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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Autores principales: Ivett Ackermann, Reiner Ulrich, Kerstin Tauscher, Olanrewaju I. Fatola, Markus Keller, James C. Shawulu, Mark Arnold, Stefanie Czub, Martin H. Groschup, Anne Balkema-Buschmann
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Publicado: MDPI AG 2021
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BSE
Acceso en línea:https://doaj.org/article/a13d8f1186a444bca4f51ad6092fc8d2
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spelling 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)
institution DOAJ
collection DOAJ
language EN
topic prion protein
BSE
infectivity
PrP<sup>BSE</sup>
cattle
peripheral and central nervous system
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle 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
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