Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection
- Autores
- Liu, Shumei; Rodriguez, Ana Virginia; Tosteson, Magdalena T.
- Año de publicación
- 2006
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Cells exposed to simvastatin or to methyl-β-cyclodextrin show reduced poliovirus infection, without alteration in virus binding or on the kinetics of genome entry, suggesting that the steps which are altered are those post uncoating and genome entry. Reduction of infection by cyclodextrin is reversed by increasing MOI whereas that produced by simvastatin treatment is not, suggesting that the effects on infection are not due to a reduction in cholesterol. The differences in the characteristics of inhibition can be explained by the differential effects of the compounds. Cyclodextrin inhibits the store-operated calcium channels, suggesting that reduction in infection is through translational inhibition. Simvastatin produces vesicles from internal membranes which cannot sustain viral RNA synthesis, reducing infection through reduced transcription. The results indicate that the impact on viral infection by the cholesterol-modifying agents is due to the cellular changes produced rather than due to disruption of the cholesterol-rich domains.
Fil: Liu, Shumei. Harvard Medical School; Estados Unidos
Fil: Rodriguez, Ana Virginia. Harvard Medical School; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Tosteson, Magdalena T.. Harvard Medical School; Estados Unidos - Materia
-
Cholesterol
Cyclodextrin
Poliovirus Infection
Simvastatin
Socc - 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:11336/56496
Ver los metadatos del registro completo
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Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infectionLiu, ShumeiRodriguez, Ana VirginiaTosteson, Magdalena T.CholesterolCyclodextrinPoliovirus InfectionSimvastatinSocchttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Cells exposed to simvastatin or to methyl-β-cyclodextrin show reduced poliovirus infection, without alteration in virus binding or on the kinetics of genome entry, suggesting that the steps which are altered are those post uncoating and genome entry. Reduction of infection by cyclodextrin is reversed by increasing MOI whereas that produced by simvastatin treatment is not, suggesting that the effects on infection are not due to a reduction in cholesterol. The differences in the characteristics of inhibition can be explained by the differential effects of the compounds. Cyclodextrin inhibits the store-operated calcium channels, suggesting that reduction in infection is through translational inhibition. Simvastatin produces vesicles from internal membranes which cannot sustain viral RNA synthesis, reducing infection through reduced transcription. The results indicate that the impact on viral infection by the cholesterol-modifying agents is due to the cellular changes produced rather than due to disruption of the cholesterol-rich domains.Fil: Liu, Shumei. Harvard Medical School; Estados UnidosFil: Rodriguez, Ana Virginia. Harvard Medical School; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; ArgentinaFil: Tosteson, Magdalena T.. Harvard Medical School; Estados UnidosAcademic Press Inc Elsevier Science2006-08-18info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/56496Liu, Shumei; Rodriguez, Ana Virginia; Tosteson, Magdalena T.; Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection; Academic Press Inc Elsevier Science; Biochemical and Biophysical Research Communications; 347; 1; 18-8-2006; 51-590006-291X1090-2104CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.bbrc.2006.06.107info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0006291X06013155info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:45:46Zoai:ri.conicet.gov.ar:11336/56496instacron: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:34982025-09-29 10:45:46.261CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
title |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
spellingShingle |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection Liu, Shumei Cholesterol Cyclodextrin Poliovirus Infection Simvastatin Socc |
title_short |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
title_full |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
title_fullStr |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
title_full_unstemmed |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
title_sort |
Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection |
dc.creator.none.fl_str_mv |
Liu, Shumei Rodriguez, Ana Virginia Tosteson, Magdalena T. |
author |
Liu, Shumei |
author_facet |
Liu, Shumei Rodriguez, Ana Virginia Tosteson, Magdalena T. |
author_role |
author |
author2 |
Rodriguez, Ana Virginia Tosteson, Magdalena T. |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Cholesterol Cyclodextrin Poliovirus Infection Simvastatin Socc |
topic |
Cholesterol Cyclodextrin Poliovirus Infection Simvastatin Socc |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Cells exposed to simvastatin or to methyl-β-cyclodextrin show reduced poliovirus infection, without alteration in virus binding or on the kinetics of genome entry, suggesting that the steps which are altered are those post uncoating and genome entry. Reduction of infection by cyclodextrin is reversed by increasing MOI whereas that produced by simvastatin treatment is not, suggesting that the effects on infection are not due to a reduction in cholesterol. The differences in the characteristics of inhibition can be explained by the differential effects of the compounds. Cyclodextrin inhibits the store-operated calcium channels, suggesting that reduction in infection is through translational inhibition. Simvastatin produces vesicles from internal membranes which cannot sustain viral RNA synthesis, reducing infection through reduced transcription. The results indicate that the impact on viral infection by the cholesterol-modifying agents is due to the cellular changes produced rather than due to disruption of the cholesterol-rich domains. Fil: Liu, Shumei. Harvard Medical School; Estados Unidos Fil: Rodriguez, Ana Virginia. Harvard Medical School; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina Fil: Tosteson, Magdalena T.. Harvard Medical School; Estados Unidos |
description |
Cells exposed to simvastatin or to methyl-β-cyclodextrin show reduced poliovirus infection, without alteration in virus binding or on the kinetics of genome entry, suggesting that the steps which are altered are those post uncoating and genome entry. Reduction of infection by cyclodextrin is reversed by increasing MOI whereas that produced by simvastatin treatment is not, suggesting that the effects on infection are not due to a reduction in cholesterol. The differences in the characteristics of inhibition can be explained by the differential effects of the compounds. Cyclodextrin inhibits the store-operated calcium channels, suggesting that reduction in infection is through translational inhibition. Simvastatin produces vesicles from internal membranes which cannot sustain viral RNA synthesis, reducing infection through reduced transcription. The results indicate that the impact on viral infection by the cholesterol-modifying agents is due to the cellular changes produced rather than due to disruption of the cholesterol-rich domains. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-08-18 |
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/11336/56496 Liu, Shumei; Rodriguez, Ana Virginia; Tosteson, Magdalena T.; Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection; Academic Press Inc Elsevier Science; Biochemical and Biophysical Research Communications; 347; 1; 18-8-2006; 51-59 0006-291X 1090-2104 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/56496 |
identifier_str_mv |
Liu, Shumei; Rodriguez, Ana Virginia; Tosteson, Magdalena T.; Role of simvastatin and methyl-β-cyclodextin on inhibition of poliovirus infection; Academic Press Inc Elsevier Science; Biochemical and Biophysical Research Communications; 347; 1; 18-8-2006; 51-59 0006-291X 1090-2104 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.bbrc.2006.06.107 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0006291X06013155 |
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/pdf |
dc.publisher.none.fl_str_mv |
Academic Press Inc Elsevier Science |
publisher.none.fl_str_mv |
Academic Press Inc Elsevier Science |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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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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13.070432 |