Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates

Risk for human exposure to bovine spongiform encephalopathy (BSE)-inducing agent was estimated in a nonhuman primate model. To determine attack rates, incubation times, and molecular signatures, we orally exposed 18 macaques to 1 high dose of brain material from cattle with BSE. Several macaques were euthanized at regular intervals starting at 1 year postinoculation, and others were observed until clinical signs developed. Among those who received >5 g BSE-inducing agent, attack rates were 100% and prions could be detected in peripheral tissues from 1 year postinoculation onward. The overall median incubation time was 4.6 years (3.7-5.3). However, for 3 macaques orally exposed on multiple occasions, incubation periods were at least 7-10 years. Before clinical signs were noted, we detected a non-type 2B signature, indicating the existence of atypical prion protein during the incubation period. This finding could affect diagnosis of variant Creutzfeldt-Jakob disease in humans and might be relevant for retrospective studies of positive tonsillectomy or appendectomy specimens because time of infection is unknown.

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Main Authors: Holznagel, E., Yutzy, B., Schulz-Schaeffer, W., Kruip, C., Hahmann, U., Bierke, P., Torres, J. M., Kim, Y. S., Thomzig, A., Beekes, M., Hunsmann, G., Loewer, J.
Format: journal article biblioteca
Language:eng
Published: 2013
Online Access:http://hdl.handle.net/20.500.12792/2123
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spelling dig-inia-es-20.500.12792-21232020-12-15T09:54:26Z Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates Holznagel, E. Yutzy, B. Schulz-Schaeffer, W. Kruip, C. Hahmann, U. Bierke, P. Torres, J. M. Kim, Y. S. Thomzig, A. Beekes, M. Hunsmann, G. Loewer, J. Risk for human exposure to bovine spongiform encephalopathy (BSE)-inducing agent was estimated in a nonhuman primate model. To determine attack rates, incubation times, and molecular signatures, we orally exposed 18 macaques to 1 high dose of brain material from cattle with BSE. Several macaques were euthanized at regular intervals starting at 1 year postinoculation, and others were observed until clinical signs developed. Among those who received >5 g BSE-inducing agent, attack rates were 100% and prions could be detected in peripheral tissues from 1 year postinoculation onward. The overall median incubation time was 4.6 years (3.7-5.3). However, for 3 macaques orally exposed on multiple occasions, incubation periods were at least 7-10 years. Before clinical signs were noted, we detected a non-type 2B signature, indicating the existence of atypical prion protein during the incubation period. This finding could affect diagnosis of variant Creutzfeldt-Jakob disease in humans and might be relevant for retrospective studies of positive tonsillectomy or appendectomy specimens because time of infection is unknown. 2020-10-22T12:34:40Z 2020-10-22T12:34:40Z 2013 journal article http://hdl.handle.net/20.500.12792/2123 10.3201/eid1905.120274 eng Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ open access
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country España
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libraryname Biblioteca del INIA España
language eng
description Risk for human exposure to bovine spongiform encephalopathy (BSE)-inducing agent was estimated in a nonhuman primate model. To determine attack rates, incubation times, and molecular signatures, we orally exposed 18 macaques to 1 high dose of brain material from cattle with BSE. Several macaques were euthanized at regular intervals starting at 1 year postinoculation, and others were observed until clinical signs developed. Among those who received >5 g BSE-inducing agent, attack rates were 100% and prions could be detected in peripheral tissues from 1 year postinoculation onward. The overall median incubation time was 4.6 years (3.7-5.3). However, for 3 macaques orally exposed on multiple occasions, incubation periods were at least 7-10 years. Before clinical signs were noted, we detected a non-type 2B signature, indicating the existence of atypical prion protein during the incubation period. This finding could affect diagnosis of variant Creutzfeldt-Jakob disease in humans and might be relevant for retrospective studies of positive tonsillectomy or appendectomy specimens because time of infection is unknown.
format journal article
author Holznagel, E.
Yutzy, B.
Schulz-Schaeffer, W.
Kruip, C.
Hahmann, U.
Bierke, P.
Torres, J. M.
Kim, Y. S.
Thomzig, A.
Beekes, M.
Hunsmann, G.
Loewer, J.
spellingShingle Holznagel, E.
Yutzy, B.
Schulz-Schaeffer, W.
Kruip, C.
Hahmann, U.
Bierke, P.
Torres, J. M.
Kim, Y. S.
Thomzig, A.
Beekes, M.
Hunsmann, G.
Loewer, J.
Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
author_facet Holznagel, E.
Yutzy, B.
Schulz-Schaeffer, W.
Kruip, C.
Hahmann, U.
Bierke, P.
Torres, J. M.
Kim, Y. S.
Thomzig, A.
Beekes, M.
Hunsmann, G.
Loewer, J.
author_sort Holznagel, E.
title Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
title_short Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
title_full Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
title_fullStr Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
title_full_unstemmed Foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
title_sort foodborne transmission of bovine spongiform encephalopathy to nonhuman primates
publishDate 2013
url http://hdl.handle.net/20.500.12792/2123
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