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Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection

Prions are unique infectious agents that replicate without a genome and cause neurodegenerative diseases that include chronic wasting disease (CWD) of cervids. Immunohistochemistry (IHC) is currently considered the gold standard for diagnosis of a prion infection but may be insensitive to early or s...

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Autores principales: Wyckoff, A. Christy, Galloway, Nathan, Meyerett-Reid, Crystal, Powers, Jenny, Spraker, Terry, Monello, Ryan J., Pulford, Bruce, Wild, Margaret, Antolin, Michael, VerCauteren, Kurt, Zabel, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389033/
https://www.ncbi.nlm.nih.gov/pubmed/25665713
http://dx.doi.org/10.1038/srep08358
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author Wyckoff, A. Christy
Galloway, Nathan
Meyerett-Reid, Crystal
Powers, Jenny
Spraker, Terry
Monello, Ryan J.
Pulford, Bruce
Wild, Margaret
Antolin, Michael
VerCauteren, Kurt
Zabel, Mark
author_facet Wyckoff, A. Christy
Galloway, Nathan
Meyerett-Reid, Crystal
Powers, Jenny
Spraker, Terry
Monello, Ryan J.
Pulford, Bruce
Wild, Margaret
Antolin, Michael
VerCauteren, Kurt
Zabel, Mark
author_sort Wyckoff, A. Christy
collection PubMed
description Prions are unique infectious agents that replicate without a genome and cause neurodegenerative diseases that include chronic wasting disease (CWD) of cervids. Immunohistochemistry (IHC) is currently considered the gold standard for diagnosis of a prion infection but may be insensitive to early or sub-clinical CWD that are important to understanding CWD transmission and ecology. We assessed the potential of serial protein misfolding cyclic amplification (sPMCA) to improve detection of CWD prior to the onset of clinical signs. We analyzed tissue samples from free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) and used hierarchical Bayesian analysis to estimate the specificity and sensitivity of IHC and sPMCA conditional on simultaneously estimated disease states. Sensitivity estimates were higher for sPMCA (99.51%, credible interval (CI) 97.15–100%) than IHC of obex (brain stem, 76.56%, CI 57.00–91.46%) or retropharyngeal lymph node (90.06%, CI 74.13–98.70%) tissues, or both (98.99%, CI 90.01–100%). Our hierarchical Bayesian model predicts the prevalence of prion infection in this elk population to be 18.90% (CI 15.50–32.72%), compared to previous estimates of 12.90%. Our data reveal a previously unidentified sub-clinical prion-positive portion of the elk population that could represent silent carriers capable of significantly impacting CWD ecology.
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spelling pubmed-53890332017-04-14 Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection Wyckoff, A. Christy Galloway, Nathan Meyerett-Reid, Crystal Powers, Jenny Spraker, Terry Monello, Ryan J. Pulford, Bruce Wild, Margaret Antolin, Michael VerCauteren, Kurt Zabel, Mark Sci Rep Article Prions are unique infectious agents that replicate without a genome and cause neurodegenerative diseases that include chronic wasting disease (CWD) of cervids. Immunohistochemistry (IHC) is currently considered the gold standard for diagnosis of a prion infection but may be insensitive to early or sub-clinical CWD that are important to understanding CWD transmission and ecology. We assessed the potential of serial protein misfolding cyclic amplification (sPMCA) to improve detection of CWD prior to the onset of clinical signs. We analyzed tissue samples from free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) and used hierarchical Bayesian analysis to estimate the specificity and sensitivity of IHC and sPMCA conditional on simultaneously estimated disease states. Sensitivity estimates were higher for sPMCA (99.51%, credible interval (CI) 97.15–100%) than IHC of obex (brain stem, 76.56%, CI 57.00–91.46%) or retropharyngeal lymph node (90.06%, CI 74.13–98.70%) tissues, or both (98.99%, CI 90.01–100%). Our hierarchical Bayesian model predicts the prevalence of prion infection in this elk population to be 18.90% (CI 15.50–32.72%), compared to previous estimates of 12.90%. Our data reveal a previously unidentified sub-clinical prion-positive portion of the elk population that could represent silent carriers capable of significantly impacting CWD ecology. Nature Publishing Group 2015-02-10 /pmc/articles/PMC5389033/ /pubmed/25665713 http://dx.doi.org/10.1038/srep08358 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wyckoff, A. Christy
Galloway, Nathan
Meyerett-Reid, Crystal
Powers, Jenny
Spraker, Terry
Monello, Ryan J.
Pulford, Bruce
Wild, Margaret
Antolin, Michael
VerCauteren, Kurt
Zabel, Mark
Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection
title Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection
title_full Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection
title_fullStr Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection
title_full_unstemmed Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection
title_short Prion Amplification and Hierarchical Bayesian Modeling Refine Detection of Prion Infection
title_sort prion amplification and hierarchical bayesian modeling refine detection of prion infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389033/
https://www.ncbi.nlm.nih.gov/pubmed/25665713
http://dx.doi.org/10.1038/srep08358
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