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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 tiss...

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Detalles Bibliográficos
Autores principales: Arnold, Mark Edward, Hawkins, Stephen Anthony Charles, Green, Robert, Dexter, Ian, Wells, Gerald Arthur Henry
Formato: Texto
Lenguaje:English
Publicado: EDP Sciences 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695012/
https://www.ncbi.nlm.nih.gov/pubmed/18950589
http://dx.doi.org/10.1051/vetres:2008046
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author Arnold, Mark Edward
Hawkins, Stephen Anthony Charles
Green, Robert
Dexter, Ian
Wells, Gerald Arthur Henry
author_facet Arnold, Mark Edward
Hawkins, Stephen Anthony Charles
Green, Robert
Dexter, Ian
Wells, Gerald Arthur Henry
author_sort Arnold, Mark Edward
collection PubMed
description 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.
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spelling pubmed-26950122010-01-01 Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§ Arnold, Mark Edward Hawkins, Stephen Anthony Charles Green, Robert Dexter, Ian Wells, Gerald Arthur Henry Vet Res Original Article 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. EDP Sciences 2009 2008-10-28 /pmc/articles/PMC2695012/ /pubmed/18950589 http://dx.doi.org/10.1051/vetres:2008046 Text en © INRA, EDP Sciences, 2008
spellingShingle Original Article
Arnold, Mark Edward
Hawkins, Stephen Anthony Charles
Green, Robert
Dexter, Ian
Wells, Gerald Arthur Henry
Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§
title Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§
title_full Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§
title_fullStr Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§
title_full_unstemmed Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§
title_short Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period§
title_sort pathogenesis of experimental bovine spongiform encephalopathy (bse): estimation of tissue infectivity according to incubation period§
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695012/
https://www.ncbi.nlm.nih.gov/pubmed/18950589
http://dx.doi.org/10.1051/vetres:2008046
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