Multiplex RT-PCR for detection and identification of three necroviruses that infect olive trees
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , |
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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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 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
127340 bytes application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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