Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Choy, Milly M., Zhang, Summer L., Costa, Vivian V., Tan, Hwee Cheng, Horrevorts, Sophie, Ooi, Eng Eong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
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
_version_ 1782400592752148480
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
work_keys_str_mv AT choymillym proteasomeinhibitionsuppressesdenguevirusegressinantibodydependentinfection
AT zhangsummerl proteasomeinhibitionsuppressesdenguevirusegressinantibodydependentinfection
AT costavivianv proteasomeinhibitionsuppressesdenguevirusegressinantibodydependentinfection
AT tanhweecheng proteasomeinhibitionsuppressesdenguevirusegressinantibodydependentinfection
AT horrevortssophie proteasomeinhibitionsuppressesdenguevirusegressinantibodydependentinfection
AT ooiengeong proteasomeinhibitionsuppressesdenguevirusegressinantibodydependentinfection