1887

Abstract

In order to begin to elucidate the genomic basis of the attenuation of mouse-adapted, poliovirus type 2 strain W-2 (PV2/W-2), we have cloned and sequenced the virus and compared it with the virulent, mouse-adapted PV2/Lansing strain. In addition, we have performed computer-generated comparisons of PV2/W-2 to the non-mouse-adapted, attenuated PV2/Sabin strain to determine whether mutational patterns occur that result in attenuation. The PV2/W-2 genome is 7434 nucleotides in length, which is three bases shorter than PV2/Lansing. The 5′ non-coding region of PV2/W-2 is 747 nucleotides in length (compared to 744 in PV2/Lansing) and shares 98·8% identity with PV2/Lansing and 82·3% identity with PV2/Sabin. Overall, the PV2/W-2 polyprotein (2205 amino acids) is two amino acids shorter than that of either PV2/Lansing or PV2/Sabin (2207 amino acids). These contiguous deletions fall within the P3-D region (polymerase). Within these 2205 amino acid residues only 26 differences were observed between PV2/W-2 and PV2/Lansing (98-8% identity), whereas 92 occurred between PV2/W-2 and PV2/Sabin (95·8% identity). The 3′ non-coding region of PV2/W-2 is 72 nucleotides in length and shares 100% identity with PV2/Lansing and 98-6% identity with PV2/Sabin. Amino acid changes in the capsid protein region occurred in neutralization sites 1 and 3, areas previously shown to be important for pathogenicity. The cleavage site between non-structural proteins P2-C/P3- A consisted of a glutamine-serine pair, in contrast to other sequenced polioviruses which have a glutamine- glycine dipeptide.

Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-71-1-43
1990-01-01
2024-04-16
Loading full text...

Full text loading...

/deliver/fulltext/jgv/71/1/JV0710010043.html?itemId=/content/journal/jgv/10.1099/0022-1317-71-1-43&mimeType=html&fmt=ahah

References

  1. Armstrong C. 1939; Successful transfer of the Lansing strain of poliomyelitis virus from the cotton rat to the white mouse. Public Health Reports 54:2302–2305
    [Google Scholar]
  2. Carp R. I., Plotkin S. A., Norton T. W., Kowprowski H. 1963; Modification of an attenuated type 2 polio vaccine following passage at 23 °C. Proceedings of the Society for Experimental Biology and Medicine 112:251–256
    [Google Scholar]
  3. Cohen J. I., Ticehurst J. R., Purcell R. H., Buckler-White A., Baroudy B. M. 1987; Complete nucleotide sequence of wild-type hepatitis A virus: comparison with different strains of hepatitis A virus and other picomaviruses. Journal of Virology 61:50–59
    [Google Scholar]
  4. Dale R. M. K., Mcclure B. A., Houchins J. P. 1985; A rapid single-stranded cloning strategy for producing a sequential series of overlapping clones for use in DNA sequencing: application to sequencing the com mitocondrial 18S rDNA. Plasmid 13:31–40
    [Google Scholar]
  5. Devereux J., Haeberli P., Smithies O. 1984; A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Research 12:387–395
    [Google Scholar]
  6. Duechler M., Skern T., Sommergruber W., Neubauer C., Gruendler P., Fogy I., Blaas D., Kuechler E. 1987; Evolutionary relationships within the human rhinovirus genus: comparison of serotypes 89, 2, and 14. Proceedings of the National Academy of Sciences U.S.A.: 842605–2609
    [Google Scholar]
  7. Emini E. A., Elizinga M., Wimmer E. 1982; Carboxy-terminal analysis of poliovirus proteins: termination of poliovirus RNA translation and location of unique poliovirus polyprotein cleavage sites. Journal of Virology 42:194–199
    [Google Scholar]
  8. Evans D. M. A., Dunn G., Minor P. D., Schild G. C., Cann A. J., Stanway G., Almond J. W., Currey K., Maizel J. V. Jr 1985; Increased neurovirulence associated with a single nucleotide change in a noncoding region of the Sabin type 3 poliovaccine genome. Nature; London: 314548–550
    [Google Scholar]
  9. Hanahan D. 1983; Studies on transformation of Escherichia coliwith plasmids. Journal of Molecular Biology 166:557–580
    [Google Scholar]
  10. Hanecak R., Semler B. L., Anderson C. W., Wimmer E. 1982; Proteolytic processing of poliovirus polypeptides: antibodies to polypeptide P3-7C inhibit cleavage at glutamine-glycine pairs. Proceedings of the National Academy of Sciences U.S.A.: 793973–3977
    [Google Scholar]
  11. Hogle J. M., Chow M., Filman D. J. 1985; Three-dimensional structure of poliovirus at 2.9 Å resolution. Science 229:1358–1365
    [Google Scholar]
  12. Iizuka N., Kuge S., Nomoto A. 1987; Complete nucleotide sequence of the genome of coxsackievirus Bl. Virology 156:64–73
    [Google Scholar]
  13. Jenkins O., Booth J. D., Minor P. D., Almond J. W. 1987; The complete nucleotide sequence of coxsackievirus B4 and its comparison to other members of the Picomaviridae. Journal of General Virology 68:1835–1848
    [Google Scholar]
  14. Jubelt B., Lipton H. L. 1987; Lansing poliovirus infection in mice: antibody demonstrable by enzyme linked immunosorbent assay (ELISA) and immunoprecipitation but not by neutralization. Journal of Neuroimmunology 14:109–121
    [Google Scholar]
  15. Jubelt B., Meagher J. B. 1984a; Poliovirus infection of cyclophosphamide-treated mice results in persistence and late paralysis: I. Clinical, pathologic, and immunologic studies. Neurology 34:486–493
    [Google Scholar]
  16. Jubelt B., Meagher J. B. 1984b; Poliovirus infection of cyclophosphamide-treated mice results in persistence and late paralysis: II. Virologic studies. Neurology 34:494–499
    [Google Scholar]
  17. Jubelt B., Gallez-Hawkins G., Narayan O., Johnson R. T. 1980a; Pathogenesis of human poliovirus infection in mice. I. Clinical and pathological studies. Journal of Neuropathology and Experimental Neurology 39:138–148
    [Google Scholar]
  18. Jubelt B., Narayan O., Johnson R. T. 1980b; Pathogenesis of human poliovirus infection in mice. II. Age dependency of paralysis. Journal of Neuropathology and Experimental Neurology 39:149–159
    [Google Scholar]
  19. Kandolf R., Hofschneider P. H. 1985; Molecular cloning of the genome of a cardiotropic coxsackie B3 virus: full-length reverse- transcribed recombinant cDNA generates infectious virus in mammalian cells. Proceedings of the National Academy of Sciences U.S.A.: 824818–4822
    [Google Scholar]
  20. Kawamura N., Kohara M., Abe S., Komatsu T., Tago K., Arita M., Nomoto A. 1989; Determinants in the 5ʹ noncoding regions of poliovirus Sabin 1 RNA that influence the attenuated phenotype. Journal of Virology 63:1302–1309
    [Google Scholar]
  21. Kitamura N., Semler B. L., Rothberg P. G., Larsen G. R., Adler C. J., Dorner A. J., Emini E. A., Hanecak R., Lee J. J., Vanderwerf S., Anderson C. W., Wimmer E. 1981; Primary structure, gene organization and polypeptide expression of poliovirus RNA. Nature; London: 291547–553
    [Google Scholar]
  22. Koprowski H., Norton T. W., Jervis G. A. 1951; Studies on rodent adapted poliomyelitis virus. I. Cerebral resistance induced in the rhesus monkey. Bacteriological Proceedings 92 (abstract)
    [Google Scholar]
  23. Koprowski H., Norton T. W., Jervis G. A. 1952; Immune response in human volunteers upon oral administration of a rodent- adapted strain of poliomyelitis virus. American Journal of Hygiene 55:108–126
    [Google Scholar]
  24. La Monica N., Meriam C., Racaniello V. R. 1986; Mapping of sequences required for mouse neurovirulence of poliovirus type 2 Lansing. Journal of Virology 57:515–525
    [Google Scholar]
  25. La Monica N., Almond J. W., Racaniello V. R. 1987a; A mouse model for poliovirus neurovirulence identifies mutations that attenuate the virus for humans. Journal Of Virology 61:2917–2920
    [Google Scholar]
  26. Lamonica N., Kupsky W. J., Racaniello V. R. 1987b; Reduced mouse neurovirulence of poliovirus type 2 Lansing antigenic variants selected with monoclonal antibodies. Journal of Virology 161:429–437
    [Google Scholar]
  27. Lindberg A. M., Stalhandske P. O. K., Pettersson U. 1987; Genome of coxsackievirus B3. Virology 156:50–63
    [Google Scholar]
  28. Maniatis T., Fritsch E. F., Sambrook J. 1982 Molecular Cloning: A Laboratory Manual New York: Cold Spring Harbor Laboratory;
    [Google Scholar]
  29. Martin A., Wychowski C., Couderc T., Crainic R., Hogle J., Girard M. 1988; Engineering a poliovirus type 2 antigenic site on a type 1 capsid results in a chimaeric virus which is neurovirulent for mice. EMBO Journal 7:2839–2847
    [Google Scholar]
  30. Miller J. R. 1981; Prolonged intracerebral infection with poliovirus in asymptomatic mice. Annals of Neurology 9:590–596
    [Google Scholar]
  31. Minor P. D., Ferguson M., Evans D. M. A., Almond J. W., Icenogle J. P. 1986; Antigenic structure of polioviruses of serotypes 1, 2 and 3. Journal of General Virology 67:1283–1291
    [Google Scholar]
  32. Moss E. G., O’Neill R. E., Racaniello V. R. 1989; Mapping of attenuating sequences of an avirulent poliovirus type 2 strain. Journal of Virology 63:1884–1890
    [Google Scholar]
  33. Murray M. G., Bradley J., Yang X.-F., Wimmer E., Moss E. G., Racaniello V. R. 1988; Poliovirus host range is determined by a short amino acid sequence in neutralization antigenic site 1. Science 241:213–215
    [Google Scholar]
  34. Ohara Y., Stein S., Fu J., Stillman L., Klaman L., Roos R. P. 1988; Molecular cloning and sequence determination of DA strain of Theiler's murine encephalomyelitis viruses. Virology 164:245–255
    [Google Scholar]
  35. Pallansch M. A., Kew O. M., Semler B. L., Omilianowski D. R., Anderson C. W., Wimmer E., Rueckert R. R. 1984; Protein processing map of poliovirus. Journal of Virology 49:873–880
    [Google Scholar]
  36. Palmenberg A. C., Kirby E. M., Janda M. R., Drake N. L., Duke G. M., Potratz K. F., Collett M. S. 1984; The nucleotide and deduced amino acid sequences of the encephalomyo- carditis viral polyprotein coding region. Nucleic Acids Research 12:2969–2985
    [Google Scholar]
  37. Pevear D. C., Calenoff M., Rozhon E., Lipton H. L. 1987; Analysis of the complete nucleotide sequence of the picomavirus Theiler’s murine encephalomyelitis virus indicates that it is closely related to cardioviruses. Journal of Virology 61:1507–1516
    [Google Scholar]
  38. Pevear D. C., Borkowski J., Calenoff M., Oh C. K., Ostrowski B., Lipton H. L. 1988; Insights into Theiler’s virus neurovirulence based on a genomic comparison of the neurovirulent GDVII and less virulent BeAn strains. Virology 165:1–12
    [Google Scholar]
  39. Racaniello V. R. 1984; Poliovirus type II produced from cloned cDNA is infectious in mice. Virus Research 1:669–675
    [Google Scholar]
  40. Rozhon E. J., Wilson A. K., Jubelt B. 1984; Characterization of genetic changes occurring in attenuated poliovirus 2 during persistent infection in mouse central nervous systems. Journal of Virology 50:137–144
    [Google Scholar]
  41. Rueckert R. R., Wimmer E. 1984; Systematic nomenclature of picomavirus proteins. Journal of Virology 50:957–959
    [Google Scholar]
  42. Sabin A. B. 1950; Relative resistance of newborn mice to poliomyelitis virus. Proceedings of the Society for Experimental Biology and Medicine 73:394–399
    [Google Scholar]
  43. Sanger F., Nicklen S., Coulson A. R. 1977; DNA sequencing with chain-terminating inhibitors. Proceedings of the National Academy Of Sciences U.S.A.: 745463–5477
    [Google Scholar]
  44. Semler B. L., Anderson C. W., Kitamura N., Rothberg P. C., Wishart W. L., Wimmer E. 1981; Poliovirus replication proteins: RNA sequence encoding P3-lb and the site of proteolytic processing. Proceedings of the National Academy of Sciences U.S.A.: 783464–3468
    [Google Scholar]
  45. Staden R. 1980; A new computer method for the storage and manipulation of DNA gel reading data. Nucleic Acids Research 8:3673–3694
    [Google Scholar]
  46. Stanway G., Hughes P. J., Mountford R. C., Reeve P., Minor P. D., Schild G. C., Almond J. W. 1984; Comparison of the complete nucleotide sequences of the genomes of the neurovirulent poliovirus P3/Leon/37 and its attenuated Sabin vaccine derivative P3/Leon 12a1b. Proceedings of the National Academy of Sciences U.S.A.: 811539–1543
    [Google Scholar]
  47. Toyoda H., Kohara M., Kataoka Y., Suganuma T., Omata T., Imura N., Nomoto A. 1984; Complete nucleotide sequences of all three poliovirus serotype genomes: implication for genetic relationship, gene function and antigenic determinants. Journal of Molecular Biology 174:561–585
    [Google Scholar]
  48. Ziola B. R., Scraba D. G. 1974; Structure of the Mengo virion. 1. Polypeptide and ribonucleate components of the virus particle. Virology 57:531–542
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jgv/10.1099/0022-1317-71-1-43
Loading
/content/journal/jgv/10.1099/0022-1317-71-1-43
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error