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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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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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 |
work_keys_str_mv |
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