Skip to main content

Coxsackievirus B5 and the Relationship to Swine Vesicular Disease Virus

  • Chapter
The Coxsackie B Viruses

Part of the book series: Current Topics in Microbiology and Immunology ((CT MICROBIOLOGY,volume 223))

Abstract

Coxsackieviruses are divided into two groups (A and B) based largely on their pathogenicity and replication in newborn mice. Both groups have been associated with a wide variety of neurological, cardiovascular, gastroenteric, ophthalmic, and exanthematic diseases. The main natural hosts of coxsackieviruses are humans but several studies have established that coxsackievirus B5 (CVB5) and swine vesicular disease virus (SVDV) are antigenically closely related.

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

Access this chapter

eBook
USD 16.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Similar content being viewed by others

References

  • Bergelson JM, Chan M, Solomon KR, St. John NF, Lin H, Finberg RW (1994) Decay-accelerating factor (CD55), a glycosylphosphatidylinositol-anchored complement regulatory protein, is a receptor for several echoviruses. Proc Natl Acad Sci USA 91:6245–6248

    Article  PubMed  CAS  Google Scholar 

  • Bergelson JM, Mohanty JG, Crowell RL, St. John NF, Lublin DM, Finberg RW (1995) Coxsackievirus B3 adapted to growth in RD cells binds to decay-accelerating factor (CD55). J Virol 69:1903–1906

    PubMed  CAS  Google Scholar 

  • Brown F, Talbot P, Burrows R (1973) Antigenic differences between isolates of swine vesicular disease virus and their relationship to coxsackie B5 virus. Nature 245:315–316

    Article  PubMed  CAS  Google Scholar 

  • Brown F, Wild F (1974) Variation in the coxsackievirus type B5 and its possible role in the etiology of swine vesicular disease. Intervirology 3:125–128

    Article  PubMed  CAS  Google Scholar 

  • Brown F, Goodridge D, Burrows R (1976a) Infection of man by swine vesicular disease virus. J Comp Path 86:409–414

    Article  PubMed  CAS  Google Scholar 

  • Brown F, Wild TF, Rowe LW, Underwood BO, Harris TJR (1976b) Comparison of swine vesicular disease virus and coxsackie B5 virus by serological and RNA hybridization methods. J Gen Virol 31:231–237

    Article  PubMed  Google Scholar 

  • Burrows R, Greig A, Goodridge D (1973) Swine vesicular disease. Research in Veterinary Science 15:141–144

    PubMed  CAS  Google Scholar 

  • Chang KH, Auvinen P, Hyypia T, Stanway G (1989) The nucleotide sequence of coxsackievirus A9; implications for receptor binding and enterovirus classification. J Gen Virol 70:3269–3280

    Article  PubMed  CAS  Google Scholar 

  • Dunne HW (1975) Porcine enteroviruses. 4 edn. In: Dunne HWLeman AD (eds)Diseases of Swine. Iowa State University Press,Ames, Iowa pp 353–368

    Google Scholar 

  • Garland AJM, Mann JA (1974) Attempts to infect pigs with coxsackie virus type B5. J Hyg Cambs 73:85–96

    Article  CAS  Google Scholar 

  • Graves JH (1973) Serological relationship of swine vesicular disease virus and coxsackie B5 virus. Nature 245:314–315

    Article  PubMed  CAS  Google Scholar 

  • Harris TJR, Brown F (1975) Correlation of polypeptide composition with antigenic variation in the swine vesicular disease and coxsackie B5 viruses. Nature 258:758–760

    Article  PubMed  CAS  Google Scholar 

  • Harris TJR, Doel TR, Brown F (1977) Molecular aspects of the antigenic variation of swine vesicular disease and coxsackie B5 viruses. J Gen Virol 35:299–315

    Article  PubMed  CAS  Google Scholar 

  • Harris TJR, Underwood BO, Knowles NJ, Crowther JR, Brown F (1979) Molecular approach to the epidemiology of swine vesicular disease: correlation of variation in the virus structural polypeptides with serological properties. Infect Immun 24:593–599

    PubMed  CAS  Google Scholar 

  • Huttenen P, Santti J, Pulli T, Hyypia T (1996) The major echovirus group is genetically coherent and related to coxsackie B viruses. J Gen Virol 77:715–725

    Article  Google Scholar 

  • IizukaN, Kuge S, Nomoto A (1987) Complete nucleotide sequence of the genome of coxsackievirus Bl. Virology 156:64–73

    Article  PubMed  CAS  Google Scholar 

  • Inoue T, Suzuki T, Sekiguchi K (1989) The complete nucleotide sequence of swine vesicular disease virus. J Gen Virol 70:919–934.

    Article  PubMed  CAS  Google Scholar 

  • Jenkins O, Booth JD, Minor PD, Almond JW (1987) The complete nucleotide sequence of coxsackievirus B4 and its comparison to other members of the Picornaviridae. J Gen Virol 68:1835–1848

    Article  PubMed  Google Scholar 

  • Kanno T, Inoue T, Wang YF, Sarai A, Yamaguchi S (1995) Identification of the location of antigenic sites of swine vesicular disease virus with neutralization-resistant mutants. J Gen Virol 76:3099–3106

    Article  PubMed  CAS  Google Scholar 

  • Kitamura N, Semler BL, Rothberg PG, Larsen GR, Adler CJ, Dorner AJ, Emini EA, Hanecak R, Lee JJ, Van derWerf S, Anderson CW, Wimmer E (1981) Primary structure, gene organization and polypeptide expression of poliovirus RNA. Nature 291:547–553

    Article  PubMed  CAS  Google Scholar 

  • Klump WM, Bergmann I, Mueller BC, Ameis D, Kandolf R (1990) Complete nucleotide sequence of infectious coxsackievirus B3 cDNA: two initial 5’ uridine residues are regained during plus-strand RNA synthesis. J Virol 64:1573–1583

    PubMed  CAS  Google Scholar 

  • Knowles NJ, Buckley LS, Pereira HG (1979) Classification of porcine enteroviruses by antigenic analysis and cytopathic effects in tissue culture: description of 3 new serotypes. Arch Virol 62:201–208

    Article  PubMed  CAS  Google Scholar 

  • Kodama M (1976) Outline of studies on swine vesicular disease in Japan. Bull Off Int Epiz 86:423–432

    Google Scholar 

  • Kopecka H, Brown B, Pallansch M (1995) Genotypic variation in coxsackievirus B5 isolates from three different outbreaks in the United States. Virus Res 38:125–136

    Article  PubMed  CAS  Google Scholar 

  • Lai SS, McKercher PD, Moore DM, Gillespie JH (1980) Response of pigs to recent isolates of coxsackievirus B5. Comp Immun Microbiol Infect Dis 2:459–468

    Article  Google Scholar 

  • Loxam JG, Hedger RS (1983) Swine vesicular disease: clinical signs, diagnosis, epidemiology and control. Rev sci tech Off Int Epiz 2:11–24

    Google Scholar 

  • Mann JA, Burrows R, Goodridge D (1975) Mild and sub-clinical infections with swine vesicular disease virus. Bull Off Int Epiz 83:117–122

    Google Scholar 

  • McKercher PB, Graves JH (1981) Swine Vesicular Disease. In: Beran GW (ed)Handbook of Zoonoses. Section B: Viral Zoonoses, Vol. 2. CRC Press, Boca Raton pp 161–167

    Google Scholar 

  • Monlux WS, McKercher PD, Graves JH (1975) Brain and spinal cord lesions in pigs inoculated with swine vesicular disease (UKG strain) virus and coxsackievirus B5. Am J Vet Res 36:1745–1749

    PubMed  CAS  Google Scholar 

  • Muckelbauer JK, Kremer M, Minor I, Diana G, Dutko FJ, Groarke J, Pevear DC, Rossmann MG (1995) The structure of coxsackievirus B3 at 3.5 Angstrom resolution. Structure 3:653–667

    Article  PubMed  CAS  Google Scholar 

  • Nardelli L, Lodetti E, Gualandi GL, Burrows R, Goodridge D, Brown F, Cartwright B (1968) A foot-andmouth disease syndrome in pigs caused by an enterovirus. Nature 219:1275–1276

    Article  PubMed  CAS  Google Scholar 

  • Page GS, Mosser AG, Hogle JM, Filman SJ, Rueckert RR, Chow M (1988) Three-dimensional structure of poliovirus serotype 1 neutralizing determinants. J Virol 62:1781–1794

    PubMed  CAS  Google Scholar 

  • Racaniellio VR, Baltimore D (1981) Molecular cloning of poliovirus cDNA and determination of the complete nucleotide sequence of the viral genome. Proc Natl Acad Sci USA 78:4887-891

    Article  Google Scholar 

  • Sayle RA, Milner-White EJ (1995) RasMol: biomolecular graphics for all. Trends in Biochemical Sciences 20:374–376

    Article  PubMed  CAS  Google Scholar 

  • Schmidt NJ, Melnick JL, Wenner HA, Ho HH, Burkhardt MA (1971) Evaluation of enterovirus immune horse serum pools for identification of virus field strains. Bull Wrld Hlth Org 45:317–330

    CAS  Google Scholar 

  • Seechurn P, Knowles NJ, McCauley JW (1990) The complete nucleotide sequence of a pathogenic swine vesicular disease virus. Virus Res 16:255–274

    Article  PubMed  CAS  Google Scholar 

  • Sellers RF. (1984). Vesicular Diseases. In: Brown FWilson G (eds)Topley and Wilson’s Principles of Bacteriology, Virology and Immunity, Vol 4, Virology. Edward Arnold, London pp 213–232

    Google Scholar 

  • Sellers RF, Herniman KAJ (1974) The airborne excretion by pigs of swine vesicular disease virus. J Hyg Cambs 72:61–65

    Article  CAS  Google Scholar 

  • Shafren DR, Bates RC, Agrez MV, Herd RL, Burns GF, Barry RD (1995) Coxsackievirus Bl, B3, and B5 use decay-accelerating factor as a receptor for cell attachment. J Virol 69:3873–3877

    PubMed  CAS  Google Scholar 

  • Sherry B, Mosser AG, Colonno RJ, Rueckert RR (1986) Use of monoclonal antibodies to identify four neutralization immunogens on a common cold picornavirus, human rhinovirus 14. J Virol 57:246–257

    PubMed  CAS  Google Scholar 

  • Ward T, Pipkin PA, Clarkson NA, Stone DM, Minor PD, Almond JW (1994) Decay-accelerating factor CD55 is identified as the receptor for echovirus 7 using CELICS, a rapid immuno-focal cloning method. EMBO J 13:5070–5074

    PubMed  CAS  Google Scholar 

  • Watson WA (1981) Swine vesicular disease in Great Britain. Can Vet J 22:195–200

    PubMed  CAS  Google Scholar 

  • Zhang G, Wilsden G, Knowles NJ, McCauley JW (1993a) Complete nucleotide sequence of a coxsackie B5 virus and its relationship to swine vesicular disease virus. J Gen Virol 74:845–853

    Article  PubMed  CAS  Google Scholar 

  • Zhang G, Wilsden G, Knowles NJ, McCauley JW (1993b) Nucleotide sequence diversity in a range of swine vesicular disease virus isolates and coxsackievirus B5 isolates. Abstract of a poster presented at the IXth International Congress of Virology, Glasgow, August 8-13, P28-24 p 221

    Google Scholar 

  • Zimmermann H, Eggers HJ, Kraus W, Nelsen-Salz B (1995) Complete nucleotide sequence and biological properties of an infectious clone of prototype echovirus 9. Virus Res 39:311–320

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1997 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Knowles, N.J., McCauley, J.W. (1997). Coxsackievirus B5 and the Relationship to Swine Vesicular Disease Virus. In: Tracy, S., Chapman, N.M., Mahy, B.W.J. (eds) The Coxsackie B Viruses. Current Topics in Microbiology and Immunology, vol 223. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60687-8_7

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-60687-8_7

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-64507-5

  • Online ISBN: 978-3-642-60687-8

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics