In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells

We have found out that transfection of the RTG-2 cell line with the viral haemorrhagic septicaemia virus (VHSV) glycoprotein G (GVHSV)-coding plasmid induces an anti-VHSV state, similar to that induced by poly IC. Taking the advantage of the constitutive expression of toll-like receptor 9 gene (tlr9) in RTG-2 cells, we have investigated whether this antiviral state was induced by the cytosine-phosphodiester-guanine (CpG) motifs present in the plasmid DNA, by the endogenous expression of GVHSV protein or by both elements. For that, we have analysed the expression profile of the rainbow trout tlr9 and several genes related to TLR9-mediated immune response in the absence or presence of a lysosomotropic drug that specifically blocks TLR9-CpG DNA interaction. The results suggested that the high levels of cell protection conferred by a plasmid encoding GVHSV gene are due to GVHSV rather than to the CpG motifs within plasmid DNA. Therefore, plasmid DNA might not play a key role in the immune response elicited by DNA vaccines or perhaps other receptors instead TLR9 could be implicated in CpG motifs recognition and signalling. In addition, since RTG-2 cells express tlr9 gene, this cell line could be a good tool for screening TLR9 agonists, such as the immunomodulatory oligonucleotides (IMOs), as fish DNA vaccine adjuvants. © 2010 Elsevier Ltd.

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Main Authors: Ortega-Villaizan, M., Chico, V., Martinez-Lopez, A., Falco, A., Perez, L., Coll, J. M., Estepa, A.
Format: artículo biblioteca
Language:English
Published: Elsevier 2011
Subjects:Innate immunity, Toll-like receptor, TLR9, DNA vaccine, Viral glycoproteins, VHSV, Rhabdovirus, Rainbow trout, RTG-2 cell line, TNF, IL1, IRF3, IRF7, Mx, Unmethylated CpG motifs,
Online Access:http://hdl.handle.net/20.500.12792/3229
http://hdl.handle.net/10261/290925
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spelling dig-inia-es-10261-2909252023-02-17T12:31:00Z In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells Ortega-Villaizan, M. Chico, V. Martinez-Lopez, A. Falco, A. Perez, L. Coll, J. M. Estepa, A. Innate immunity Toll-like receptor TLR9 DNA vaccine Viral glycoproteins VHSV Rhabdovirus Rainbow trout RTG-2 cell line TNF IL1 IRF3 IRF7 Mx Unmethylated CpG motifs We have found out that transfection of the RTG-2 cell line with the viral haemorrhagic septicaemia virus (VHSV) glycoprotein G (GVHSV)-coding plasmid induces an anti-VHSV state, similar to that induced by poly IC. Taking the advantage of the constitutive expression of toll-like receptor 9 gene (tlr9) in RTG-2 cells, we have investigated whether this antiviral state was induced by the cytosine-phosphodiester-guanine (CpG) motifs present in the plasmid DNA, by the endogenous expression of GVHSV protein or by both elements. For that, we have analysed the expression profile of the rainbow trout tlr9 and several genes related to TLR9-mediated immune response in the absence or presence of a lysosomotropic drug that specifically blocks TLR9-CpG DNA interaction. The results suggested that the high levels of cell protection conferred by a plasmid encoding GVHSV gene are due to GVHSV rather than to the CpG motifs within plasmid DNA. Therefore, plasmid DNA might not play a key role in the immune response elicited by DNA vaccines or perhaps other receptors instead TLR9 could be implicated in CpG motifs recognition and signalling. In addition, since RTG-2 cells express tlr9 gene, this cell line could be a good tool for screening TLR9 agonists, such as the immunomodulatory oligonucleotides (IMOs), as fish DNA vaccine adjuvants. © 2010 Elsevier Ltd. 2023-02-17T12:31:00Z 2023-02-17T12:31:00Z 2011 artículo Vaccine 29: 737-743 (2011) 0264-410X http://hdl.handle.net/20.500.12792/3229 http://hdl.handle.net/10261/290925 10.1016/j.vaccine.2010.11.021 en none 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 Innate immunity
Toll-like receptor
TLR9
DNA vaccine
Viral glycoproteins
VHSV
Rhabdovirus
Rainbow trout
RTG-2 cell line
TNF
IL1
IRF3
IRF7
Mx
Unmethylated CpG motifs
Innate immunity
Toll-like receptor
TLR9
DNA vaccine
Viral glycoproteins
VHSV
Rhabdovirus
Rainbow trout
RTG-2 cell line
TNF
IL1
IRF3
IRF7
Mx
Unmethylated CpG motifs
spellingShingle Innate immunity
Toll-like receptor
TLR9
DNA vaccine
Viral glycoproteins
VHSV
Rhabdovirus
Rainbow trout
RTG-2 cell line
TNF
IL1
IRF3
IRF7
Mx
Unmethylated CpG motifs
Innate immunity
Toll-like receptor
TLR9
DNA vaccine
Viral glycoproteins
VHSV
Rhabdovirus
Rainbow trout
RTG-2 cell line
TNF
IL1
IRF3
IRF7
Mx
Unmethylated CpG motifs
Ortega-Villaizan, M.
Chico, V.
Martinez-Lopez, A.
Falco, A.
Perez, L.
Coll, J. M.
Estepa, A.
In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells
description We have found out that transfection of the RTG-2 cell line with the viral haemorrhagic septicaemia virus (VHSV) glycoprotein G (GVHSV)-coding plasmid induces an anti-VHSV state, similar to that induced by poly IC. Taking the advantage of the constitutive expression of toll-like receptor 9 gene (tlr9) in RTG-2 cells, we have investigated whether this antiviral state was induced by the cytosine-phosphodiester-guanine (CpG) motifs present in the plasmid DNA, by the endogenous expression of GVHSV protein or by both elements. For that, we have analysed the expression profile of the rainbow trout tlr9 and several genes related to TLR9-mediated immune response in the absence or presence of a lysosomotropic drug that specifically blocks TLR9-CpG DNA interaction. The results suggested that the high levels of cell protection conferred by a plasmid encoding GVHSV gene are due to GVHSV rather than to the CpG motifs within plasmid DNA. Therefore, plasmid DNA might not play a key role in the immune response elicited by DNA vaccines or perhaps other receptors instead TLR9 could be implicated in CpG motifs recognition and signalling. In addition, since RTG-2 cells express tlr9 gene, this cell line could be a good tool for screening TLR9 agonists, such as the immunomodulatory oligonucleotides (IMOs), as fish DNA vaccine adjuvants. © 2010 Elsevier Ltd.
format artículo
topic_facet Innate immunity
Toll-like receptor
TLR9
DNA vaccine
Viral glycoproteins
VHSV
Rhabdovirus
Rainbow trout
RTG-2 cell line
TNF
IL1
IRF3
IRF7
Mx
Unmethylated CpG motifs
author Ortega-Villaizan, M.
Chico, V.
Martinez-Lopez, A.
Falco, A.
Perez, L.
Coll, J. M.
Estepa, A.
author_facet Ortega-Villaizan, M.
Chico, V.
Martinez-Lopez, A.
Falco, A.
Perez, L.
Coll, J. M.
Estepa, A.
author_sort Ortega-Villaizan, M.
title In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells
title_short In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells
title_full In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells
title_fullStr In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells
title_full_unstemmed In vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein G in transfected trout cells
title_sort in vitro analysis of the factors contributing to the antiviral state induced by a plasmid encoding the viral haemorrhagic septicaemia virus glycoprotein g in transfected trout cells
publisher Elsevier
publishDate 2011
url http://hdl.handle.net/20.500.12792/3229
http://hdl.handle.net/10261/290925
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