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      Stress responses in flavivirus-infected cells: activation of unfolded protein response and autophagy

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          Abstract

          The Flavivirus is a genus of RNA viruses that includes multiple long known human, animal, and zoonotic pathogens such as Dengue virus, yellow fever virus, West Nile virus, or Japanese encephalitis virus, as well as other less known viruses that represent potential threats for human and animal health such as Usutu or Zika viruses. Flavivirus replication is based on endoplasmic reticulum-derived structures. Membrane remodeling and accumulation of viral factors induce endoplasmic reticulum stress that results in activation of a cellular signaling response termed unfolded protein response (UPR), which can be modulated by the viruses for their own benefit. Concomitant with the activation of the UPR, an upregulation of the autophagic pathway in cells infected with different flaviviruses has also been described. This review addresses the current knowledge of the relationship between endoplasmic reticulum stress, UPR, and autophagy in flavivirus-infected cells and the growing evidences for an involvement of these cellular pathways in the replication and pathogenesis of these viruses.

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          Most cited references43

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          Composition and Three-Dimensional Architecture of the Dengue Virus Replication and Assembly Sites

          Summary Positive-strand RNA viruses are known to rearrange cellular membranes to facilitate viral genome replication. The biogenesis and three-dimensional organization of these membranes and the link between replication and virus assembly sites is not fully clear. Using electron microscopy, we find Dengue virus (DENV)-induced vesicles, convoluted membranes, and virus particles to be endoplasmic reticulum (ER)-derived, and we detect double-stranded RNA, a presumed marker of RNA replication, inside virus-induced vesicles. Electron tomography (ET) shows DENV-induced membrane structures to be part of one ER-derived network. Furthermore, ET reveals vesicle pores that could enable release of newly synthesized viral RNA and reveals budding of DENV particles on ER membranes directly apposed to vesicle pores. Thus, DENV modifies ER membrane structure to promote replication and efficient encapsidation of the genome into progeny virus. This architecture of DENV replication and assembly sites could explain the coordination of distinct steps of the flavivirus replication cycle.
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              The endoplasmic reticulum provides the membrane platform for biogenesis of the flavivirus replication complex.

              The cytoplasmic replication of positive-sense RNA viruses is associated with a dramatic rearrangement of host cellular membranes. These virus-induced changes result in the induction of vesicular structures that envelop the virus replication complex (RC). In this study, we have extended our previous observations on the intracellular location of West Nile virus strain Kunjin virus (WNV(KUN)) to show that the virus-induced recruitment of host proteins and membrane appears to occur at a pre-Golgi step. To visualize the WNV(KUN) replication complex, we performed three-dimensional (3D) modeling on tomograms from WNV(KUN) replicon-transfected cells. These analyses have provided a 3D representation of the replication complex, revealing the open access of the replication complex with the cytoplasm and the fluidity of the complex to the rough endoplasmic reticulum. In addition, we provide data that indicate that a majority of the viral RNA species housed within the RC is in a double-stranded RNA (dsRNA) form.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                03 June 2014
                2014
                : 5
                : 266
                Affiliations
                [1] 1Departamento de Biotecnología, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria Madrid, Spain
                [2] 2Departamento de Virología y Microbiología, Centro de Biología Molecular “Severo Ochoa”, Consejo Superior de Investigaciones Científicas – Universidad Autónoma de Madrid Madrid, Spain
                Author notes

                Edited by: Shiu-Wan Chan, The University of Manchester, UK

                Reviewed by: Hengli Tang, Florida State University, USA; Sara Louise Cosby, Queen’s University Belfast, UK

                *Correspondence: Miguel A. Martín-Acebes, Departamento de Virología y Microbiología, Centro de Biología Molecular “Severo Ochoa”, Consejo Superior de Investigaciones Científicas – Universidad Autónoma de Madrid, Nicolas Cabrera 1, Campus de Cantoblanco UAM, Madrid 28049, Spain e-mail: mamartin@ 123456cbm.csic.es ; martin.mangel@ 123456inia.es

                This articlewas submitted toVirology, a section of the journal Frontiers inMicrobiology.

                Article
                10.3389/fmicb.2014.00266
                4042264
                24478763
                38c508ec-3e4e-4edd-af23-631376e37faf
                Copyright © 2014 Blázquez, Escribano-Romero, Merino-Ramos, Saiz and Martín-Acebes.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 24 March 2014
                : 15 May 2014
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 63, Pages: 7, Words: 0
                Categories
                Microbiology
                Mini Review Article

                Microbiology & Virology
                flavivirus,unfolded protein response,autophagy,dengue virus,west nile virus,endoplasmic reticulum stress,virus replication

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