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      Study of Usutu virus neuropathogenicity in mice and human cellular models

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          Abstract

          Usutu virus (USUV), an African mosquito-borne flavivirus closely related to West Nile virus, was first isolated in South Africa in 1959. USUV emerged in Europe two decades ago, causing notably massive mortality in Eurasian blackbirds. USUV is attracting increasing attention due to its potential for emergence and its rapid spread in Europe in recent years. Although mainly asymptomatic or responsible for mild clinical signs, USUV was recently described as being associated with neurological disorders in humans such as encephalitis and meningoencephalitis, highlighting the potential health threat posed by the virus. Despite this, USUV pathogenesis remains largely unexplored. The aim of this study was to evaluate USUV neuropathogenicity using in vivo and in vitro approaches. Our results indicate that USUV efficiently replicates in the murine central nervous system. Replication in the spinal cord and brain is associated with recruitment of inflammatory cells and the release of inflammatory molecules as well as induction of antiviral-responses without major modulation of blood-brain barrier integrity. Endothelial cells integrity is also maintained in a human model of the blood-brain barrier despite USUV replication and release of pro-inflammatory cytokines. Furthermore, USUV-inoculated mice developed major ocular defects associated with inflammation. Moreover, USUV efficiently replicates in human retinal pigment epithelium. Our results will help to better characterize the physiopathology related to USUV infection in order to anticipate the potential threat of USUV emergence.

          Author summary

          Number of emerging arboviruses involved in human infections has increased considerably in the past years. Among them, Usutu virus (USUV) is an African mosquito-borne virus first isolated in South Africa that recently emerged. USUV infection in humans is considered to be most often asymptomatic or to cause mild clinical signs. Nonetheless, increased cases of neurological complications such as encephalitis or meningoencephalitis have been reported in Europe but the mechanisms behind this neuropathogenesis remain largely unclear. In this study we showed that USUV can infect efficiently several organs and cells of the central nervous system associated with a drastic inflammation and various deleterious effects. Our results contribute to the characterization of the neurotropism related to USUV infection.

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          Most cited references55

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          Beitrag zur kollektiven Behandlung pharmakologischer Reihenversuche

          G. Kärber (1931)
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            The retinal pigment epithelium in health and disease.

            Retinal pigment epithelial cells (RPE) constitute a simple layer of cuboidal cells that are strategically situated behind the photoreceptor (PR) cells. The inconspicuousness of this monolayer contrasts sharply with its importance [1]. The relationship between the RPE and PR cells is crucial to sight; this is evident from basic and clinical studies demonstrating that primary dysfunctioning of the RPE can result in visual cell death and blindness. RPE cells carry out many functions including the conversion and storage of retinoid, the phagocytosis of shed PR outer segment membrane, the absorption of scattered light, ion and fluid transport and RPE-PR apposition. The magnitude of the demands imposed on this single layer of cells in order to execute these tasks, will become apparent to the reader of this review as will the number of clinical disorders that take origin from these cells.
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              Alpha/beta interferon protects against lethal West Nile virus infection by restricting cellular tropism and enhancing neuronal survival.

              West Nile virus (WNV) is a mosquito-borne flavivirus that is neurotropic in humans, birds, and other animals. While adaptive immunity plays an important role in preventing WNV spread to the central nervous system (CNS), little is known about how alpha/beta interferon (IFN-alpha/beta) protects against peripheral and CNS infection. In this study, we examine the virulence and tropism of WNV in IFN-alpha/beta receptor-deficient (IFN- alpha/betaR-/-) mice and primary neuronal cultures. IFN-alpha/betaR-/- mice were acutely susceptible to WNV infection through subcutaneous inoculation, with 100% mortality and a mean time to death (MTD) of 4.6 +/- 0.7 and 3.8+/- 0.5 days after infection with 10(0) and 10(2) PFU, respectively. In contrast, congenic wild-type 129Sv/Ev mice infected with 10(2) PFU showed 62% mortality and a MTD of 11.9 +/- 1.9 days. IFN-alpha/betaR-/- mice developed high viral loads by day 3 after infection in nearly all tissues assayed, including many that were not infected in wild-type mice. IFN-alpha/betaR-/- mice also demonstrated altered cellular tropism, with increased infection in macrophages, B cells, and T cells in the spleen. Additionally, treatment of primary wild-type neurons in vitro with IFN-beta either before or after infection increased neuronal survival independent of its effect on WNV replication. Collectively, our data suggest that IFN-alpha/beta controls WNV infection by restricting tropism and viral burden and by preventing death of infected neurons.
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                Author and article information

                Contributors
                Role: InvestigationRole: MethodologyRole: Writing – review & editing
                Role: Investigation
                Role: InvestigationRole: Methodology
                Role: InvestigationRole: MethodologyRole: ResourcesRole: Writing – review & editing
                Role: Investigation
                Role: InvestigationRole: MethodologyRole: Validation
                Role: Resources
                Role: InvestigationRole: Resources
                Role: ConceptualizationRole: MethodologyRole: ValidationRole: Writing – review & editing
                Role: ResourcesRole: Writing – review & editing
                Role: ResourcesRole: Writing – review & editing
                Role: InvestigationRole: MethodologyRole: Writing – review & editing
                Role: Investigation
                Role: ResourcesRole: Writing – review & editing
                Role: Methodology
                Role: Funding acquisition
                Role: ConceptualizationRole: Funding acquisitionRole: InvestigationRole: Writing – review & editing
                Role: ConceptualizationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – original draft
                Role: Editor
                Journal
                PLoS Negl Trop Dis
                PLoS Negl Trop Dis
                plos
                plosntds
                PLoS Neglected Tropical Diseases
                Public Library of Science (San Francisco, CA USA )
                1935-2727
                1935-2735
                23 April 2020
                April 2020
                : 14
                : 4
                : e0008223
                Affiliations
                [1 ] Pathogenesis and Control of Chronic Infections, University of Montpellier, INSERM, EFS, Montpellier, France
                [2 ] BioCommunication en CardioMétabolique (BC2M), University of Montpellier, Montpellier, France
                [3 ] Inserm U1051, Institute for Neurosciences of Montpellier. University of Montpellier, Montpellier, France
                [4 ] UPE, Anses Animal Health Laboratory, INRA, Anses, ENVA, Maisons-Alfort, France
                [5 ] BCM, University of Montpellier, CNRS, INSERM, Montpellier, France
                [6 ] IRCM, University of Montpellier, ICM INSERM, Montpellier, France
                [7 ] University of Artois, Blood-Brain Barrier Laboratory (BBB Lab), France
                [8 ] RAM-ECE, BioCampus Montpellier, CNRS, INSERM, University of Montpellier, Montpellier France
                [9 ] Centre Hospitalier Universitaire de Montpellier, Montpellier, France
                Center for Disease Control and Prevention, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0002-5072-7078
                http://orcid.org/0000-0003-4492-2093
                http://orcid.org/0000-0002-3475-1369
                Article
                PNTD-D-19-02018
                10.1371/journal.pntd.0008223
                7179837
                32324736
                48781ffa-178a-4f64-b1b0-060458428793
                © 2020 Clé et al

                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 credited.

                History
                : 6 December 2019
                : 16 March 2020
                Page count
                Figures: 7, Tables: 0, Pages: 27
                Funding
                Funded by: Reacting
                Award ID: YY/FC/2018-032
                Award Recipient :
                Funded by: Board of College and University Development, Savitribai Phule Pune University (IN)
                Award ID: ANR-16-IDEX-0006
                Award Recipient :
                This work was funded by REACTing (reference: YY/FC/2018-032) and Montpellier University of Excellence (MUSE) through ANR (the French National Research Agency) under the "Investissements d’avenir" programme with the reference ANR-16-IDEX-0006. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
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