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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.)

Early detection of Neophysopella tropicalis in grapevine leaves and on spore traps by qPCR

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Autor(es):
Primiano, Isabela V. [1, 2] ; Cia, Mariana C. [1] ; Camargo, Luis E. A. [1] ; Amorim, Lilian [1]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Luiz de Queiroz Agr Sch, ESALQ Dept Plant Pathol & Nematol, Av Padua Dias 11, BR-13418900 Piracicaba, SP - Brazil
[2] Fund Citrus Protect FUNDECITRUS, Araraquara, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: PLANT PATHOLOGY; v. 70, n. 2 OCT 2020.
Citações Web of Science: 0
Resumo

Neophysopella tropicalis, one of the causal agents of Asian grapevine leaf rust (AGLR), can cause severe epidemics in Brazil that lead to yield losses in commercial vineyards. An early detection of the pathogen by air sampling of urediniospores on spore traps or in symptomless leaves would be valuable to multiple studies, such as epidemics modelling, risk forecasting, monitoring of pathogen introductions in rust-free areas, and predicting the beginning of epidemics. This study developed a quantitative PCR (qPCR) protocol to quantify N. tropicalis urediniospores attached to adhesive tapes and in grapevine leaves before symptom appearance. A specific primer pair was designed based on the internal transcribed spacer (ITS) sequence region of the AGLR pathogen. Standard amplification curves using genomic DNA from urediniospores of N. tropicalis and from urediniospores attached to adhesive tapes were established. Grapevine leaves inoculated with N. tropicalis were collected at 2, 5, and 7 days postinoculation (dpi). One primer pair (580F/720R) amplified a 140 bp product in all AGLR isolates but did not amplify products of other rust genera, such as Phakopsora, Puccinia, Hemileia, Tranzschelia, Cerotelium, and Coleosporium. As little as 0.1 pg DNA and 10 urediniospores of N. tropicalis attached to adhesive tapes could be detected. qPCR enabled the detection of the pathogen as early as 2 dpi, before symptom appearance. This method can be used to monitor N. tropicalis inoculum in grapevine-growing areas and to quantify symptomless infections of the AGLR pathogen. (AU)

Processo FAPESP: 13/24003-9 - Epidemiologia, avaliação de danos e controle de doenças da videira
Beneficiário:Lilian Amorim
Linha de fomento: Auxílio à Pesquisa - Temático