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. 1996 Mar;70(3):1745–1750. doi: 10.1128/jvi.70.3.1745-1750.1996

Entry kinetics and mouse virulence of Ross River virus mutants altered in neutralization epitopes.

S Vrati 1, P J Kerr 1, R C Weir 1, L Dalgarno 1
PMCID: PMC189999  PMID: 8627696

Abstract

Previously we identified the locations of three neutralization epitopes (a, b1 and b2) of Ross River virus (RRV) by sequencing a number of variants resistant to monoclonal antibody neutralization which were found to have single amino acid substitutions in the E2 protein (S. Vrati, C.A. Fernon, L. Dalgarno, and R.C. Weir, Virology 162:346-353, 1988). We have now studied the biological properties of these variants in BHK cells and their virulence in mice. While variants altered in epitopes a and/or b1 showed no difference, variants altered in epitope b2, including a triple variant altered in epitopes a, b1, and b2, showed rapid penetration but retarded kinetics of growth and RNA and protein synthesis in BHK cells compared with RRV T48, the parent virus. Variants altered in epitopes a and/or b1 showed no change in mouse virulence. However, two of the six epitope b2 variants examined had attenuated mouse virulence. They had a four- to fivefold-higher 50% lethal dose (LD50), although no change in the average survival time of infected mice was observed. These variants grew to titers in mouse tissues similar to those of RRV T48. The ID50 of the triple variant was unchanged, but infected mice had an increased average survival time. This variant produced lower levels of viremia in infected mice. On the basis of these findings we propose that both the receptor binding site and neutralization epitopes of RRV are nearby or in the same domain of the E2 protein.

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Selected References

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  1. Baric R. S., Trent D. W., Johnston R. E. A Sindbis virus variant with a cell-determined latent period. Virology. 1981 Apr 15;110(1):237–242. doi: 10.1016/0042-6822(81)90029-5. [DOI] [PubMed] [Google Scholar]
  2. Bassel-Duby R., Spriggs D. R., Tyler K. L., Fields B. N. Identification of attenuating mutations on the reovirus type 3 S1 double-stranded RNA segment with a rapid sequencing technique. J Virol. 1986 Oct;60(1):64–67. doi: 10.1128/jvi.60.1.64-67.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baxt B., Morgan D. O., Robertson B. H., Timpone C. A. Epitopes on foot-and-mouth disease virus outer capsid protein VP1 involved in neutralization and cell attachment. J Virol. 1984 Aug;51(2):298–305. doi: 10.1128/jvi.51.2.298-305.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Dalgarno L., Rice C. M., Strauss J. H. Ross River virus 26 s RNA: complete nucleotide sequence and deduced sequence of the encoded structural proteins. Virology. 1983 Aug;129(1):170–187. doi: 10.1016/0042-6822(83)90404-x. [DOI] [PubMed] [Google Scholar]
  5. Davis N. L., Fuller F. J., Dougherty W. G., Olmsted R. A., Johnston R. E. A single nucleotide change in the E2 glycoprotein gene of Sindbis virus affects penetration rate in cell culture and virulence in neonatal mice. Proc Natl Acad Sci U S A. 1986 Sep;83(18):6771–6775. doi: 10.1073/pnas.83.18.6771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dietzschold B., Wunner W. H., Wiktor T. J., Lopes A. D., Lafon M., Smith C. L., Koprowski H. Characterization of an antigenic determinant of the glycoprotein that correlates with pathogenicity of rabies virus. Proc Natl Acad Sci U S A. 1983 Jan;80(1):70–74. doi: 10.1073/pnas.80.1.70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Doherty R. L., Barrett E. J., Gorman B. M., Whitehead R. H. Epidemic polyarthritis in Eastern Australia, 1959-1970. Med J Aust. 1971 Jan 2;1(1):5–8. [PubMed] [Google Scholar]
  8. Emini E. A., Kao S. Y., Lewis A. J., Crainic R., Wimmer E. Functional basis of poliovirus neutralization determined with monospecific neutralizing antibodies. J Virol. 1983 May;46(2):466–474. doi: 10.1128/jvi.46.2.466-474.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Faragher S. G., Marshall I. D., Dalgarno L. Ross River virus genetic variants in Australia and the Pacific Islands. Aust J Exp Biol Med Sci. 1985 Aug;63(Pt 4):473–488. doi: 10.1038/icb.1985.52. [DOI] [PubMed] [Google Scholar]
  10. Faragher S. G., Meek A. D., Rice C. M., Dalgarno L. Genome sequences of a mouse-avirulent and a mouse-virulent strain of Ross River virus. Virology. 1988 Apr;163(2):509–526. doi: 10.1016/0042-6822(88)90292-9. [DOI] [PubMed] [Google Scholar]
  11. Fuller S. D. The T=4 envelope of Sindbis virus is organized by interactions with a complementary T=3 capsid. Cell. 1987 Mar 27;48(6):923–934. doi: 10.1016/0092-8674(87)90701-x. [DOI] [PubMed] [Google Scholar]
  12. Gard G., Marshall I. D., Woodroofe G. M. Annually recurrent epidemic polyarthritis and Ross River virus activity in a coastal area of New South Wales. II. Mosquitoes, viruses, and wildlife. Am J Trop Med Hyg. 1973 Jul;22(4):551–560. doi: 10.4269/ajtmh.1973.22.551. [DOI] [PubMed] [Google Scholar]
  13. Glasgow G. M., Killen H. M., Liljeström P., Sheahan B. J., Atkins G. J. A single amino acid change in the E2 spike protein of a virulent strain of Semliki Forest virus attenuates pathogenicity. J Gen Virol. 1994 Mar;75(Pt 3):663–668. doi: 10.1099/0022-1317-75-3-663. [DOI] [PubMed] [Google Scholar]
  14. Johnson B. J., Brubaker J. R., Roehrig J. T., Trent D. W. Variants of Venezuelan equine encephalitis virus that resist neutralization define a domain of the E2 glycoprotein. Virology. 1990 Aug;177(2):676–683. doi: 10.1016/0042-6822(90)90533-w. [DOI] [PubMed] [Google Scholar]
  15. Johnston R. E., Smith J. F. Selection for accelerated penetration in cell culture coselects for attenuated mutants of Venezuelan equine encephalitis virus. Virology. 1988 Feb;162(2):437–443. doi: 10.1016/0042-6822(88)90484-9. [DOI] [PubMed] [Google Scholar]
  16. Kerr P. J., Weir R. C., Dalgarno L. Ross River virus variants selected during passage in chick embryo fibroblasts: serological, genetic, and biological changes. Virology. 1993 Mar;193(1):446–449. doi: 10.1006/viro.1993.1143. [DOI] [PubMed] [Google Scholar]
  17. Kinney R. M., Chang G. J., Tsuchiya K. R., Sneider J. M., Roehrig J. T., Woodward T. M., Trent D. W. Attenuation of Venezuelan equine encephalitis virus strain TC-83 is encoded by the 5'-noncoding region and the E2 envelope glycoprotein. J Virol. 1993 Mar;67(3):1269–1277. doi: 10.1128/jvi.67.3.1269-1277.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lustig S., Jackson A. C., Hahn C. S., Griffin D. E., Strauss E. G., Strauss J. H. Molecular basis of Sindbis virus neurovirulence in mice. J Virol. 1988 Jul;62(7):2329–2336. doi: 10.1128/jvi.62.7.2329-2336.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Löve A., Rydbeck R., Kristensson K., Orvell C., Norrby E. Hemagglutinin-neuraminidase glycoprotein as a determinant of pathogenicity in mumps virus hamster encephalitis: analysis of mutants selected with monoclonal antibodies. J Virol. 1985 Jan;53(1):67–74. doi: 10.1128/jvi.53.1.67-74.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Meek A. D., Faragher S. G., Weir R. C., Dalgarno L. Genetic and phenotypic studies on Ross River virus variants of enhanced virulence selected during mouse passage. Virology. 1989 Oct;172(2):399–407. doi: 10.1016/0042-6822(89)90182-7. [DOI] [PubMed] [Google Scholar]
  21. Murgita R. A., Wigzell H. Regulation of immune functions in the fetus and newborn. Prog Allergy. 1981;29:54–133. [PubMed] [Google Scholar]
  22. Newton S. E., Short N. J., Dalgarno L. Bunyamwera virus replication in cultured Aedes albopictus (mosquito) cells: establishment of a persistent viral infection. J Virol. 1981 Jun;38(3):1015–1024. doi: 10.1128/jvi.38.3.1015-1024.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Olmsted R. A., Meyer W. J., Johnston R. E. Characterization of Sindbis virus epitopes important for penetration in cell culture and pathogenesis in animals. Virology. 1986 Jan 30;148(2):245–254. doi: 10.1016/0042-6822(86)90322-3. [DOI] [PubMed] [Google Scholar]
  24. Pence D. F., Davis N. L., Johnston R. E. Antigenic and genetic characterization of Sindbis virus monoclonal antibody escape mutants which define a pathogenesis domain on glycoprotein E2. Virology. 1990 Mar;175(1):41–49. doi: 10.1016/0042-6822(90)90184-s. [DOI] [PubMed] [Google Scholar]
  25. Polo J. M., Davis N. L., Rice C. M., Huang H. V., Johnston R. E. Molecular analysis of Sindbis virus pathogenesis in neonatal mice by using virus recombinants constructed in vitro. J Virol. 1988 Jun;62(6):2124–2133. doi: 10.1128/jvi.62.6.2124-2133.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Prehaud C., Coulon P., LaFay F., Thiers C., Flamand A. Antigenic site II of the rabies virus glycoprotein: structure and role in viral virulence. J Virol. 1988 Jan;62(1):1–7. doi: 10.1128/jvi.62.1.1-7.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Rice C. M., Strauss J. H. Association of sindbis virion glycoproteins and their precursors. J Mol Biol. 1982 Jan 15;154(2):325–348. doi: 10.1016/0022-2836(82)90067-5. [DOI] [PubMed] [Google Scholar]
  28. Rossmann M. G., Arnold E., Erickson J. W., Frankenberger E. A., Griffith J. P., Hecht H. J., Johnson J. E., Kamer G., Luo M., Mosser A. G. Structure of a human common cold virus and functional relationship to other picornaviruses. Nature. 1985 Sep 12;317(6033):145–153. doi: 10.1038/317145a0. [DOI] [PubMed] [Google Scholar]
  29. Russell D. L., Dalrymple J. M., Johnston R. E. Sindbis virus mutations which coordinately affect glycoprotein processing, penetration, and virulence in mice. J Virol. 1989 Apr;63(4):1619–1629. doi: 10.1128/jvi.63.4.1619-1629.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Sabara M., Gilchrist J. E., Hudson G. R., Babiuk L. A. Preliminary characterization of an epitope involved in neutralization and cell attachment that is located on the major bovine rotavirus glycoprotein. J Virol. 1985 Jan;53(1):58–66. doi: 10.1128/jvi.53.1.58-66.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Santagati M. G., Mättä J. A., Itäranta P. V., Salmi A. A., Hinkkanen A. E. The Semliki Forest virus E2 gene as a virulence determinant. J Gen Virol. 1995 Jan;76(Pt 1):47–52. doi: 10.1099/0022-1317-76-1-47. [DOI] [PubMed] [Google Scholar]
  32. Schoepp R. J., Johnston R. E. Directed mutagenesis of a Sindbis virus pathogenesis site. Virology. 1993 Mar;193(1):149–159. doi: 10.1006/viro.1993.1111. [DOI] [PubMed] [Google Scholar]
  33. Seif I., Coulon P., Rollin P. E., Flamand A. Rabies virulence: effect on pathogenicity and sequence characterization of rabies virus mutations affecting antigenic site III of the glycoprotein. J Virol. 1985 Mar;53(3):926–934. doi: 10.1128/jvi.53.3.926-934.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Strauss E. G., Stec D. S., Schmaljohn A. L., Strauss J. H. Identification of antigenically important domains in the glycoproteins of Sindbis virus by analysis of antibody escape variants. J Virol. 1991 Sep;65(9):4654–4664. doi: 10.1128/jvi.65.9.4654-4664.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Taylor W. P., Marshall I. D. Adaptation studies with Ross River virus: laboratory mice and cell cultures. J Gen Virol. 1975 Jul;28(1):59–72. doi: 10.1099/0022-1317-28-1-59. [DOI] [PubMed] [Google Scholar]
  36. Tucker P. C., Griffin D. E. Mechanism of altered Sindbis virus neurovirulence associated with a single-amino-acid change in the E2 Glycoprotein. J Virol. 1991 Mar;65(3):1551–1557. doi: 10.1128/jvi.65.3.1551-1557.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Vrati S., Faragher S. G., Weir R. C., Dalgarno L. Ross River virus mutant with a deletion in the E2 gene: properties of the virion, virus-specific macromolecule synthesis, and attenuation of virulence for mice. Virology. 1986 Jun;151(2):222–232. doi: 10.1016/0042-6822(86)90044-9. [DOI] [PubMed] [Google Scholar]
  38. Vrati S., Fernon C. A., Dalgarno L., Weir R. C. Location of a major antigenic site involved in Ross River virus neutralization. Virology. 1988 Feb;162(2):346–353. doi: 10.1016/0042-6822(88)90474-6. [DOI] [PubMed] [Google Scholar]
  39. Wiley D. C., Wilson I. A., Skehel J. J. Structural identification of the antibody-binding sites of Hong Kong influenza haemagglutinin and their involvement in antigenic variation. Nature. 1981 Jan 29;289(5796):373–378. doi: 10.1038/289373a0. [DOI] [PubMed] [Google Scholar]
  40. Ziemiecki A., Garofff H. Subunit composition of the membrane glycoprotein complex of Semliki Forest virus. J Mol Biol. 1978 Jul 5;122(3):259–269. doi: 10.1016/0022-2836(78)90189-4. [DOI] [PubMed] [Google Scholar]

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