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Dengue virus NS1 secretion is regulated via importin-subunit ?1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin
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Document Title
Dengue virus NS1 secretion is regulated via importin-subunit ?1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin
Author
Denolly S. Guo H. Martens M. P?aszczyca A. Scaturro P. Prasad V. Kongmanas K. Punyadee N. Songjaeng A. Mairiang D. Pichlmair A. Avirutnan P. Bartenschlager R.
Affiliations
Department of Infectious Diseases Molecular Virology Center for Integrative Infectious Disease Research Heidelberg University Medical Faculty Heidelberg Heidelberg Germany; Technical University of Munich School of Medicine Institute of Virology Munich Germany; Leibniz Institute of Virology Hamburg Germany; Division of Dengue Hemorrhagic Fever Research Department of Research and Development Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand; Siriraj Center of Research Excellence in Dengue and Emerging Pathogens Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand; Molecular Biology of Dengue and Flaviviruses Research Team National Center for Genetic Engineering and Biotechnology National Science and Technology Development Agency Pathumthani Thailand; Department of Immunology Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand
Type
Article
Source Title
mBio
ISSN
21612129
Year
2023
Volume
14
Issue
5
Open Access
All Open Access Gold Green
Publisher
American Society for Microbiology
DOI
10.1128/mbio.01441-23
Abstract
Dengue virus (DENV) is a major human pathogen. An important pathogenicity factor is non-structural protein 1 (NS1) required for viral replication and secreted from infected cells. A clinical study indicated that the anti-parasitic drug ivermectin lowers NS1 blood levels without affecting viremia. Ivermectin targets nuclear transport by binding to importin-? but how NS1 secretion in patients is suppressed by this drug is unknown. We show that ivermectin impairs folding and secretion of endoplasmic reticulum-luminal glycoproteins including NS1. Proteomic analysis identified chaperones interacting with NS1 including GRp78 (78-kDa glucose-regulated protein also known as HSPA5 or BIP). This chaperone increased in abundance on DENV infection via activation of the unfolded protein response (UPR). Ivermectin blocked the nuclear transport of transcription factors required for UPR thus impairing GRp78 upregulation and NS1 secretion. Reduction of GRp78 and NS1 secretion was also observed in patients treated with ivermectin. These results link nuclear transport and its inhibition by ivermectin to folding and secretion of luminal glycoproteins including DENV NS1. IMPORTANCE Dengue virus (DENV) is a major human pathogen that can cause hemorrhagic fever and shock syndrome. One important factor of DENV pathogenicity is non-structural protein 1 (NS1) a glycoprotein that is secreted from infected cells. Here we study the mode of action of the widely used drug ivermectin used to treat parasitic infections and recently shown to lower NS1 blood levels in DENV-infected patients. We found that ivermectin blocks the nuclear transport of transcription factors required for the expression of chaperones that support the folding and secretion of glycoproteins including NS1. Impairing nuclear transport of these transcription factors by ivermectin or depleting them from infected cells dampens NS1 folding and thus its secretion. These results reveal a novel mode of action of ivermectin that might apply to other flaviviruses as well. Copyright ? 2023 Denolly et al.
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
License
CC BY
Rights
Authors
Publication Source
WOS