First Report of Target Spot of Soybean Caused by Corynespora cassiicola in the Colombian Eastern Plains
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https://doi.org/10.1094/PDIS-07-20-1586-PDNhttps://apsjournals.apsnet.org/doi/full/10.1094/PDIS-07-20-1586-PDNFecha
2020Autor
Lopez Cardona, Nathali
Guevara Castro, Yudy Alejandra
Gañan, Lederson
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Ministerio de Agricultura y Desarrollo Rural - MADRPalabras clave
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Resumen
Soybean (Glycine max L. Merr.) is an important leguminous crop for Colombia, given the growing demand from the livestock, poultry, and aquaculture industries. About 80% of Colombian soybean production is in the State (or Department) of Meta, located in the Eastern Plains region, or Llanos Orientales, where the crop has an average yield of 2.5 t/ha (FENALCE 2020). In July 2017, foliar symptoms, including rounded to irregular reddish-brown spots surrounded by a yellowish halo progressing to irregular spots with concentric rings, and in severe cases defoliation, were observed in a production field of Soyica P-34 soybean cultivar in Puerto López, Meta (Colombia). Dark brown lesions on stems and dark-brown to black spots on pods were also observed, and the incidence of symptomatic plants was recorded as 50%. Four infected plants were arbitrarily sampled from different locations across the field and used for pathogen isolation. Specimen collection was conducted according to the permit conferred to AGROSAVIA under ANLAS resolution number 1466 of December 3, 2014, Colombia. Symptomatic leaf pieces (~5 mm2) were rinsed with tap water for 1 min, dipped in a 0.5% sodium hypochlorite for 2 min, rinsed with sterile distilled water for 1 min, and then plated on potato dextrose agar (PDA, 39 g/liter). Plates were incubated at 25°C for 2 weeks with a 12-h/12-h light/dark cycle using dark light. Four monoconidial isolates with similar morphological characteristics were obtained. Observations under the light microscope showed that conidia (n = 50) were hyaline, elongated, 65 to 120 × 9 to 12 µm, with three to 10 pseudosepta, corresponding with those characteristics described for Corynespora cassiicola (Berk. & M. A. Curtis) C. T. Wei (Ellis and Holliday 1971). Colonies on PDA medium were dark gray with abundant aerial mycelia growth. To confirm the morphological identification, extracted DNA from isolates AGSV13 and AGSV15 was used as a template to obtain partial sequences of the internal transcribed spacer (ITS) region of ribosomal DNA using the primer pair ITS 5/ITS 4 (White et al. 1990). Results from an NCBI-BLASTn search revealed that the ITS sequences (GenBank accessions MN298749 and MN298751) were 100% identical to those of C. cassiicola in GenBank (accessions MN945374 and AB873045). A phylogenetic analysis, using the maximum likelihood method, based on ITS sequences from voucher specimens of Corynespora spp. available at GenBank, revealed that the two isolates were placed in the same clade as C.
Parte del recurso
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Plant Disease; Vol. 105, Núm 2 (2020): Plant Disease Vol. 105, Núm 2 (2020); p.1.
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