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Molecular Mechanisms of Poliovirus Pathogenesis

  • Chapter
Molecular Neurovirology

Abstract

Poliomyelitis, an acute disease of the central nervous system (CNS), is caused by poliovirus. Poliovirus is a human enterovirus belonging to the Picornaviridae, and is classified into three stable serotypes (types 1, 2, and 3). Poliovirus strains, except for type 2 virulent strains, infect only primates. The poliovirus infection is initiated by ingestion of a virus and its primary multiplication in the alimentary mucosa. The tonsils and Peyer’s patches are invaded early in the course of infection, and extensive viral multiplication occurs in these loci. From these primary sites, the virus moves into deep cervical and mesenteric lymph nodes, and then into the blood. When effective viremia is established, the virus spreads into the CNS, and then paralytic poliomyelitis occurs as a result of destruction of motor neurons in the brain and spinal cord through lytic viral replication.

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References

  1. Paul, J. R. (1971) A history of poliomyelitis. Yale University Press, New Haven, CT.

    Google Scholar 

  2. Salk, J. E. (1960) Persistence of immunity after administration of Formalin-treated poliovirus vaccine. Lancet ii, 715–723.

    Google Scholar 

  3. Melnick, J. L. (1984) Live attenuated oral poliovirus vaccine. Rev. Infect. Dis. 6(Suppl. ), 323–327.

    Google Scholar 

  4. Sabin, A. B. and L. R. Boulger (1973) History of Sabin attenuated poliovirus oral live vaccine strains. J. Biol. Stand. 1, 115–118.

    Google Scholar 

  5. Omata, T., M. Kohara, Y. Sakai, A. Kameda, N. Imura, and A. Nomoto (1984) Cloned infectious complementary DNA of the poliovirus Sabin 1 genome: Biochemical and biological properties of the recovered virus. Gene 32, 1–10.

    PubMed  CAS  Google Scholar 

  6. Racaniello, V. R. and D. Baltimore (1981) Cloned poliovirus complementary DNA is infectious in mammalian cells. Science 214, 916–919.

    PubMed  CAS  Google Scholar 

  7. Semler, B. L., A. J. Dorner, and E. Wimmer (1984) Production of infectious poliovirus from cloned cDNA is dramatically increased by SV40 transcription and replication signals. Nucleic Acids Res. 12, 5123–5141.

    PubMed  CAS  Google Scholar 

  8. van der Werf, S., J. Bradley, E. Wimmer, F. W. Studier, and J. J. Dunn (1986) Synthesis of infectious poliovirus RNA by purified T7 RNA polymerase. Proc. Natl. Acad. Sci. USA 83, 2330–2334.

    PubMed  Google Scholar 

  9. Kitamura, N., B. L. Semler, P. G. Rothberg, G. R. Larsen, C. J. Adler, A. J. Dorner, E. A. Emini, R. Hanecak, J. J. Lee, S. van der Werf, C. W. Anderson, and E. Wimmer (1981) Primary structure, gene organization and polypeptide expression of poliovirus RNA. Nature 291, 547–553.

    PubMed  CAS  Google Scholar 

  10. Racaniello, V. R. and D. Baltimore (1981) Molecular cloning of poliovirus cDNA and determination of the complete nucleotide sequence of the viral genome. Proc. Natl. Acad. Sci. USA 78, 4887–4891.

    PubMed  CAS  Google Scholar 

  11. Hogle, J. M., M. Chow, and D. J. Filman (1985) Three-dimensional structure of poliovirus at 2. 9 Å resolution. Science 229, 1358–1363.

    PubMed  CAS  Google Scholar 

  12. LaMonica, N., C. Meriam, and V. R. Racaniello (1986) Mapping of sequences required for mouse neurovirulence of poliovirus type 2 Lansing. J. Virol. 57, 515–525.

    CAS  Google Scholar 

  13. Nomoto, A., T. Omata, H. Toyoda, S. Kuge, H. Horie, Y. Kataoka, Y. Genba, Y. Nakano, and N. Imura (1982) Complete nucleotide sequence of the attenuated poliovirus Sabin 1 strain genome. Proc. Natl. Acad. Sci. USA 79, 5793–5797.

    PubMed  CAS  Google Scholar 

  14. Stanway, G., P. J. Hughes, R. C. Mountford, P. Reeve, P. D. Minor, G. C. Schild, and J. W. Almond (1984) Comparison of the complete nucleotide sequences of the genomes of the neurovirulent poliovirus P3/ Leon 37 and its attenuated Sabin vaccine derivative P2/Leon 12a1b. Proc. Natl. Acad. Sci. USA 81, 1539–1543.

    PubMed  CAS  Google Scholar 

  15. Toyoda, H., M. Kohara, Y. Kataoka, T. Suganuma, T. Omata, N. Imura, and A. Nomoto (1984) Complete nucleotide sequences of all three poliovirus serotype genomes: Implication for genetic relationship, gene function and antigenic determinants. J. Mol. Biol. 174, 561–585.

    PubMed  CAS  Google Scholar 

  16. Nomoto, A. and E. Wimmer (1987) Genetic studies of the antigenicity and the attenuation phenotype of poliovirus, in SGM40, Molecular Basis of Virus Disease. Russell, W. C. and J. W. Almond, eds., Cambridge University Press, Cambridge, pp. 107–137.

    Google Scholar 

  17. Rueckert, R. R.} (1976) On the structure and morphogenesis of picornaviruses. Compr. Virol. 6, 131–213.

    CAS  Google Scholar 

  18. Rossmann, M. G., E. Arnold, J. W. Erickson, E. A. Frankenberger, J. P. Griffith, H.-J. Hecht, J. Johnson, G. Kamer, M. Luo, A. Mosser, R. R. Rueckert, B. Sherry, and G. Vriend (1985) Structure of a human common cold virus and functional relationship to other picornaviruses. Nature 317, 145–153.

    PubMed  CAS  Google Scholar 

  19. Nomoto, A., N. Kitamura, F. Golini, and E. Wimmer (1977) The 5′-terminal structures of poliovirion RNA and poliovirus mRNA differ only in the genome-linked protein VPg. Proc. Natl. Acad. Sci. USA 74, 5345–5349.

    PubMed  CAS  Google Scholar 

  20. Nomoto, A., Y. F. Lee, and E. Wimmer (1976) The 5′ end of poliovirus mRNA is not capped with m7G(5′)ppp(5′)Np. Proc. Natl. Acad. Sci. USA 73, 375–380.

    PubMed  CAS  Google Scholar 

  21. Pelletier, J. and N. Sonenberg (1988) Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA. Nature 334, 320–325.

    PubMed  CAS  Google Scholar 

  22. Pelletier, J. and N. Sonenberg (1989) Internal binding of eucaryotic ribosomes on poliovirus RNA: Translation in HeLa cell extracts. J. Virol. 63, 441–444.

    PubMed  CAS  Google Scholar 

  23. Jang, S. K., H.-G. Kräusslich, M. J. H. Nicklin, G. M. Duke, A. C. Palmenberg, and E. Wimmer (1988) A segment of the 5′ nontranslated region of encephalomyocarditis virus RNA directs internal entry of ribosomes during in vitro translation. J. Virol. 62, 2636–2643.

    PubMed  CAS  Google Scholar 

  24. Jang, S. K., M. V. Davies, R. J. Kaufman, and E. Wimmer (1989) Initiation of protein synthesis by internal entry of ribosomes into the 5′ nontranslated region of encephalomyocarditis virus RNA in vivo. J. Virol. 63, 1651–1660.

    PubMed  CAS  Google Scholar 

  25. Kaminski, A., M. T. Howell, and R. J. Jackson (1990) Initiation of encephalomyocarditis virus RNA translation: The authentic initiation site is not selected by a scanning mechanism. EMBO J. 9, 3753–3759.

    PubMed  CAS  Google Scholar 

  26. Pelletier, J., M. E. Flynn, G. Kaplan, V. Racaniello, and N. Sonenberg (1988) Mutational analysis of upstream AUG codons of poliovirus RNA. J. Virol. 62, 4486–4492.

    PubMed  CAS  Google Scholar 

  27. Iizuka, N., M. Kohara, K. Hagino-Yamagishi, S. Abe, T. Komatsu, K. Tago, M. Arita, and A. Nomoto (1989) Construction of less neurovirulent polioviruses by introducing deletions into the 5′ noncoding sequence of the genome. J. Virol. 63, 5354–5363.

    PubMed  CAS  Google Scholar 

  28. Kuge, S. and A. Nomoto (1987) Construction of viable deletion and insertion mutants of the Sabin strain of type 1 poliovirus: Function of the 5′ noncoding sequence in viral replication. J. Virol. 61, 1478–1487.

    PubMed  CAS  Google Scholar 

  29. Kuge, S., N. Kawamura, and A. Nomoto (1989) Genetic variation ocurring on the genome of an in vitro insertion mutant of poliovirus type 1. J. Virol. 63, 1069–1075.

    PubMed  CAS  Google Scholar 

  30. Kuge, S., N. Kawamura, and A. Nomoto (1989) Strong inclination toward transition mutation in nucleotide substitutions by poliovirus replicase. J. Mol. Biol. 207, 175–182.

    PubMed  CAS  Google Scholar 

  31. Jang, S. K. and E. Wimmer (1990) Cap-independent translation of encephalomyocarditis virus RNA: Structural elements of the internal ribosomal entry site and involvement of a cellular 57-kD RNA-binding protein. Genes Dev. 4, 1560–1572.

    PubMed  CAS  Google Scholar 

  32. Meerovitch, K., J. Pelletier, and N. Sonenberg (1989) A cellular protein that binds to the 5′-noncoding region of poliovirus RNA: Implications for internal translation initiation. Genes Dev. 3, 1026–1034.

    PubMed  CAS  Google Scholar 

  33. Hanecak, R., B. L. Semler, C. W. Anderson, and E. Wimmer (1982) Proteolytic processing of poliovirus polypeptides: Antibodies to polypeptide P3-7c inhibit cleavage at glutamine-glycine pairs. Proc. Natl. Acad. Sci. USA 79, 3973–3977.

    PubMed  CAS  Google Scholar 

  34. Kräusslich, H.-G. and E. Wimmer (1988) Viral proteinases. Ann. Rev. Biochem. 57, 701–754.

    PubMed  Google Scholar 

  35. Toyoda, H., M. J. H. Nicklin, M. G. Murray, C. W. Anderson, J. J. Dunn, F. W. Studier, and E. Wimmer (1986) A second virus-encoded proteinase involved in proteolytic processing of poliovirus polyprotein. Cell 45, 761–770.

    PubMed  CAS  Google Scholar 

  36. Nicklin, M. J. H., K. S. Harris, P. V. Pallai, and E. Wimmer (1988) Poliovirus proteinase 3C: Large-scale expression, purification, and specific cleavage activity on natural and synthetic substrates in vitro. J. Virol. 62, 4586–4593.

    PubMed  CAS  Google Scholar 

  37. Takahara, Y., N. Ando, M. Kohara, K. Hagino-Yamagishi, A. Nomoto, H. Itoh, N. Numao, and E. Wimmer (1989) Purification of enzymatically active poliovirus proteinase 3C produced in Escherichia coli. Gene 79, 249–258.

    PubMed  CAS  Google Scholar 

  38. Ypma-Wong, M. F., P. G. Dewalt, V. H. Johnson, J. G. Lamb, and B. L. Semler (1988) Protein 3CD is the major proteinase responsible for cleavage of the PI capsid precursor. Virology 166, 265–270.

    PubMed  CAS  Google Scholar 

  39. Arnold, E., M. Luo, G. Vriend, M. G. Rossmann, A. C. Palmenberg, G._D. Parks, M. J. H. Nicklin, and E. Wimmer (1987) Implications of the picornavirus capsid structure for polyprotein processing. Proc. Natl. Acad. Sci. USA 84, 21–25.

    PubMed  CAS  Google Scholar 

  40. Yogo, Y. and E. Wimmer (1972) Polyadenylic acid at 3′-terminus of poliovirus RNA. Proc. Natl. Acad. Sci. USA 69, 1877–1882.

    PubMed  CAS  Google Scholar 

  41. Lee, Y. F., A. Nomoto, B. M. Detjen, and E. Wimmer (1977) A protein covalently linked to poliovirus genome RNA. Proc. Natl. Acad. Sci. USA 74, 59–63.

    PubMed  CAS  Google Scholar 

  42. Nomoto, A., B. M. Detjen, R. Pozzatti, and E. Wimmer (1977) The location of the polio genome protein in viral RNAs and its implication for RNA synthesis. Nature 268, 208–213.

    PubMed  CAS  Google Scholar 

  43. Wimmer, E. (1982) Genome-linked protein of viruses. Cell 28, 199–201.

    PubMed  CAS  Google Scholar 

  44. Dasgupta, A., P. Zabel, and D. Baltimore (1980) Dependence of the activity of poliovirus replicase on a host cell protein. Cell 19, 423–429.

    PubMed  CAS  Google Scholar 

  45. Flanegan J. B. and D. Baltimore (1977) Poliovirus-specific primer-dependent RNA polymerase able to copy poly(A). Proc. Natl. Acad. Sci. USA 74, 3677–3680.

    PubMed  CAS  Google Scholar 

  46. Kuhn, R. J. and E. Wimmer (1987) The replication of picornaviruses, in The Molecular Biology of Positive Strand RNA Viruses. Rowlands, D. J., B. W. J. Mahy, and M. Mayo, eds., Academic, New York, pp. 17–51.

    Google Scholar 

  47. Semler, B. L., R. J. Kuhn, and E. Wimmer (1988) Replication of poliovirus genome, in RNA Genetics, vol 1. Domingo, E., J. J. Holland, and P. Ahlquist, eds., CRC, Boca Raton, FL, pp. 23–48.

    Google Scholar 

  48. Van Dyke, T. A., R. J. Rickles, and J. B. Flanegan (1982) Genome-length copies of poliovirus RNA are synthesized in vitro by poliovirus RNA-dependent RNA polymerase. J. Biol. Chem. 257, 4610–4617.

    PubMed  Google Scholar 

  49. Hey, T. D., O. C. Richards, and E. Ehrenfeld (1986) Synthesis of plus-and minus-strand RNA from poliovirion RNA template in vitro. J. Virol. 58, 790–796.

    PubMed  CAS  Google Scholar 

  50. Young, D. C., D. M. Tuschall, and J. B. Flanegan (1985) Poliovirus RNA-dependent RNA polymerase and host cell protein synthesize product RNA twice the size of poliovirus RNA in vitro. J. Virol. 54, 256–264.

    PubMed  CAS  Google Scholar 

  51. Andrews, N. C. and D. Baltimore (1986) Purification of a terminal uridylyl-transferase that acts as host factor in the in vitro poliovirus replicase reaction. Proc. Natl. Acad. Sci. USA 83, 221–225.

    PubMed  CAS  Google Scholar 

  52. Tobin, G. J., D. C. Young, and J. B. Flanegan (1989) Self-catalyzed linkage of poliovirus terminal protein VPg to poliovirus RNA. Cell 59, 511–519.

    PubMed  CAS  Google Scholar 

  53. Hey, T. D., O. C. Richards, and E. Ehrenfeld (1987) Poliovirus RNA templates utilized by the viral polymerase in vitro. J. Virol. 61, 802–811.

    PubMed  CAS  Google Scholar 

  54. Lubinski, J. M., G. Kaplan, V. R. Racaniello, and A. Dasgupta (1986) Mechanism of in vitro synthesis of covalently linked dimeric RNA molecules by the poliovirus replicase. J. Virol. 58, 459–467.

    PubMed  CAS  Google Scholar 

  55. Bienz, K., D. Egger, and L. Pasamontes (1987) Association of polioviral proteins of the P2 genomic region with the viral replication complex and virus-induced membrane synthesis as visualized by electron microscopic immunocytochemistry and autoradiography. Virology 160, 220–226.

    PubMed  CAS  Google Scholar 

  56. Bienz, K., D. Egger, Y. Rasser, and W. Bossart (1980) Kinetics and location of poliovirus macromolecular synthesis in correlation to virus-induced cytopathology. Virology 100, 390–399.

    PubMed  CAS  Google Scholar 

  57. Bienz, K., D. Egger, Y. Rasser, and W. Bossart (1983) Intracellular distribution of poliovirus proteins and the induction of virus-specific cytoplasmic structure. Virology 131, 39–48.

    PubMed  CAS  Google Scholar 

  58. Caliguiri, L. A. and I. Tamm (1970) Characterization of poliovirus-specific structures associated with cytoplasmic membranes. Virology 42, 112–122.

    PubMed  CAS  Google Scholar 

  59. Caliguiri, L. A. and I. Tamm (1970) The role of cytoplasmic membranes in poliovirus biosynthesis. Virology 42, 100–111.

    PubMed  CAS  Google Scholar 

  60. Caliguiri, L. A. and R. W. Compans (1973) The formation of poliovirus particles in association with the RNA replication complexes. J. Gen. Virol. 21, 99–108.

    PubMed  CAS  Google Scholar 

  61. Etchison, D. and E. Ehrenfeld (1981) Comparison of replication complexes synthesizing poliovirus RNA. Virology 111, 33–46.

    PubMed  CAS  Google Scholar 

  62. McDonnel, J. P. and L. Levintow (1970) Kinetics of appearance of the products of poliovirus-induced RNA polymerase. Virology 42, 999–1006.

    Google Scholar 

  63. Takegami, T., R. J. Kuhn, C. W., Anderson, and E. Wimmer (1983) Membrane-dependent uridylylation of the genome-linked protein VPg of poliovirus. Proc. Natl. Acad. Sci. USA 80, 7447–7451.

    PubMed  CAS  Google Scholar 

  64. Takeda, N., R. J. Kuhn, C.-F. Yang, T. Takegami, and E. Wimmer (1986) Initiation of poliovirus plus-strand RNA synthesis in a membrane complex of infected HeLa cells. J. Virol. 60, 43–53.

    PubMed  CAS  Google Scholar 

  65. Guinea, R. and L. Carrasco (1990) Phospholipid biosynthesis and poliovirus genome replication, two coupled phenomena. EMBO J. 9, 2011–2016.

    PubMed  CAS  Google Scholar 

  66. Wimmer, E., R. Kuhn, S. Pincus, C. F. Yang, H. Toyoda, M. J. H. Nicklin, and N. Takeda (1987) Molecular events leading to picornavirus genome replication. J. Cell Sci. (Suppl. )7, 251–276.

    Google Scholar 

  67. Fenner, F., B. R. McAuslan, C. A. Mims, J. Sambrook, and D. O. White (1974) Adaptation to new host, in The Biology of Animal Viruses, 2nd Ed., Academic, New York, pp. 317, 318.

    Google Scholar 

  68. Nakano, J. H., M. H. Hatch, M. L. Thieme, and B. Nottay (1978) Parameters for differentiating vaccine-derived and wild poliovirus strains. Prog. Med. Virol. 24, 178–206.

    PubMed  CAS  Google Scholar 

  69. World Health Oganization (1983) Requirements for poliomyelitis vaccine (oral). WHO Expert Committee on Biological Standardization. Annex 4. Tech. Rep. Ser. 687, 134.

    Google Scholar 

  70. Nomoto, A., M. Kohara, S. Kuge, N. Kawamura, M. Arita, T. Komatsu, S. Abe, B. L. Semler, E. Wimmer, and H. Itoh (1987) Study on virulence of poliovirus type 1 using in vitro modified viruses. UCLA Symp. Mol. Cell. Biol. New Ser. 54, 437–452.

    Google Scholar 

  71. Kawamura, N., M. Kohara, S. Abe, T. Komatsu, K. Tago, M. Arita, and A. Nomoto (1989) Determinants in the 5′ noncoding region of poliovirus Sabin 1 RNA that influence the attenuation phenotype. J. Virol. 63, 1302–1309.

    PubMed  CAS  Google Scholar 

  72. Kohara, M., S. Abe, T. Komatsu, K. Tago, M. Arita, and A. Nomoto (1988) A recombinant virus between the Sabin 1 and Sabin 3 vaccine strains of poliovirus as a possible candidate for a new type 3 poliovirus live vaccine strain. J. Virol. 62, 2828–2835.

    PubMed  CAS  Google Scholar 

  73. Omata, T., M. Kohara, S. Kuge, T. Komatsu, S. Abe, B. L. Semler, A. Kameda, H. Itoh, M. Arita, E. Wimmer, and A. Nomoto (1986) Genetic analysis of the attenuation phenotype of poliovirus type 1. J. Virol. 58, 348–358.

    PubMed  CAS  Google Scholar 

  74. Agol, V. I., S. G. Drozdov, M. P. Frolova, V. P. Grachev, M. S. Kolesnikova, V. G. Kozlov, N. M. Ralph, L. I. Romanova, E. A. Tolskaya, and E. G. Viktorova (1985) Neurovirulence of the intertypic poliovirus recombinant v3/al-25: Characterization of strains isolated from the spinal cord of diseased monkeys and evaluation of the contribution of the 3′ half of the genome. J. Gen. Virol. 66, 309–316.

    PubMed  CAS  Google Scholar 

  75. Agol, V. I., S. G. Drozdov, V. P. Grachev, M. S. Kolesnikova, V. G. Kozlov, N. M. Ralph, L. I. Romanova, E. A. Tolskaya, A. V. Tyufanov, and E. G. Viktorova (1985) Recombination between attenuated and virulent strains of poliovirus type 1: Derivation and characterization of recombinants with centrally located crossover points. Virology 143, 467–477.

    PubMed  CAS  Google Scholar 

  76. Agol, V. I., V. P. Grachev, S. G. Drozdov, M. S. Kolesnikova, V. G. Kozlov, N. M. Ralph, L. I. Romanova, E. A. Tolskaya, A. V. Tyufanov, and E. G. Viktorova (1984) Construction and properties of intertypic poliovirus recombinants: First approximation mapping of the major determinants of neurovirulence. Virology 136, 41–55.

    PubMed  CAS  Google Scholar 

  77. Kohara, M., T. Omata, A. Kameda, B. L. Semler, H. Itoh, E. Wimmer, and A. Nomoto (1985) In vitro phenotypic markers of a poliovirus recombinant constructed from infectious cDNA clones of the neurovirulent Mahoney strain and the attenuated Sabin 1 strain. J. Virol. 53, 786–792.

    PubMed  CAS  Google Scholar 

  78. Evans, D. M. A., G. Dunn, P. D. Minor, G. C. Schild, A. J. Cann, G. Stanway, J. W. Almond, K. Currey, and J. V. Maizel, Jr. (1985) Increased neurovirulence associated with a single nucleotide change in a non-coding region of the Sabin type 3 poliovaccine genome. Nature 314, 548–550.

    PubMed  CAS  Google Scholar 

  79. Pilipenko, E. V., V. M. Blinov, L. I. Romanova, A. N. Sinyakov, S. V. Maslova, and V. I. Agol (1989) Conserved structural domains in the 5′ untranslated region of picornaviral genomes: An analysis of the segment controlling translation and neurovirulence. Virology 168, 201–209.

    PubMed  CAS  Google Scholar 

  80. Skinner, M. A., V. R. Racaniello, G. Dunn, J. Cooper, P. D. Minor, and J. W. Almond (1989) New model for the secondary structure of the 5′ noncoding RNA of poliovirus is supported by biochemical and genetic data that also show that RNA secondary structure is important in neurovirulence. J. Mol. Biol. 207, 379–392.

    PubMed  CAS  Google Scholar 

  81. Svitkin, Y. V., S. V. Maslova, and V. I. Agol (1985) The genomes of attenuated and virulent poliovirus strains differ in their in vitro translation efficiencies. Virology 147, 243–252.

    PubMed  CAS  Google Scholar 

  82. Crowell, R. L. and B. J. Landau (1983) Receptors in the initiation of picornavirus infections. Compr. Virol. 18, 1–42.

    CAS  Google Scholar 

  83. Holland, J. J. (1961) Receptor affinities as major determinants of enterovirus tissue tropisms in humans. Virology 15, 312–326.

    PubMed  CAS  Google Scholar 

  84. Holland, J. J., J. C. McLaren, and J. T. Syverton (1959) The mammalian cell-virus relationship. IV. Infection of naturally insusceptible cells with enterovirus ribonucleic acid. J. Exp. Med. 110, 65–80.

    PubMed  CAS  Google Scholar 

  85. Crowell, R. L., K.-H. L. Hsu, M. Shultz, and B. J. Landau (1987) Cellular receptors in coxsackievirus infections. UCLA Symp. Mol. Cell. Biol. New Ser. 54, 453–466.

    Google Scholar 

  86. Koike, S., H. Horie, I. Ise, A. Okitsu, M. Yoshida, N. Iizuka, K. Takeuchi, T. Takegami, and A. Nomoto (1990) The poliovirus receptor protein is produced both as membrane-bound and secreted forms. EMBO J. 9, 3217–3224.

    PubMed  CAS  Google Scholar 

  87. Minor, P. D., P. A. Pipkin, D. Hockley, G. C. Schild, and J. W. Almond (1984) Monoclonal antibodies which block cellular receptors of poliovirus. Virus Res. 1, 203–212.

    PubMed  CAS  Google Scholar 

  88. Nobis, P., R. Zibbire, G. Meyer, J. Kuhne, G. Warnecke, and G. Koch (1985) Production of a monoclonal antibodies against an epitope on HeLa cells that is the functional poliovirus binding site. J. Gen. Virol. 66, 2563–2569.

    PubMed  Google Scholar 

  89. Shepley, M. P., B. Sherry, and H. L. Weiner (1988) Monoclonal antibody identification of a 100-kDa membrane protein in HeLa cells and human spinal cord involved in poliovirus attachment. Proc. Natl. Acad. Sci. USA 85, 7743–7747.

    PubMed  CAS  Google Scholar 

  90. Koike, S., I. Ise, and A. Nomoto (1991) Functional domains of the poliovirus receptor. Proc. Natl. Acad. Sci. USA, 88, 4104–4108.

    PubMed  CAS  Google Scholar 

  91. Mendelsohn, C. L., E. Wimmer, and V. R. Racaniello (1989) Cellular receptor for poliovirus: Molecular cloning, nucleotide sequence, and expression of a new member of the immunoglobulin superfamily. Cell 56, 855–865.

    PubMed  CAS  Google Scholar 

  92. Williams, A. F. and A. N. Barclay (1988) The immunoglobulin superfamily-domains for cell surface recognition. Ann. Rev. Immunol. 6, 381–405.

    CAS  Google Scholar 

  93. Fricks, C. E. and J. M. Hogle (1990) Cell-induced conformational change in poliovirus: Externalization of the amino terminus of VP1 is responsible for liposome binding. J. Virol. 64, 1934–1945.

    PubMed  CAS  Google Scholar 

  94. Kaplan, G., M. S. Freistadt, and V. R. Racaniello (1990) Neutralization of poliovirus by cell receptors expressed in insect cells. J. Virol. 64, 4697–4702.

    PubMed  CAS  Google Scholar 

  95. Madshus, I. H., S. Olsnes, and K. Sandvig (1984) Mechanism of entry into the cytosol of poliovirus type 1: Requirement for low pH. J. Cell Biol. 98, 1194–1200.

    PubMed  CAS  Google Scholar 

  96. Willingmann, P., H. Barnert, H. Zeichhardt, and K.-D. Habermehl (1989) Recovery of structurally intact and infectious poliovirus type 1 from HeLa cells during receptor mediated endocytosis. Virology 168, 417–420.

    PubMed  CAS  Google Scholar 

  97. Zeichhardt, H., K. Wetz, P. Willingmann, and K.-O. Habermehl (1985) Entry of poliovirus type 1 and mouse elberfeld (ME) virus into HEp-2 cells: Receptor-mediated endocytosis and endosomal or lysosomal uncoating. J. Gen. Virol. 66, 483–492.

    PubMed  CAS  Google Scholar 

  98. Lehrman, M. A., J. L. Goldstein, M. S. Brown, D. W. Russell, and W. J. Schneider (1985) Internalization-defective LDL receptors produced by genes with nonsense and frameshift mutations that truncate the cytoplasmic domain. Cell 41, 735–743.

    PubMed  CAS  Google Scholar 

  99. Mostov, K. E., A. de Bruyn Kops, and D. L. Deitcher (1986) Deletion of the cytoplasmic domain of the polymeric immunoglobulin receptor prevents basilateral localization and endocytosis. Cell 47, 359–364.

    PubMed  CAS  Google Scholar 

  100. Prywes, R., E. Livneh, A. Ullrich, and J. Schlessinger (1986) Mutations in the cytoplasmic domain of EGF receptor affect EGF binding and receptor internalization. EMBO J. 5, 2179–2190.

    PubMed  CAS  Google Scholar 

  101. Rothenberger, S., B. J. Lacopetta, and L. C. Kuhn (1987) Endocytosis of the transferrin receptor requires the cytoplasmic domain but not its phosphorylation site. Cell 49, 423–431.

    PubMed  CAS  Google Scholar 

  102. Bedinger, P., A. Moriaty, R. C. von Borstel, N. J. Donovan, K. S. Steimer, and D. R. Littman (1988) Internalization of human immunodeficiency virus does not require the cytoplasmic domain of CD4. Nature 334, 162–165.

    PubMed  CAS  Google Scholar 

  103. Maddon, P. J., J. S. McDougal, P. R. Clapham, A. G. Dalgleish, S. Jamal, R. A. Weiss, and R. Axel (1988) HIV infection does not require endocytosis of its receptor, CD4. Cell 54, 865–874.

    PubMed  CAS  Google Scholar 

  104. Koike, S., C. Taya, T. Kurata, S. Abe, I. Ise, H. Yonekawa, and A. Nomoto (1991) Transgenic mice susceptible to poliovirus. Proc. Natl. Acad. Sci. USA, 88, 951–955.

    PubMed  CAS  Google Scholar 

  105. Ren, R., F. Costantini, E. J. Gorgacz, J. J. Lee, and V. R. Racaniello (1990) Transgenic mice expressing a human poliovirus receptor: A new model for poliomyelitis. Cell 63, 353–362.

    PubMed  CAS  Google Scholar 

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© 1992 Springer Science+Business Media New York

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Nomoto, A., Koike, S. (1992). Molecular Mechanisms of Poliovirus Pathogenesis. In: Roos, R.P. (eds) Molecular Neurovirology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-4612-0407-7_6

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  • DOI: https://doi.org/10.1007/978-1-4612-0407-7_6

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-4612-6748-5

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