Article ; Online: Valosin-containing protein ATPase activity regulates the morphogenesis of Zika virus replication organelles and virus-induced cell death.
2021 Volume 23, Issue 4, Page(s) e13302
Abstract: With no available therapies, infections with Zika virus (ZIKV) constitute a major public health concern as they can lead to congenital microcephaly. In order to generate an intracellular environment favourable to viral replication, ZIKV induces ... ...
| Abstract | With no available therapies, infections with Zika virus (ZIKV) constitute a major public health concern as they can lead to congenital microcephaly. In order to generate an intracellular environment favourable to viral replication, ZIKV induces endomembrane remodelling and the morphogenesis of replication factories via enigmatic mechanisms. In this study, we identified the AAA+ type ATPase valosin-containing protein (VCP) as a cellular interaction partner of ZIKV non-structural protein 4B (NS4B). Importantly, its pharmacological inhibition as well as the expression of a VCP dominant-negative mutant impaired ZIKV replication. In infected cells, VCP is relocalised to large ultrastructures containing both NS4B and NS3, which are reminiscent of dengue virus convoluted membranes. Moreover, short treatment with the VCP inhibitors NMS-873 or CB-5083 drastically decreased the abundance and size of ZIKV-induced convoluted membranes. Furthermore, NMS-873 treatment inhibited ZIKV-induced mitochondria elongation previously reported to be physically and functionally linked to convoluted membranes in case of the closely related dengue virus. Finally, VCP inhibition resulted in enhanced apoptosis of ZIKV-infected cells strongly suggesting that convoluted membranes limit virus-induced cytopathic effects. Altogether, this study identifies VCP as a host factor required for ZIKV life cycle and more precisely, for the maintenance of viral replication factories. Our data further support a model in which convoluted membranes regulate ZIKV life cycle by impacting on mitochondrial functions and ZIKV-induced death signals in order to create a cytoplasmic environment favourable to viral replication. |
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| MeSH term(s) | Acetanilides/pharmacology ; Adenosine Triphosphatases/genetics ; Adenosine Triphosphatases/metabolism ; Animals ; Apoptosis ; Benzothiazoles/pharmacology ; Cell Line, Tumor ; Chlorocebus aethiops ; Gene Expression Regulation ; HEK293 Cells ; Host Microbial Interactions/drug effects ; Host Microbial Interactions/genetics ; Humans ; Indoles/pharmacology ; Mitochondria/drug effects ; Mitochondria/metabolism ; Mitochondria/virology ; Pyrimidines/pharmacology ; Valosin Containing Protein/antagonists & inhibitors ; Valosin Containing Protein/genetics ; Valosin Containing Protein/metabolism ; Vero Cells ; Zika Virus/genetics ; Zika Virus/physiology |
| Chemical Substances | Acetanilides ; Benzothiazoles ; CB-5083 ; Indoles ; NMS-873 ; Pyrimidines ; Adenosine Triphosphatases (EC 3.6.1.-) ; Valosin Containing Protein (EC 3.6.4.6) |
| Language | English |
| Publishing date | 2021-01-11 |
| Publishing country | England |
| Document type | Journal Article ; Research Support, Non-U.S. Gov't |
| ZDB-ID | 1468320-9 |
| ISSN | 1462-5822 ; 1462-5814 |
| ISSN (online) | 1462-5822 |
| ISSN | 1462-5814 |
| DOI | 10.1111/cmi.13302 |
| Database | MEDical Literature Analysis and Retrieval System OnLINE |
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