Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2

ABSTARCT: It has been reported that treatment of DENV-infected cultures with Lovastatin (LOV), can affect viral assembly. The objective of this study was to evaluate the effect of LOV on the survival rate and viremia levels of DENV-2-infected AG129 mice. Methodology/Principal Findings: Mice were ino...

Full description

Autores:
Martínez Gutiérrez, Marlén
Castellanos Parra, Jaime Eduardo
Gallego Gómez, Juan Carlos
Osorio Benitez, Jorge Emilio
Correa Londoño, Luis Alfonso
Tipo de recurso:
Article of investigation
Fecha de publicación:
2014
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/11578
Acceso en línea:
http://hdl.handle.net/10495/11578
Palabra clave:
Virus del dengue
Dengue
Treatment outcome
Lovastatina
Agente antiviral
Viremia
Virus assembly
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
id UDEA2_329379f711f1ed4de0baeb2cd2c684e4
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/11578
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
title Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
spellingShingle Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
Virus del dengue
Dengue
Treatment outcome
Lovastatina
Agente antiviral
Viremia
Virus assembly
title_short Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
title_full Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
title_fullStr Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
title_full_unstemmed Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
title_sort Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2
dc.creator.fl_str_mv Martínez Gutiérrez, Marlén
Castellanos Parra, Jaime Eduardo
Gallego Gómez, Juan Carlos
Osorio Benitez, Jorge Emilio
Correa Londoño, Luis Alfonso
dc.contributor.author.none.fl_str_mv Martínez Gutiérrez, Marlén
Castellanos Parra, Jaime Eduardo
Gallego Gómez, Juan Carlos
Osorio Benitez, Jorge Emilio
Correa Londoño, Luis Alfonso
dc.contributor.researchgroup.spa.fl_str_mv Programa de Estudio y Control de Enfermedades Tropicales (PECET)
Centro de de Investigaciones Dermatológicas
Grupo Ingeniería de Tejidos y Terapias Celulares
Grupo Medicina Molecular y de Translación
dc.subject.none.fl_str_mv Virus del dengue
Dengue
Treatment outcome
Lovastatina
Agente antiviral
Viremia
Virus assembly
topic Virus del dengue
Dengue
Treatment outcome
Lovastatina
Agente antiviral
Viremia
Virus assembly
description ABSTARCT: It has been reported that treatment of DENV-infected cultures with Lovastatin (LOV), can affect viral assembly. The objective of this study was to evaluate the effect of LOV on the survival rate and viremia levels of DENV-2-infected AG129 mice. Methodology/Principal Findings: Mice were inoculated with 16106 plaque-forming units (PFU/ml) of DENV-2 and treated with LOV (200 mg/kg/day). Pre-treatment with one or three doses of LOV increased the survival rate compared to untreated mice (7.3 and 7.1 days, respectively, compared to 4.8 days). Viremia levels also decreased by 21.8% compared to untreated mice, but only in the group administered three doses prior to inoculation. When LOV was administered after viral inoculation, the survival rate increased (7.3 days in the group treated at 24 hpi, 6.8 days in the group treated at 48 hpi and 6.5 days in the group treated with two doses) compared to the untreated group (4.8 days). Interestingly, the serum viral titer increased by 24.6% in mice treated at 48 hpi with a single dose of LOV and by 21.7% in mice treated with two doses (at 24 and 48 hpi) of LOV compared to untreated mice. Finally histopathological changes in the liver and spleen in infected and untreated mice included massive extramedullary erythropoiesis foci and inflammatory filtration, and these characteristics were decreased or absent in LOV-treated mice. Conclusions/Significance: Our results suggest that the effect of LOV on viremia depends on the timing of treatment and on the number of doses administered. We observed a significant increase in the survival rate in both schemes due to a delay in the progression of the disease. However, the results obtained in the post-treatment scheme must be handled carefully because this treatment scheme increases viremia and we do not know how this increase could affect disease progression in humans.
publishDate 2014
dc.date.issued.none.fl_str_mv 2014
dc.date.accessioned.none.fl_str_mv 2019-07-30T20:00:16Z
dc.date.available.none.fl_str_mv 2019-07-30T20:00:16Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.version.spa.fl_str_mv info:eu-repo/semantics/publishedVersion
format http://purl.org/coar/resource_type/c_2df8fbb1
status_str publishedVersion
dc.identifier.citation.spa.fl_str_mv Martínez-Gutierrez M, Correa-Londoño LA, Castellanos JE, Gallego-Gómez JC, Osorio JE. Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2. PLoS One. 2014 Feb 21;9(2):e87412
dc.identifier.issn.none.fl_str_mv 1932-6203
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/11578
dc.identifier.doi.none.fl_str_mv 10.1371/journal.pone.0087412
identifier_str_mv Martínez-Gutierrez M, Correa-Londoño LA, Castellanos JE, Gallego-Gómez JC, Osorio JE. Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2. PLoS One. 2014 Feb 21;9(2):e87412
1932-6203
10.1371/journal.pone.0087412
url http://hdl.handle.net/10495/11578
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv PLoS One
dc.relation.citationendpage.spa.fl_str_mv 11
dc.relation.citationissue.spa.fl_str_mv 2
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 9
dc.relation.ispartofjournal.spa.fl_str_mv PLoS One
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by/2.5/co/
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by/4.0/
dc.rights.accessrights.*.fl_str_mv Atribución 2.5
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.coar.spa.fl_str_mv http://purl.org/coar/access_right/c_abf2
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/co/
https://creativecommons.org/licenses/by/4.0/
Atribución 2.5
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.extent.spa.fl_str_mv 10
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Public Library of Science
dc.publisher.place.spa.fl_str_mv San Francisco, Estados Unidos
institution Universidad de Antioquia
bitstream.url.fl_str_mv https://bibliotecadigital.udea.edu.co/bitstreams/fab7c17a-b0db-4ddf-9029-3c2270611828/download
https://bibliotecadigital.udea.edu.co/bitstreams/fe75aaed-5c0c-45a5-aa80-d3409ea7fcbf/download
https://bibliotecadigital.udea.edu.co/bitstreams/84e4db71-025b-478d-9d5d-b27f220eaf6b/download
https://bibliotecadigital.udea.edu.co/bitstreams/4f53739c-d8b3-40d2-a6fd-70191f6431a0/download
https://bibliotecadigital.udea.edu.co/bitstreams/c47ab2a4-7ca4-40e3-bf77-fbcbf483c1a6/download
https://bibliotecadigital.udea.edu.co/bitstreams/2f149ac0-65d9-4528-80b5-31797e4c79ee/download
https://bibliotecadigital.udea.edu.co/bitstreams/37c2db93-954e-4436-a74c-162ba0c7c83c/download
bitstream.checksum.fl_str_mv 1ea2e125400b722587f4a21799fae9e6
4afdbb8c545fd630ea7db775da747b2f
d41d8cd98f00b204e9800998ecf8427e
d41d8cd98f00b204e9800998ecf8427e
8a4605be74aa9ea9d79846c1fba20a33
1995043c6046867e3bf328c52b11ba18
bf832bb1069a0c716ff75ca9a3d6859c
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv Repositorio Institucional de la Universidad de Antioquia
repository.mail.fl_str_mv aplicacionbibliotecadigitalbiblioteca@udea.edu.co
_version_ 1851052393794371584
spelling Martínez Gutiérrez, MarlénCastellanos Parra, Jaime EduardoGallego Gómez, Juan CarlosOsorio Benitez, Jorge EmilioCorrea Londoño, Luis AlfonsoPrograma de Estudio y Control de Enfermedades Tropicales (PECET)Centro de de Investigaciones DermatológicasGrupo Ingeniería de Tejidos y Terapias CelularesGrupo Medicina Molecular y de Translación2019-07-30T20:00:16Z2019-07-30T20:00:16Z2014Martínez-Gutierrez M, Correa-Londoño LA, Castellanos JE, Gallego-Gómez JC, Osorio JE. Lovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2. PLoS One. 2014 Feb 21;9(2):e874121932-6203http://hdl.handle.net/10495/1157810.1371/journal.pone.0087412ABSTARCT: It has been reported that treatment of DENV-infected cultures with Lovastatin (LOV), can affect viral assembly. The objective of this study was to evaluate the effect of LOV on the survival rate and viremia levels of DENV-2-infected AG129 mice. Methodology/Principal Findings: Mice were inoculated with 16106 plaque-forming units (PFU/ml) of DENV-2 and treated with LOV (200 mg/kg/day). Pre-treatment with one or three doses of LOV increased the survival rate compared to untreated mice (7.3 and 7.1 days, respectively, compared to 4.8 days). Viremia levels also decreased by 21.8% compared to untreated mice, but only in the group administered three doses prior to inoculation. When LOV was administered after viral inoculation, the survival rate increased (7.3 days in the group treated at 24 hpi, 6.8 days in the group treated at 48 hpi and 6.5 days in the group treated with two doses) compared to the untreated group (4.8 days). Interestingly, the serum viral titer increased by 24.6% in mice treated at 48 hpi with a single dose of LOV and by 21.7% in mice treated with two doses (at 24 and 48 hpi) of LOV compared to untreated mice. Finally histopathological changes in the liver and spleen in infected and untreated mice included massive extramedullary erythropoiesis foci and inflammatory filtration, and these characteristics were decreased or absent in LOV-treated mice. Conclusions/Significance: Our results suggest that the effect of LOV on viremia depends on the timing of treatment and on the number of doses administered. We observed a significant increase in the survival rate in both schemes due to a delay in the progression of the disease. However, the results obtained in the post-treatment scheme must be handled carefully because this treatment scheme increases viremia and we do not know how this increase could affect disease progression in humans.COL0015099COL0130733COL0027213COL014013910application/pdfengPublic Library of ScienceSan Francisco, Estados Unidoshttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/Atribución 2.5info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Virus del dengueDengueTreatment outcomeLovastatinaAgente antiviralViremiaVirus assemblyLovastatin delays infection and increases survival rates in AG129 mice infected with dengue virus serotype 2Artículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPLoS One11219PLoS OnePublicationORIGINALMartinezMarlen_2014_LovastatinInfectionIncreases.pdfMartinezMarlen_2014_LovastatinInfectionIncreases.pdfArtículo de investigaciónapplication/pdf14180057https://bibliotecadigital.udea.edu.co/bitstreams/fab7c17a-b0db-4ddf-9029-3c2270611828/download1ea2e125400b722587f4a21799fae9e6MD51trueAnonymousREADCC-LICENSElicense_urllicense_urltext/plain; charset=utf-849https://bibliotecadigital.udea.edu.co/bitstreams/fe75aaed-5c0c-45a5-aa80-d3409ea7fcbf/download4afdbb8c545fd630ea7db775da747b2fMD52falseAnonymousREADlicense_textlicense_texttext/html; charset=utf-80https://bibliotecadigital.udea.edu.co/bitstreams/84e4db71-025b-478d-9d5d-b27f220eaf6b/downloadd41d8cd98f00b204e9800998ecf8427eMD53falseAnonymousREADlicense_rdflicense_rdfapplication/rdf+xml; charset=utf-80https://bibliotecadigital.udea.edu.co/bitstreams/4f53739c-d8b3-40d2-a6fd-70191f6431a0/downloadd41d8cd98f00b204e9800998ecf8427eMD54falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/c47ab2a4-7ca4-40e3-bf77-fbcbf483c1a6/download8a4605be74aa9ea9d79846c1fba20a33MD55falseAnonymousREADTEXTMartinezMarlen_2014_LovastatinInfectionIncreases.pdf.txtMartinezMarlen_2014_LovastatinInfectionIncreases.pdf.txtExtracted texttext/plain55105https://bibliotecadigital.udea.edu.co/bitstreams/2f149ac0-65d9-4528-80b5-31797e4c79ee/download1995043c6046867e3bf328c52b11ba18MD56falseAnonymousREADTHUMBNAILMartinezMarlen_2014_LovastatinInfectionIncreases.pdf.jpgMartinezMarlen_2014_LovastatinInfectionIncreases.pdf.jpgGenerated Thumbnailimage/jpeg17542https://bibliotecadigital.udea.edu.co/bitstreams/37c2db93-954e-4436-a74c-162ba0c7c83c/downloadbf832bb1069a0c716ff75ca9a3d6859cMD57falseAnonymousREAD10495/11578oai:bibliotecadigital.udea.edu.co:10495/115782025-03-26 21:36:22.994http://creativecommons.org/licenses/by/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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