In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells

Present DNA vaccines against fish rhabdoviruses require intramuscular injection (fish-to-fish vaccination) of their G-protein gene under the control of the human immediate early cytomegalovirus (IE-CMV) promoter, while immersion delivery (mass DNA vaccination), for instance, by using fish epithelial-specific promoters, would be more practical for aquaculture. To find fish epithelial-specific promoters alternative to the IE-CMV, a comparative study of the effectiveness of different fish promoters constitutively expressing the G gene of the viral haemorrhagic septicemia virus (VHSV) in the epithelial papulosum cyprini (EPC) cell line was performed. The study included MCV1.4 (an alternative IE-CMV promoter version), AE6 (a version of the carp β-actin promoter), long terminal repeats (LTR) of zebrafish or walleye retroviruses, trout Mx1, carp myosin-heavy-chain and flatfish pleurocidin promoters and salmonid sleeping beauty (SB)/medaka Tol2 transposon repeats. The G-protein expression in transfected EPC cells was studied by estimating the number of cells expressing the G-protein in their membrane and the average expression level per cell. In addition, in an attempt to reduce their sizes, some regions of the MCV1.4 and AE6 promoters were deleted and expression levels compared to those observed for full-length promoters. Since both zebrafish LTR and carp AE6 promoters were the most effective regulatory sequences for expressing the VHSV G-protein in EPC cells, these sequences might be candidates for new DNA vaccine vectors for fish epithelial tissues avoiding the IE-CMV promoter. Furthermore, known transcription factor binding sites (TFBS) common to most of the fish G-expressing promoters, might enable the future design of fully synthetic or hybrid promoters with improved efficacy of VHSV G-protein expression in epithelial fish cells. © 2008 Elsevier Ltd. All rights reserved.

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Main Authors: Ruiz, Sophie, Tafalla, Carolina, Cuesta, Alberto, Estepa, Amparo, Coll Morales, Julio
Other Authors: Tafalla, Carolina [0000-0002-0860-2976]
Format: artículo biblioteca
Language:English
Published: Elsevier 2008
Subjects:VHSV, Viral haemorrhagic septicemia viruses, G-protein, Fish DNA vaccines, Epithelial vaccines, Promoters, Transcription binding sites,
Online Access:http://hdl.handle.net/10261/292572
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spelling dig-inia-es-10261-2925722024-10-24T13:01:11Z In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells Ruiz, Sophie Tafalla, Carolina Cuesta, Alberto Estepa, Amparo Coll Morales, Julio Tafalla, Carolina [0000-0002-0860-2976] Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] VHSV Viral haemorrhagic septicemia viruses G-protein Fish DNA vaccines Epithelial vaccines Promoters Transcription binding sites Present DNA vaccines against fish rhabdoviruses require intramuscular injection (fish-to-fish vaccination) of their G-protein gene under the control of the human immediate early cytomegalovirus (IE-CMV) promoter, while immersion delivery (mass DNA vaccination), for instance, by using fish epithelial-specific promoters, would be more practical for aquaculture. To find fish epithelial-specific promoters alternative to the IE-CMV, a comparative study of the effectiveness of different fish promoters constitutively expressing the G gene of the viral haemorrhagic septicemia virus (VHSV) in the epithelial papulosum cyprini (EPC) cell line was performed. The study included MCV1.4 (an alternative IE-CMV promoter version), AE6 (a version of the carp β-actin promoter), long terminal repeats (LTR) of zebrafish or walleye retroviruses, trout Mx1, carp myosin-heavy-chain and flatfish pleurocidin promoters and salmonid sleeping beauty (SB)/medaka Tol2 transposon repeats. The G-protein expression in transfected EPC cells was studied by estimating the number of cells expressing the G-protein in their membrane and the average expression level per cell. In addition, in an attempt to reduce their sizes, some regions of the MCV1.4 and AE6 promoters were deleted and expression levels compared to those observed for full-length promoters. Since both zebrafish LTR and carp AE6 promoters were the most effective regulatory sequences for expressing the VHSV G-protein in EPC cells, these sequences might be candidates for new DNA vaccine vectors for fish epithelial tissues avoiding the IE-CMV promoter. Furthermore, known transcription factor binding sites (TFBS) common to most of the fish G-expressing promoters, might enable the future design of fully synthetic or hybrid promoters with improved efficacy of VHSV G-protein expression in epithelial fish cells. © 2008 Elsevier Ltd. All rights reserved. Peer reviewed 2023-02-20T07:30:18Z 2023-02-20T07:30:18Z 2008 artículo http://purl.org/coar/resource_type/c_6501 Vaccine 26(51): 6620-6629 (2008) 0264-410X http://hdl.handle.net/10261/292572 10.1016/j.vaccine.2008.09.048 en Departamento de Biotecnología Sí open Elsevier
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic VHSV
Viral haemorrhagic septicemia viruses
G-protein
Fish DNA vaccines
Epithelial vaccines
Promoters
Transcription binding sites
VHSV
Viral haemorrhagic septicemia viruses
G-protein
Fish DNA vaccines
Epithelial vaccines
Promoters
Transcription binding sites
spellingShingle VHSV
Viral haemorrhagic septicemia viruses
G-protein
Fish DNA vaccines
Epithelial vaccines
Promoters
Transcription binding sites
VHSV
Viral haemorrhagic septicemia viruses
G-protein
Fish DNA vaccines
Epithelial vaccines
Promoters
Transcription binding sites
Ruiz, Sophie
Tafalla, Carolina
Cuesta, Alberto
Estepa, Amparo
Coll Morales, Julio
In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells
description Present DNA vaccines against fish rhabdoviruses require intramuscular injection (fish-to-fish vaccination) of their G-protein gene under the control of the human immediate early cytomegalovirus (IE-CMV) promoter, while immersion delivery (mass DNA vaccination), for instance, by using fish epithelial-specific promoters, would be more practical for aquaculture. To find fish epithelial-specific promoters alternative to the IE-CMV, a comparative study of the effectiveness of different fish promoters constitutively expressing the G gene of the viral haemorrhagic septicemia virus (VHSV) in the epithelial papulosum cyprini (EPC) cell line was performed. The study included MCV1.4 (an alternative IE-CMV promoter version), AE6 (a version of the carp β-actin promoter), long terminal repeats (LTR) of zebrafish or walleye retroviruses, trout Mx1, carp myosin-heavy-chain and flatfish pleurocidin promoters and salmonid sleeping beauty (SB)/medaka Tol2 transposon repeats. The G-protein expression in transfected EPC cells was studied by estimating the number of cells expressing the G-protein in their membrane and the average expression level per cell. In addition, in an attempt to reduce their sizes, some regions of the MCV1.4 and AE6 promoters were deleted and expression levels compared to those observed for full-length promoters. Since both zebrafish LTR and carp AE6 promoters were the most effective regulatory sequences for expressing the VHSV G-protein in EPC cells, these sequences might be candidates for new DNA vaccine vectors for fish epithelial tissues avoiding the IE-CMV promoter. Furthermore, known transcription factor binding sites (TFBS) common to most of the fish G-expressing promoters, might enable the future design of fully synthetic or hybrid promoters with improved efficacy of VHSV G-protein expression in epithelial fish cells. © 2008 Elsevier Ltd. All rights reserved.
author2 Tafalla, Carolina [0000-0002-0860-2976]
author_facet Tafalla, Carolina [0000-0002-0860-2976]
Ruiz, Sophie
Tafalla, Carolina
Cuesta, Alberto
Estepa, Amparo
Coll Morales, Julio
format artículo
topic_facet VHSV
Viral haemorrhagic septicemia viruses
G-protein
Fish DNA vaccines
Epithelial vaccines
Promoters
Transcription binding sites
author Ruiz, Sophie
Tafalla, Carolina
Cuesta, Alberto
Estepa, Amparo
Coll Morales, Julio
author_sort Ruiz, Sophie
title In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells
title_short In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells
title_full In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells
title_fullStr In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells
title_full_unstemmed In vitro search for alternative promoters to the human immediate early cytomegalovirus (IE-CMV) to express the G gene of viral haemorrhagic septicemia virus (VHSV) in fish epithelial cells
title_sort in vitro search for alternative promoters to the human immediate early cytomegalovirus (ie-cmv) to express the g gene of viral haemorrhagic septicemia virus (vhsv) in fish epithelial cells
publisher Elsevier
publishDate 2008
url http://hdl.handle.net/10261/292572
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