Blueberries (Vaccinium corymbosum) have recently become an important alternative crop in different ecological regions of Argentina. In surveys, a new disease characterized by leaf spots and twig and shoot blight has been observed on plants cultivated in Arrecifes, Mercedes, and San Pedro (provinces of Buenos Aires) and Concordia (province of Entre Ríos) since July 2004. Spots initially appear brown, circular, 1 to 2 mm in diameter, and irregularly distributed on the leaves and they eventually coalesce. Fruiting twig and shoot blight developed from the tips toward the base. Affected plants of cvs. O'Neal and Reveille were distributed randomly in the field and with a low incidence (average of 2%). The objective of this work was to identify the causal agent of this disease. Symptomatic plant material was surface disinfested with 0.2% NaOCl for 1 min and 70% ethanol for 1 min, washed once with sterile distilled water, blotted dry with paper towels, and plated on potato dextrose agar. Colonies were initially white, becoming light to dark gray with the onset of sporulation with black, sphaerical to subsphaerical conidia that measured 14 to 19 × 12 to 16 μm. These characteristics agree with published descriptions of Nigrospora sphaerica (Sacc.) Mason (1,4). To evaluate pathogenicity, all leaves, petioles, and stems of seven healthy potted plants of cv. O'Neal were punctured with flamed needles and sprayed with a suspension of 1 × 108 spores of the fungus per milliliter of sterile distilled water. Another seven nonwounded plants were sprayed with the spore suspension. Seven plants similarly injured and seven nonwounded plants were sprayed with sterile distilled water and served as controls. Each plant was covered with a water-sprayed polyethylene bag and maintained in a controlled environment chamber at 20°C with a 12-h photoperiod. The bags were removed after 3 days. All wounded inoculated plants began to show disease symptoms similar to those observed in the field 20 days after inoculation. Controls and nonwounded inoculated plants remained symptomless. The pathogen was reisolated from diseased tissues fulfilling Koch's postulates. N. sphaerica is a well-known saprophyte on many plant species but has been mentioned as pathogen on many hosts (2,3). To our knowledge, this is the first reference of N. sphaerica as a wound pathogen of blueberry. In the field, the fungus would have gained access to the plant through wounds caused by insects or frost after a long-term wetness duration. References: (1) M. B. Ellis. Dematiaceous Hyphomycetes. CMI, Kew, Surrey, UK, 1971. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. American Phytopathological Society, St. Paul, MN, 1989. (3) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory. Online publication. ARS, USDA. 2007. (4) E. W. Mason. Trans. Brit. Mycol. Soc. 12:152, 1927.
Night-blooming cereus (Hylocereus undatus A. Berger) is generally used as rootstock of ornamental cactus because of its rapid growth and tolerance to humid substrates. Since 2002, in Gran Buenos Aires, a new disease has been observed in grafted crops in all production stages. Incidence was as much as 30% in many greenhouses. Symptoms consisted of soft rot that started near the soil line and developed upward until it affected all the rootstock. The scion was not rotten, but died as a consequence of rootstock infection. All the roots were symptomless. For pathogen isolation, symptomatic tissues were surface disinfected by a 1-min immersion in 0.2% NaOCl, placed on potato dextrose agar (PDA), and incubated at 22 ± 2°C. Only a Fusarium spp. was consistently isolated in pure culture. Twenty healthy potted night-blooming cereus plants, 10 of them previously injured with needles on the rootstock near the soil line, were gently removed from the substrate and inoculated by a 1-min immersion of their base in a suspension of 1.4 × 106 conidia per ml of sterile distilled water, prepared from 15-day-old cultures. Ten control plants, five of them previously injured, were immersed in sterile distilled water. Inoculated and noninoculated plants were replanted in the original substrate, placed in a climatic chamber at 22 ± 2°C, and monitored for disease expression. Basal rot was observed on all injured inoculated plants 12 days after inoculation. Symptoms on undamaged plants appeared 22 days after inoculation. After 72 days of incubation, all inoculated plants were totally rotten. Control plants remained symptomless. The same pathogen was reisolated to fulfill Koch's postulates. For species identification, single-spore cultures were grown on PDA and carnation leaf agar in a climatic chamber at 23 ± 2°C with a 12-h darkness/near ultraviolet light regimen. The micromorphology and culture features, mainly conidial ontogeny, were consistent with descriptions of Fusarium oxysporum Schlechtend.:Fr. (1). The pathogen was able to penetrate undamaged tissues. Needle injuries accelerated infection. To our knowledge, this is the first report of Fusarium oxysporum on H. undatus in Gran Buenos Aires, Argentina. A culture of the pathogen was deposited at the fungal collection of PRHIDEB-CONICET (University of Buenos Aires) as BAFCult 3158. Reference: (1) P. E. Nelson et al. Fusarium species. An Illustrated Manual for Identification. The Pennsylvania State University Press, University Park, PA, 1983.
Bluebeny is a relatively new crop cultivated in the provinces of Buenos Aires, Cbrdoba, RioNegro and Santa Fe (AR). In 1996, an unknown disease was observed. Plants ready to be planted near Buenos Aires and plants growing in a glasshouse in Buenos Aires, both imported from USA, had their stems blighted. P esfalotiopsis guepini and Glomerella cingulata were determined as causal agents of the symptoms.
Disease symptoms have been observed since October 1997 on highbush blueberry (Vaccinium corymbosum L.) cvs. Georgia Gem, O'Neal, and Sharpblue cultivated in Buenos Aires. Lesions were observed on recently planted, as well as mature plants, in commercial fields. Circular-to-irregular, light brown-to-gray leaf spots with brownish red borders, initially 3 to 7 mm in diameter, enlarged and coalesced. Blight developed on twigs. Reddish circular spots appeared on stems, developing small cankers. Dark sunken lesions were observed on attached ripening berries. During December 2002, postharvest fruit rot was noted. Small pieces of diseased leaves, twigs, stems, and fruits were surface sterilized with 0.2% NaOCl, plated on 2% potato dextrose agar (pH 7), and incubated at 20 ± 3°C. Symptomatic fruits were placed in plastic trays in humid chambers. In all cases, olive mycelium developed after 3 days with septate hyphae and abundant ovoid and obclavate muriformly septate conidia. The isolate obtained from diseased leaves of cv. O'Neal was used to test pathogenicity on micropropagated potted plants of 20-cm height and ripe fruits contained in plastic trays. Both plants and fruits belonged to cv. O'Neal. A suspension of 2 × 105 conidia per ml was sprayed on needle-punctured young stems, fully expanded leaves, and mature fruits. Plants and trays were covered with polyethylene bags and kept at 24 ± 3°C under fluorescent light (12-hr photoperiod). The bags were removed after 72 hr. Symptoms appeared after 3 days on fruits and 8 days on leaves and stems. Controls remained symptomless. The inoculated pathogen was recovered from diseased organs and identified as Alternaria tenuissima (Kunze:Fr.) Wiltshire (1). To our knowledge, this is the first report on the presence of A. tenuissima affecting blueberry crops in Argentina. Reference: (1) E. G. Simmons. Mycotaxon 70:325, 1999.
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