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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Quick and accurate detection of Sclerotinia sclerotiorum and Phomopsis spp. in soybean seeds using qPCR and seed-soaking method

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Autor(es):
Ramiro, Juliana [1] ; Ciampi-Guillardi, Maisa [1] ; Gomes Caldas, Danielle Gregorio [2] ; Duarte de Moraes, Maria Heloisa [1] ; Goldoni Barbieri, Marina Coan [1] ; Pereira, Wagner Vicente [3] ; Massola, Jr., Nelson Sidnei [1]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Dept Plant Pathol & Nemathol, ESALQ, Piracicaba, SP - Brazil
[2] Univ Sao Paulo, Ctr Nucl Energy Agr, Piracicaba, SP - Brazil
[3] Univ Fed Parana, Dept Crop Sci, Curitiba, PR - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF PHYTOPATHOLOGY; v. 167, n. 5, p. 273-282, MAY 2019.
Citações Web of Science: 0
Resumo

Seed-borne pathogenic fungi can cause serious damage to soybean crops by reducing the germination, vigour and emergence of the seeds. Special attention should be paid to pathogen detection in seeds to prevent its introduction in disease-free areas. Considering the importance of rapid and successful diagnosis of seed-borne pathogenic fungi in soybeans, this study evaluated a method to detect Sclerotinia sclerotiorum and Phomopsis spp. in seeds using quantitative polymerase chain reaction (qPCR). Naturally infested samples were subjected to detection using qPCR and blotter test, and the findings were compared. Using soybean seeds soaked in water, both pathogens were detected at an infestation level up a 0.0625% (one infected seed out of 1,599 healthy seeds) by qPCR. This technique allowed the detection of 300 fg of S. sclerotiorum and 30 fg of Phomopsis spp. DNA in the seed samples. Phomopsis spp. was detected in 40.7% of the evaluated seed batches (81 batches) and S. sclerotiorum was detected in 32.1% of the evaluated batches, although most of the seeds had low infestation levels. It was up to 28.5 times more efficient to use qPCR rather than blotter test to detect pathogens with a low incidence of occurrence in soybean seeds. If routinely used to test healthy seeds, qPCR would contribute to reducing soybean losses due to diseases as well as decreasing the costs required to control those diseases. (AU)

Processo FAPESP: 13/16726-0 - Detecção molecular de fungos fitopatogênicos associados às sementes de soja
Beneficiário:Nelson Sidnei Massola Júnior
Modalidade de apoio: Auxílio à Pesquisa - Regular