A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging

ABSTRACT: Dengue virus (DENV) infection is the most arbovirosis in the world. However, medications have not been approved for its treatment. Drug discovery based on the host-targeted antiviral (HTA) constitutes a new promising strategy, considering their high genetic barrier to resistance and the lo...

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Autores:
Miranda Brand, Yaneth
Roa Linares, Vicky Constanza
Santiago Dugarte, Carolina
Del Olmo, Esther
López Pérez, José Luis
Betancur Galvis, Liliana Amparo
Gallego Gómez, Juan Carlos
San Feliciano, Arturo
Tipo de recurso:
Article of investigation
Fecha de publicación:
2023
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/43349
Acceso en línea:
https://hdl.handle.net/10495/43349
Palabra clave:
Antivirales
Antiviral Agents
Técnicas de Cultivo de Célula
Cell Culture Techniques
Virus del Dengue
Dengue Virus
Virosis
Virus Diseases
Replicación Viral
Virus Replication
https://id.nlm.nih.gov/mesh/D000998
https://id.nlm.nih.gov/mesh/D018929
https://id.nlm.nih.gov/mesh/D003716
https://id.nlm.nih.gov/mesh/D014777
https://id.nlm.nih.gov/mesh/D014779
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
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repository_id_str
dc.title.spa.fl_str_mv A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
title A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
spellingShingle A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
Antivirales
Antiviral Agents
Técnicas de Cultivo de Célula
Cell Culture Techniques
Virus del Dengue
Dengue Virus
Virosis
Virus Diseases
Replicación Viral
Virus Replication
https://id.nlm.nih.gov/mesh/D000998
https://id.nlm.nih.gov/mesh/D018929
https://id.nlm.nih.gov/mesh/D003716
https://id.nlm.nih.gov/mesh/D014777
https://id.nlm.nih.gov/mesh/D014779
title_short A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
title_full A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
title_fullStr A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
title_full_unstemmed A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
title_sort A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging
dc.creator.fl_str_mv Miranda Brand, Yaneth
Roa Linares, Vicky Constanza
Santiago Dugarte, Carolina
Del Olmo, Esther
López Pérez, José Luis
Betancur Galvis, Liliana Amparo
Gallego Gómez, Juan Carlos
San Feliciano, Arturo
dc.contributor.author.none.fl_str_mv Miranda Brand, Yaneth
Roa Linares, Vicky Constanza
Santiago Dugarte, Carolina
Del Olmo, Esther
López Pérez, José Luis
Betancur Galvis, Liliana Amparo
Gallego Gómez, Juan Carlos
San Feliciano, Arturo
dc.contributor.researchgroup.spa.fl_str_mv GRID - Grupo de Investigación Dermatológica
Grupo Medicina Molecular y de Translación
dc.subject.decs.none.fl_str_mv Antivirales
Antiviral Agents
Técnicas de Cultivo de Célula
Cell Culture Techniques
Virus del Dengue
Dengue Virus
Virosis
Virus Diseases
Replicación Viral
Virus Replication
topic Antivirales
Antiviral Agents
Técnicas de Cultivo de Célula
Cell Culture Techniques
Virus del Dengue
Dengue Virus
Virosis
Virus Diseases
Replicación Viral
Virus Replication
https://id.nlm.nih.gov/mesh/D000998
https://id.nlm.nih.gov/mesh/D018929
https://id.nlm.nih.gov/mesh/D003716
https://id.nlm.nih.gov/mesh/D014777
https://id.nlm.nih.gov/mesh/D014779
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000998
https://id.nlm.nih.gov/mesh/D018929
https://id.nlm.nih.gov/mesh/D003716
https://id.nlm.nih.gov/mesh/D014777
https://id.nlm.nih.gov/mesh/D014779
description ABSTRACT: Dengue virus (DENV) infection is the most arbovirosis in the world. However, medications have not been approved for its treatment. Drug discovery based on the host-targeted antiviral (HTA) constitutes a new promising strategy, considering their high genetic barrier to resistance and the low probability of selecting drug resistance strains. In this study, we have tested fifty-seven podophyllotoxin-related cyclolignans on DENV-2 infected cells and found the most promising compound was S.71. Using cellular and molecular biology experiments, we have discovered that the new lignan altered the distribution of microtubules, induced changes in cell morphology, and caused retraction of the rough endoplasmic reticulum. In addition, the compound alters the viral envelope protein and the double-stranded RNA, while there is a decrease in negative-strand RNA synthesis; especially when the compound was added between 6- and 12-hours post-infection. Altogether, S.71 decreases the viral yield through an HTA-related mechanism of action, possibly altering the DENV genome replication and/or polyprotein translation, through the alteration of microtubule distribution and endoplasmic reticulum deterioration. Finally, pharmacokinetic predictors show that S.71 falls within the standard ranges established for drugs.
publishDate 2023
dc.date.issued.none.fl_str_mv 2023
dc.date.accessioned.none.fl_str_mv 2024-11-10T21:18:13Z
dc.date.available.none.fl_str_mv 2024-11-10T21:18:13Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Brand YM, Roa-Linares V, Santiago-Dugarte C, Del Olmo E, López-Pérez JL, Betancur-Galvis L, Gallego-Gómez JC, Feliciano AS. A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging. Virus Res. 2023 Jan 2;323:198995. doi: 10.1016/j.virusres.2022.198995.
dc.identifier.issn.none.fl_str_mv 0168-1702
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/43349
dc.identifier.doi.none.fl_str_mv 10.1016/j.virusres.2022.198995
dc.identifier.eissn.none.fl_str_mv 1872-7492
identifier_str_mv Brand YM, Roa-Linares V, Santiago-Dugarte C, Del Olmo E, López-Pérez JL, Betancur-Galvis L, Gallego-Gómez JC, Feliciano AS. A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging. Virus Res. 2023 Jan 2;323:198995. doi: 10.1016/j.virusres.2022.198995.
0168-1702
10.1016/j.virusres.2022.198995
1872-7492
url https://hdl.handle.net/10495/43349
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Virus. Res.
dc.relation.citationendpage.spa.fl_str_mv 11
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 323
dc.relation.ispartofjournal.spa.fl_str_mv Virus Research
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dc.format.extent.spa.fl_str_mv 11 páginas
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dc.publisher.spa.fl_str_mv Elsevier
dc.publisher.place.spa.fl_str_mv Ámsterdam, Países Bajos
institution Universidad de Antioquia
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spelling Miranda Brand, YanethRoa Linares, Vicky ConstanzaSantiago Dugarte, CarolinaDel Olmo, EstherLópez Pérez, José LuisBetancur Galvis, Liliana AmparoGallego Gómez, Juan CarlosSan Feliciano, ArturoGRID - Grupo de Investigación DermatológicaGrupo Medicina Molecular y de Translación2024-11-10T21:18:13Z2024-11-10T21:18:13Z2023Brand YM, Roa-Linares V, Santiago-Dugarte C, Del Olmo E, López-Pérez JL, Betancur-Galvis L, Gallego-Gómez JC, Feliciano AS. A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging. Virus Res. 2023 Jan 2;323:198995. doi: 10.1016/j.virusres.2022.198995.0168-1702https://hdl.handle.net/10495/4334910.1016/j.virusres.2022.1989951872-7492ABSTRACT: Dengue virus (DENV) infection is the most arbovirosis in the world. However, medications have not been approved for its treatment. Drug discovery based on the host-targeted antiviral (HTA) constitutes a new promising strategy, considering their high genetic barrier to resistance and the low probability of selecting drug resistance strains. In this study, we have tested fifty-seven podophyllotoxin-related cyclolignans on DENV-2 infected cells and found the most promising compound was S.71. Using cellular and molecular biology experiments, we have discovered that the new lignan altered the distribution of microtubules, induced changes in cell morphology, and caused retraction of the rough endoplasmic reticulum. In addition, the compound alters the viral envelope protein and the double-stranded RNA, while there is a decrease in negative-strand RNA synthesis; especially when the compound was added between 6- and 12-hours post-infection. Altogether, S.71 decreases the viral yield through an HTA-related mechanism of action, possibly altering the DENV genome replication and/or polyprotein translation, through the alteration of microtubule distribution and endoplasmic reticulum deterioration. Finally, pharmacokinetic predictors show that S.71 falls within the standard ranges established for drugs.Universidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODICOL0050839COL014013911 páginasapplication/pdfengElsevierÁmsterdam, Países Bajoshttp://creativecommons.org/licenses/by-nc-nd/2.5/co/https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. 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