Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/224237 |
Resumo: | Background: Several types and subtypes of bovine herpesviruses 1 and 5 (BoHV-1 and BoHV-5) have been associated to different clinical conditions of cattle, making type/subtype differentiation essential to understand the pathogenesis and epidemiology of BoHV infections. BoHV-5 subtyping is currently carried out by BstEII restriction enzyme analysis (REA) of the complete virus genome. This method allowed the description of three subtypes, one of which is the most widespread while the remaining two have so far only been found in South America. The present work describes a multiplex PCR followed by REA for BoHV-5 subtyping. Results: The method consists in the simultaneous amplification of glycoprotein B and UL54 gene fragments of 534 and 669 base pairs (bp), respectively, BstEII digestion of amplicons, separation of products in 1% agarose gels, and analysis of fragment length polymorphims. The multiplex PCR detected up to 227 BoHV-5 genome copies and 9.2 × 105 BoHV-5 genome copies when DNA was extracted from purified virus or infected tissue homogenates, respectively. The applicability of multiplex PCR-REA was demonstrated on 3 BoHV-5 reference strains. In addition, subtyping of two new isolates and seventeen previously reported ones (17 BHV-5a and 2 BHV-5b) by this method gave coincident results with those obtained with the classic BstEII REA assay. Conclusions: Multiplex PCR-REA provides a new tool for the fast and simple diagnosis and subtyping of BoHV-5. |
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Maidana, Silvina SoledadMorano, Cintia DeboraCianfrini, DanielaCampos, Fabrício SouzaRoehe, Paulo MichelSiedler, Bianca SicaDe Stefano, GabrielMauroy, AxelThiry, EtienneRomera, Sonia Alejandra2021-07-21T04:23:39Z20131746-6148http://hdl.handle.net/10183/224237000902718Background: Several types and subtypes of bovine herpesviruses 1 and 5 (BoHV-1 and BoHV-5) have been associated to different clinical conditions of cattle, making type/subtype differentiation essential to understand the pathogenesis and epidemiology of BoHV infections. BoHV-5 subtyping is currently carried out by BstEII restriction enzyme analysis (REA) of the complete virus genome. This method allowed the description of three subtypes, one of which is the most widespread while the remaining two have so far only been found in South America. The present work describes a multiplex PCR followed by REA for BoHV-5 subtyping. Results: The method consists in the simultaneous amplification of glycoprotein B and UL54 gene fragments of 534 and 669 base pairs (bp), respectively, BstEII digestion of amplicons, separation of products in 1% agarose gels, and analysis of fragment length polymorphims. The multiplex PCR detected up to 227 BoHV-5 genome copies and 9.2 × 105 BoHV-5 genome copies when DNA was extracted from purified virus or infected tissue homogenates, respectively. The applicability of multiplex PCR-REA was demonstrated on 3 BoHV-5 reference strains. In addition, subtyping of two new isolates and seventeen previously reported ones (17 BHV-5a and 2 BHV-5b) by this method gave coincident results with those obtained with the classic BstEII REA assay. Conclusions: Multiplex PCR-REA provides a new tool for the fast and simple diagnosis and subtyping of BoHV-5.application/pdfengBMC veterinary research. London. Vol. 9 (4 June 2013), p. 111 [7 p.]Herpesvírus bovino tipo 5Reação em cadeia da polimerasePolimorfismoMultiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolatesEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT000902718.pdf.txt000902718.pdf.txtExtracted Texttext/plain29108http://www.lume.ufrgs.br/bitstream/10183/224237/2/000902718.pdf.txt8167792ea1df0e5373f430f1de4999dbMD52ORIGINAL000902718.pdfTexto completo (inglês)application/pdf731152http://www.lume.ufrgs.br/bitstream/10183/224237/1/000902718.pdf4b05ec48d7f139740105ad354283ee3fMD5110183/2242372021-08-18 04:32:36.350425oai:www.lume.ufrgs.br:10183/224237Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2021-08-18T07:32:36Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
title |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
spellingShingle |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates Maidana, Silvina Soledad Herpesvírus bovino tipo 5 Reação em cadeia da polimerase Polimorfismo |
title_short |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
title_full |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
title_fullStr |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
title_full_unstemmed |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
title_sort |
Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates |
author |
Maidana, Silvina Soledad |
author_facet |
Maidana, Silvina Soledad Morano, Cintia Debora Cianfrini, Daniela Campos, Fabrício Souza Roehe, Paulo Michel Siedler, Bianca Sica De Stefano, Gabriel Mauroy, Axel Thiry, Etienne Romera, Sonia Alejandra |
author_role |
author |
author2 |
Morano, Cintia Debora Cianfrini, Daniela Campos, Fabrício Souza Roehe, Paulo Michel Siedler, Bianca Sica De Stefano, Gabriel Mauroy, Axel Thiry, Etienne Romera, Sonia Alejandra |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Maidana, Silvina Soledad Morano, Cintia Debora Cianfrini, Daniela Campos, Fabrício Souza Roehe, Paulo Michel Siedler, Bianca Sica De Stefano, Gabriel Mauroy, Axel Thiry, Etienne Romera, Sonia Alejandra |
dc.subject.por.fl_str_mv |
Herpesvírus bovino tipo 5 Reação em cadeia da polimerase Polimorfismo |
topic |
Herpesvírus bovino tipo 5 Reação em cadeia da polimerase Polimorfismo |
description |
Background: Several types and subtypes of bovine herpesviruses 1 and 5 (BoHV-1 and BoHV-5) have been associated to different clinical conditions of cattle, making type/subtype differentiation essential to understand the pathogenesis and epidemiology of BoHV infections. BoHV-5 subtyping is currently carried out by BstEII restriction enzyme analysis (REA) of the complete virus genome. This method allowed the description of three subtypes, one of which is the most widespread while the remaining two have so far only been found in South America. The present work describes a multiplex PCR followed by REA for BoHV-5 subtyping. Results: The method consists in the simultaneous amplification of glycoprotein B and UL54 gene fragments of 534 and 669 base pairs (bp), respectively, BstEII digestion of amplicons, separation of products in 1% agarose gels, and analysis of fragment length polymorphims. The multiplex PCR detected up to 227 BoHV-5 genome copies and 9.2 × 105 BoHV-5 genome copies when DNA was extracted from purified virus or infected tissue homogenates, respectively. The applicability of multiplex PCR-REA was demonstrated on 3 BoHV-5 reference strains. In addition, subtyping of two new isolates and seventeen previously reported ones (17 BHV-5a and 2 BHV-5b) by this method gave coincident results with those obtained with the classic BstEII REA assay. Conclusions: Multiplex PCR-REA provides a new tool for the fast and simple diagnosis and subtyping of BoHV-5. |
publishDate |
2013 |
dc.date.issued.fl_str_mv |
2013 |
dc.date.accessioned.fl_str_mv |
2021-07-21T04:23:39Z |
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Estrangeiro info:eu-repo/semantics/article |
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1746-6148 |
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000902718 |
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http://hdl.handle.net/10183/224237 |
dc.language.iso.fl_str_mv |
eng |
language |
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dc.relation.ispartof.pt_BR.fl_str_mv |
BMC veterinary research. London. Vol. 9 (4 June 2013), p. 111 [7 p.] |
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