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. 2008 Feb 4;153(2):351–356. doi: 10.1007/s00705-007-1094-y

Characterization of equine arteritis virus particles and demonstration of their hemolytic activity

M Veit 1,, A Kabatek 1, C Tielesch 1, A Hermann 2
PMCID: PMC7086761  PMID: 18219439

Summary

Equine arteritis virus (EAV), a member of the newly established family Arteriviridae, is a small, positive-stranded RNA virus. It carries two protein complexes in its envelope, gp5/M and the recently described gp2b/gp3/gp4 complex. We report here on several basic features of EAV replication in cell culture and on the protein composition of virus particles. We have also characterized gp2b, gp3, and gp4 expressed using a baculovirus system in insect cells. Finally, we provide evidence that EAV possess hemagglutinating and hemolytic activity. The hemolysis assay might be useful for determining which of the surface proteins carries the receptor-binding and membrane fusion activity of EAV.

Keywords: Virus Particle, Newcastle Disease Virus, Hemolytic Activity, Cell Culture Supernatant, Virus Preparation

Footnotes

Correspondence: Michael Veit, Department of Immunology and Molecular Biology, Veterinary Faculty, Free University Berlin, Philippstraße 13, D-10115 Berlin, Germany

References

  1. Burnet FM. Haemolysis by Newcastle disease virus. Nature. 1949;164:1008. doi: 10.1038/1641008a0. [DOI] [PubMed] [Google Scholar]
  2. de Vries AA, Chirnside ED, Horzinek MC, Rottier PJ. Structural proteins of equine arteritis virus. J Virol. 1992;66:6294–6303. doi: 10.1128/jvi.66.11.6294-6303.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. de Vries AA, Post SM, Raamsman MJ, Horzinek MC, Rottier PJ. The two major envelope proteins of equine arteritis virus associate into disulfide-linked heterodimers. J Virol. 1995;69:4668–4674. doi: 10.1128/jvi.69.8.4668-4674.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. de Vries AA, Raamsman MJ, van Dijk HA, Horzinek MC, Rottier PJ. The small envelope glycoprotein (GS) of equine arteritis virus folds into three distinct monomers and a disulfide-linked dimer. J Virol. 1995;69:3441–3448. doi: 10.1128/jvi.69.6.3441-3448.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dobbe JC, van der Meer Y, Spaan WJ, Snijder EJ. Construction of chimeric arteriviruses reveals that the ectodomain of the major glycoprotein is not the main determinant of equine arteritis virus tropism in cell culture. Virology. 2001;288:283–294. doi: 10.1006/viro.2001.1074. [DOI] [PubMed] [Google Scholar]
  6. Hedges JF, Balasuriya UB, MacLachlan NJ. The open reading frame 3 of equine arteritis virus encodes an immunogenic glycosylated, integral membrane protein. Virology. 1999;264:92–98. doi: 10.1006/viro.1999.9982. [DOI] [PubMed] [Google Scholar]
  7. Huang RT, Rott R, Klenk HD. Influenza viruses cause hemolysis and fusion of cells. Virology. 1981;110:243–247. doi: 10.1016/0042-6822(81)90030-1. [DOI] [PubMed] [Google Scholar]
  8. Hyllseth B. A plaque assay of equine arteritis virus in BHK-21 cells. Arch Gesamte Virusforsch. 1969;28:26–33. doi: 10.1007/BF01250842. [DOI] [PubMed] [Google Scholar]
  9. Hyllseth B. Structural proteins of equine arteritis virus. Arch Gesamte Virusforsch. 1973;40:177–188. doi: 10.1007/BF01242536. [DOI] [PubMed] [Google Scholar]
  10. Kubota T, Inaba Y, Uwatoko K, Akashi H, Fukunaga Y. Hemagglutination with equine arteritis virus. J Vet Med Sci. 1997;59:943–945. doi: 10.1292/jvms.59.943. [DOI] [PubMed] [Google Scholar]
  11. Lamb RA, Paterson RG, Jardetzky TS. Paramyxovirus membrane fusion: lessons from the F and HN atomic structures. Virology. 2006;344:30–37. doi: 10.1016/j.virol.2005.09.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Maeda T, Ohnishi S. Activation of influenza virus by acidic media causes hemolysis and fusion of erythrocytes. FEBS Lett. 1980;122:283–287. doi: 10.1016/0014-5793(80)80457-1. [DOI] [PubMed] [Google Scholar]
  13. Sano Y, Inaba Y, Uwatoko K, Kubota T, Asagoe T, Kanaya J, Pan IJ, Akashi H, Fukunaga Y. Effect of heparin on hemagglutination by equine arteritis virus. J Vet Med Sci. 1998;60:447–450. doi: 10.1292/jvms.60.447. [DOI] [PubMed] [Google Scholar]
  14. Snijder EJ, Meulenberg JJ. The molecular biology of arteriviruses. J Gen Virol. 1998;79(Pt 5):961–979. doi: 10.1099/0022-1317-79-5-961. [DOI] [PubMed] [Google Scholar]
  15. Snijder EJ, van Tol H, Pedersen KW, Raamsman MJ, de Vries AA. Identification of a novel structural protein of arteriviruses. J Virol. 1999;73:6335–6345. doi: 10.1128/jvi.73.8.6335-6345.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Vaananen P, Kaariainen L. Haemolysis by two alphaviruses: Semliki Forest and Sindbis virus. J Gen Virol. 1979;43:593–601. doi: 10.1099/0022-1317-43-3-593. [DOI] [PubMed] [Google Scholar]
  17. Verheije MH, Welting TJ, Jansen HT, Rottier PJ, Meulenberg JJ. Chimeric arteriviruses generated by swapping of the M protein ectodomain rule out a role of this domain in viral targeting. Virology. 2002;303:364–373. doi: 10.1006/viro.2002.1711. [DOI] [PubMed] [Google Scholar]
  18. Wieringa R, de Vries AA, Raamsman MJ, Rottier PJ. Characterization of two new structural glycoproteins, GP(3) and GP(4), of equine arteritis virus. J Virol. 2002;76:10829–10840. doi: 10.1128/JVI.76.21.10829-10840.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wieringa R, De Vries AA, Post SM, Rottier PJ. Intra- and intermolecular disulfide bonds of the GP2b glycoprotein of equine arteritis virus: relevance for virus assembly and infectivity. J Virol. 2003;77:12996–13004. doi: 10.1128/JVI.77.24.12996-13004.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Wieringa R, de Vries AA, Rottier PJ. Formation of disulfide-linked complexes between the three minor envelope glycoproteins (GP2b, GP3, and GP4) of equine arteritis virus. J Virol. 2003;77:6216–6226. doi: 10.1128/JVI.77.11.6216-6226.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Wieringa R, de Vries AA, van der Meulen J, Godeke GJ, Onderwater JJ, van Tol H, Koerten HK, Mommaas AM, Snijder EJ, Rottier PJ. Structural protein requirements in equine arteritis virus assembly. J Virol. 2004;78:13019–13027. doi: 10.1128/JVI.78.23.13019-13027.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]

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