A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds

Autores
Consolo, Verónica Fabiana; Albani, Clara María; Berón, Corina M.; Salerno, Graciela Lidia; Cordo, Cristina Alicia
Año de publicación
2009
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A PCR assay was developed for detection of wheat seed naturally contaminated with Septoria tritici. S. tritici specific primers were derived from strict alignment of ITS and α-tubulin sequences of the pathogen. The specificity of four sets of synthesised oligonucleotide pairs (A, B, C and D) were tested using isolates from S. tritici, other selected fungi and wheat seeds. A single DNA fragment was amplified from S. tritici isolates with all primer pairs, whereas no product was generated from other DNA sources. S. tritici was also detected in wheat seed lots collected from plants with variable pycnidial coverage on the upper two leaves. PCR detection of as little as 0.5 pg of S. tritici genomic DNAwas possible. This is the first report on the detection of S. tritici DNA in naturally infested wheat seeds. This PCR based assay is simple, rapid, specific, sensitive and suitable for routine detection of the wheat pathogen in infested wheat seeds.
Centro de Investigaciones en Fitopatología
Materia
Ciencias Agrarias
Ciencias Naturales
Mycosphaerella graminicola
seedborne pathogen
Septoria leaf blotch
wheat
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/136109

id SEDICI_bff9c19fea91ada6d86c9bb5cc740b35
oai_identifier_str oai:sedici.unlp.edu.ar:10915/136109
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seedsConsolo, Verónica FabianaAlbani, Clara MaríaBerón, Corina M.Salerno, Graciela LidiaCordo, Cristina AliciaCiencias AgrariasCiencias NaturalesMycosphaerella graminicolaseedborne pathogenSeptoria leaf blotchwheatA PCR assay was developed for detection of wheat seed naturally contaminated with <i>Septoria tritici</i>. <i>S. tritici</i> specific primers were derived from strict alignment of ITS and α-tubulin sequences of the pathogen. The specificity of four sets of synthesised oligonucleotide pairs (A, B, C and D) were tested using isolates from S. tritici, other selected fungi and wheat seeds. A single DNA fragment was amplified from <i>S. tritici</i> isolates with all primer pairs, whereas no product was generated from other DNA sources. <i>S. tritici</i> was also detected in wheat seed lots collected from plants with variable pycnidial coverage on the upper two leaves. PCR detection of as little as 0.5 pg of <i>S. tritici</i> genomic DNAwas possible. This is the first report on the detection of <i>S. tritici</i> DNA in naturally infested wheat seeds. This PCR based assay is simple, rapid, specific, sensitive and suitable for routine detection of the wheat pathogen in infested wheat seeds.Centro de Investigaciones en Fitopatología2009-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf222-227http://sedici.unlp.edu.ar/handle/10915/136109enginfo:eu-repo/semantics/altIdentifier/issn/0815-3191info:eu-repo/semantics/altIdentifier/issn/1448-6032info:eu-repo/semantics/altIdentifier/issn/0310-1266info:eu-repo/semantics/altIdentifier/doi/10.1071/ap08099info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-17T10:14:41Zoai:sedici.unlp.edu.ar:10915/136109Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-17 10:14:41.936SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
title A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
spellingShingle A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
Consolo, Verónica Fabiana
Ciencias Agrarias
Ciencias Naturales
Mycosphaerella graminicola
seedborne pathogen
Septoria leaf blotch
wheat
title_short A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
title_full A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
title_fullStr A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
title_full_unstemmed A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
title_sort A conventional PCR technique to detect <i>Septoria tritici</i> in wheat seeds
dc.creator.none.fl_str_mv Consolo, Verónica Fabiana
Albani, Clara María
Berón, Corina M.
Salerno, Graciela Lidia
Cordo, Cristina Alicia
author Consolo, Verónica Fabiana
author_facet Consolo, Verónica Fabiana
Albani, Clara María
Berón, Corina M.
Salerno, Graciela Lidia
Cordo, Cristina Alicia
author_role author
author2 Albani, Clara María
Berón, Corina M.
Salerno, Graciela Lidia
Cordo, Cristina Alicia
author2_role author
author
author
author
dc.subject.none.fl_str_mv Ciencias Agrarias
Ciencias Naturales
Mycosphaerella graminicola
seedborne pathogen
Septoria leaf blotch
wheat
topic Ciencias Agrarias
Ciencias Naturales
Mycosphaerella graminicola
seedborne pathogen
Septoria leaf blotch
wheat
dc.description.none.fl_txt_mv A PCR assay was developed for detection of wheat seed naturally contaminated with <i>Septoria tritici</i>. <i>S. tritici</i> specific primers were derived from strict alignment of ITS and α-tubulin sequences of the pathogen. The specificity of four sets of synthesised oligonucleotide pairs (A, B, C and D) were tested using isolates from S. tritici, other selected fungi and wheat seeds. A single DNA fragment was amplified from <i>S. tritici</i> isolates with all primer pairs, whereas no product was generated from other DNA sources. <i>S. tritici</i> was also detected in wheat seed lots collected from plants with variable pycnidial coverage on the upper two leaves. PCR detection of as little as 0.5 pg of <i>S. tritici</i> genomic DNAwas possible. This is the first report on the detection of <i>S. tritici</i> DNA in naturally infested wheat seeds. This PCR based assay is simple, rapid, specific, sensitive and suitable for routine detection of the wheat pathogen in infested wheat seeds.
Centro de Investigaciones en Fitopatología
description A PCR assay was developed for detection of wheat seed naturally contaminated with <i>Septoria tritici</i>. <i>S. tritici</i> specific primers were derived from strict alignment of ITS and α-tubulin sequences of the pathogen. The specificity of four sets of synthesised oligonucleotide pairs (A, B, C and D) were tested using isolates from S. tritici, other selected fungi and wheat seeds. A single DNA fragment was amplified from <i>S. tritici</i> isolates with all primer pairs, whereas no product was generated from other DNA sources. <i>S. tritici</i> was also detected in wheat seed lots collected from plants with variable pycnidial coverage on the upper two leaves. PCR detection of as little as 0.5 pg of <i>S. tritici</i> genomic DNAwas possible. This is the first report on the detection of <i>S. tritici</i> DNA in naturally infested wheat seeds. This PCR based assay is simple, rapid, specific, sensitive and suitable for routine detection of the wheat pathogen in infested wheat seeds.
publishDate 2009
dc.date.none.fl_str_mv 2009-05
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/136109
url http://sedici.unlp.edu.ar/handle/10915/136109
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0815-3191
info:eu-repo/semantics/altIdentifier/issn/1448-6032
info:eu-repo/semantics/altIdentifier/issn/0310-1266
info:eu-repo/semantics/altIdentifier/doi/10.1071/ap08099
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
222-227
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
_version_ 1843532785535418368
score 13.001348