Skip to main content
Log in

Sequence Comparison of the Large Genomic RNA Segments of Two Strains of Lymphocytic Choriomeningitis Virus Differing in Pathogenic Potential for Guinea Pigs

  • Published:
Virus Genes Aims and scope Submit manuscript

Abstract

Two strains of lymphocytic choriomeningitis virus (LCMV) differ in their ability to cause a lethal disease in outbred guinea pigs: the Armstrong (ARM) strain is not lethal at high doses (106 PFU), whereas the WE strain is lethal at less than 10 PFU inoculated intraperitoneally. The high pathogenic potential of LCMV WE has been mapped to the larger (L) of the two genomic RNA segments by genetic reassortment analysis (Riviere, Y., Ahmed, R., Southern, P.J., Buchmeier, M. J. and Oldstone, M. B. A., J. Virol. 55, 704–709, 1985). Here we describe the completed sequence of the LCMV WE L RNA, and its comparison to the L RNA of the non-virulent strain, LCMV ARM. Similar to the L RNA of LCMV ARM, the L RNA of WE is 7.2 kb long and contains two open reading frames (ORFs): the 5′ ORF encodes a small RING finger (zinc-binding) protein, p11 Z, and the 3′ ORF encodes the putative RNA-dependent RNA polymerase (RdRp or L protein). Comparison of nucleotide sequences for both viruses revealed 84% L RNA homology. At the amino acid level similarity between the two strains is 87% in the Z ORF, and 88% in the RdRp ORF. The most divergent regions are found in the N-terminal parts of the RdRp and Z proteins and are most likely to account for differences in pathogenic potential.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Salvato M.S. and Rai K.S., in Mahy B. and Collier L. (eds) “Toply and Wilson's Microbiology and Microbial Infections 9th edition”, Arnold Publishing, London, 1998, pp. 629-650.

    Google Scholar 

  2. Dutko F.J. and Oldstone M.B.A., J Gen Virol 64, 1689-1698, 1983.

    PubMed  CAS  Google Scholar 

  3. Lehmann-Grube F., Virol Monogr 10, 78-81, 1971.

    Google Scholar 

  4. Buchmeier M.J., Welsh R.M., Dutko F.J., and Oldstone M.B.A., Adv Immunol 30, 275-331, 1980.

    PubMed  CAS  Google Scholar 

  5. Riviere Y., Ahmed R., Southern P., Buchmeier M.J., and Oldstone M.B., J Virol 55, 704-709, 1985.

    PubMed  CAS  Google Scholar 

  6. Martinez Peralta L.A., Laguens M., Ponzinibbio C., and Laguens R.P., Medicina 50, 225-229, 1990.

    PubMed  CAS  Google Scholar 

  7. Gonzalez P.H., Ponzinibbio C., and Laguens R.P., J Med Virol 22, 289-297, 1987.

    PubMed  CAS  Google Scholar 

  8. Peters C.J., Jahrling P.B., Liu C.T., Kenyon R.H., McKee K.T., Jr., and Barrera Oro J.G., Cur Top Microbiol Immunol 134, 5-68, 1987.

    CAS  Google Scholar 

  9. Qian C., Jahrling P.B., Peters C.J., and Liu C.T., Lab An Sci 44, 600-607, 1994.

    CAS  Google Scholar 

  10. Aronson J.F., Herzog N.K., and Jerrells T.R., Am J Pathol 145, 228-235, 1994.

    PubMed  CAS  Google Scholar 

  11. Aronson J.F., Herzog N.K., and Jerrells T.R., Am J Trop Med Hyg 52, 262-269, 1995.

    PubMed  CAS  Google Scholar 

  12. Salvato M., Shimomaye E., Southern P., and Oldstone M.B., Virol 164, 517-522, 1988.

    Article  CAS  Google Scholar 

  13. Salvato M., Shimomaye E., and Oldstone M.B., Virol 169, 377-384, 1989.

    Article  CAS  Google Scholar 

  14. Salvato M. and Shimomaye E., Virol 173, 1-10, 1989.

    Article  CAS  Google Scholar 

  15. Romanowski V., Matsuura Y., and Bishop D.H., Virus Res 3, 101-114, 1985.

    Article  PubMed  CAS  Google Scholar 

  16. Lukashevich I.S., Djavani M., Shapiro K., Sanchez A., Ravkov E., Nichol S.T., and Salvato M.S., J Gen Virol 78, 547-551, 1997.

    PubMed  CAS  Google Scholar 

  17. Djavani M., Lukashevich I.S., Sanchez A., and Salvato M.S., Virol 235, 414-418, 1997.

    Article  CAS  Google Scholar 

  18. Romanowski V. and Bishop D.H., Virus Res 2, 35-51, 1985.

    Article  PubMed  CAS  Google Scholar 

  19. Singh M.K., Fuller-Pace F.V., Buchmeier M.J., and Southern P.J., Virol 161, 448-456, 1987.

    Article  CAS  Google Scholar 

  20. Salvato M.S., in M.S. Salvato (ed). “The Arenaviridae.” Plenum Press, New York 1993, pp. 133-156.

    Google Scholar 

  21. Shimomaye E. and Salvato M., Gen Anal Tech 6, 25-28, 1989.

    Article  CAS  Google Scholar 

  22. Lovering R., Hanson I.M., Borden K.L., Martin S., O'Reilly N.J., Evan G.I., Rahman D., Pappin D.J., Trowsdale J., and Freemont P.S., Proc Natl Acad Sci USA 90, 2112-2116, 1993.

    Article  PubMed  CAS  Google Scholar 

  23. Borden K.L. and Freemont P.S., Cur Opin Structural Biol 6, 395-401, 1996.

    Article  CAS  Google Scholar 

  24. Poch O., Blumberg B.M., Bougueleret L., and Tordo N., J Gen Virol 71, 1153-1162, 1990.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Djavani, M., Lukashevich, I.S. & Salvato, M.S. Sequence Comparison of the Large Genomic RNA Segments of Two Strains of Lymphocytic Choriomeningitis Virus Differing in Pathogenic Potential for Guinea Pigs. Virus Genes 17, 151–155 (1998). https://doi.org/10.1023/A:1008016724243

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1008016724243

Navigation