Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype
- Autores
- Carlucci, Maria Josefina; Scolaro, Luis Alberto; Damonte, Elsa Beatriz
- Año de publicación
- 2002
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Natural carrageenans of diverse structural types isolated from the red seaweed Gigartina skottsbergii have been recently identified as potent and selective inhibitors of herpes simplex virus (HSV) types 1 and 2. The m/n carrageenan 1C3 was tested in vitro for its ability to select resistant variants. After serial passages of HSV-1 strain F in Vero cells in the presence of increasing concentrations of 1C3, there emerged viruses which were approximately 2-10 fold more resistant to 1C3 inhibition than parental virus and formed large plaques with an altered syncytial phenotype (1C3-syn). Plaque-purified syncytial variants isolated from passages 13 and 14 have shown variable levels of resistance to 1C3 as well as to the other antiviral carrageenans isolated from G. skottsbergii, and to other sulfated polysaccharides with known antiviral activity, such as heparin and dextran sulfate 8000, but all the clones were susceptible to acyclovir. The syn phenotype was not related to polysaccharide-resistance. All the 1C3-syn variants formed large syncytia in Vero and CV-1 cells, but did not induce fusion in other cell types. The growth efficiency in Vero cells as well as the virulence for mice by intracerebral or intraperitoneal inoculation of 1C3-syn variants showed no significative alterations in comparison to the parental virus. The syncytial properties were not affected by cyclosporin A or melittin, suggesting that an alteration on glycoprotein gB could be responsible of the syn phenotype induced by 1C3.
Fil: Carlucci, Maria Josefina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina
Fil: Scolaro, Luis Alberto. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Damonte, Elsa Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina - Materia
-
herpes simplex virus
carrageenan
viral variant - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/102827
Ver los metadatos del registro completo
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spelling |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotypeCarlucci, Maria JosefinaScolaro, Luis AlbertoDamonte, Elsa Beatrizherpes simplex viruscarrageenanviral varianthttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Natural carrageenans of diverse structural types isolated from the red seaweed Gigartina skottsbergii have been recently identified as potent and selective inhibitors of herpes simplex virus (HSV) types 1 and 2. The m/n carrageenan 1C3 was tested in vitro for its ability to select resistant variants. After serial passages of HSV-1 strain F in Vero cells in the presence of increasing concentrations of 1C3, there emerged viruses which were approximately 2-10 fold more resistant to 1C3 inhibition than parental virus and formed large plaques with an altered syncytial phenotype (1C3-syn). Plaque-purified syncytial variants isolated from passages 13 and 14 have shown variable levels of resistance to 1C3 as well as to the other antiviral carrageenans isolated from G. skottsbergii, and to other sulfated polysaccharides with known antiviral activity, such as heparin and dextran sulfate 8000, but all the clones were susceptible to acyclovir. The syn phenotype was not related to polysaccharide-resistance. All the 1C3-syn variants formed large syncytia in Vero and CV-1 cells, but did not induce fusion in other cell types. The growth efficiency in Vero cells as well as the virulence for mice by intracerebral or intraperitoneal inoculation of 1C3-syn variants showed no significative alterations in comparison to the parental virus. The syncytial properties were not affected by cyclosporin A or melittin, suggesting that an alteration on glycoprotein gB could be responsible of the syn phenotype induced by 1C3.Fil: Carlucci, Maria Josefina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; ArgentinaFil: Scolaro, Luis Alberto. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Damonte, Elsa Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; ArgentinaWiley-liss, Div John Wiley & Sons Inc2002-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/mswordapplication/mswordapplication/pdfhttp://hdl.handle.net/11336/102827Carlucci, Maria Josefina; Scolaro, Luis Alberto; Damonte, Elsa Beatriz; Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype; Wiley-liss, Div John Wiley & Sons Inc; Journal of Medical Virology; 68; 1; 9-2002; 92-980146-6615CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/jmv.10174info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jmv.10174info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:56:00Zoai:ri.conicet.gov.ar:11336/102827instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:56:00.496CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
title |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
spellingShingle |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype Carlucci, Maria Josefina herpes simplex virus carrageenan viral variant |
title_short |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
title_full |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
title_fullStr |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
title_full_unstemmed |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
title_sort |
Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype |
dc.creator.none.fl_str_mv |
Carlucci, Maria Josefina Scolaro, Luis Alberto Damonte, Elsa Beatriz |
author |
Carlucci, Maria Josefina |
author_facet |
Carlucci, Maria Josefina Scolaro, Luis Alberto Damonte, Elsa Beatriz |
author_role |
author |
author2 |
Scolaro, Luis Alberto Damonte, Elsa Beatriz |
author2_role |
author author |
dc.subject.none.fl_str_mv |
herpes simplex virus carrageenan viral variant |
topic |
herpes simplex virus carrageenan viral variant |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Natural carrageenans of diverse structural types isolated from the red seaweed Gigartina skottsbergii have been recently identified as potent and selective inhibitors of herpes simplex virus (HSV) types 1 and 2. The m/n carrageenan 1C3 was tested in vitro for its ability to select resistant variants. After serial passages of HSV-1 strain F in Vero cells in the presence of increasing concentrations of 1C3, there emerged viruses which were approximately 2-10 fold more resistant to 1C3 inhibition than parental virus and formed large plaques with an altered syncytial phenotype (1C3-syn). Plaque-purified syncytial variants isolated from passages 13 and 14 have shown variable levels of resistance to 1C3 as well as to the other antiviral carrageenans isolated from G. skottsbergii, and to other sulfated polysaccharides with known antiviral activity, such as heparin and dextran sulfate 8000, but all the clones were susceptible to acyclovir. The syn phenotype was not related to polysaccharide-resistance. All the 1C3-syn variants formed large syncytia in Vero and CV-1 cells, but did not induce fusion in other cell types. The growth efficiency in Vero cells as well as the virulence for mice by intracerebral or intraperitoneal inoculation of 1C3-syn variants showed no significative alterations in comparison to the parental virus. The syncytial properties were not affected by cyclosporin A or melittin, suggesting that an alteration on glycoprotein gB could be responsible of the syn phenotype induced by 1C3. Fil: Carlucci, Maria Josefina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina Fil: Scolaro, Luis Alberto. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Damonte, Elsa Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Biológica. Laboratorio de Virología; Argentina |
description |
Natural carrageenans of diverse structural types isolated from the red seaweed Gigartina skottsbergii have been recently identified as potent and selective inhibitors of herpes simplex virus (HSV) types 1 and 2. The m/n carrageenan 1C3 was tested in vitro for its ability to select resistant variants. After serial passages of HSV-1 strain F in Vero cells in the presence of increasing concentrations of 1C3, there emerged viruses which were approximately 2-10 fold more resistant to 1C3 inhibition than parental virus and formed large plaques with an altered syncytial phenotype (1C3-syn). Plaque-purified syncytial variants isolated from passages 13 and 14 have shown variable levels of resistance to 1C3 as well as to the other antiviral carrageenans isolated from G. skottsbergii, and to other sulfated polysaccharides with known antiviral activity, such as heparin and dextran sulfate 8000, but all the clones were susceptible to acyclovir. The syn phenotype was not related to polysaccharide-resistance. All the 1C3-syn variants formed large syncytia in Vero and CV-1 cells, but did not induce fusion in other cell types. The growth efficiency in Vero cells as well as the virulence for mice by intracerebral or intraperitoneal inoculation of 1C3-syn variants showed no significative alterations in comparison to the parental virus. The syncytial properties were not affected by cyclosporin A or melittin, suggesting that an alteration on glycoprotein gB could be responsible of the syn phenotype induced by 1C3. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002-09 |
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 |
http://hdl.handle.net/11336/102827 Carlucci, Maria Josefina; Scolaro, Luis Alberto; Damonte, Elsa Beatriz; Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype; Wiley-liss, Div John Wiley & Sons Inc; Journal of Medical Virology; 68; 1; 9-2002; 92-98 0146-6615 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/102827 |
identifier_str_mv |
Carlucci, Maria Josefina; Scolaro, Luis Alberto; Damonte, Elsa Beatriz; Herpes simplex virus type 1 variants arising after selection with an antiviral carrageenan: Lack of correlation between drug susceptibility and syn phenotype; Wiley-liss, Div John Wiley & Sons Inc; Journal of Medical Virology; 68; 1; 9-2002; 92-98 0146-6615 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1002/jmv.10174 info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jmv.10174 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/msword application/msword application/pdf |
dc.publisher.none.fl_str_mv |
Wiley-liss, Div John Wiley & Sons Inc |
publisher.none.fl_str_mv |
Wiley-liss, Div John Wiley & Sons Inc |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269376859865088 |
score |
13.13397 |