A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo de conferência |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10174/24415 |
Resumo: | Sensitive detection of viruses in olive orchards is actually of main importance since these pathogenic agents cannot be treated, their dissemination is quite easy, and they can have negative effects on olive oil quality. Traditionally, techniques based on serology have been used widely for the detection of olive viruses, but more recently, molecular biology-based methods that include the highly laborious dsRNA analysis, have started to be performed. The low viral titres in olive tissues is the major constrain of the techniques and do not always allow the successful, accurate and reproducible detection. Phytosanitary certification programs depend on a reliable and sensitive detection of these viruses. In plant virology, real-time PCR (qPCR) is increasingly being used to improve the sensitivity and accuracy while maintaining reliability. The work describes the development and application of new SYBRGreen qPCR assays for the detection of the Olive leaf yellowing-associated virus, Olive latent virus-1, Tobacco necrosis virus-D and Olive mild mosaic virus, the main viruses that affect the olive trees. The main goal is to increase the accuracy of detection of olive viruses and, consequently, to improve their control. The work involves i) design of specific primers for each target virus; ii) studies on the sensitivity of the technique and primers specificity; iii) validation of the technique with plant material from different orchards. This work enables for the first time a reliable, sensitive and reproducible estimation of virus accumulation in infected olive trees that will allow gaining new insights in virus biology essential for disease control. |
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A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDSSensitive detection of viruses in olive orchards is actually of main importance since these pathogenic agents cannot be treated, their dissemination is quite easy, and they can have negative effects on olive oil quality. Traditionally, techniques based on serology have been used widely for the detection of olive viruses, but more recently, molecular biology-based methods that include the highly laborious dsRNA analysis, have started to be performed. The low viral titres in olive tissues is the major constrain of the techniques and do not always allow the successful, accurate and reproducible detection. Phytosanitary certification programs depend on a reliable and sensitive detection of these viruses. In plant virology, real-time PCR (qPCR) is increasingly being used to improve the sensitivity and accuracy while maintaining reliability. The work describes the development and application of new SYBRGreen qPCR assays for the detection of the Olive leaf yellowing-associated virus, Olive latent virus-1, Tobacco necrosis virus-D and Olive mild mosaic virus, the main viruses that affect the olive trees. The main goal is to increase the accuracy of detection of olive viruses and, consequently, to improve their control. The work involves i) design of specific primers for each target virus; ii) studies on the sensitivity of the technique and primers specificity; iii) validation of the technique with plant material from different orchards. This work enables for the first time a reliable, sensitive and reproducible estimation of virus accumulation in infected olive trees that will allow gaining new insights in virus biology essential for disease control.International Conference on Olive Tree and Olive Products - OliveBioteq182019-02-01T12:57:07Z2019-02-012018-10-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjecthttp://hdl.handle.net/10174/24415http://hdl.handle.net/10174/24415engCampos et al., 2018b95naonaosimFitotecniamdcc@uevora.ptzellama.mohamed.salem@gmail.comcarlavaranda@uevora.ptpmateratski@uevora.ptapeixe@uevora.ptmaher.chaouachi@gmail.commrff@uevora.pt581Campos, Maria DoroteiaZellama, Mohamed SalemVaranda, CarlaMateratski, PatrickPeixe, AugustoChaouachi, MaherFélix, Maria do Rosárioinfo: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:RCAAP2024-01-03T19:17:11Zoai:dspace.uevora.pt:10174/24415Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:15:00.174158Repositório 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 |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
title |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
spellingShingle |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS Campos, Maria Doroteia |
title_short |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
title_full |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
title_fullStr |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
title_full_unstemmed |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
title_sort |
A NEW REAL-TIME PCR METHOD DEVELOPED FOR THE DETECTION OF THE MAIN VIRUSES PRESENT IN OLIVE ORCHARDS |
author |
Campos, Maria Doroteia |
author_facet |
Campos, Maria Doroteia Zellama, Mohamed Salem Varanda, Carla Materatski, Patrick Peixe, Augusto Chaouachi, Maher Félix, Maria do Rosário |
author_role |
author |
author2 |
Zellama, Mohamed Salem Varanda, Carla Materatski, Patrick Peixe, Augusto Chaouachi, Maher Félix, Maria do Rosário |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Campos, Maria Doroteia Zellama, Mohamed Salem Varanda, Carla Materatski, Patrick Peixe, Augusto Chaouachi, Maher Félix, Maria do Rosário |
description |
Sensitive detection of viruses in olive orchards is actually of main importance since these pathogenic agents cannot be treated, their dissemination is quite easy, and they can have negative effects on olive oil quality. Traditionally, techniques based on serology have been used widely for the detection of olive viruses, but more recently, molecular biology-based methods that include the highly laborious dsRNA analysis, have started to be performed. The low viral titres in olive tissues is the major constrain of the techniques and do not always allow the successful, accurate and reproducible detection. Phytosanitary certification programs depend on a reliable and sensitive detection of these viruses. In plant virology, real-time PCR (qPCR) is increasingly being used to improve the sensitivity and accuracy while maintaining reliability. The work describes the development and application of new SYBRGreen qPCR assays for the detection of the Olive leaf yellowing-associated virus, Olive latent virus-1, Tobacco necrosis virus-D and Olive mild mosaic virus, the main viruses that affect the olive trees. The main goal is to increase the accuracy of detection of olive viruses and, consequently, to improve their control. The work involves i) design of specific primers for each target virus; ii) studies on the sensitivity of the technique and primers specificity; iii) validation of the technique with plant material from different orchards. This work enables for the first time a reliable, sensitive and reproducible estimation of virus accumulation in infected olive trees that will allow gaining new insights in virus biology essential for disease control. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-10-01T00:00:00Z 2019-02-01T12:57:07Z 2019-02-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/conferenceObject |
format |
conferenceObject |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10174/24415 http://hdl.handle.net/10174/24415 |
url |
http://hdl.handle.net/10174/24415 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Campos et al., 2018b 95 nao nao sim Fitotecnia mdcc@uevora.pt zellama.mohamed.salem@gmail.com carlavaranda@uevora.pt pmateratski@uevora.pt apeixe@uevora.pt maher.chaouachi@gmail.com mrff@uevora.pt 581 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
International Conference on Olive Tree and Olive Products - OliveBioteq18 |
publisher.none.fl_str_mv |
International Conference on Olive Tree and Olive Products - OliveBioteq18 |
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 |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799136631664410624 |