Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge
After oral exposure of cattle with classical bovine spongiform encephalopathy (C-BSE), the infectious agent ascends from the gut to the central nervous system (CNS) primarily via the autonomic nervous system. However, the timeline of this progression has thus far remained widely undetermined. Previo...
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2021
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oai:doaj.org-article:a13d8f1186a444bca4f51ad6092fc8d22021-11-11T16:48:03ZPrion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge10.3390/ijms2221113101422-00671661-6596https://doaj.org/article/a13d8f1186a444bca4f51ad6092fc8d22021-10-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11310https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067After oral exposure of cattle with classical bovine spongiform encephalopathy (C-BSE), the infectious agent ascends from the gut to the central nervous system (CNS) primarily via the autonomic nervous system. However, the timeline of this progression has thus far remained widely undetermined. Previous studies were focused on later time points after oral exposure of animals that were already 4 to 6 months old when challenged. In contrast, in this present study, we have orally inoculated 4 to 6 weeks old unweaned calves with high doses of BSE to identify any possible BSE infectivity and/or PrP<sup>BSE</sup> in peripheral nervous tissues during the first eight months post-inoculation (mpi). For the detection of BSE infectivity, we used a bovine PrP transgenic mouse bioassay, while PrP<sup>BSE</sup> depositions were analyzed by immunohistochemistry (IHC) and by protein misfolding cyclic amplification (PMCA). We were able to show that as early as 8 mpi the thoracic spinal cord as well as the parasympathetic nodal ganglion of these animals contained PrP<sup>BSE</sup> and BSE infectivity. This shows that the centripetal prion spread starts early after challenge at least in this age group, which represents an essential piece of information for the risk assessments for food, feed, and pharmaceutical products produced from young calves.Ivett AckermannReiner UlrichKerstin TauscherOlanrewaju I. FatolaMarkus KellerJames C. ShawuluMark ArnoldStefanie CzubMartin H. GroschupAnne Balkema-BuschmannMDPI AGarticleprion proteinBSEinfectivityPrP<sup>BSE</sup>cattleperipheral and central nervous systemBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11310, p 11310 (2021) |
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prion protein BSE infectivity PrP<sup>BSE</sup> cattle peripheral and central nervous system Biology (General) QH301-705.5 Chemistry QD1-999 |
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prion protein BSE infectivity PrP<sup>BSE</sup> cattle peripheral and central nervous system Biology (General) QH301-705.5 Chemistry QD1-999 Ivett Ackermann Reiner Ulrich Kerstin Tauscher Olanrewaju I. Fatola Markus Keller James C. Shawulu Mark Arnold Stefanie Czub Martin H. Groschup Anne Balkema-Buschmann Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge |
description |
After oral exposure of cattle with classical bovine spongiform encephalopathy (C-BSE), the infectious agent ascends from the gut to the central nervous system (CNS) primarily via the autonomic nervous system. However, the timeline of this progression has thus far remained widely undetermined. Previous studies were focused on later time points after oral exposure of animals that were already 4 to 6 months old when challenged. In contrast, in this present study, we have orally inoculated 4 to 6 weeks old unweaned calves with high doses of BSE to identify any possible BSE infectivity and/or PrP<sup>BSE</sup> in peripheral nervous tissues during the first eight months post-inoculation (mpi). For the detection of BSE infectivity, we used a bovine PrP transgenic mouse bioassay, while PrP<sup>BSE</sup> depositions were analyzed by immunohistochemistry (IHC) and by protein misfolding cyclic amplification (PMCA). We were able to show that as early as 8 mpi the thoracic spinal cord as well as the parasympathetic nodal ganglion of these animals contained PrP<sup>BSE</sup> and BSE infectivity. This shows that the centripetal prion spread starts early after challenge at least in this age group, which represents an essential piece of information for the risk assessments for food, feed, and pharmaceutical products produced from young calves. |
format |
article |
author |
Ivett Ackermann Reiner Ulrich Kerstin Tauscher Olanrewaju I. Fatola Markus Keller James C. Shawulu Mark Arnold Stefanie Czub Martin H. Groschup Anne Balkema-Buschmann |
author_facet |
Ivett Ackermann Reiner Ulrich Kerstin Tauscher Olanrewaju I. Fatola Markus Keller James C. Shawulu Mark Arnold Stefanie Czub Martin H. Groschup Anne Balkema-Buschmann |
author_sort |
Ivett Ackermann |
title |
Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge |
title_short |
Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge |
title_full |
Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge |
title_fullStr |
Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge |
title_full_unstemmed |
Prion Infectivity and PrP<sup>BSE</sup> in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge |
title_sort |
prion infectivity and prp<sup>bse</sup> in the peripheral and central nervous system of cattle 8 months post oral bse challenge |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/a13d8f1186a444bca4f51ad6092fc8d2 |
work_keys_str_mv |
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