Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period

This paper reports the results of tissue infectivity assays of bovine spongiform encephalopathy (BSE) agent in orally exposed cattle at stages during the incubation period. Estimations of the titre of infectivity in central nervous system (CNS), certain peripheral nerve ganglia and distal ileum tissue were made according to time post exposure from the relationship between incubation period and dose for RIII mice and C57bl mice using data from titrations of brain material from cases of BSE. The rate of increase of infectivity in the bovine CNS was then estimated, taking into account these tissue infectivity titres, the variability of the brain titre of clinical field cases of BSE, and the probability density of the expected number of months before clinical onset of each infected bovine. The doubling time for CNS was shown to equal 1.2 months. The titre in the thoracic dorsal root ganglia (DRG) was, on average, approximately 1 log units less than CNS, and cervical DRG approximately 0.5 log less than thoracic DRG. The pattern of increase of infectivity in the distal ileum is that of an initial increase up to 14–18 months post exposure, followed by a decrease, which is likely to be highly variable between animals. These results will be informative for future risk assessments of BSE, especially in relation to reviewing current control measures.

[1]  N M Ferguson,et al.  Epidemiological determinants of the pattern and magnitude of the vCJD epidemic in Great Britain , 1998, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[2]  Arieyeh J Austin,et al.  Infectivity in the ileum of cattle challenged orally with bovine spongiform encephalopathy , 1994, Veterinary Record.

[3]  Christian Ducrot,et al.  Review on the epidemiology and dynamics of BSE epidemics. , 2008, Veterinary research.

[4]  A. Buschmann,et al.  Prions spread via the autonomic nervous system from the gut to the central nervous system in cattle incubating bovine spongiform encephalopathy. , 2007, The Journal of general virology.

[5]  J. Spiropoulos,et al.  Pathogenesis of experimental bovine spongiform encephalopathy: preclinical infectivity in tonsil and observations on the distribution of lingual tonsil in slaughtered cattle , 2005, Veterinary Record.

[6]  J. Wilesmith,et al.  Bovine spongiform encephalopathy: the effect of oral exposure dose on attack rate and incubation period in cattle. , 2007, The Journal of general virology.

[7]  T. Yokoyama,et al.  Prions in the peripheral nerves of bovine spongiform encephalopathy-affected cattle. , 2007, The Journal of general virology.

[8]  G. Wells,et al.  Preliminary observations on the pathogenesis of experimental bovine spongiform encephalopathy (BSE): an update. , 1998, The Veterinary record.

[9]  H. Fraser,et al.  Identification of a gene which controls the incubation period of some strains of scrapie agent in mice. , 1968, Journal of comparative pathology.

[10]  Christl A Donnelly,et al.  Assessment of the risk posed by bovine spongiform encephalopathy in cattle in Great Britain and the impact of potential changes to current control measures , 2003, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[11]  M. Czub,et al.  Pathogenesis of scrapie: study of the temporal development of clinical symptoms, of infectivity titres and scrapie-associated fibrils in brains of hamsters infected intraperitoneally. , 1986, The Journal of general virology.

[12]  Quantifying BSE control by calculating the basic reproduction ratio R0 for the infection among cattle , 2004, Journal of mathematical biology.

[13]  H. Fraser,et al.  Genetical control of the concentration of ME7 scrapie agent in the brain of mice. , 1969, Journal of comparative pathology.

[14]  M. Dawson,et al.  Preliminary observations on the pathogenesis of experimental bovine spongiform encephalopathy (BSE): an update , 1998, Veterinary Record.

[15]  Neil M. Ferguson,et al.  Estimation of the basic reproduction number of BSE: the intensity of transmission in British cattle , 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[16]  G. Wells,et al.  Limited detection of sternal bone marrow infectivity in the clinical phase of experimental bovine spongiform encephalopathy (BSE) , 1999, Veterinary Record.

[17]  P. Comer,et al.  TSE risk assessments: a decision support tool , 2003, Statistical methods in medical research.

[18]  J. Gorham,et al.  Organ-specific modification of the dose-response relationship of scrapie infectivity. , 1990, The Journal of infectious diseases.

[19]  R H Kimberlin,et al.  Pathogenesis of experimental scrapie. , 1988, Ciba Foundation symposium.

[20]  M. Simmons,et al.  Estimating the temporal relationship between PrPSc detection and incubation period in experimental bovine spongiform encephalopathy of cattle. , 2007, The Journal of general virology.

[21]  L. Terry,et al.  Detection of disease-specific PrP in the distal ileum of cattle exposed orally to the agent of bovine spongiform encephalopathy , 2003, Veterinary Record.

[22]  S. Bird,et al.  UK dietary exposure to BSE in head meat: by birth cohort and gender. , 2002, Journal of cancer epidemiology and prevention.

[23]  S. Prusiner,et al.  Measurement of the scrapie agent using an incubation time interval assay , 1982, Annals of neurology.

[24]  D. Taylor,et al.  Decontamination studies with the agents of bovine spongiform encephalopathy and scrapie , 2005, Archives of Virology.

[25]  M. Beekes,et al.  Sequential appearance and accumulation of pathognomonic markers in the central nervous system of hamsters orally infected with scrapie. , 1996, The Journal of general virology.

[26]  A. Ghani,et al.  Assessment of the prevalence of vCJD through testing tonsils and appendices for abnormal prion protein , 2000, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[27]  J. Castilla,et al.  Progression of prion infectivity in asymptomatic cattle after oral bovine spongiform encephalopathy challenge. , 2007, The Journal of general virology.

[28]  P. Comer,et al.  Exposure of the human population to BSE infectivity over the course of the BSE epidemic in Great Britain and the impact of changes to the Over Thirty Month Rule , 2004 .

[29]  A. Buschmann,et al.  Highly bovine spongiform encephalopathy-sensitive transgenic mice confirm the essential restriction of infectivity to the nervous system in clinically diseased cattle. , 2005, The Journal of infectious diseases.

[30]  G. Kärber,et al.  Beitrag zur kollektiven Behandlung pharmakologischer Reihenversuche , 1931, Naunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie.

[31]  N M Ferguson,et al.  The epidemiology of BSE in cattle herds in Great Britain. II. Model construction and analysis of transmission dynamics. , 1997, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[32]  Cooper Jd,et al.  UK dietary exposure to BSE in head meat: by birth cohort and gender. , 2002 .

[33]  A. Ghani,et al.  Feed-borne transmission and case clustering of BSE , 2000, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[34]  H. Fraser,et al.  Transmission of bovine spongiform encephalopathy and scrapie to mice. , 1992, The Journal of general virology.