Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin
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 vi...
| Main Authors: | , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
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American Society for Microbiology
2023-10-01
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| Series: | mBio |
| Subjects: | |
| Online Access: | https://journals.asm.org/doi/10.1128/mbio.01441-23 |
| _version_ | 1827150325776121856 |
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| author | Solène Denolly Hongbo Guo Miriam Martens Anna Płaszczyca Pietro Scaturro Vibhu Prasad Kessiri Kongmanas Nuntaya Punyadee Adisak Songjaeng Dumrong Mairiang Andreas Pichlmair Panisadee Avirutnan Ralf Bartenschlager |
| author_facet | Solène Denolly Hongbo Guo Miriam Martens Anna Płaszczyca Pietro Scaturro Vibhu Prasad Kessiri Kongmanas Nuntaya Punyadee Adisak Songjaeng Dumrong Mairiang Andreas Pichlmair Panisadee Avirutnan Ralf Bartenschlager |
| author_sort | Solène Denolly |
| collection | DOAJ |
| description | 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-α, 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. |
| first_indexed | 2024-03-11T08:30:48Z |
| format | Article |
| id | doaj.art-c84d4923c84b4095923cbf7f1fc0ba2d |
| institution | Directory Open Access Journal |
| issn | 2150-7511 |
| language | English |
| last_indexed | 2025-03-20T21:32:17Z |
| publishDate | 2023-10-01 |
| publisher | American Society for Microbiology |
| record_format | Article |
| series | mBio |
| spelling | doaj.art-c84d4923c84b4095923cbf7f1fc0ba2d2024-08-11T18:20:46ZengAmerican Society for MicrobiologymBio2150-75112023-10-0114510.1128/mbio.01441-23Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectinSolène Denolly0Hongbo Guo1Miriam Martens2Anna Płaszczyca3Pietro Scaturro4Vibhu Prasad5Kessiri Kongmanas6Nuntaya Punyadee7Adisak Songjaeng8Dumrong Mairiang9Andreas Pichlmair10Panisadee Avirutnan11Ralf Bartenschlager12Department of Infectious Diseases, Molecular Virology, Center for Integrative Infectious Disease Research, Heidelberg University, Medical Faculty Heidelberg , Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, Center for Integrative Infectious Disease Research, Heidelberg University, Medical Faculty Heidelberg , Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, Center for Integrative Infectious Disease Research, Heidelberg University, Medical Faculty Heidelberg , Heidelberg, GermanyDepartment of Infectious Diseases, Molecular Virology, Center for Integrative Infectious Disease Research, Heidelberg University, Medical Faculty Heidelberg , Heidelberg, GermanyTechnical University of Munich, School of Medicine, Institute of Virology , Munich, GermanyDepartment of Infectious Diseases, Molecular Virology, Center for Integrative Infectious Disease Research, Heidelberg University, Medical Faculty Heidelberg , Heidelberg, GermanyDivision of Dengue Hemorrhagic Fever Research, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University , Bangkok, ThailandDivision of Dengue Hemorrhagic Fever Research, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University , Bangkok, ThailandDivision of Dengue Hemorrhagic Fever Research, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University , Bangkok, ThailandSiriraj Center of Research Excellence in Dengue and Emerging Pathogens, Faculty of Medicine Siriraj Hospital, Mahidol University , Bangkok, ThailandTechnical University of Munich, School of Medicine, Institute of Virology , Munich, GermanyDivision of Dengue Hemorrhagic Fever Research, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University , Bangkok, ThailandDepartment of Infectious Diseases, Molecular Virology, Center for Integrative Infectious Disease Research, Heidelberg University, Medical Faculty Heidelberg , Heidelberg, GermanyABSTRACT 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-α, 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.https://journals.asm.org/doi/10.1128/mbio.01441-23flavivirusnuclear transportprotein secretionnonstructural proteinhost targeting therapyglycoproteins |
| spellingShingle | Solène Denolly Hongbo Guo Miriam Martens Anna Płaszczyca Pietro Scaturro Vibhu Prasad Kessiri Kongmanas Nuntaya Punyadee Adisak Songjaeng Dumrong Mairiang Andreas Pichlmair Panisadee Avirutnan Ralf Bartenschlager Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin mBio flavivirus nuclear transport protein secretion nonstructural protein host targeting therapy glycoproteins |
| title | Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin |
| title_full | Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin |
| title_fullStr | Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin |
| title_full_unstemmed | Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin |
| title_short | Dengue virus NS1 secretion is regulated via importin-subunit β1 controlling expression of the chaperone GRp78 and targeted by the clinical drug ivermectin |
| title_sort | dengue virus ns1 secretion is regulated via importin subunit β1 controlling expression of the chaperone grp78 and targeted by the clinical drug ivermectin |
| topic | flavivirus nuclear transport protein secretion nonstructural protein host targeting therapy glycoproteins |
| url | https://journals.asm.org/doi/10.1128/mbio.01441-23 |
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