Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells
- Autores
- Mignaqui, Ana Clara; Ruiz, Vanesa; Wigdorovitz, Andres
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Foot-and-mouth disease is a highly contagious disease that produces severe economic losses in the livestock industry. This disease is being controlled by the use of an inactivated vaccine. However, the use of recombinant empty capsids as a subunit vaccine has been reported to be a promising candidate because it avoids the use of virus in the vaccine production. A plasmid containing the capsid precursor P12A and protease 3C sequences of foot-and-mouth disease virus (FMDV) was constructed and used to compare transient and stable expression in mammalian cells. When BHK-21 cells were transfected with the recombinant vector, protease 3C cleaved the capsid precursor P12A into the structural proteins VP0, VP1 and VP3. A sucrose gradient demonstrated that the structural proteins assembled into different subviral particles. Attempts to generate a stable cell line only allowed isolating low-level-expressing clones, probably due to the effect of protease 3C on the cells. Moreover, the recombinant protein yield achieved in transient expression assays was much higher than the one achieved in stable expression assays. Results indicate that mammalian cells are a good strategy to produce recombinant FMDV subviral particles. However, the alternative approach of transient gene expression in scalable systems should be used instead of the standard method that involves the generation of a stable cell line.
Instituto de Virología
Fil: Mignaqui, Ana Clara. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina.
Fil: Ruiz, Vanesa. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina
Fil: Wigdorovitz, Andres. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina - Fuente
- Advances in Bioscience and Biotechnology 4 (12) : 1024-1029 (December 2013)
- Materia
-
Enfermedades de los Animales
Fiebre Aftosa
Expresión Génica
Células
Mamíferos
Proteínas
Animal Diseases
Foot and Mouth Disease
Gene Expression
Cells
Mammals
Proteins - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Instituto Nacional de Tecnología Agropecuaria
- OAI Identificador
- oai:localhost:20.500.12123/4278
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Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cellsMignaqui, Ana ClaraRuiz, VanesaWigdorovitz, AndresEnfermedades de los AnimalesFiebre AftosaExpresión GénicaCélulasMamíferosProteínasAnimal DiseasesFoot and Mouth DiseaseGene ExpressionCellsMammalsProteinsFoot-and-mouth disease is a highly contagious disease that produces severe economic losses in the livestock industry. This disease is being controlled by the use of an inactivated vaccine. However, the use of recombinant empty capsids as a subunit vaccine has been reported to be a promising candidate because it avoids the use of virus in the vaccine production. A plasmid containing the capsid precursor P12A and protease 3C sequences of foot-and-mouth disease virus (FMDV) was constructed and used to compare transient and stable expression in mammalian cells. When BHK-21 cells were transfected with the recombinant vector, protease 3C cleaved the capsid precursor P12A into the structural proteins VP0, VP1 and VP3. A sucrose gradient demonstrated that the structural proteins assembled into different subviral particles. Attempts to generate a stable cell line only allowed isolating low-level-expressing clones, probably due to the effect of protease 3C on the cells. Moreover, the recombinant protein yield achieved in transient expression assays was much higher than the one achieved in stable expression assays. Results indicate that mammalian cells are a good strategy to produce recombinant FMDV subviral particles. However, the alternative approach of transient gene expression in scalable systems should be used instead of the standard method that involves the generation of a stable cell line.Instituto de VirologíaFil: Mignaqui, Ana Clara. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina.Fil: Ruiz, Vanesa. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; ArgentinaFil: Wigdorovitz, Andres. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; ArgentinaScientific Research2019-01-16T17:03:09Z2019-01-16T17:03:09Z2013-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttps://www.scirp.org/journal/PaperInformation.aspx?PaperID=41054http://hdl.handle.net/20.500.12123/42782156-84562156-8502https://doi.org/10.4236/abb.2013.412137Advances in Bioscience and Biotechnology 4 (12) : 1024-1029 (December 2013)reponame:INTA Digital (INTA)instname:Instituto Nacional de Tecnología Agropecuariaenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)2025-09-29T13:44:33Zoai:localhost:20.500.12123/4278instacron:INTAInstitucionalhttp://repositorio.inta.gob.ar/Organismo científico-tecnológicoNo correspondehttp://repositorio.inta.gob.ar/oai/requesttripaldi.nicolas@inta.gob.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:l2025-09-29 13:44:33.461INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuariafalse |
dc.title.none.fl_str_mv |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
title |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
spellingShingle |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells Mignaqui, Ana Clara Enfermedades de los Animales Fiebre Aftosa Expresión Génica Células Mamíferos Proteínas Animal Diseases Foot and Mouth Disease Gene Expression Cells Mammals Proteins |
title_short |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
title_full |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
title_fullStr |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
title_full_unstemmed |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
title_sort |
Comparison of transient and stable expression of foot-and-mouth disease virus capsid proteins in mammalian cells |
dc.creator.none.fl_str_mv |
Mignaqui, Ana Clara Ruiz, Vanesa Wigdorovitz, Andres |
author |
Mignaqui, Ana Clara |
author_facet |
Mignaqui, Ana Clara Ruiz, Vanesa Wigdorovitz, Andres |
author_role |
author |
author2 |
Ruiz, Vanesa Wigdorovitz, Andres |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Enfermedades de los Animales Fiebre Aftosa Expresión Génica Células Mamíferos Proteínas Animal Diseases Foot and Mouth Disease Gene Expression Cells Mammals Proteins |
topic |
Enfermedades de los Animales Fiebre Aftosa Expresión Génica Células Mamíferos Proteínas Animal Diseases Foot and Mouth Disease Gene Expression Cells Mammals Proteins |
dc.description.none.fl_txt_mv |
Foot-and-mouth disease is a highly contagious disease that produces severe economic losses in the livestock industry. This disease is being controlled by the use of an inactivated vaccine. However, the use of recombinant empty capsids as a subunit vaccine has been reported to be a promising candidate because it avoids the use of virus in the vaccine production. A plasmid containing the capsid precursor P12A and protease 3C sequences of foot-and-mouth disease virus (FMDV) was constructed and used to compare transient and stable expression in mammalian cells. When BHK-21 cells were transfected with the recombinant vector, protease 3C cleaved the capsid precursor P12A into the structural proteins VP0, VP1 and VP3. A sucrose gradient demonstrated that the structural proteins assembled into different subviral particles. Attempts to generate a stable cell line only allowed isolating low-level-expressing clones, probably due to the effect of protease 3C on the cells. Moreover, the recombinant protein yield achieved in transient expression assays was much higher than the one achieved in stable expression assays. Results indicate that mammalian cells are a good strategy to produce recombinant FMDV subviral particles. However, the alternative approach of transient gene expression in scalable systems should be used instead of the standard method that involves the generation of a stable cell line. Instituto de Virología Fil: Mignaqui, Ana Clara. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina. Fil: Ruiz, Vanesa. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina Fil: Wigdorovitz, Andres. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina |
description |
Foot-and-mouth disease is a highly contagious disease that produces severe economic losses in the livestock industry. This disease is being controlled by the use of an inactivated vaccine. However, the use of recombinant empty capsids as a subunit vaccine has been reported to be a promising candidate because it avoids the use of virus in the vaccine production. A plasmid containing the capsid precursor P12A and protease 3C sequences of foot-and-mouth disease virus (FMDV) was constructed and used to compare transient and stable expression in mammalian cells. When BHK-21 cells were transfected with the recombinant vector, protease 3C cleaved the capsid precursor P12A into the structural proteins VP0, VP1 and VP3. A sucrose gradient demonstrated that the structural proteins assembled into different subviral particles. Attempts to generate a stable cell line only allowed isolating low-level-expressing clones, probably due to the effect of protease 3C on the cells. Moreover, the recombinant protein yield achieved in transient expression assays was much higher than the one achieved in stable expression assays. Results indicate that mammalian cells are a good strategy to produce recombinant FMDV subviral particles. However, the alternative approach of transient gene expression in scalable systems should be used instead of the standard method that involves the generation of a stable cell line. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-12 2019-01-16T17:03:09Z 2019-01-16T17:03:09Z |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://www.scirp.org/journal/PaperInformation.aspx?PaperID=41054 http://hdl.handle.net/20.500.12123/4278 2156-8456 2156-8502 https://doi.org/10.4236/abb.2013.412137 |
url |
https://www.scirp.org/journal/PaperInformation.aspx?PaperID=41054 http://hdl.handle.net/20.500.12123/4278 https://doi.org/10.4236/abb.2013.412137 |
identifier_str_mv |
2156-8456 2156-8502 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Scientific Research |
publisher.none.fl_str_mv |
Scientific Research |
dc.source.none.fl_str_mv |
Advances in Bioscience and Biotechnology 4 (12) : 1024-1029 (December 2013) reponame:INTA Digital (INTA) instname:Instituto Nacional de Tecnología Agropecuaria |
reponame_str |
INTA Digital (INTA) |
collection |
INTA Digital (INTA) |
instname_str |
Instituto Nacional de Tecnología Agropecuaria |
repository.name.fl_str_mv |
INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuaria |
repository.mail.fl_str_mv |
tripaldi.nicolas@inta.gob.ar |
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12.559606 |