Skip to main content
Log in

Analysis of sites of foot and mouth disease virus persistence in carrier cattle via the polymerase chain reaction

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

This study was undertaken in order to explore possible sites of foot-and-mouth disease virus (FMDV) persistence during the carrier state. Tissue samples taken from experimentally infected animals at different times post-infection (p.i) were examined by conventional viral isolation and the polymerase chain reaction (PCR) technique. The analysis of samples from several organs taken from 17 bovines between 3 and 270 days p.i. allowed the following conclusions: 1) Virus present in oesophageal-pharyngeal fluids (OPF) during the carrier state originates in the pharynx as shown by the detection of antisense FMDV RNA by PCR, 2) PCR is more sensitive than standard virus isolation techniques and may be used for the rapid detection of FMDV in specimens obtained during the acute stage of FMD and for identification of persistently infected cattle.

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. Bachrach HL (1968) Foot-and-mouth disease virus. Annu Rev Microbiol 22: 201–244

    Google Scholar 

  2. Burrows R (1966) Studies on the carrier state of cattle exposed to FMDV. Hyg 64: 81–90

    Google Scholar 

  3. Straver PJ, Bool PH, Claessens AM, Van Bekkum JG (1970) Some properties of carrier strains of FMDV. Arch Ges Virusforsch 29: 113–126

    Google Scholar 

  4. Van Bekkum JG, Straver PJ, Bool P, Frenkel S (1959) Further information on the persistence of infective FMDV. Tijdschr Diergeneekunde 84: 1159–1164

    Google Scholar 

  5. Van Bekkum JG, Straver PJ, Bool P, Frenkel S (1960) Further information on the persistence of infective FMDV in cattle exposed to virulent virus strain. Bull Off Int Epiz 65: 1949–1965

    Google Scholar 

  6. Rossi MS, Sadir AM, Schudel AA Palma EL (1988) Detection of FMDV with DNA probes in bovine esophageal-pharingeal fluids. Arch Virol 99: 67–74

    Google Scholar 

  7. Sutmoller P, Gaggero CA (1965) Foot and mouth disease carriers. Vet Rec 77: 968–969

    Google Scholar 

  8. Donaldson Al and Kitching RP (1989) Transmission of FMDV by vaccinated cattle following natural challenge. Res Vet Sci 46: 9–14

    Google Scholar 

  9. Terpstra C, Van Maanen C, Van Bekkum JG (1990) Endurance of immunity against FMDV in cattle after three consecutive annual vaccinations. Res Vet Sci 49: 236–242

    Google Scholar 

  10. Burrows R, Mann JA, Garland JM, Greig A, Goodridge D (1981) The pathogenesis of natural and simulated natural FMD infection in cattle. J Comp Pathol 91: 599–609

    Google Scholar 

  11. Eskildsen MK (1969) Experimental pulmonary infection of cattle with FMDV. Nord Vet Med 21: 86–91

    Google Scholar 

  12. Sutmoller P, Mc Vicar (1976) Pathogenesis of FMD: the lung as an additional portal of entry of the virus. J Hyg 77: 235–243

    Google Scholar 

  13. Meyer RF, Brown CC, House C, Molitor TW (1991) Rapid and sensitive detection of FMDV in tissues by enzymatic RNA amplification of the polymerase gene. J Virol Methods 34: 161–172

    Google Scholar 

  14. Snowdon WA (1966) Growth of FMDV in monolayer cultures of calf thyroid cells. Nature 210: 1079–1080

    Google Scholar 

  15. House C, House JA (1989) Evaluation of techniques to demostrate FMDV in bovine tongue epithelium: comparison of the sensitivity of cattle, mice, primary cell cultures, cryopreserved cell cultures and established cell lines. Vet Microbiol 20: 99–109

    Google Scholar 

  16. Brown F, Cartwright B (1960) Purification of the virus of foot and mouth disease by fluorocarbon treatment and its dissociation from neutralizing antibody. J Immunol 85: 309–313

    Google Scholar 

  17. Reed L, Muench H (1938) A simple method of estimating fifty percent end point. Am J Hygiene 27: 493–495

    Google Scholar 

  18. Martinez Salas E, Ortin J, Domingo E (1985) Sequence of viral replicase gene from FMDV C1-Santa Pau (C-S8). Gene 35: 55–61

    Google Scholar 

  19. Schmitz G, Walter T, Seibl R, Kessler (1991) Nonradioactive labeling of oligonucleotides in vitro with hapten digoxigenin by tailling with terminal transferase. Anal Biochem 192: 222–231

    Google Scholar 

  20. Sambrook J, Fritsch EF Maniatis T (1989) Molecular cloning. A laboratory manual 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor

    Google Scholar 

  21. Kitching RP (1992) The application of biotechnology to the control of foot-and-mouth disease virus. Br Vet J 148: 375–388

    Google Scholar 

  22. Mullis KB, Fallons FA (1987) Specific synthesis of DNA in vitro via a polymerase chain reaction. Methods Enzymol 155: 335–350

    Google Scholar 

  23. Saiki RK, Gelfand DH, Stoffel S, Scharf SJ, Higuchi R, Horn GT, Mullis KB, Erlich HA (1988) Primer directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239: 487–491

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Prato Murphy, M.L., Meyer, R.F., Mebus, C. et al. Analysis of sites of foot and mouth disease virus persistence in carrier cattle via the polymerase chain reaction. Archives of Virology 136, 299–307 (1994). https://doi.org/10.1007/BF01321059

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01321059

Keywords

Navigation