scholarly journals First report of Neurospora on Corylus avellana in natural forest of Iran

2015 ◽  
Vol 6 (4) ◽  
pp. 31-36
Author(s):  
Rahnama Kamran ◽  
Habibi Roghaieh
Author(s):  
Vincenzo Tagliavento ◽  
Federico de Santis ◽  
Serena Ciarroni ◽  
Giorgio Mariano Balestra ◽  
Valerio Cristofori ◽  
...  

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

2020 ◽  
Vol 42 ◽  
pp. 14
Author(s):  
H. Voglmayr ◽  
T. Zankl ◽  
I. Krisai-Greilhuber ◽  
T. Kirisits

Plant Disease ◽  
2018 ◽  
Vol 102 (12) ◽  
pp. 2636-2636 ◽  
Author(s):  
N. Mehle ◽  
M. Ravnikar ◽  
M. Dermastia ◽  
A. Solar ◽  
B. Matko ◽  
...  

Plant Disease ◽  
2021 ◽  
Author(s):  
Muhammad Waqas ◽  
Vladimiro Guarnaccia ◽  
Davide Spadaro

Hazelnut (Corylus avellana L.), which is native to Europe and Western Asia, is a widely distributed and economically important crop in Italy, cultivated on 82,104 ha and its production is 110,618 t (ISTAT 2021). A total of one hundred and eleven black rotted nuts (incidence: 41%) with sunken lesions from Lu and Cuccaro (45°00'21.8"N/8°28'59.6"E), north-western Italy, were collected during the ripening stage of hazelnuts during October-December 2020. Symptomatic half cut kernels were sterilized in 1% NaClO for 1 min, washed in sterile water twice, and dried on sterile filter paper. The fragments were placed onto potato dextrose agar (PDA) containing streptomycin. After 48 to 72 h of incubation at 25°C, fast-growing white colonies with abundant aerial mycelia were observed. On the opposite side of the plates, colonies were initially white, then turned to dark-grayish olive after one week of incubation. Dark colonies produced globose, hyaline, ellipsoidal, unicellular conidia ranging from 12.23-15 μm x 5-6.71 μm. Morphologically, the causal agent was identified as Neofusicoccum parvum (Pennycook & Samuels) Crous, Slippers & A.J.L. Phillips (Crous et al. 2006; Zhang et al. 2021). The DNA from the isolates HMa-19-2 and Hwb-4b-2 was extracted with the E.Z.N.A. Fungal DNA mini kit (Omega Bio-tek) according to manufacturer instructions. Molecular identification was confirmed by sequencing of rDNA internal transcribed spacer (ITS) using primers ITS1/ITS4 (White et al. 1990) and translation elongation factor 1-alpha (tef-1α) gene by using the primers EF1-728F/EF1-986R (Carbone & Kohn, 1999). The sequences of both isolates were deposited in GenBank for ITS (accession numbers MZ848132 and MZ848133) and for tef-1α gene (accession numbers MZ913266 and MZ913267). The BLAST analysis showed 99% identity with ex-type strain of N. parvum (CMW9081) for ITS and tef-1α. Maximum likelihood method based on combined sequences of ITS and tef-1α genes was performed and the isolates of N. parvum clustered with ex-type strain of N. parvum (CMW9081; eXtra file). Pathogenicity of both isolates were tested on ripening hazelnuts (BBCH: 85) to evaluate Koch’s postulates. Three nuts per isolate, and per three replicates, were surface disinfected with 1% NaClO. A piece of shell (5 mm diameter) from nuts was removed with a sterile cork borer, then nuts were inoculated with PDA mycelium plugs of the same diameter cut from 7 days old PDA colony (Seddaiu et al. 2021). The control nuts were treated with sterilized PDA plugs. All inoculated nuts produced black lesions with softening pulp (eXtra file). Additionally, abundant white-gray mycelium developed on the inoculation sites. Control nuts showed no symptoms. Neofusicoccum parvuwas recently reported in Italy on chestnut (Seddaiu et al. 2021) and blueberry (Guarnaccia et al. 2021). The fungal pathogen was also reported as agent of grey necrosis of hazelnut in Chile (Duran et al. 2020). However, this is the first report of N. parvum on hazelnut nut in Italy. The findings suggest that N. parvum could severely affect hazelnut production in Italy. Accurate identification of the pathogen will support the growers to manage the disease.


2017 ◽  
Vol 47 (5) ◽  
pp. e12355 ◽  
Author(s):  
S. R. Mohali ◽  
F. Castro-Medina ◽  
J. R. Úrbez-Torres ◽  
W. D. Gubler

Plant Disease ◽  
2013 ◽  
Vol 97 (12) ◽  
pp. 1657-1657 ◽  
Author(s):  
J. Guerrero ◽  
S. Pérez

European hazelnut (Corylus avellana L.) is an emerging crop for export, mainly in southern Chile. Stem cankers and dieback of twigs on six-year-old European hazelnut cultivar Barcelona were observed during the 2012 growing season on plantations in Panguipulli (39° 38′ 37.12″ S and 72° 20′ 10.87″ W), Region de Los Rios, Chile. The incidence has been variable according to the place of plantation; it was estimated at approximately 15%. Cankers were characterized by brownish-gray and brown to reddish discoloration of the vascular stem system. Hazelnut plants between 1 and 3 years old developed stem basal canker, especially at conditions of high humidity and overpopulation of weeds; at critical conditions, the affected plants generally die. Small pieces of cankered stems, selected from 10 European hazelnuts, were surface sterilized in 0.5% sodium hypochlorite for 2 min and rinsed twice in sterile distilled water prior to incubation in a humid chamber for 7 days (25 ± 2°C) to stimulate production of reproductive bodies. Black sub-epidermal perithecia with unitunicate, cylindrical-clavate, 8-spored asci (n = 20) were obtained. Ascospores were septated, hyaline, multigutulate, and slightly constricted at the septum, the average measurements were (n = 20) 13.4 ± 0.6 μm × 3.9 ± 0.2 μm. The ascospores were transferred to potato dextrose agar (PDA) and incubated for 6 days at 25°C in the dark, then hyphal tips were transferred to fresh PDA and obtained a mycelia with white, cottony, and sparse colonies. Pycnidia and smooth, unicellular, hyaline, and biguttulate alpha conidia of 6.1 to 7.2 μm × 2.8 to 3.1 μm (n = 40) were observed. Beta conidia were not observed in culture media. Mature pycnidia were also detected on hazelnut shells remaining on the soil from the previous season. The identification of the species (isolate IMI-501237) was confirmed at CABI, United Kingdom, using an internal transcribed spacer (ITS), rDNA, BLASTn analysis of the 524-bp fragment, and showed 100% identity with Diaporthe australafricana Crous & J.M. van Niekerk (accessions KC343039, KC343038). These molecular and morphological characteristics were similar that reported from Vitis vinifera (2) and Chilean blueberry (3). The sequence obtained was deposited in GenBank (Accession No. JX316218.1). A pathogenicity test was conducted with isolate IMI-501237 on four 1-year-old plants from the hazelnut cultivar Barcelona. Plants were maintained in individual bags in greenhouse conditions (14/10 h dark/light, 20°C; 70% relative humidity). Prior to inoculation, plant tissues were surface disinfected with 2% sodium hypochlorite and rinsed with sterile distilled water. Each plant was inoculated at fresh wound sites on three stems and three vegetative buds on twigs. The inoculum consisted of an agar plug with mycelia (5 mm) from the edge of an actively growing colony cultured on PDA for 6 days. Each inoculation was covered with moistened cotton and sealed with Parafilm; a control plant was inoculated in the same way with agar only. After 30 days, necrotic lesions and discolored vascular tissue were only observed on inoculated stems and twigs. Symptomatic tissues were removed and incubated on PDA. D. australafricana was consistently recovered from these tissues, satisfying Koch's postulates. The control plant showed no symptoms of the disease. D. australafricana were previously reported on Vitis vinifera in Australia and South Africa (2,4), and Vaccinium corymbosum in Chile (1,3). To our knowledge, this is the first report of Diaporthe australafricana on Corylus avellana cultivar Barcelona in worldwide. References: (1) K. Elfar et al. Plant Dis. 97:1042, 2013. (2) R. Gomes et al. Persoonia 31:1, 2013. (3) B. Latorre et al. Plant Dis. 96:5, 2012. (4) J. M. van Niekerk et al. Australas. Plant Pathol. 34:27, 2005.


Plant Disease ◽  
2010 ◽  
Vol 94 (10) ◽  
pp. 1265-1265 ◽  
Author(s):  
T. J. Molnar ◽  
J. Capik ◽  
S. Zhao ◽  
N. Zhang

Eastern filbert blight (EFB) is a serious disease of European hazelnut, Corylus avellana L., which causes economic losses in Oregon (OR) where 99% of the U.S. crop is produced. The causal organism, Anisogramma anomala (Peck) E. Müller, is native east of the Rocky Mountains where it is found in association with C. americana Marshall. While C. americana is tolerant, EFB causes cankering, branch dieback, and death of C. avellana (3). EFB was first discovered in Washington State in the late 1960s (1). Since then, it has spread throughout the Willamette Valley of OR. In OR, ‘Gasaway’, an obsolete pollinizer, shows complete resistance to EFB, conferred by a dominant allele at a single locus (4). ‘Gasaway’ has been widely used in breeding at Oregon State University (OSU) to develop resistant cultivars that are used in most new orchards. In January 2008, cankers containing rows of dark brown elliptical stroma, characteristic of EFB, were first observed on more than 25 trees of ‘Gasaway’ growing at the Rutgers University research farms in Adelphia and North Brunswick, NJ. At that time, cankers were also found on 18 trees of ‘VR20-11’ growing on the research farms. ‘VR20-11,’ an offspring of ‘Gasaway’ that carries the same resistance gene, was released by OSU for use as a pollinizer for ‘Barcelona’, an EFB-susceptible but widely grown cultivar in OR. Additional cankers were observed on the New Jersey trees in January 2009 and 2010. To our knowledge, this is the first report of EFB on either cultivar under field conditions. The cankers are smaller than those on susceptible cultivars. Of 61 cankers on 10 trees of ‘Gasaway’, the average length was 11 cm with a range of 4 to 42 cm. Canker lengths on susceptible trees are typically 20 to 100 cm. The cankers appear otherwise alike with stromata, 2 to 4 × 2 mm, up to 2 mm high; perithecia upright, in the lower part of stroma; asci ellipsoid, 35 to 45 × 9 to 12 μm; and ascospores 8 to 11 × 4 to 5.5 μm, hyaline, smooth, ellipsoid, 2-celled, with the lower cell very short (1 to 1.5 μm long and wide). Genomic DNA was isolated from ascospores excised from cankers of ‘Gasaway’ and ‘VR20-11’. ITS1F and ITS2 primers were used to amplify and sequence the internal transcribed spacer 1 region (ITS1) of the rRNA genes (GenBank Accession Nos. HM565133 and HM565132). BLAST analysis of the 238-bp segments showed 99% homology with a sequence of A. anomala (EU683064). Phylogenetic analysis also confirmed that the two isolates are A. anomala. To test viability, ‘Gasaway’ cankers were excised and ascospore suspensions (1 × 106 spores ml–1) were applied to 15 trees of susceptible ‘Barcelona’ in March 2008 following the protocol of Johnson et al. (2). In December 2009, 12 of 15 inoculated trees expressed EFB. ‘Gasaway’ has shown no signs or symptoms of infection by A. anomala over several decades of exposure in OR, which is believed to have a limited diversity of the fungus due to a single-point introduction. Our findings suggest quarantine efforts must be bolstered to prevent further introductions of A. anomala into the Pacific Northwest to protect the viability of the U.S hazelnut industry. References: (1) A. D. Davison and R. M. Davidson, Jr. Plant Dis. Rep. 57:522, 1973. (2) K. B. Johnson et al. Phytopathology 84:1465, 1994. (3) K. B. Johnson and J. N. Pinkerton. Eastern filbert blight. Page 44 in: Compendium of Nut Crop Diseases in Temperate Zones. B. L. Teviotdale et al., eds. The American Phytopathological Society. St. Paul, MN. 2002. (4) S. A. Mehlenbacher et al. HortScience 26:410, 1991.


1988 ◽  
Vol 62 (01) ◽  
pp. 141-143 ◽  
Author(s):  
Gerard M. Thomas ◽  
George O. Poinar

A sporulating Aspergillus is described from a piece of Eocene amber originating from the Dominican Republic. The Aspergillus most closely resembles a form of the white spored phase of Aspergillus janus Raper and Thom. This is the first report of a fossil species of Aspergillus.


2005 ◽  
Vol 173 (4S) ◽  
pp. 377-378
Author(s):  
Yasunori Hiraoka ◽  
Kazuhiko Yamada ◽  
Yuji Shimizu ◽  
Hiroyuki Abe
Keyword(s):  

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