Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds

Bibliographic Details
Main Author: Grabicoski, Edilaine Mauricia Gelinski
Publication Date: 2015
Other Authors: Jaccoud Filho, David de Souza, Pileggi, Marcos, Henneberg, Luciane, Pierre, Marcelo Luiz Cunha, Vrisman, Cláudio Mauricio, Dabul, Audrei Nisio Gebieluca
Format: Article
Language: eng
Source: Scientia Agrícola (Online)
Download full: https://www.revistas.usp.br/sa/article/view/100171
Summary: Caused by Sclerotinia sclerotiorum, white mold is an important seed-transmitted disease of soybean (Glycine max). Incubation-based methods available for the detection and quantification of seed-borne inoculum such as the blotter test, paper roll and Neon-S assay are time-consuming, laborious, and not always sensitive. In this study, we developed and evaluated a molecular assay for the detection of S. sclerotiorum in soybean seeds using a species-specific PCR (polymerase chain reaction) primer set and seed soaking (without DNA extraction) for up to 72 h. The PCR products were amplified in all the samples infected with the pathogen, but not in the other samples of plant material or the other seed-borne fungi DNA. The minimum amount of DNA detected was 10 pg, or one artificially infested seed in a 400-seed sample (0.25 % fungal incidence) and one naturally infected seed in a 300-seed sample (0.33 % incidence). The PCR-based assay was rapid (< 9 h), did not require DNA extraction and was very sensitive.
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spelling Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds Caused by Sclerotinia sclerotiorum, white mold is an important seed-transmitted disease of soybean (Glycine max). Incubation-based methods available for the detection and quantification of seed-borne inoculum such as the blotter test, paper roll and Neon-S assay are time-consuming, laborious, and not always sensitive. In this study, we developed and evaluated a molecular assay for the detection of S. sclerotiorum in soybean seeds using a species-specific PCR (polymerase chain reaction) primer set and seed soaking (without DNA extraction) for up to 72 h. The PCR products were amplified in all the samples infected with the pathogen, but not in the other samples of plant material or the other seed-borne fungi DNA. The minimum amount of DNA detected was 10 pg, or one artificially infested seed in a 400-seed sample (0.25 % fungal incidence) and one naturally infected seed in a 300-seed sample (0.33 % incidence). The PCR-based assay was rapid (< 9 h), did not require DNA extraction and was very sensitive. Universidade de São Paulo. Escola Superior de Agricultura Luiz de Queiroz2015-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/sa/article/view/10017110.1590/0103-9016-2013-0395Scientia Agricola; v. 72 n. 1 (2015); 69-74Scientia Agricola; Vol. 72 Núm. 1 (2015); 69-74Scientia Agricola; Vol. 72 No. 1 (2015); 69-741678-992X0103-9016reponame:Scientia Agrícola (Online)instname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/sa/article/view/100171/98836Copyright (c) 2015 Scientia Agricolainfo:eu-repo/semantics/openAccessGrabicoski, Edilaine Mauricia Gelinski Jaccoud Filho, David de Souza Pileggi, Marcos Henneberg, Luciane Pierre, Marcelo Luiz Cunha Vrisman, Cláudio Mauricio Dabul, Audrei Nisio Gebieluca 2015-08-31T11:54:04Zoai:revistas.usp.br:article/100171Revistahttp://revistas.usp.br/sa/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpscientia@usp.br||alleoni@usp.br1678-992X0103-9016opendoar:2015-08-31T11:54:04Scientia Agrícola (Online) - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
title Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
spellingShingle Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
Grabicoski, Edilaine Mauricia Gelinski
title_short Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
title_full Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
title_fullStr Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
title_full_unstemmed Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
title_sort Rapid PCR-based assay for Sclerotinia sclerotiorum detection on soybean seeds
author Grabicoski, Edilaine Mauricia Gelinski
author_facet Grabicoski, Edilaine Mauricia Gelinski
Jaccoud Filho, David de Souza
Pileggi, Marcos
Henneberg, Luciane
Pierre, Marcelo Luiz Cunha
Vrisman, Cláudio Mauricio
Dabul, Audrei Nisio Gebieluca
author_role author
author2 Jaccoud Filho, David de Souza
Pileggi, Marcos
Henneberg, Luciane
Pierre, Marcelo Luiz Cunha
Vrisman, Cláudio Mauricio
Dabul, Audrei Nisio Gebieluca
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Grabicoski, Edilaine Mauricia Gelinski
Jaccoud Filho, David de Souza
Pileggi, Marcos
Henneberg, Luciane
Pierre, Marcelo Luiz Cunha
Vrisman, Cláudio Mauricio
Dabul, Audrei Nisio Gebieluca
description Caused by Sclerotinia sclerotiorum, white mold is an important seed-transmitted disease of soybean (Glycine max). Incubation-based methods available for the detection and quantification of seed-borne inoculum such as the blotter test, paper roll and Neon-S assay are time-consuming, laborious, and not always sensitive. In this study, we developed and evaluated a molecular assay for the detection of S. sclerotiorum in soybean seeds using a species-specific PCR (polymerase chain reaction) primer set and seed soaking (without DNA extraction) for up to 72 h. The PCR products were amplified in all the samples infected with the pathogen, but not in the other samples of plant material or the other seed-borne fungi DNA. The minimum amount of DNA detected was 10 pg, or one artificially infested seed in a 400-seed sample (0.25 % fungal incidence) and one naturally infected seed in a 300-seed sample (0.33 % incidence). The PCR-based assay was rapid (< 9 h), did not require DNA extraction and was very sensitive.
publishDate 2015
dc.date.none.fl_str_mv 2015-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/sa/article/view/100171
10.1590/0103-9016-2013-0395
url https://www.revistas.usp.br/sa/article/view/100171
identifier_str_mv 10.1590/0103-9016-2013-0395
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/sa/article/view/100171/98836
dc.rights.driver.fl_str_mv Copyright (c) 2015 Scientia Agricola
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2015 Scientia Agricola
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Escola Superior de Agricultura Luiz de Queiroz
publisher.none.fl_str_mv Universidade de São Paulo. Escola Superior de Agricultura Luiz de Queiroz
dc.source.none.fl_str_mv Scientia Agricola; v. 72 n. 1 (2015); 69-74
Scientia Agricola; Vol. 72 Núm. 1 (2015); 69-74
Scientia Agricola; Vol. 72 No. 1 (2015); 69-74
1678-992X
0103-9016
reponame:Scientia Agrícola (Online)
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Scientia Agrícola (Online)
collection Scientia Agrícola (Online)
repository.name.fl_str_mv Scientia Agrícola (Online) - Universidade de São Paulo (USP)
repository.mail.fl_str_mv scientia@usp.br||alleoni@usp.br
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