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Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection
The mosquito-borne dengue virus (DENV) is a cause of significant global health burden, with an estimated 390 million infections occurring annually. However, no licensed vaccine or specific antiviral treatment for dengue is available. DENV interacts with host cell factors to complete its life cycle a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643959/ https://www.ncbi.nlm.nih.gov/pubmed/26565697 http://dx.doi.org/10.1371/journal.pntd.0004058 |
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author | Choy, Milly M. Zhang, Summer L. Costa, Vivian V. Tan, Hwee Cheng Horrevorts, Sophie Ooi, Eng Eong |
author_facet | Choy, Milly M. Zhang, Summer L. Costa, Vivian V. Tan, Hwee Cheng Horrevorts, Sophie Ooi, Eng Eong |
author_sort | Choy, Milly M. |
collection | PubMed |
description | The mosquito-borne dengue virus (DENV) is a cause of significant global health burden, with an estimated 390 million infections occurring annually. However, no licensed vaccine or specific antiviral treatment for dengue is available. DENV interacts with host cell factors to complete its life cycle although this virus-host interplay remains to be fully elucidated. Many studies have identified the ubiquitin proteasome pathway (UPP) to be important for successful DENV production, but how the UPP contributes to DENV life cycle as host factors remains ill defined. We show here that proteasome inhibition decouples infectious virus production from viral RNA replication in antibody-dependent infection of THP-1 cells. Molecular and imaging analyses in β-lactone treated THP-1 cells suggest that proteasome function does not prevent virus assembly but rather DENV egress. Intriguingly, the licensed proteasome inhibitor, bortezomib, is able to inhibit DENV titers at low nanomolar drug concentrations for different strains of all four serotypes of DENV in primary monocytes. Furthermore, bortezomib treatment of DENV-infected mice inhibited the spread of DENV in the spleen as well as the overall pathological changes. Our findings suggest that preventing DENV egress through proteasome inhibition could be a suitable therapeutic strategy against dengue. |
format | Online Article Text |
id | pubmed-4643959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46439592015-11-18 Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection Choy, Milly M. Zhang, Summer L. Costa, Vivian V. Tan, Hwee Cheng Horrevorts, Sophie Ooi, Eng Eong PLoS Negl Trop Dis Research Article The mosquito-borne dengue virus (DENV) is a cause of significant global health burden, with an estimated 390 million infections occurring annually. However, no licensed vaccine or specific antiviral treatment for dengue is available. DENV interacts with host cell factors to complete its life cycle although this virus-host interplay remains to be fully elucidated. Many studies have identified the ubiquitin proteasome pathway (UPP) to be important for successful DENV production, but how the UPP contributes to DENV life cycle as host factors remains ill defined. We show here that proteasome inhibition decouples infectious virus production from viral RNA replication in antibody-dependent infection of THP-1 cells. Molecular and imaging analyses in β-lactone treated THP-1 cells suggest that proteasome function does not prevent virus assembly but rather DENV egress. Intriguingly, the licensed proteasome inhibitor, bortezomib, is able to inhibit DENV titers at low nanomolar drug concentrations for different strains of all four serotypes of DENV in primary monocytes. Furthermore, bortezomib treatment of DENV-infected mice inhibited the spread of DENV in the spleen as well as the overall pathological changes. Our findings suggest that preventing DENV egress through proteasome inhibition could be a suitable therapeutic strategy against dengue. Public Library of Science 2015-11-13 /pmc/articles/PMC4643959/ /pubmed/26565697 http://dx.doi.org/10.1371/journal.pntd.0004058 Text en © 2015 Choy et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Choy, Milly M. Zhang, Summer L. Costa, Vivian V. Tan, Hwee Cheng Horrevorts, Sophie Ooi, Eng Eong Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection |
title | Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection |
title_full | Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection |
title_fullStr | Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection |
title_full_unstemmed | Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection |
title_short | Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection |
title_sort | proteasome inhibition suppresses dengue virus egress in antibody dependent infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643959/ https://www.ncbi.nlm.nih.gov/pubmed/26565697 http://dx.doi.org/10.1371/journal.pntd.0004058 |
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