Animal virus receptors

. 1999 ; 44 (5) : 467-86.

Jazyk angličtina Země Spojené státy americké Médium print

Typ dokumentu časopisecké články, práce podpořená grantem, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid10997129

The term 'receptor' is generally accepted as the cell-surface component that participates in virus binding and facilitates subsequent viral infection. Recent advances in technology have permitted the identification of several virus receptors, increasing our understanding of the significance of this initial virus-cell and virus-host interaction. Virus binding was previously considered to involve simple recognition and attachment to a single cell surface molecule by virus attachment proteins. The classical concept of these as single entities that participate in a lock-and-key-type process has been superseded by new data indicating that binding can be a multistep process, often involving different virus-attachment proteins and more than one host-cell receptor.

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Air G.M., Laver W.G. The neuraminidase of influenza virus. Proteins. 1989;6:341–356. doi: 10.1002/prot.340060402. PubMed DOI

Albritton L.M., Tseng L., Scadden D., Cunningham J.M. A putative murine ecotropic retrovirus receptor gene encodes a multiple membrane-spanning protein and confers susceptibility to virus infection. Cell. 1989;57:659–666. doi: 10.1016/0092-8674(89)90134-7. PubMed DOI

Alcamí A., Carrascosa A.L., Vinuela E. Saturable binding sites mediate the entry of African swine fever virus into Vero cells. Virology. 1989;168:393–398. doi: 10.1016/0042-6822(89)90281-X. PubMed DOI

Alcamí A., Carrascosa A.L., Vinuela E. Interaction of African swine fever virus with macrophages. Virus Res. 1990;17:93–104. doi: 10.1016/0168-1702(90)90071-I. PubMed DOI

Allaway G.P., Pardoe U.I., Tavakkol A., Burness A.T.H. Encephalomyocarditis virus attachment. In: Crowell R.L., Lonberg-Holm K., editors. Virus Attachment and Entry into Cells. Washington (DC): American Society for Microbiology; 1986. pp. 116–125.

Anderson L.W., Anderson P.K., Liggitt H.D. Susceptibility of blood-derived monocytes and macrophages to caprine arthritis-encephalitis virus. Infect. Immun. 1983;41:837–840. PubMed PMC

Angulo A., Alcamí A., Vinuela E. Virus-host interactions in African swine fever: the attachment to cellular receptors. Arch. Virol. (Suppl.) 1993;7:169–183. PubMed

Ardman B., Khiroya R.H., Schwartz R.S. Recognition of a leukemia-related antigen by an anti-idiotypic antiserum to an anti-gp70 monoclonal antibody. J. Exp. Med. 1985;161:669–686. doi: 10.1084/jem.161.4.669. PubMed DOI PMC

Arthur L.O., Bess J.W.J., Sowder R.C., Benveniste R.E., Mann D.L., Chermann J.C., Henderson L.E. Cellular proteins bound to immunodeficiency viruses: implications for pathogenesis and vaccines. Science. 1992;258:1935–1938. doi: 10.1126/science.1470916. PubMed DOI

Bahraoui E., Benjouard A., Guetard D., Kolbe H., Gluckman J.-C., Montagnier L. Study of the interaction of HIV-1 and HIV-2 envelope glycoproteins with the CD4 receptors and role of N-glycans. AIDS Res. Hum. Retrovir. 1992;8:565–573. PubMed

Baker A.T., Varghese J.N., Laver W.G., Air G.M., Colman P.M. Three-dimensional structure of neuraminidase of subtype N9 from an avian virus. Proteins. 1987;2:111–117. doi: 10.1002/prot.340020205. PubMed DOI

Balzarini J., Schls D., Neyts J., Van Damme E., Peumans W., De Clerq E. Alpha-1,3- and alpha-1,6-d-mannose-specific plant lectins are markedly inhibitory to human immunodeficiency virus and cytomegalovirus infectionin vitro. Antimicrob. Agents Chemother. 1991;35:410–416. PubMed PMC

Ban J., Portetelle D., Altaner C., Horion B., Milan D., Krchnak V., Burny A., Kettmann R. Isolation and characterization of a 2.3-kilobase-pair cDNA fragment encoding the binding domain of the bovine leukemia virus cell receptor. J. Virol. 1993;67:1050–1057. PubMed PMC

Bass D.M., Mackow E.R., Greenberg H.B. Identification and partial characterization of a rhesus rotavirus binding glycoprotein on murine enterocytes. Virology. 1991;183:602–610. doi: 10.1016/0042-6822(91)90989-O. PubMed DOI

Bates P., Young J.A.T., Varmus H.E. A receptor for subgroup A Rous sarcoma virus is related to the low density lipoprotein receptor. Cell. 1993;74:1043–1051. doi: 10.1016/0092-8674(93)90726-7. PubMed DOI

Becker S., Spiess M., Klenk H.-D. The asialoglycoprotein receptor is a potential liver-specific receptor for Marburg virus. J. Gen. Virol. 1995;76:393–399. PubMed

Benkirane M., Corbeau P., Housset V., Devaux C. An antibody that binds the immunoglobulin CDR3-like region of the CD4 molecule inhibits provirus transcription in HIV-infected T cells. EMBO J. 1993;12:4909–4921. PubMed PMC

Bergelson J.M., Krithivas A., Celi L., Droguett G., Horwitz M.S., Wickham T., Crowell R.L., Finberg R.W. The murine CAR homolog is a receptor for coxsackie B viruses and adenoviruses. J. Virol. 1998;72:415–419. PubMed PMC

Bergelson J.M., Shepley M.P., Chan M.C., Hemler M.E., Finberg R.W. Identification of the integrin VLA-2 as a receptor for echovirus 1. Science. 1992;255:1718–1720. doi: 10.1126/science.1553561. PubMed DOI

Bergelson J.M., St. John N., Kawaguchi S., Chan M.C., Stubdal H., Modlin J., Finberg R.W. Infection by echoviruses 1 and 8 depends on the α2 subunit of human VLA-2. J. Virol. 1993;67:6847–6852. PubMed PMC

Bergelson J.M., Chan M., Solomon K.R., St. John N.F., Lin J.H., Finberg R.W. Decay-accelerating factor (CD55), a glycosylphosphatidylinositol-anchored complement regulatory protein, is a receptor for several echoviruses. Proc. Nat. Acad. Sci. USA. 1994;91:6245–6248. doi: 10.1073/pnas.91.13.6245. PubMed DOI PMC

Berinstein A., Roivainen M., Hovi T., Mason P.W., Baxt B. Antibodies to the vitronectin receptor (integrin αVβ3) inhibit binding and infection of foot-and-mouth disease virus to cultured cells. J. Virol. 1995;69:2664–2666. PubMed PMC

Bhat S., Spitalnik S.L., Gonzalez-Scarano F., Silberberg D.H. Galactosylceramide or a derivative is an essential component of the neural receptor for HIV-1 envelope glycoprotein gp120. Proc. Nat. Acad. Sci. USA. 1991;88:7131–7134. doi: 10.1073/pnas.88.16.7131. PubMed DOI PMC

Bork P., Holm L., Sander C. The immunoglobulin fold. Structural classification, sequence patterns and common core. J. Mol. Biol. 1994;242:309–320. PubMed

Braun J.M.A., Gras G., Chapuis F., Sommerfelt M.A., Clapham P.R., Weiss R.A., Asjo B., Gluckman J.-C., Dormont D., Barre-Sinoussi F. In: Leucocyte Typing V: White Cell Differentiation Antigens. Schlossman S.F., editor. Oxford-New York: Oxford University Press; 1995. pp. 465–468.

Breau W.C., Atwood W.J., Norkin L.C. Class I major histocompatibility proteins are an essential component of the simian virus 40 receptor. J. Virol. 1992;66:2037–2045. PubMed PMC

Broder C.C., Collman R.G. Chemokine receptors and HIV. J. Leukocyt. Biol. 1997;62:20–29. PubMed

Brossmer R., Isecke R., Herrler G. A sialic acid analogue acting as a receptor determinant for binding but not for infection by influenza C virus. FEBS Lett. 1993;323:96–98. doi: 10.1016/0014-5793(93)81456-A. PubMed DOI

Broughan J.H., Wunner W.H. Characterization of protein involvement in rabies virus binding to BHK-21 cells. Arch. Virol. 1995;140:75–93. doi: 10.1007/BF01309725. PubMed DOI

Brown K.E., Anderson S.M., Young N.S. Erythrocyte P antigen: cellular receptor for B19 parvovirus. Science. 1993;262:114–117. doi: 10.1126/science.8211117. PubMed DOI

Buckland R., Wild T.F. Is CD46 the cellular receptor for measles virus? Virus Res. 1997;48:1–9. doi: 10.1016/S0168-1702(96)01421-9. PubMed DOI

Bullough P.A., Hugson F.M., Skehel J.J., Wiley D.C. Structure of influenza hemagglutinin at the pH of membrane fusion. Nature. 1994;371:37–43. doi: 10.1038/371037a0. PubMed DOI

Burmeister W.P., Ruigrok R.W.H., Cusack S. The 2.2 Å resolution crystal structure of influenza B neuraminidase and its complex with sialic acid. EMBO J. 1992;11:49–56. PubMed PMC

Chattopadhyay S.K., Lander M.R., Gupta S., Rands E., Lowy D.R. Origin of mink cytopathic focus-forming (MCF) viruses: comparison with ecotropic and xenotropic murine leukemia virus genomes. Virology. 1981;113:465–483. doi: 10.1016/0042-6822(81)90175-6. PubMed DOI

Crane S.E., Buzy J., Clements J.E. Identification of cell membrane proteins that bind visna virus. J. Virol. 1991;65:6137–6143. PubMed PMC

Crowell R.L., Tomko R.P. Receptors for picornaviruses. In: Wimmer E., editor. Cellular Receptors for Animal Viruses. Cold Spring Harbor: Cold Spring Harbor Laboratory Press; 1994. pp. 75–79.

Dalgleish A.G., Beverley P.C., Clapham P.R., Crawford D.H., Greaves M.F., Weiss A. The CD4 (T4) antigen is an essential component of the receptor for the AIDS retrovirus. Nature (London) 1984;312:763–767. doi: 10.1038/312763a0. PubMed DOI

Dallocchio F., Tomasi M., Bellini T. Activation of the Sendai virus fusion protein by receptor binding. Biochem. Biophys. Res. Commun. 1995;208:36–41. doi: 10.1006/bbrc.1995.1301. PubMed DOI

Dalziel K.G., Hopkins J., Watt N.J., Dutia B.M., Clarke M.A.K., McConnell I. Identification of a putative cellular receptor for the lentivirus visna virus. J. Gen. Virol. 1991;72:1905–1911. PubMed

Delmas B., Gelfi J., L'Haridon R., Vogel L.K., Sjostrom H., Noren O., Laude H. Aminopeptidase N is a major receptor for the enteropathogenic coronavirus TGEV. Nature (London) 1992;357:417–422. doi: 10.1038/357417a0. PubMed DOI PMC

Delmas G., Gelfi H., Sjostrom H., Noren O., Laude H. Further characterization of aminopeptidase N as a receptor for coronaviruses. Adv. Exp. Med. Biol. 1993;342:293–298. PubMed

De Meyer S., Gong Z.J., Suwandhi W., van Pelt J., Soumillion A., Yap S.H. Organ and species specificity of hepatitis B virus (HBV) infection: a review of literature with a special reference to preferential attachment of HBV to human hepatocytes. J. Virol. Hepat. 1997;4:145–153. doi: 10.1046/j.1365-2893.1997.00126.x. PubMed DOI

Doring R.E., Marcil A., Chopra A., Richardson C.D. The human CD46 molecule is a receptor for measles virus (Edmonston strain) Cell. 1993;75:295–305. doi: 10.1016/0092-8674(93)80071-L. PubMed DOI

Dunster L.M., Schneider-Schaulies J., Loffler S., Lankes W., Schwartz-Albiez R., Lottspeich F., ter Meulen V. Moesin: a cell membrane protein linked with susceptibility to measles virus infection. Virology. 1994;198:265–274. doi: 10.1006/viro.1994.1029. PubMed DOI

Durrer P., Gaudin Y., Ruigrok R.W.H., Graf R., Brunner J. Photolabeling identifies a putative fusion domain in the envelope glycoprotein of rabies and vesicular stomatitis viruses. J. Biol. Chem. 1995;270:17575–17581. doi: 10.1074/jbc.270.29.17575. PubMed DOI

Dveksler G.S., Dieffenbach C.W., Cardellichio C.B., McCuaig K., Pensiero M.N., Jiang G.-S., Beauchemin N., Holmes K.V. Several members of the mouse carcinoembryonic antigen-related glycoprotein family are functional receptors for the coronavirus mouse hepatitis virus-A59. J. Virol. 1993;67:1–8. PubMed PMC

Dveksler G.S., Pensiero M.N., Cardellichio C.B., Williams R.K., Jiang G.-S., Holmes K.V., Dieffenbach C.W. Cloning of the mouse hepatitis virus (MHV) receptor: expression in human and hamster cell lines confers susceptibility to MHV. J. Virol. 1991;65:6881–6891. PubMed PMC

Dveksler G.S., Pensiero M.N., Dieffenbach C.W., Cardellichio C.B., Basile A.A., Elias P.E., Holmes K.V. Mouse coronavirus MHV-A59 and blocking anti-receptor monoclonal antibody bind to the N-terminal domain of cellular receptor MHVR. Proc. Nat. Acad. Sci. USA. 1993;90:1716–1720. doi: 10.1073/pnas.90.5.1716. PubMed DOI PMC

Eglitis M.A., Eiden M.V., Wilson C.A. Gibbon ape leukemia virus and the amphotropic murine leukemia virus 4070A exhibit an unusual interference pattern on E36 Chinese hamster cells. J. Virol. 1993;67:5472–5477. PubMed PMC

Epand R.M., Nir S., Parolini M., Flanagan T.D. The role of the ganglioside GD1a as a receptor for Sendai virus. Biochemistry. 1995;34:1084–1089. doi: 10.1021/bi00003a045. PubMed DOI

Evander M., Frazer I.H., Payne E., Qi Y.M., Hengst K., McMillan N.A.J. Identification of the α6 integrin as a candidate receptor for papillomaviruses. J. Virol. 1997;71:2449–2456. PubMed PMC

Fantini J., Cook D.G., Nathanson N., Spitalnik S.L., Gonzalez-Scarano F. Infection of colonic epithelial cell lines by type 1 human immunodeficiency virus is associated with cell surface expression of galactosylceramide, a potential pg120 receptor. Proc. Nat. Acad. Sci. USA. 1993;90:2700–2704. doi: 10.1073/pnas.90.7.2700. PubMed DOI PMC

Feng Y., Broder C.C., Kennedy P.E., Berger E.A. HIV-1 entry co-factor: functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor. Science. 1996;272:872–877. doi: 10.1126/science.272.5263.872. PubMed DOI

Fenouillet E., Gluckman J.-C., Jones I.M.: Biological roles of HIV-1 glycoprotein glycans. Paper presented atGlyco XII: 12th Internat. Symp. on Glycoconjugates, Kraków (Poland) 1993.

Fenouillet E., Gluckman J.-C., Jones I.M. Functions of HIV envelope glycans. TIBS. 1994;19:65–71. PubMed

Fischinger P.J., Nomura S., Bolognesi D.P. A novel murine oncornavirus with dual eco- and xenotropic properties. Proc. Nat. Acad. Sci. USA. 1975;72:5150–5155. doi: 10.1073/pnas.72.12.5150. PubMed DOI PMC

Fukudome K., Yoshie O., Konno T. Comparison of human, simian, and bovine rotaviruses for requirement of sialic acid in hemagglutination and cell adsorption. Virology. 1989;172:196–205. doi: 10.1016/0042-6822(89)90121-9. PubMed DOI

Furuta Y., Eriksson K., Svennerholm B., Fredman P., Horal P., Jeansson S., Vahlne A., Holmgren J., Czerkinsky C. Infection of vaginal and colonic epithelial cells by the human immunodeficiency virus type 1 is neutralized by antibodies raised against conserved epitopes on the envelope glycoprotein gp120. Proc. Nat. Acad. Sci. USA. 1994;91:12559–12563. doi: 10.1073/pnas.91.26.12559. PubMed DOI PMC

Gastka M., Morvath J., Lentz T. Rabies virus binding to the nicotinic acetylcholine receptor α subunit demonstrated by virus overlay protein binding assay. J. Gen. Virol. 1996;77:2437–2440. PubMed

Gattegno L., Ramdani A., Jouault T., Saffar L., Gluckman J.-C. Lectin-carbohydrate interactions and infectivity of human immunodeficiency virus type 1 (HIV-1) AIDS Res. Hum. Retrovir. 1992;8:27–37. doi: 10.1089/aid.1992.8.27. PubMed DOI

Geyer H., Holschbach C., Hunsmann G., Schneider J. Carbohydrates of human immunodeficiency virus. J. Biol. Chem. 1988;263:11760–11767. PubMed

Gomez-Puertas P., Rodríguez F., Oviedo J.M., Ramiro-Ibánez F., Ruiz-Gonzalvo F., Covadonga A., Escribano J.M. Neutralizing antibodies to different proteins of African swine fever virus inhibit both virus attachment and internalization. J. Virol. 1996;70:5689–5694. PubMed PMC

Gonda M.A., Luther D.G., Fong S.E., Tobin G.J. Bovine immunodeficiency virus: molecular biology and virus-host interactions. Virus Res. 1994;32:155–181. doi: 10.1016/0168-1702(94)90040-X. PubMed DOI

Gonzales-Scarano F., Pobjecky N., Nathanson N. La Crosse bunyavirus can mediate pH-dependent fusion from without. Virology. 1984;132:222–225. doi: 10.1016/0042-6822(84)90107-7. PubMed DOI

Gratama J.W., Ernberg I. Molecular epidemiology of Epstein-Barr virus infection. Adv. Cancer Res. 1995;67:197–255. PubMed

Greve J.M., Davis G., Meyer A.M., Forte C.P., Yost S.C., Marlor C.W., Kamarck M.E., McClelland A. The major human rhinovirus receptor is ICAM-1. Cell. 1989;56:839–847. doi: 10.1016/0092-8674(89)90688-0. PubMed DOI

Grewal K.K., Hamid J., Pardoe I.U., Burness A.T.H.: Transfection of bovine cells with glycophorin A cDNA induces susceptibility to encephalomyocarditis virus infection. Abstr. A-11, 7th Eur. Study Group Mol. Biol. Picornaviruses, 1991.

Gyu Y., King D.S., Shin Y.K. Insertion of a coiled-coil peptide from influenza virus hemagglutinin into membranes. Science. 1994;266:274–276. doi: 10.1126/science.7939662. PubMed DOI

Hammar L., Hirsch I., Machado A.A., De Mareuil J., Baillon J.G., Bolmont C., Chermann J.-C. Lectin-mediated effects on HIV type 1 infectionin vitro. AIDS Res. Hum. Retrovir. 1995;11:87–95. PubMed

Harouse J.M., Kunsch C., Hartle H.T., Laughlin M.A., Hoxie J.A., Wigdahl B., Gonzalez-Scarano F. CD4-independent infection of human neural cells by human immunodeficiency virus type 1. J. Virol. 1989;63:2527–2533. PubMed PMC

Harrowe G., Mitsuhashi M., Payan D.G. Measles virus-substance P receptor interactions. J. Clin. Invest. 1990;85:1324–1327. PubMed PMC

Harrowe G., Sudduth-Klinger J., Payan D.G. Measles virus-substance P receptor interaction: Jurkat lymphocytes transfected with substance P receptor cDNA enhance measles virus fusion and replication. Cell. Mol. Neurobiol. 1992;12:397–409. doi: 10.1007/BF00711541. PubMed DOI PMC

Hartley J.W., Wolford N.K., Old L.J., Rowe W.P. A new class of murine leukemia virus associated with development of spontaneous lymphomas. Proc. Nat. Acad. Sci. USA. 1977;74:789–792. doi: 10.1073/pnas.74.2.789. PubMed DOI PMC

Hartshorn K.L., Sastry K., Brown D., White M.R., Okarma T.B., Lee Y.-M., Tauber A.I. Conglutinin acts as an opsonin for influenza A viruses. J. Immunol. 1993;151:6265–6273. PubMed

Haywood A.M. Virus receptors: binding, adhesion strengthening, and changes in viral structure. J. Virol. 1994;68:1–5. PubMed PMC

Helenius A., Kartenbeck J., Simons K., Fries E. On the entry of Semliki forest virus into BHK-21 cells. J. Cell. Biol. 1980;84:404–420. doi: 10.1083/jcb.84.2.404. PubMed DOI PMC

Helenius A., Morein B., Fries E., Simons K., Robinson P., Schirrmacher V., Terhorst C., Strominger J.L. Human (HLA-A and HLA-B) and murine (H-2K and H2D) histocompatibility antigens are cell surface receptors for Semliki forest virus. Proc. Nat. Acad. Sci. USA. 1978;75:3846–3850. doi: 10.1073/pnas.75.8.3846. PubMed DOI PMC

Herrler G. Transmissible gastroenteritis virus, but not the related porcine respiratory coronavirus, has a sialic acid (N-glycolylneuraminic acid) binding activity. J. Virol. 1996;70:5634–5637. PubMed PMC

Hertogs K., Leenders W.P., Depla E., De Bruin W.C., Meheus L., Raymackers J., Moshage H., Yap S.H. Endonexin II, present on human liver plasma membranes, is a specific binding protein of small hepatitis B virus (HBV) envelope protein. Virology. 1993;197:549–557. doi: 10.1006/viro.1993.1628. PubMed DOI

Hirsch V.M., Johnson P.R. Pathogenic diversity of simian immunodeficiency viruses. Virus Res. 1994;32:183–203. doi: 10.1016/0168-1702(94)90041-8. PubMed DOI

Hofer F., Gruenberger M., Kowalski H., Machat H., Huettinger M., Kuechler E., Blaas D. Members of the low density lipoprotein receptor family mediate cell entry of a minor group common cold virus. Proc. Nat. Acad. Sci. USA. 1994;91:1839–1842. doi: 10.1073/pnas.91.5.1839. PubMed DOI PMC

Holschbach C., Schneider J., Geyer H. Glycosylation of the envelope glycoprotein gp130 of simian immunodeficiency virus from sooty mangabey (Cercocebus atys) Biochem. J. 1990;267:759–766. PubMed PMC

Horuk R., Hesselgesser J., Zhou Y., Faulds D., Halks-Miller M., Harvey S., Taub D., Samson M., Parmentier M., Rucker J., Doranz B.J., Doms R.W. The CC chemokine I-309 inhibits CCR8-dependent infection by diverse HIV-1 strains. J. Biol. Chem. 1998;273:386–391. doi: 10.1074/jbc.273.1.386. PubMed DOI

Hosie M.J., Willett B.J., Dunsford T.H., Jarrett O., Neil J.C. A monoclonal antibody which blocks infection with feline immunodeficiency virus identifies a possible non-CD4 receptor. J. Virol. 1993;67:1667–1671. PubMed PMC

Huang T., Campadelli-Fiume G. Anti-idiotypic antibodies mimicking glycoprotein D of herpes simplex virus identify a cellular protein required for virus spread from cell to cell and virus-induced polykaryocytosis. Proc. Nat. Acad. Sci. USA. 1996;93:1836–1840. doi: 10.1073/pnas.93.5.1836. PubMed DOI PMC

Huang R.T.C., Lichtenberg B., Rick O. Involvement of annexin V in the entry of influenza viruses and role of phospholipids in infection. FEBS Lett. 1996;392:59–62. doi: 10.1016/0014-5793(96)00783-1. PubMed DOI

Huber S.A. VCAM-1 is a receptor for encephalomyocarditis virus on murine vascular endothelial cells. J. Virol. 1994;68:3453–3458. PubMed PMC

Jackson T., Ellard F.M., Ghazaleh R.A., Brookes S.M., Blakemore W.E., Corteyn A.H., Stuart D.I., Newman J.W.I., King A.M.Q. Efficient infection of cells in culture by type O foot-and-mouth disease virus requires binding to cell surface heparan sulfate. J. Virol. 1996;70:5282–5287. PubMed PMC

Ito T., Couceiro J.N.S.S., Kelm S., Baum L.G., Krauss S., Castrucci M.R., Donatelli I., Kida H., Paulson J.C., Webster R.G., Kawaoka Y. Molecular basis for the generation in pigs of influenza A viruses with pandemic potential. J. Virol. 1998;72:7667–7376. PubMed PMC

Jin Y.-M., Pardoe I.U., Burness A.T., Michalak T.I. Identification and characterization of the cell surface 70-kilodalton sialoglycoprotein(s) as a candidate receptor for encephalomyocarditis virus on human nucleated cells. J. Virol. 1994;68:7308–7319. PubMed PMC

Jones P.L.S.J., Korte T., Blumenthal R. Conformational changes in cell surface HIV-1 envelope glycoproteins are triggered by cooperation between cell surface CD4 and co-receptors. J. Biol. Chem. 1998;273:404–409. doi: 10.1074/jbc.273.1.404. PubMed DOI

Jungeblut C.W., Kodza H. Studies of propagation of Col SK group of viruses in various tissue culture media. Proc. Soc. Exp. Biol. Med. 1957;96:133–139. PubMed

Kaplan G., Totsuka A., Thompson P., Akatsuka A., Moritsugu Y., Feinstone S.M. Identification of a surface glycoprotein on African green monkey kidney cells as a receptor for hepatitis A virus. EMBO J. 1996;15:4282–4296. PubMed PMC

Karlsson K.A., Stromberg N. Overlay and solid-phase analysis of glycolipid receptors for bacteria and viruses. Meth. Enzymol. 1987;138:220–232. PubMed

Karlsson K.A., Angstrom J., Bergstrom J., Lanne B. Microbial interaction with animal cell surface carbohydrates. Acta Pathol. Microbiol. Immunol. 1992;100:71–83. PubMed

Kauffman R.S., Noseworthy J.H., Nepom J.T., Finberg R., Fields B.N., Greene M.I. Cell receptors for the mammalian reovirus. II. Monoclonal anti-idiotypic antibody blocks viral binding to cells. J. Immunol. 1983;131:2539–2541. PubMed

Kavanaugh M.P., Miller D.G., Zhang W., Law W., Kozak S.L., Kebat D., Miller A.D. Cell-surface receptors for gibbon ape leukemia virus and amphotropic murine retrovirus are inducible sodium-dependent phosphate symporters. Proc. Nat. Acad. Sci. USA. 1994;91:7071–7075. doi: 10.1073/pnas.91.15.7071. PubMed DOI PMC

Keljo D.J., Smith A.K. Characterization of binding of simian rotavirus SA11 to cultured epithelial cells. J. Pediatr. Gastroenterol. Nutr. 1988;7:249–256. PubMed

Kim J.W., Closs E.I., Albritton L.M., Cunningham J.M. Transport of cationic amino acids by the mouse ecotropic retrovirus receptor. Nature (London) 1991;352:725–728. doi: 10.1038/352725a0. PubMed DOI

Kimura T., Kimura-Kuroda J., Nagashima K., Yasui K. Analysis of virus-cell binding characteristics on the determination of Japanese encephalitis virus susceptibility. Arch. Virol. 1994;139:239–251. doi: 10.1007/BF01310788. PubMed DOI

Klatzmann D., Champagne E., Chamaret S., Gruest J., Guetard D., Hercend T., Gluckman J.-C., Montagnier L. T-lymphocyte T4 molecule behaves as the receptor for human retrovirus LAV. Nature (London) 1984;312:767–768. doi: 10.1038/312767a0. PubMed DOI

Kopecký J., Grubhoffer L., Kovář V., Jindrák L., Vokurková D. A putative host-cell receptor for tick-borne encephalitis virus identified by anti-idiotypic antibodies and virus affinoblotting. Intervirology. 1999;42:9–16. doi: 10.1159/000024954. PubMed DOI

Lankes W.T., Furthmayer H. Moesin: a member of the protein 4.1-talin-ezrin family of proteins. Proc. Nat. Acad. Sci. USA. 1991;88:8297–8301. doi: 10.1073/pnas.88.19.8297. PubMed DOI PMC

Lankes W.T., Griesmacher A., Grunwald J., Schwartz-Albiez R., Keller R. A heparin-binding protein involved in inhibition of smooth muscle cell proliferation. Biochem. J. 1988;251:831–842. PubMed PMC

Lawlence M.B., Springer T.A. Leukocytes roll on a selection at physiologic flow rates: distinction from and prerequisite for adhesion through integrins. Cell. 1991;65:859–873. doi: 10.1016/0092-8674(91)90393-D. PubMed DOI

Leonard C.K., Spellman M.W., Riddle L., Harris R.J., Thomas J.N., Gregory T.J. Assignment of intrachain disulfide bonds and characterization of potential glycosylation sites of the type 1 recombinant human immunodeficiency virus envelope glycoprotein (gp120) expressed in Chinese hamster ovary cells. J. Biol. Chem. 1990;265:10373–10382. PubMed

Li Y., Luo L., Rasool N., Kang C.Y. Glycosylation is necessary for the correct folding of human immunodeficiency virus gp120 in CD4 binding. J. Virol. 1993;67:584–588. PubMed PMC

Liu C., Eichelberger M.C., Compans R.W., Air G.M. Influenza type A virus neuraminidase does not play a role in viral entry, replication, assembly, or budding. J. Virol. 1995;69:1099–1106. PubMed PMC

Ludwig G.V., Kondig J.P., Smith J.F. A putative receptor for Venezuelan equine encephalitis virus from mosquito cells. J. Virol. 1996;70:5592–5599. PubMed PMC

Maddon P.J., Dalgleish A.G., McDougal J.S., Clapham R.A., Weiss R.A., Axel R. The T4 gene encodes for the AIDS virus receptor and is expressed in the immune system and in the brain. Cell. 1986;47:333–348. doi: 10.1016/0092-8674(86)90590-8. PubMed DOI

Maldov D.G., Karganova G.G., Timofeev A.V. Tick-borne encephalitis virus interaction with the target cells. Arch. Virol. 1992;127:321–325. doi: 10.1007/BF01309594. PubMed DOI

Marriott S.J., Roeder D.J., Consigli R.A. Anti-idiotypic antibodies to a polyomavirus monoclonal antibody recognize cell surface components of mouse kidney cells and prevent polyomavirus infection. J. Virol. 1987;61:2747–2753. PubMed PMC

Marsh M., Helenius A. Adsorptive endocytosis of Semliki forest virus. J. Mol. Biol. 1980;142:439–454. doi: 10.1016/0022-2836(80)90281-8. PubMed DOI

Marsh M., Bolzau E., Helenius A. Penetration of Semliki forest virus from acidic prelysosomal vacuoles. Cell. 1983;32:931–940. doi: 10.1016/0092-8674(83)90078-8. PubMed DOI

Marsh M., Matlin K., Simons K., Reggio H., White J., Kartenbeck J., Helenius A. Are lysosomes a site of enveloped-virus penetration? Cold Spring Harbor Symp. Quant. Biol. 1982;46:835–843. PubMed

Matlin K.S., Reggio J., Helenius A., Simons K. Entry pathway of influenza virus in a canine kidney cell line. J. Cell Biol. 1981;91:601–613. doi: 10.1083/jcb.91.3.601. PubMed DOI PMC

Matrosovich M., Miller Podraza H., Teneberg S., Robertson J., Karlsson K.A. Influenza viruses display high-affinity binding to human polyglycosylceramides represented on a solid-phase assay surface. Virology. 1996;223:413–416. doi: 10.1006/viro.1996.0498. PubMed DOI

Mecham R.P. Receptors for laminin on mammalian cells. FASEB J. 1991;5:2538–2546. PubMed

Mendelsohn C.L., Wimmer E., Racaniello V.R. Cellular receptor for poliovirus: molecular cloning, nucleotide sequence, and expression of a new member of the immunoglobulin superfamily. Cell. 1989;56:855–865. doi: 10.1016/0092-8674(89)90690-9. PubMed DOI

Mendez E., Barias C.F., Lopez S. Binding to sialic acids is not an essential step for the entry of animal rotaviruses to epithelial cells in culture. J. Virol. 1993;67:5253–5259. PubMed PMC

McClintock P.R., Billups L.C., Notkins A.L. Receptors for encephalomyocarditis virus on murine and human cells. Virology. 1980;106:261–272. doi: 10.1016/0042-6822(80)90249-4. PubMed DOI

Miller D.G., Miller A.D. Tunicamycin treatment of CHO cells abrogates multiple blocks to retrovirus infection, one of which is due to a secreted inhibitor. J. Virol. 1992;66:78–84. PubMed PMC

Miller D.G., Miller D. A family of retroviruses that utilize related phosphate transporters for cell entry. J. Virol. 1994;68:8270–8276. PubMed PMC

Miller D.G., Edwards R.H., Miller A.D. Cloning of the cellular receptor for amphotropic murine retroviruses reveals homology to that for gibbon ape leukemia virus. Proc. Nat. Acad. Sci. USA. 1994;91:78–82. doi: 10.1073/pnas.91.1.78. PubMed DOI PMC

Mizuochi T., Spellman M.W., Larkin M., Solomon J., Basa L., Feizi T. Carbohydrate structures of the human immunodeficiency virus (HIV) recombinant envelope glycoprotein gp120 produced in Chinese-hamster ovary cells. Biochem. J. 1988;254:599–603. PubMed PMC

Mizuochi T., Matthews T.J., Kato M., Hamako J., Titani K., Solomon J., Feizi T. Diversity of oligosaccharide structures on the envelope glycoprotein gp120 of human immunodeficiency virus 1 from the lymphoblastoid cell line H9. Presence of complex-type oligosaccharides with bisecting N-acetylglucosamine residues. J. Biol. Chem. 1990;265:8519–8524. PubMed

Moore J.P., Trkola A., Dragic T. Co-receptors for HIV-1 entry. Curr. Opin. Immunol. 1997;9:551–562. doi: 10.1016/S0952-7915(97)80110-0. PubMed DOI

Myers G., Lenroot R. HIV variation studies; HIV glycosylation: What does it portend? AIDS Res. Hum. Retrovir. 1992;8:1459–1460. PubMed

Naito S., Matsumoto S. Identification of cellular actin within the rabies virus. Virology. 1978;91:151–163. doi: 10.1016/0042-6822(78)90363-X. PubMed DOI

Nandi P., Charpilienne A., Cohen J. Interaction of rotavirus particles with liposomes. J. Virol. 1992;66:3363–3367. PubMed PMC

Naniche D., Varior-Krishnan G., Cervoni F., Wild T.F., Rossi B., Rabourdin-Combe C., Gerlier D. Human membrane cofactor protein (CD46) acts as a cellular receptor for measles virus. J. Virol. 1993;67:6025–6032. PubMed PMC

Naniche D., Wild C., Rabourdin-Combe C., Gerlier D. Measles virus hæmagglutinin induces down-regulation of gp57/67, a molecule involved in virus binding. J. Gen. Virol. 1993;74:1073–1079. PubMed

Narayan O., Kennedy-Stoskopf S., Sheffer D., Griffin D.E., Clements J.E. Activation of caprine arthritis-encephalitis virus expression during maturation of monocytes to macrophages. Infect. Immun. 1983;41:67–73. PubMed PMC

Nėdellec P., Dveksler G.S., Daniels E., Turbide C., Chow B., Basile A.A., Holmes K.V., Beauchemin N. Bgp2, a new member of the carcinoembryonic antigen-related gene family, encodes an alternative receptor for mouse hepatitis viruses. J. Virol. 1994;68:4525–4537. PubMed PMC

Neurath A.R., Strick N. The putative cell receptors for hepatitis B virus (HBV), annexin V and apolipoprotein, H, bind to lipid components of HBV. Virology. 1994;204:475–447. doi: 10.1006/viro.1994.1558. PubMed DOI

Nicholson-Weller A., Burge J., Fearon D.T., Weller P.F., Austen K.F. Isolation of a human erythrocyte membrane glyco-protein with decay accelerating activity for C3 convertases of the complement system. J. Immunol. 1982;129:184–189. PubMed

Nieva J.L., Bron R., Corver J., Wilschut J. Membrane fusion of Semliki forest virus requires sphingolipids in the target membrane. EMBO J. 1994;13:2797–2808. PubMed PMC

Norkin L.C. Virus receptors: implication for pathogenesis and the design of antiviral agents. Clin. Microbiol. Rev. 1995;8:293–315. PubMed PMC

Noseworthy J.H., Fields B.N., Dichter M.A., Sobotka C., Pizer E., Perry L.L., Nepom J.T., Greene M.I. Cell receptors for the mammalian reovirus. I. Syngeneic monoclonal anti-idiotypic antibody identifies a cell surface receptor for reovirus. J. Immunol. 1983;131:2533–2538. PubMed

O'Hara B., Johann S.V., Klinger H.P., Blair D.G., Rubinson H., Dunn K.J., Sass P., Vitek S.M., Robins T. Characterization of a human gene conferring sensitivity to infection by gibbon ape leukemia virus. Cell. Growth Differ. 1990;1:119–127. PubMed

Okhuma S., Poole B. Fluorescence probe measurement of the intralysosomal pH in living cells and the perturbation of pH by various agents. Proc. Nat. Acad. Sci. USA. 1978;75:3327–3331. doi: 10.1073/pnas.75.7.3327. PubMed DOI PMC

Pardoe I.U., Grewal K.K., Baldeh P., Hamid J., Burnes A.T.H. Persistent infection of K562 cells by encephalomyocarditis virus. J. Virol. 1990;64:6040–6044. PubMed PMC

Payne H.R., Storz J., Henk W.G. Initial events in bovine coronavirus infection: analysis through immunogold probes and lysosomotropic inhibitors. Arch. Virol. 1990;114:175–189. doi: 10.1007/BF01310747. PubMed DOI PMC

Pifat D.Y., Ennis W.H., Ward J.M., Oberste M.S., Gonda M.A. Persistent infection of rabbits with the bovine immunodeficiency-like virus. J. Virol. 1992;66:4518–4524. PubMed PMC

Pileri P., Uematsu Y., Gampagnoli S., Galli G., Falugi F., Petracca R., Weiner A.J., Houghton M., Rosa D., Grandi G., Abrignani S. Binding of hepatitis C virus to CD81. Science. 1998;282:938–940. doi: 10.1126/science.282.5390.938. PubMed DOI

Poste G., Pasternak C.A. Virus-induced cell fusion. In: Poste G., Nicholson G.L., editors. Cell Surface Reviews, Vol. 4. Amsterdam: Elsevier/North-Holland; 1978. pp. 305–357.

Price P. Are MHC proteins cellular receptors for CMV? Immunol. Today. 1994;15:295–296. doi: 10.1016/0167-5699(94)90011-6. PubMed DOI

Protopopova E.V., Konavalova S.N., Loktev V.B. Isolation of a cellular receptor for tick-borne encephalitis virus using anti-idiotypic antibodies. Vopr. Virusol. 1997;42:264–268. PubMed

Qingxue L., Spriggs M.K., Kovats S., Turk S.M., Comeau M.R., Nepom B., Hutt-Fletcher L.M. Epstein-Barr virus uses HLA class II as a cofactor for infection of B lymphocytes. J. Virol. 1997;71:4657–4662. PubMed PMC

Ramos-Castaneda J., Imbert J.L., Barron B.L., Ramos C. A 65-kDa trypsin-sensible membrane cell protein as a possible receptor for dengue virus in cultured neuroblastoma cells. J. Neurovirol. 1997;3:435–440. doi: 10.3109/13550289709031189. PubMed DOI

Rey F.A., Heinz F.X., Mandl C., Kunz C., Harrison S.C. The envelope glycoprotein from tick-borne encephalitis virus at 2 Å resolution. Nature. 1995;375:291–298. doi: 10.1038/375291a0. PubMed DOI

Roivainen M., Piirainen L., Hovi T., Virtanen I., Riikonen T., Heino J., Hyypia T. Entry of coxsackievirus A9 into host cells: specific interactions with αVβ3 integrin, the vitronectin receptor. Virology. 1994;203:357–365. doi: 10.1006/viro.1994.1494. PubMed DOI

Roivainen M., Piirainen L., Hovi T. Efficient RGD-independent entry process of coxsackievirus A9. Arch. Virol. 1996;141:1909–1919. doi: 10.1007/BF01718203. PubMed DOI

Ruiz M.-C., Alonso-Torre S.R., Charpilienne A., Vasseur M., Michelangeli F., Cohen J., Alvarado F. Rotavirus interaction with isolated membrane vesicles. J. Virol. 1994;68:4009–4016. PubMed PMC

Sattentau Q.J., Clapham P.R., Weiss R.A., Beverley P.C., Montagnier L., Alhalabi M.F., Gluckman J.-C., Klatzmann D. The human and simian immunodeficiency viruses HIV-1, HIV-2, and SIV interact with similar epitopes on their cellular receptor, the CD4 molecule. AIDS. 1988;2:101–105. doi: 10.1097/00002030-198804000-00005. PubMed DOI

Sauter N.K., Glick G.D., Crowther R.L., Park S-J., Eisen M.B., Skehel J.J., Knowles J.R., Wiley D.C. Crystallographic detection of a second ligand binding site in influenza virus hemagglutinin. Proc. Nat. Acad. Sci. USA. 1992;89:324–328. doi: 10.1073/pnas.89.1.324. PubMed DOI PMC

Sharma A., Rao Z., Fry E., Booth T., Jones E.Y., Rowlands D.J., Simmons D.L., Stuart D.I. Specific interactions between human integrin αVβ3 and chimeric hepatitis B virus core particles bearing the receptor-binding epitope of foot-and-mouth disease virus. Virology. 1997;239:150–157. doi: 10.1006/viro.1997.8833. PubMed DOI

Schultze B., Krempl C., Ballesteros M.L., Shaw L., Schauer R., Enjuanes L., Herrler G. Transmissible gastroenteritis virus, but not the related porcine respiratory coronavirus, has a sialic acid (N-glycolylneuraminic acid) binding activity. J. Virol. 1996;70:5634–5637. PubMed PMC

Simeoni L., Forte P., Auiti A., Candido A., Campese A.F., Fedele G., Di Tomaso F., Navarra M., Fantoni A. Transgenic mice expressing human HIV receptors become persistently recipient of HIV DNA after injection with infected human cell lines. Folia Microbiol. 1998;43:525–526. doi: 10.1007/BF02820812. PubMed DOI

Staunton D.E., Merluzzi V.J., Rothlein R., Barton S.D., Springer T.A. A cell adhesion molecule, ICAM-1, is the major surface receptor for rhinoviruses. Cell. 1989;56:849–853. doi: 10.1016/0092-8674(89)90689-2. PubMed DOI

Svensson L. Group C rotavirus requires sialic acid for erythrocyte and cell receptor binding. J. Virol. 1992;66:5582–5585. PubMed PMC

Sagara J., Tsukita S., Yonemura S., Kawai A. Cellular actin-binding ezrin-radixin-moesin (ERM) family proteins are incorporated into the rabies virion and closely associated with viral envelope proteins in the cell. Virology. 1994;206:485–494. doi: 10.1016/S0042-6822(95)80064-6. PubMed DOI

Sagara J., Kawai A. Identification of heat shock protein 70 in the rabies virion. Virology. 1992;190:845–848. doi: 10.1016/0042-6822(92)90923-D. PubMed DOI

Schelp C., Greiser-Wilke I., Wolf G., Beer M., Moennig V., Liess B. Identification of cell membrane proteins linked to susceptibility to bovine viral diarrhoea virus infection. Arch. Virol. 1995;140:1997–2009. doi: 10.1007/BF01322688. PubMed DOI

Schnittler H.-J., Mahner F., Drenckhahn D., Klenk H.-D., Feldmann H. Replication of Marburg virus in human endothelial cells: a possible mechanism for the development of viral hemorrhagic disease. J. Clin. Invest. 1993;91:1301–1309. PubMed PMC

Smith A.L., Tignor G.H. Host cell receptors for two strains of Sindbis virus. Arch. Virol. 1980;66:11–26. doi: 10.1007/BF01315041. PubMed DOI

Sommerfelt M.A., Weiss R.A. Receptor interference groups of 20 retroviruses plating on human cells. Virology. 1990;176:58–69. doi: 10.1016/0042-6822(90)90230-O. PubMed DOI

Srnka C.A., Tiemeyer M., Gilbert J.H., Moreland M., Schweingruber H., de Lappe B.W., James P.G., Gant T., Willough R.E., Yolken R.H., Nashed M.A., Abbas S.A., Laine R.A. Cell surface ligands for rotavirus mouse intestinal glycolipids and synthetic carbohydrate analogs. Virology. 1992;190:794–805. doi: 10.1016/0042-6822(92)90917-E. PubMed DOI

Svensson L. Group C rotavirus requires sialic acid for erythrocyte and cell receptor binding. J. Virol. 1992;66:5582–5585. PubMed PMC

Stehle T., Yan Y., Benjamin T.L., Harrison S.C. Structure of murine polyomavirus complexed with an oligosaccharide receptor fragment. Nature. 1994;369:160–163. doi: 10.1038/369160a0. PubMed DOI

Tavakkol A., Burness A.T.H. Evidence for a direct role for sialic acid in the attachment of encephalomyocarditis virus to human erythrocytes. Biochemistry. 1990;29:10684–10690. doi: 10.1021/bi00499a016. PubMed DOI

Takeuchi Y., Vile R.G., Simpson G., O'Hara B., Collins M.K., Weiss R.A. Feline leukemia virus subgroup B uses the same cell surface receptor as gibbon ape leukemia virus. J. Virol. 1992;66:1219–1222. PubMed PMC

Tomassini J.E., Graham D., DeWitt C.M., Lineberger D.W., Rodkey J.A., Colonno R.J. cDNA cloning reveals that the major group rhinovirus receptor on HeLa cells is intercellular adhesion molecule 1. Proc. Nat. Acad. Sci. USA. 1989;86:4907–4911. doi: 10.1073/pnas.86.13.4907. PubMed DOI PMC

Tycko B., Maxfield F.R. Rapid acidification of endocytic vesicles containing α-2-macroglobulin. Cell. 1982;28:643–651. doi: 10.1016/0092-8674(82)90219-7. PubMed DOI

Ubol S., Griffin D.E. Identification of a putative alphavirus receptor on mouse neural cells. J. Virol. 1991;65:6913–6921. PubMed PMC

Varghese J.N., Laver W.G., Colman P.M. Structure of the influenza virus glycoprotein antigen neuraminidase at 2.9 Å resolution. Nature. 1983;303:35–40. doi: 10.1038/303035a0. PubMed DOI

Varghese J.N., McKimm-Breschkin J.L., Caldwell J.B., Kortt A.A., Colman P.M. The structure of the complex influenza virus neuraminidase and sialic acid, the viral receptor. Proteins. 1992;14:327–332. doi: 10.1002/prot.340140302. PubMed DOI

Vlasak R., Lnytzes W., Leider J., Spaan W., Palese P. The E3 protein of bovine coronavirus is a receptor-destroying enzyme with acetylesterase activity. J. Virol. 1988;62:4686–4690. PubMed PMC

van Zeijl M., Johann S.V., Closs E., Cunningham J., Eddy R., Shows T.B., O'Hara B. A human amphotropic retrovirus receptor is a second member of the gibbon ape leukemia virus receptor family. Proc. Nat. Acad. Sci. USA. 1994;91:1168–1172. doi: 10.1073/pnas.91.3.1168. PubMed DOI PMC

Vinuela E. Molecular biology of African swine fever virus. In: Becker Y., editor. African Swine Fever. Boston: Martinus Nijhoff Publishing; 1987. pp. 31–49.

Wang K.S., Kuhn R.J., Strauss E.G., Ou S., Strauss J.H. High-affinity laminin receptor is a receptor for Sindbis virus in mammalian cells. J. Virol. 1992;66:4992–5001. PubMed PMC

Wang H., Kavanaugh M.P., North R.A., Kabat D. Cell-surface receptor for ecotropic murine retroviruses is a basic amino-acid transporter. Nature (London) 1991;352:729–731. doi: 10.1038/352729a0. PubMed DOI

Ward T., Pipkin P.A., Clarkson N.A., Stone D.M., Minor P.D., Almond J.W. Decay-accelerating factor CD55 is identified as the receptor for echovirus 7 using CELICS, a rapid immuno-focal cloning method. EMBO J. 1994;13:5070–5074. PubMed PMC

Watanabe S. The receptor and pathways for human cytomegalovirus entry. Nippon Rinsho. 1998;56:44–49. PubMed

Watowich S.J., Skehel J.J., Wiley D.C. Crystal structures of influenza virus hemagglutinin in complex with high-affinity receptor analogs. Structure. 1994;2:719–731. doi: 10.1016/S0969-2126(00)00073-3. PubMed DOI

Weiss R.A. Cellular receptors and viral glycoproteins involved in retroviral entry. In: Levy J., editor. The Retroviridae. New York: Plenum Press; 1993. pp. 1–108.

Weiss R.A., Tailor C.S. Retrovirus receptors. Cell. 1995;82:531–533. doi: 10.1016/0092-8674(95)90024-1. PubMed DOI

Weis W.I., Brown J.H., Cusack S., Paulson J.C., Skehel J.J., Wiley D.C. Structure of the influenza virus hæmagglutinin complexed with its receptor, sialic acid. Nature. 1988;333:426–431. doi: 10.1038/333426a0. PubMed DOI

White J., Matlin K., Helenius A. Cell fusion by Semliki forest, influenza, and vesicular stomatitis viruses. J. Cell. Biol. 1981;89:674–679. doi: 10.1083/jcb.89.3.674. PubMed DOI PMC

Wickham T.J., Mathias P., Cheresh D.A., Nemerow G.R. Integrins αVβ3 and αVβ5 promote adenovirus internalization but not virus attachment. Cell. 1993;73:309–319. doi: 10.1016/0092-8674(93)90231-E. PubMed DOI

Willett B.J., Hosie M.J., Jarrett O., Neil J.C. Identification of a putative cellular receptor for feline immunodeficiency virus as the feline homologue of CD9. Immunology. 1994;81:228–233. PubMed PMC

Willett B., Hosie M., Shaw A., Neil J. Inhibition of feline immunodeficiency virus infection by CD9 antibody operates after virus entry and is independent of virus entry and is independent of virus tropism. J. Gen. Virol. 1997;78:611–618. PubMed

Williams R.K., Jiang G.S., Holmes K.V. Receptor for mouse hepatitis virus is a member of the carcinoembryonic antigen family of glycoproteins. Proc. Nat. Acad. Sci. USA. 1991;88:5533–5536. doi: 10.1073/pnas.88.13.5533. PubMed DOI PMC

Willoughby R.E., Yolken R.H., Schnaar R.L. Rotaviruses specifically bind to the neutral glycosphingolipid. J. Virol. 1990;64:4830–4835. PubMed PMC

Wilson C.A., Eiden M.V., Anderson W.B., Lehel C., Olah Z. The dual-function hamster receptor for amphotropic murine leukemia virus (MuLV), 10A1 MuLV, and Gibbon ape leukemia virus is a phosphate symporter. J. Virol. 1995;69:534–537. PubMed PMC

Wilson C.A., Farrell K.B., Eiden M.V. Properties of a unique form of the murine amphotropic leukemia virus receptor expressed on hamster cells. J. Virol. 1994;68:7697–7703. PubMed PMC

Wimmer E. Cellular Receptors for Animal Viruses. Cold Spring Harbor: Cold Springer Harbor Laboratory Press; 1994.

Xu G., Suzuki T., Tahara H., Kiso M., Hasegawa A., Suzuki Y. Specificity of sialyl-sugar chain mediated recognition by the hemagglutinin of human influenza B virus isolates. J. Biochem. 1994;115:202–207. PubMed

Xu R., Mohanty J.G., Crowell R.L. Receptor proteins on newborn Balb/c mouse brain cells for coxsackievirus B3 are immunologically distinct from those on HeLa cells. Virus Res. 1994;35:323–340. doi: 10.1016/0168-1702(94)00100-Q. PubMed DOI

Yasukawa M. HHV-7 infection of CD4 gene transfected cells. Nippon Rinsho. 1998;56:56–61. PubMed

Yeager C.L., Ashmun R.A., Williams R.K., Cardellichio C.B., Shapiro L.H., Look A.T., Holmes K.V. Human amino peptidase N is a receptor for human coronavirus 229E. Nature (London) 1992;357:420–422. doi: 10.1038/357420a0. PubMed DOI PMC

Yi Y., Rana S., Turner J.D., Gaddis N., Collman R.G. CXCR-4 is expressed by primary macrophages and supports CCR5-independent infection by dual-tropic but not T-tropic isolates of human immunodeficiency virus type 1. J. Virol. 1998;72:772–777. PubMed PMC

Yokomori K., Lai M.M. Mouse hepatitis virus utilizes two carcinoembryonic antigens as alternative receptors. J. Virol. 1992;66:6194–6199. PubMed PMC

Yoshikawa Y., Yamanouchi K., Takasu T., Rauf S., Ahmed A. Structural homology between hemagglutinin (HA) of measles virus and the active site of long neurotoxins. Virus Genes. 1991;5:57–67. doi: 10.1007/BF00571731. PubMed DOI

Young J.A., Bates P., Varmus H.E. Isolation of a chicken gene that confers susceptibility to infection by subgroup A avian leukosis and sarcoma viruses. J. Virol. 1993;67:1811–1814. PubMed PMC

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