Multiplex PCR followed by restriction length polymorphism analysis for the subtyping of bovine herpesvirus 5 isolates

Detalhes bibliográficos
Autor(a) principal: Maidana, Silvina Soledad
Data de Publicação: 2013
Outros Autores: Morano, Cintia Debora, Cianfrini, Daniela, Campos, Fabrício Souza, Roehe, Paulo Michel, Siedler, Bianca Sica, De Stefano, Gabriel, Mauroy, Axel, Thiry, Etienne, Romera, Sonia Alejandra
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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spelling 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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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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