Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus
Main Author: | |
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Publication Date: | 2007 |
Other Authors: | , , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10174/6790 |
Summary: | The pinewood nematode (PWN), Bursaphelenchus xylophilus , is a major pathogen of conifers, which impacts on forest health, natural ecosystem stability and international trade. As a consequence, it has been listed as a quarantine organism in Europe. A real-time PCR approach based on TaqMan chemistry was developed to detect this organism. Specific probe and primers were designed based on the sequence of the Msp I satellite DNA family previously characterized in the genome of the nematode. The method proved to be specific in tests with target DNA from PWN isolates from worldwide origin. From a practical point of view, detection limit was 1 pg of target DNA or one individual nematode. In addition, PWN genomic DNA or single individuals were positively detected in mixed samples in which B. xylophilius was associated with the closely related non-pathogenic species B. mucronatus , up to the limit of 0.01% or 1% of the mixture, respectively. The real-time PCR assay was also used in conjunction with a simple DNA extraction method to detect PWN directly in artificially infested wood samples. These results demonstrate the potential of this assay to provide rapid, accurate and sensitive molecular identification of the PWN in relation to pest risk assessment in the field and quarantine regulation. |
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Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilusBursaphelenchus xylophiluspinewoodnematodeThe pinewood nematode (PWN), Bursaphelenchus xylophilus , is a major pathogen of conifers, which impacts on forest health, natural ecosystem stability and international trade. As a consequence, it has been listed as a quarantine organism in Europe. A real-time PCR approach based on TaqMan chemistry was developed to detect this organism. Specific probe and primers were designed based on the sequence of the Msp I satellite DNA family previously characterized in the genome of the nematode. The method proved to be specific in tests with target DNA from PWN isolates from worldwide origin. From a practical point of view, detection limit was 1 pg of target DNA or one individual nematode. In addition, PWN genomic DNA or single individuals were positively detected in mixed samples in which B. xylophilius was associated with the closely related non-pathogenic species B. mucronatus , up to the limit of 0.01% or 1% of the mixture, respectively. The real-time PCR assay was also used in conjunction with a simple DNA extraction method to detect PWN directly in artificially infested wood samples. These results demonstrate the potential of this assay to provide rapid, accurate and sensitive molecular identification of the PWN in relation to pest risk assessment in the field and quarantine regulation.2012-12-10T16:25:43Z2012-12-102007-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/6790http://hdl.handle.net/10174/6790eng8ICAAMndndndndndndndpvieira@uevora.ptmmtota@uevora.ptPhilippe.Castagnone@sophia.inra.fr218CECILE, FRANÇOISCASTAGNONE, CHANTALBOONHAM, NEILTOMLINSON, JENNYLAWSON, REBECCAHOCKLAND, SUEQUILL, JAMESVIEIRA, PauloMota, ManuelCASTAGNONE-SERENO, PHILIPPEinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-01-03T18:46:20Zoai:dspace.uevora.pt:10174/6790Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T11:56:19.049440Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
title |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
spellingShingle |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus CECILE, FRANÇOIS Bursaphelenchus xylophilus pinewood nematode |
title_short |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
title_full |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
title_fullStr |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
title_full_unstemmed |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
title_sort |
Satellite DNA as a target for TaqMan real-time PCR detection of the pinewood nematode, Bursaphelenchus xylophilus |
author |
CECILE, FRANÇOIS |
author_facet |
CECILE, FRANÇOIS CASTAGNONE, CHANTAL BOONHAM, NEIL TOMLINSON, JENNY LAWSON, REBECCA HOCKLAND, SUE QUILL, JAMES VIEIRA, Paulo Mota, Manuel CASTAGNONE-SERENO, PHILIPPE |
author_role |
author |
author2 |
CASTAGNONE, CHANTAL BOONHAM, NEIL TOMLINSON, JENNY LAWSON, REBECCA HOCKLAND, SUE QUILL, JAMES VIEIRA, Paulo Mota, Manuel CASTAGNONE-SERENO, PHILIPPE |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
CECILE, FRANÇOIS CASTAGNONE, CHANTAL BOONHAM, NEIL TOMLINSON, JENNY LAWSON, REBECCA HOCKLAND, SUE QUILL, JAMES VIEIRA, Paulo Mota, Manuel CASTAGNONE-SERENO, PHILIPPE |
dc.subject.por.fl_str_mv |
Bursaphelenchus xylophilus pinewood nematode |
topic |
Bursaphelenchus xylophilus pinewood nematode |
description |
The pinewood nematode (PWN), Bursaphelenchus xylophilus , is a major pathogen of conifers, which impacts on forest health, natural ecosystem stability and international trade. As a consequence, it has been listed as a quarantine organism in Europe. A real-time PCR approach based on TaqMan chemistry was developed to detect this organism. Specific probe and primers were designed based on the sequence of the Msp I satellite DNA family previously characterized in the genome of the nematode. The method proved to be specific in tests with target DNA from PWN isolates from worldwide origin. From a practical point of view, detection limit was 1 pg of target DNA or one individual nematode. In addition, PWN genomic DNA or single individuals were positively detected in mixed samples in which B. xylophilius was associated with the closely related non-pathogenic species B. mucronatus , up to the limit of 0.01% or 1% of the mixture, respectively. The real-time PCR assay was also used in conjunction with a simple DNA extraction method to detect PWN directly in artificially infested wood samples. These results demonstrate the potential of this assay to provide rapid, accurate and sensitive molecular identification of the PWN in relation to pest risk assessment in the field and quarantine regulation. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-01-01T00:00:00Z 2012-12-10T16:25:43Z 2012-12-10 |
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/10174/6790 http://hdl.handle.net/10174/6790 |
url |
http://hdl.handle.net/10174/6790 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
8 ICAAM nd nd nd nd nd nd nd pvieira@uevora.pt mmtota@uevora.pt Philippe.Castagnone@sophia.inra.fr 218 |
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info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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