On ‘Camarosa’ plants, white patches of mycelium developed on the lower leaf surface. Later, the leaf edges rolled upward, and reddish or necrotic irregular spots appeared on the lower leaf surface. Some immature fruits were abnormally hard and covered with a dense white mycelium. Symptoms were much less severe on ‘Andana’ and ‘Carisma’. Microscopic observations revealed conidia in chains, ellipsoidal to barrel-shaped, with fibrosin granules. Mean dimensions of conidia (N= 70) were 31.2 μm ± 2.8 × 20.39 μm ± 4.1. Cleistothecia were not detected. Based on these characteristics, the causal agent was identified as Sphaerotheca macularis (Wallr.:Fr.) Lind. (1). Pathogenicity was confirmed by inoculating leaves of 2-month-old potted ‘Camarosa’ plants. S. macularis obtained from field-grown plants was maintained on ‘Camarosa’ strawberry leaves in a growth chamber (20°C and 100% relative humidity). Inoculum was obtained from freshly sporulating infected leaves 11 days after inoculation. Conidia of S. macularis were gently brushed into 100-ml distilled water containing two drops of Tween 20. Ten strawberry ‘Camarosa’ plants were inoculated by misting with a conidial suspension (104 conidia per ml) (2). The plants were incubated at 100% relative humidity for 48 h in the greenhouse (15 to 25°C). Colonies of powdery mildew were observed on leaves after 18 days. To our knowledge, this is the first confirmation of S. macularis on strawberry in Spain. References: (1) K. G. Mukerji. No. 188 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, UK, 1968. (2) R. Reuveni et al. Crop Prot. 19:335, 2000.


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

Spiraea japonica is an old-fashioned shrub widely grown in Italy in parks and gardens. In the summer of 2003, severe outbreaks of a previously unknown powdery mildew were observed in some parks and gardens in the city of Torino (northern Italy). Infected leaves became covered on both sides with a white mycelium. As the disease progressed, infected leaves turned reddish and eventually dropped prematurely. The presence of powdery mildew infections on leaves sometimes caused their distortion and growth reduction. Frequently, mycelium was observed also on the stem. Conidia were hyaline, ellipsoid, cylindrical, or dol iform, born in chains, measured 21.0 to 38.4 × 10.8 to 14.4 mm, and showed fibrosin bodies. Cleistothecia were not observed. The pathogen was identified as Oidium subgenus Fibroidium (1,2). Pathogenicity was confirmed by spraying leaves of healthy potted S. japonica plants with a conidial suspension (105 conidia per ml) prepared in sterile water from diseased leaves. Three plants were inoculated and three noninoculated plants served as control. The artificial inoculation was carried out twice. After artificial inoculation, plants were maintained in a growth chamber at 25°C. After 20 days, powdery mildew symptoms developed. Microsphaera alni and Podosphaera oxyacanthae were described as causal agents of powdery mildew on S. japonica in the United States (3), while Sphaerotheca spiraeae was considered the causal agent of a powdery mildew observed in Japan (4) and more recently in Poland. References: (1) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (2) R. T. A. Cook et al. Mycol. Res. 101:975, 1997. (3) P. Pirone. Diseases and Pests of Ornamental Plants. John Wiley and Sons, NY, 1978. (4) K. Sawada. Rev. Appl. Mycol. 31:577, 1952.


2021 ◽  
Vol 44 (1) ◽  
Author(s):  
A. Mazzaglia ◽  
M.I. Drais ◽  
S. Turco ◽  
C. Silvestri ◽  
V. Cristofori ◽  
...  

Plant Disease ◽  
2014 ◽  
Vol 98 (2) ◽  
pp. 282-282
Author(s):  
K. Vrandečić ◽  
J. Ćosić ◽  
D. Jurković ◽  
I. Stanković ◽  
A. Vučurović ◽  
...  

Lavandula × intermedia Emeric ex Loiseleur, commonly known as lavandin, is an aromatic and medicinal perennial shrub widely and traditionally grown in Croatia. The lavandin essential oil is primarily used in perfumery and cosmetic industries, but also possesses anti-inflammatory, sedative, and antibacterial properties. In June 2012, severe foliar and stem symptoms were observed on approximately 40% of plants growing in a commercial lavandin crop in the locality of Banovo Brdo, Republic of Croatia. Initial symptoms on lower leaves included numerous, small, oval to irregular, grayish brown lesions with a slightly darker brown margin of necrotic tissue. Further development of the disease resulted in yellowing and necrosis of the infected leaves followed by premature defoliation. Similar necrotic oval-shaped lesions were observed on stems as well. The lesions contained numerous, dark, sub-globose pycnidia that were immersed in the necrotic tissue or partly erumpent. Small pieces of infected internal tissues were superficially disinfected with 50% commercial bleach (4% NaOCl) and placed on potato dextrose agar (PDA). A total of 10 isolates from leaves and five from stems of lavandin formed a slow-growing, dark, circular colonies with raised center that produced pycnidia at 23°C, under 12 h of fluorescent light per day. All 15 recovered isolates formed uniform hyaline, elongate, straight or slightly curved conidia with 3 to 4 septa, with average dimensions of 17.5 to 35 × 1.5 to 2.5 μm. Based on the morphological characteristics, the pathogen was identified as Septoria lavandulae Desm., the causal agent of lavender leaf spot (1,2). Pathogenicity of one selected isolate (428-12) was tested by spraying 10 lavandin seedlings (8 weeks old) with a conidial suspension (106 conidia/ml) harvested from a 4-week-old monoconidial culture on PDA. Five lavandin seedlings, sprayed with sterile distilled water, were used as negative control. After 5 to 7 days, leaf spot symptoms identical to those observed on the source plants developed on all inoculated seedlings and the pathogen was successfully re-isolated. No symptoms were observed on any of the control plants. Morphological identification was confirmed by amplification and sequencing of the internal transcribed spacer (ITS) region of rDNA (3). Total DNA was extracted directly from fungal mycelium with a DNeasy Plant Mini Kit (Qiagen, Hilden, Germany) and PCR amplification performed with primers ITS1F/ITS4. Sequence analysis of ITS region revealed at least 99% identity between the isolate 428-12 (GenBank Accession No. KF373078) and isolates of many Septoria species; however, no information was available for S. lavandulae. To our knowledge, this is the first report of Septoria leaf spot of lavandin caused by S. lavandulae in Croatia. Since the cultivation area of lavandin plants has been increasing in many continental parts of Croatia, especially in Slavonia and Baranja counties, the presence of a new and potentially harmful disease may represent a serious constraint for lavandin production and further monitoring is needed. References: (1) T. V. Andrianova and D. W. Minter. IMI Descriptions of Fungi and Bacteria, 142, Sheet 1416, 1999. (2) R. Bounaurio et al. Petria 6:183, 1996. (3) G. J. M. Verkley et al. Mycologia 96:558, 2004.


Plant Disease ◽  
2012 ◽  
Vol 96 (3) ◽  
pp. 457-457
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
P. Martini ◽  
L. Repetto ◽  
M. L. Gullino

Origanum vulgare L., common name oregano, also known as pot marjoram, Lamiaceae family, is grown for its aromatic and medicinal properties and as an ornamental. In particular, O. vulgare ‘Compactum’ is becoming popular as a potted plant. During January 2011, 3-month-old plants grown on a commercial farm located near Albenga (northern Italy) showed signs and symptoms of an unknown powdery mildew. Ninety percent of the plants were affected. 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, wilted, and eventually fell off. Mycelia were also observed on stems. Conidia were hyaline, elliptical, borne single or in short chains (three to four conidia per chain), and measured 37.9 × 19.6 (31.2 to 45.1 × 14.9 to 26.2) μm. Conidiophores were erect with a cylindrical foot cell measuring 81.1 × 9.7 (54.2 to 112.4 × 7.9 to 11.6) μm followed by two to three shorter cells measuring 26.8 × 11.8 (16.6 to 38.1 × 8.5 to 15.3) μm. Fibrosin bodies were absent. Chasmothecia were not observed in the collected samples. The internal transcribed spacer (ITS) region of rDNA was amplified with the primers ITS1F/ITS4 and sequenced (3) (GenBank Accession No. JN594608). The 560-bp amplicon had 99% homology with the sequence of Golovinomyces biocellatus (GenBank Accession No. AB307675). Pathogenicity was confirmed through inoculation by spraying a conidial suspension (6 × 104 CFU/ml) prepared from diseased leaves onto leaves of healthy O. vulgare ‘Compactum’ plants. Four plants were inoculated while the same number of noninoculated plants served as a control. Plants were maintained in a glasshouse at temperatures ranging from 23 to 28°C. Ten 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. G. biocellatus on O. vulgare has been reported in Switzerland (2) and Argentina (4) and it is present on other plant genera in Italy. In Italy, on the same host, attacks of Erysiphe galeopsis have been previously reported (1). The economic importance of this disease is currently limited due to limited planting of this species. However, in the last years, potted aromatic plants represent a steady increasing crop in Italy. Voucher specimens are available at the Agroinnova Collection, University of Torino. References: (1) K. Amano. Host Range and Geographical Distribution of the Powdery Mildew Fungi. Japan Science Society Press, Tokyo, 1986. (2) A. Bolay. Cryptog. Helv. 20:1, 2005. (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. (4) S. M. Wolcan. J. Plant Patho. 91:501, 2009.


Plant Disease ◽  
2014 ◽  
Vol 98 (10) ◽  
pp. 1443-1443
Author(s):  
J. H. Park ◽  
S. E. Cho ◽  
C. K. Lee ◽  
S. H. Lee ◽  
H. D. Shin

Dictamnus dasycarpus Turcz, known as densefruit pittany, is a perennial herbal plant belonging to the Rutaceae. In Oriental medicine, this plant is used for treatment of various ailments (4). Since the white and purple striped flowers and glossy leaves are of aesthetic value, the plant is popular in gardens throughout Korea. In July 2012, a leaf spot was observed on hundreds of D. dasycarpus with nearly 100% incidence in a garden in Gapyeong County, Korea. Lesions on leaves reaching up to 20 mm in diameter were circular to irregular, brown to dark brown, then becoming zonate with age, and finally fading to grayish brown in the center with a reddish brown margin. The disease caused premature defoliation and reduced plant vigor as well as aesthetic value. In June 2014, the same symptoms were found on D. dasycarpus in a nursery in Jinju City, Korea. Representative samples were deposited in the Korea University Herbarium (KUS). Pycnidia on lesions were epiphyllous, immersed or semi-immersed in host tissue, light brown to olive brown, and 90 to 210 μm in diameter. Ostioles were 15 to 30 μm wide and surrounded by a ring of darker cells. Conidia were hyaline, smooth, ellipsoidal to nearly reniform, straight to mildly curved, aseptate or rarely medianly 1-septate with age, 5.5 to 9.6 × 1.8 to 3.6 μm, and contained small oil drops. These characteristics were consistent with the previous descriptions of Phoma dictamnicola Boerema, Gruyter & Noordel. (1,2). A monoconidial isolate was cultured on potato dextrose agar plates and deposited in the Korea Agricultural Culture Collection (Accession No. KACC46948). Morphological identification of the fungus was confirmed by molecular data. Genomic DNA was extracted using a DNeasy Plant Mini Kit (Qiagen Inc., Valencia, CA). The internal transcribed spacer (ITS) region of rDNA was amplified using the ITS1/ITS4 primers and sequenced. The resulting sequence of 505 bp was deposited in GenBank (Accession No. KM047023). A BLAST search showed that the ITS sequence shared >99% similarity with that of P. dictamnicola (GU237877). For the pathogenicity tests, inoculum was prepared by harvesting conidia from 30-day-old cultures of KACC46948 and a conidial suspension (2 × 106 conidia/ml) was sprayed onto leaves of five healthy seedlings. Five seedlings were sprayed with sterile distilled water, serving as controls. The plants were covered with transparent plastic bags for 48 h in a 25°C glasshouse with a 12-h photoperiod. After 10 days, typical leaf spot symptoms started to develop on the leaves of the inoculated plants. The fungus, P. dictamnicola, was re-isolated from those lesions, confirming Koch's postulates. No symptoms were observed on control plants. Previously, Phoma leaf spot on Dictamnus spp. has been reported in the Netherlands and North America (3) and recently in China (1). To our knowledge, this is the first report of leaf spot on D. dasycarpus caused by P. dictamnicola in Korea. Our observations suggest that low humidity with good ventilation as well as removal of infected leaves and plant debris might be main strategies for preventing this disease. References: (1) Q. Bai et al. Plant Dis. 95:771, 2011. (2) G. H. Boerema et al. Phoma Identification Manual: Differentiation of Specific and Infra-Specific Taxa in Culture. CABI Publishing. Wallingford, UK, 2004. (3) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, USDA ARS, Retrieved June 19, 2014. (4) J. L. Yang et al. Planta Med. 77:271, 2011.


Plant Disease ◽  
2011 ◽  
Vol 95 (7) ◽  
pp. 873-873
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. T. Amatulli ◽  
M. L. Gullino

In January 2010, a fruit spot of “Clementine” (Citrus clementina Hort. ex Tan.) was observed on Italian-grown fruit in a market in northern Italy. The surface of the peel of infected fruits had black, irregular, necrotic areas that were slightly depressed, 10 mm in diameter, and surrounded by chlorotic halos. No pycnidia were observed on the necrotic spots. Tissues beneath the necrotic spots, which included the albedo (white pith), appeared dark and a black rot affected the external part of the juice vesicles. Small sections (approximately 3 mm2) of infected internal tissues were cultured on potato dextrose agar (PDA) amended with 25 ppm of streptomycin and maintained at 22 to 24°C. A slow-growing fungus with dark colored mycelium that produced pycnidia was consistently isolated. Conidia were hyaline, elongate, straight or slightly curved, unicellular, but sometimes with one septum, and measured 9.0 to 25.4 × 1.0 to 2.7 (average 17.7 × 1.8) μm. Preliminary morphological identification of the fungal isolates resembling Septoria spp. was confirmed by PCR using genomic DNA extracted from the mycelia of pure cultures. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS6 and sequenced. BLAST analysis of the 508-bp segment showed a 99% homology with the sequence of Septoria citri (GenBank Accession No. DQ897650). The nucleotide sequence has been assigned the GenBank Accession No. HQ176410. Pathogenicity of one isolate was tested by inoculating 10 fruits. These were wounded at the equatorial level (three wounds per fruit, 5 mm depth) and dipped for 10 s in a conidial suspension (1.2 × 107 conidia/ml). Ten wounded noninoculated fruits were dipped in sterilized water and served as control. Fruits were kept at 10 ± 1°C. After 50 days, dark, sunken necrosis appeared around the wounds of inoculated fruits and the same symptoms first observed were present into the tissues beneath the wounds. S. citri was consistently reisolated from the inoculated fruits. Noninoculated fruits remained healthy. The pathogenicity test was carried out twice. The same disease was observed on other fruits belonging to the Rutaceae family, such as lemon in Greece (3) and on orange and lemon in Australia (1). In Italy, S. citri has been reported on lemon (2) fruit. To our knowledge, this is the first report of the presence of this pathogen on clementine in Italy as well in the world. The presence of Septoria spot on clementine fruits is currently sporadic in Italy; however it is necessary to monitor the incidence of this disease with field and postharvest surveys. References: (1) T. G. B. Osborn and G. Samuel. Trans. R. Soc. Aust. 46:166, 1922. (2) P. Petri. Boll. Stn. Patol. Veg. Roma N.S. 16:1, 1936. (3) D. G. Zachos. FAO Plant Prot. Bull. 6:41, 1957.


Botany ◽  
2020 ◽  
Vol 98 (4) ◽  
pp. 185-195 ◽  
Author(s):  
R. Gregorio-Cipriano ◽  
D. González ◽  
R. Félix-Gastélum ◽  
S. Chacón

A novel species of powdery mildew, Neoerysiphe sechii sp. nov., has been proposed based on host, morphological characteristics, and gene sequences. The new species was found on chayote (Sechium edule) and a wild species, chayotillo (S. mexicanum), in Veracruz, Mexico. This novel species was identified as a member of Neoerysiphe, based on the morphological characteristics of the anamorph: catenescent conidia, lobed appressoria, and Striatoidium-type conidia. No teleomorph was observed. Neoerysiphe sechii is distinguished by foot cells that are frequently cylindrical with a slight widening at the base, a feature not observed previously in other species in the genus. An Erysiphales-specific primer was designed for the 5′ end of the ITS region of the nuclear rDNA. Independent and concatenated phylogenetic analyses with our rDNA sequences and sequences available in GenBank for Neoerysiphe spp. confirmed that the powdery mildew specimens found in Sechium spp. form an independent and strongly supported lineage. This is the first report of a Neoerysiphe species causing powdery mildew on members of Cucurbitaceae, and it is the second species reported from Mexico after N. cumminsiana. Neoerysiphe sechii is found on cultivated and endemic hosts in Mexico, suggesting that the fungus itself may be endemic.


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