Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees

Detalhes bibliográficos
Autor(a) principal: Varanda, Carla
Data de Publicação: 2010
Outros Autores: Cardoso, Joana M.S., Félix, M. Rosário, Oliveira, Solange, Clara, M.Ivone
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/2098
Resumo: An optimized multiplex RT-PCR assay was developed to discriminate three necrovirus (Olive latent virus 1 (OLV-1), Tobacco necrosis virus D (TNV-D) and Olive mild mosaic virus (OMMV)) that infect olive trees. An olive orchard consisting of 54 trees of cv. "Galega vulgar" in the south of Portugal was surveyed. dsRNA fraction was used as template and revealed the 3 viruses, singly or in multiple infections, present in 17 out of 54 trees in the orchard. OMMV was the most frequent occurring in 15 trees, followed by OLV-1 in 12 and TNV-D in 4 plants. The results obtained showed that necrovirus- specific dsRNAs do exist in infected tissues in amounts below the resolution permitted by gel electrophoresis analysis and that the developed multiplex PCR based assay is of much higher sensitivity. The design of the specific primers described enabled, for the first time, to discriminate between OMMV and TNV-D by means of RT-PCR assays, an indispensable tool in identification, epidemiology and survey studies
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spelling Multiplex RT-PCR for detection and identification of three necroviruses that infect olive treesMultiplex RT-PCRnecrovirusesAn optimized multiplex RT-PCR assay was developed to discriminate three necrovirus (Olive latent virus 1 (OLV-1), Tobacco necrosis virus D (TNV-D) and Olive mild mosaic virus (OMMV)) that infect olive trees. An olive orchard consisting of 54 trees of cv. "Galega vulgar" in the south of Portugal was surveyed. dsRNA fraction was used as template and revealed the 3 viruses, singly or in multiple infections, present in 17 out of 54 trees in the orchard. OMMV was the most frequent occurring in 15 trees, followed by OLV-1 in 12 and TNV-D in 4 plants. The results obtained showed that necrovirus- specific dsRNAs do exist in infected tissues in amounts below the resolution permitted by gel electrophoresis analysis and that the developed multiplex PCR based assay is of much higher sensitivity. The design of the specific primers described enabled, for the first time, to discriminate between OMMV and TNV-D by means of RT-PCR assays, an indispensable tool in identification, epidemiology and survey studies2010-09-27T14:00:54Z2010-09-272010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article127340 bytesapplication/pdfhttp://hdl.handle.net/10174/2098http://hdl.handle.net/10174/2098engpag 161-164127EUROPEAN JOURNAL OF PLANT PATHOLOGYlivrendndndndnd226Varanda, CarlaCardoso, Joana M.S.Félix, M. RosárioOliveira, SolangeClara, M.Ivoneinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-03T18:38:18Zoai:dspace.uevora.pt:10174/2098Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:57:53.465579Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
title Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
spellingShingle Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
Varanda, Carla
Multiplex RT-PCR
necroviruses
title_short Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
title_full Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
title_fullStr Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
title_full_unstemmed Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
title_sort Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
author Varanda, Carla
author_facet Varanda, Carla
Cardoso, Joana M.S.
Félix, M. Rosário
Oliveira, Solange
Clara, M.Ivone
author_role author
author2 Cardoso, Joana M.S.
Félix, M. Rosário
Oliveira, Solange
Clara, M.Ivone
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Varanda, Carla
Cardoso, Joana M.S.
Félix, M. Rosário
Oliveira, Solange
Clara, M.Ivone
dc.subject.por.fl_str_mv Multiplex RT-PCR
necroviruses
topic Multiplex RT-PCR
necroviruses
description An optimized multiplex RT-PCR assay was developed to discriminate three necrovirus (Olive latent virus 1 (OLV-1), Tobacco necrosis virus D (TNV-D) and Olive mild mosaic virus (OMMV)) that infect olive trees. An olive orchard consisting of 54 trees of cv. "Galega vulgar" in the south of Portugal was surveyed. dsRNA fraction was used as template and revealed the 3 viruses, singly or in multiple infections, present in 17 out of 54 trees in the orchard. OMMV was the most frequent occurring in 15 trees, followed by OLV-1 in 12 and TNV-D in 4 plants. The results obtained showed that necrovirus- specific dsRNAs do exist in infected tissues in amounts below the resolution permitted by gel electrophoresis analysis and that the developed multiplex PCR based assay is of much higher sensitivity. The design of the specific primers described enabled, for the first time, to discriminate between OMMV and TNV-D by means of RT-PCR assays, an indispensable tool in identification, epidemiology and survey studies
publishDate 2010
dc.date.none.fl_str_mv 2010-09-27T14:00:54Z
2010-09-27
2010-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/2098
http://hdl.handle.net/10174/2098
url http://hdl.handle.net/10174/2098
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv pag 161-164
127
EUROPEAN JOURNAL OF PLANT PATHOLOGY
livre
nd
nd
nd
nd
nd
226
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