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      Transferrin receptor 1 is a cellular receptor for New World haemorrhagic fever arenaviruses

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          Viral receptor identified

          The transferrin receptor 1 (TfR1) has been identified as the cellular receptor for four New World arenaviruses — the Junin, Machupo, Guanarito and Sabia viruses. This class of arenaviruses is important because they cause fatal haemorrhagic fevers. Treating cultured cells with an antibody against TfR1 blocks viral entry and replication. Antibodies that limit arenavirus replication without interfering with host iron metabolism may be effective in controlling outbreaks of New World haemorrhagic fever.

          Supplementary information

          The online version of this article (doi:10.1038/nature05539) contains supplementary material, which is available to authorized users.

          Abstract

          At least five arenaviruses cause viral haemorrhagic fevers in humans. Lassa virus, an Old World arenavirus, uses the cellular receptor α-dystroglycan to infect cells 1 . Machupo, Guanarito, Junin and Sabia viruses are New World haemorrhagic fever viruses that do not use α-dystroglycan 2 . Here we show a specific, high-affinity association between transferrin receptor 1 (TfR1) and the entry glycoprotein (GP) of Machupo virus. Expression of human TfR1, but not human transferrin receptor 2, in hamster cell lines markedly enhanced the infection of viruses pseudotyped with the GP of Machupo, Guanarito and Junin viruses, but not with those of Lassa or lymphocytic choriomeningitis viruses. An anti-TfR1 antibody efficiently inhibited the replication of Machupo, Guanarito, Junin and Sabia viruses, but not that of Lassa virus. Iron depletion of culture medium enhanced, and iron supplementation decreased, the efficiency of infection by Junin and Machupo but not Lassa pseudoviruses. These data indicate that TfR1 is a cellular receptor for New World haemorrhagic fever arenaviruses.

          Supplementary information

          The online version of this article (doi:10.1038/nature05539) contains supplementary material, which is available to authorized users.

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          Most cited references26

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          Canine and feline parvoviruses can use human or feline transferrin receptors to bind, enter, and infect cells.

          Canine parvovirus (CPV) enters and infects cells by a dynamin-dependent, clathrin-mediated endocytic pathway, and viral capsids colocalize with transferrin in perinuclear vesicles of cells shortly after entry (J. S. L. Parker and C. R. Parrish, J. Virol. 74:1919-1930, 2000). Here we report that CPV and feline panleukopenia virus (FPV), a closely related parvovirus, bind to the human and feline transferrin receptors (TfRs) and use these receptors to enter and infect cells. Capsids did not detectably bind or enter quail QT35 cells or a Chinese hamster ovary (CHO) cell-derived cell line that lacks any TfR (TRVb cells). However, capsids bound and were endocytosed into QT35 cells and CHO-derived TRVb-1 cells that expressed the human TfR. TRVb-1 cells or TRVb cells transiently expressing the feline TfR were susceptible to infection by CPV and FPV, but the parental TRVb cells were not. We screened a panel of feline-mouse hybrid cells for susceptibility to FPV infection and found that only those cells that possessed feline chromosome C2 were susceptible. The feline TfR gene (TRFC) also mapped to feline chromosome C2. These data indicate that cell susceptibility for these viruses is determined by the TfR.
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            Hemorrhagic Fever Viruses as Biological Weapons

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              Identification of -Dystroglycan as a Receptor for Lymphocytic Choriomeningitis Virus and Lassa Fever Virus

              W Cao (1998)
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                Author and article information

                Contributors
                hyeryun.choe@childrens.harvard.edu
                Journal
                Nature
                Nature
                Nature
                Nature Publishing Group UK (London )
                0028-0836
                1476-4687
                7 February 2007
                2007
                : 446
                : 7131
                : 92-96
                Affiliations
                [1 ]GRID grid.38142.3c, ISNI 000000041936754X, Department of Microbiology and Molecular Genetics, , Harvard Medical School, New England Primate Research Center, Southborough, Massachusetts 01772, USA, ; ,
                [2 ]Pulmonary Division, Department of Pediatrics, Children’s Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA, ,
                [3 ]GRID grid.416738.f, ISNI 0000 0001 2163 0069, Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA, ; ,
                [4 ]GRID grid.14095.39, ISNI 0000 0000 9116 4836, Department of Biology, , Chemistry, Pharmacy, Freie Universität Berlin, 14195 Berlin, Germany, ; ,
                [5 ]Division of Hematology/Oncology, Department of Pediatrics, Children’s Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA, ,
                [6 ]GRID grid.253613.0, ISNI 0000 0001 2192 5772, Montana Biotechnology Center, The University of Montana, Missoula, Montana 59812, USA, ; ,
                Article
                BFnature05539
                10.1038/nature05539
                3197705
                17287727
                66d48b9d-3a68-448c-b37a-8497921278cb
                © Nature Publishing Group 2006

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 4 November 2006
                : 18 December 2006
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                © Springer Nature Limited 2007

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