Leonardo Daniel Ploper

First report of Colletotrichum acutatum on strawberry in northwestern Argentina.

Isolates were obtained from strawberry tissue with anthracnose symptoms from several locations near Tucumán, Argentina. Isolates were characterized using several criteria. Isolates produced fusiform conidia, tapered to a point at both ends, and averaged 13.5 × 4.9 μm. On potato dextrose agar, colonies produced a white cottony mycelial colony that turned orange in older cultures. Compared with Colletotrichum fragariae, the new isolates produced fewer appressoria. Pathogenicity tests were conducted on detached leaves and plants in the greenhouse and field. Detached immature leaves of cvs. Chandler, Fern, and Sweet Charlie were inoculated with a 20-μl droplet of an aqueous conidial suspension (106 conidia per ml) placed on the adaxial surface. Control leaves were inoculated with sterile distilled water. Leaves were maintained under white light (2,000 lux, 12 h/day) at 26°C, and 100% relative humidity. Necrotic spots were visible 4 days after inoculation. Greenhouse and field plants were spray-inoculated and covered for 48 h. Disease symptoms were mainly observed on petioles and runners 9 days after inoculation. No lesions were observed on control detached leaves or plants. Kochs postulates were confirmed in all cases. Based on morphological and cultural characteristics, isolates were identified as C. acutatum Simmonds (1). This is the first report of C. acutatum causing strawberry anthracnose in northwestern Argentina. Reference: (1) B. Smith and L. L. Black. Plant Dis. 74:69, 1990.

First report of Fusarium rot caused by Fusarium oxysporum on lemon in Tucumán, Argentina.

Fusarium rot is considered a minor disease of citrus fruits. Several Fusarium species have been associated with fruit decay, most commonly F. lateritium Nees, F. moniliforme J. Sheld., F. oxysporum Schltdl., and F. solani (Mart.) Sacc. (2,3). In the winters of 2007, 2009, 2010, and 2011, lemon [Citrus limon (L.) Burm. f.] fruit with white mycelium covering the peduncle were submitted to the Phytopathology Lab at the Estación Experimental Agroindustrial Obispo Colombres. All fruit samples from Tucumán, Argentina, were stored in boxes kept in packinghouse for more than 1 month. In 2007 only, light to dark brown flavedo around the peduncle was observed in less than 1% of the sample fruit received. No internal breakdown was visible. No change in rind color was observed in the samples received in remaining years. Abundant Fusarium sp. conidia were observed on the mycelium. Colonies with white to violet fluffy aerial mycelium developed on potato dextrose agar (PDA) and produced abundant ovoid or oblong microconidia (1.9 to 3.6 × 4.8 to 10.8 μm), usually unicellular, borne in false heads on short monophialides, and loculated slightly falcate macroconidia were mostly three to five septate (2.4 to 4.8 × 19.2 to 31.2 μm). Unbranched and branched-monophialidic conidiophores were observed. Simple or paired chlamydospores developed on synthetic nutrient agar (1 g KH2PO4, 1 g KNO3, 0.5 g MgSO4.7H2O, 0.5 g KCl, 0.2 g sucrose, and 20 g agar/liter distilled water). On the basis of morphological and cultural criteria, 22 isolates were identified as F. oxysporum (4) designated as D1 to D22. Morfological identification was confirmed by PCR (1) using genomic DNA extracted from the mycelium of pure culture, and an amplified product of 70 bp, specific for the species F. oxysporum, was obtained. The internal transcribed spacer (ITS) region of rDNA was amplified using the primers ITS4/ITS5 and secuenced. BLAST analysis of the 600 bp segment showed a 100% indentity with F. oxysporum, strains CCF 4362 and 1166 (GenBank Accession Nos. HE974454 and FR731133, respectively). Pathogenicity tests were conducted twice by inoculating 10 surface-disinfected wounded lemon fruit. A rind disc (5 mm in diameter and 1 mm deep) near the stem end was removed and a 5-mm-diameter agar disc of D2 isolate (grown at 25°C for 5 days on PDA) was attached to the wound replacing the rind disc. The inoculation site was covered with moistened cotton wool and the fruit were wrapped in plastic bags to prevent the inoculum from drying out. Ten control fruit were inoculated with uncultured PDA plugs (5 mm in diameter). All fruit were maintained in a growth chamber at 25°C under humid conditions. After 5 to 6 days, all inoculated fruit showed white aerial mycelium, initially on the inoculation site and then on the peduncle, similar to that observed on naturally infected fruit. After 20 days, two fruit developed stem end dry rot and showed peduncle fall but no internal breakdown was visible. Control fruit developed any symptom as described above. F. oxysporum was consistently reisolated from infected tissues, completing Kochs postulates. To our knowledge, this is the first report of Fusarium rot caused by F. oxysporum on lemon in Tucumán, Argentina. References: (1) V. Edel et al. Mycol. Res. 104:518, 2000. (2) H. S. Fawcett. Citrus Diseases and Their Control, 1936. (3) A. Z. Joffe and M. Schiffmann-Nadel. Fruits 27:117, 1972. (4) P. E. Nelson et al. Fusarium species: An Illustrated Manual for Identification, 1983.

Frogeye Leaf Spot of Soybean Caused by Cercospora sojina in Northwestern Argentina

Frogeye leaf spot of soybean (Glycine max (L.) Merr.), caused by Cercospora sojina Hara, was first detected during the 1997-98 growing season at low incidence and severity (<1% of the leaf diseased) levels in the provinces of Tucumán, Salta, Jujuy, Catamarca, and Santiago del Estero in northwestern Argentina. During the 1998-1999 growing season, disease incidence increased and disease severity grew to 10% of the leaf surface diseased on highly susceptible cultivars in a few locations. An outbreak of frogeye leaf spot occurred throughout northwestern Argentina during the 1999-2000 growing season. Frogeye leaf spot was severe on susceptible cultivars in the provinces of Salta, Santiago del Estero and Catamarca with the greatest intensity in the northeastern part of the Province of Tucumán. Symptoms on leaves were circular lesions that ranged in size from 1 to 5 mm, were reddish-brown to gray or tan, and were bordered by a narrow, reddish-brown to purple margin. Conidiophores and conidia of C. sojina developed on the abaxial leaf surface (1,2). Severely diseased leaves were desiccated and dropped during the R6 stage of growth. Lesions also developed on stems, pods, and seeds. Field surveys indicated that this disease reduced the yields of the highly susceptible cultivars Anta 82 RR, Coker 6738, and A 6445 RG by 48, 34, and 25%, respectively. C. sojina was cultured from diseased tissue on PDA acidified with 0.2% lactic acid and maintained on V-8 juice agar amended with streptomycin sulfate (100 mg/l). Conidia were elongated, dark, 38 to 62 × 5 to 9 μm, with 2 to 6 septa, and borne on dark conidiophores with 1 to 4 septa. Pathogenicity tests were conducted on seedlings of the susceptible cultivars A 6445 RG and Coker 6738 and on the resistant cultivars A 8000 RG and Shulka. Seedlings were inoculated at the V3 growth stage by spraying the leaves with a conidial suspension (4 × 104 conidia/ml) using a hand-held atomizer. Control plants were sprayed with sterile distilled water. Plants were placed in a moist chamber at 26°C for 2 days and then transferred to a greenhouse bench where they were kept at 25 to 30°C. Symptoms identical to those observed in the field became visible after 7 to 10 days. Ratings were made 14 days after inoculation by estimating the percentage of leaf area affected using a standard area diagram. Lesions covered 60 to 65% of the leaf area of susceptible cultivars, but less than 2% on resistant cultivars. Control plants remained healthy. C. sojina was reisolated from lesions on leaves of susceptible plants. Above-average rainfall and high relative humidity in northwestern Argentina during the first three months of 2000 may have encouraged the severe outbreak of frogeye leaf spot of soybean. The outbreak was aggravated by the widespread use of notillage systems in the region and the large hectarage planted with susceptible cultivars. References: (1) S.G. Lehman J. Agric. Res. 36:811-833, 1928. (2) D. V. Philips and J. T. Yorinori. 1989. Frogeye leaf spot. Pages 19-21 in: Compendium of Soybean Diseases, 3rd ed. APS Press, St. Paul, MN.

A Study of the Sugarcane Yellow Leaf Disease in Argentina

Yellow leaf disease, caused by Sugarcane yellow leaf virus (SCYLV), is widespread around the world but very little information is available on this viral disease in Argentina. Therefore, the aims of the study were to assess the presence of SCYLV, analyze its distribution in the main sugarcane production areas of Argentina, characterize the virus, and determine histological alterations caused by its presence. For this purpose, 148 sugarcane samples with and without symptoms were collected in 2011 and 2012 from the province of Tucumán. One additional sample was collected in Salta, a different geographical, agroecological, and producing region. Results showed that SCYLV is widely distributed in commercial varieties of sugarcane throughout Tucumán in both symptomatic and asymptomatic leaves. A low but statistically significant positive correlation with virus detection and disease symptoms was found. BRA-PER was the only genotype detected by reverse-transcription polymerase chain reaction and sequence analysis of the SCYLV capsid protein gene. SCYLV-positive samples showed high starch levels in bundle sheath cells, whereas the asymptomatic ones, probably in an early stage of infection, were found to contain more chloroplasts. Symptomatic noninfected samples presented crystal formation probably associated with phytoplasma infection.