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Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood

Efforts to prevent human-to-human transmission of variant Creutzfeldt-Jakob disease (vCJD) by contaminated blood would be aided by the development of a sensitive diagnostic test that could be routinely used to screen blood donations. As blood samples from vCJD patients are extremely rare, here we de...

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Autores principales: Thomas, Charlotte M., Salamat, M. Khalid F., de Wolf, Christopher, McCutcheon, Sandra, Blanco, A. Richard Alejo, Manson, Jean C., Hunter, Nora, Houston, E. Fiona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621866/
https://www.ncbi.nlm.nih.gov/pubmed/37917783
http://dx.doi.org/10.1371/journal.pone.0293845
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author Thomas, Charlotte M.
Salamat, M. Khalid F.
de Wolf, Christopher
McCutcheon, Sandra
Blanco, A. Richard Alejo
Manson, Jean C.
Hunter, Nora
Houston, E. Fiona
author_facet Thomas, Charlotte M.
Salamat, M. Khalid F.
de Wolf, Christopher
McCutcheon, Sandra
Blanco, A. Richard Alejo
Manson, Jean C.
Hunter, Nora
Houston, E. Fiona
author_sort Thomas, Charlotte M.
collection PubMed
description Efforts to prevent human-to-human transmission of variant Creutzfeldt-Jakob disease (vCJD) by contaminated blood would be aided by the development of a sensitive diagnostic test that could be routinely used to screen blood donations. As blood samples from vCJD patients are extremely rare, here we describe the optimisation of real-time quaking-induced conversion (RT-QuIC) for detection of PrP(Sc) (misfolded prion protein, a marker of prion infection) in blood samples from an established large animal model of vCJD, sheep experimentally infected with bovine spongiform encephalopathy (BSE). Comparative endpoint titration experiments with RT-QuIC, miniaturized bead protein misfolding cyclic amplification (mb-PMCA) and intracerebral inoculation of a transgenic mouse line expressing sheep PrP (tgOvARQ), demonstrated highly sensitive detection of PrP(Sc) by RT-QuIC in a reference sheep brain homogenate. Upon addition of a capture step with iron oxide beads, the RT-QuIC assay was able to detect PrP(Sc) in whole blood samples from BSE-infected sheep up to two years before disease onset. Both RT-QuIC and mb-PMCA also demonstrated sensitive detection of PrP(Sc) in a reference vCJD-infected human brain homogenate, suggesting that either assay may be suitable for application to human blood samples. Our results support the further development and evaluation of RT-QuIC as a diagnostic or screening test for vCJD.
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spelling pubmed-106218662023-11-03 Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood Thomas, Charlotte M. Salamat, M. Khalid F. de Wolf, Christopher McCutcheon, Sandra Blanco, A. Richard Alejo Manson, Jean C. Hunter, Nora Houston, E. Fiona PLoS One Research Article Efforts to prevent human-to-human transmission of variant Creutzfeldt-Jakob disease (vCJD) by contaminated blood would be aided by the development of a sensitive diagnostic test that could be routinely used to screen blood donations. As blood samples from vCJD patients are extremely rare, here we describe the optimisation of real-time quaking-induced conversion (RT-QuIC) for detection of PrP(Sc) (misfolded prion protein, a marker of prion infection) in blood samples from an established large animal model of vCJD, sheep experimentally infected with bovine spongiform encephalopathy (BSE). Comparative endpoint titration experiments with RT-QuIC, miniaturized bead protein misfolding cyclic amplification (mb-PMCA) and intracerebral inoculation of a transgenic mouse line expressing sheep PrP (tgOvARQ), demonstrated highly sensitive detection of PrP(Sc) by RT-QuIC in a reference sheep brain homogenate. Upon addition of a capture step with iron oxide beads, the RT-QuIC assay was able to detect PrP(Sc) in whole blood samples from BSE-infected sheep up to two years before disease onset. Both RT-QuIC and mb-PMCA also demonstrated sensitive detection of PrP(Sc) in a reference vCJD-infected human brain homogenate, suggesting that either assay may be suitable for application to human blood samples. Our results support the further development and evaluation of RT-QuIC as a diagnostic or screening test for vCJD. Public Library of Science 2023-11-02 /pmc/articles/PMC10621866/ /pubmed/37917783 http://dx.doi.org/10.1371/journal.pone.0293845 Text en © 2023 Thomas et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Thomas, Charlotte M.
Salamat, M. Khalid F.
de Wolf, Christopher
McCutcheon, Sandra
Blanco, A. Richard Alejo
Manson, Jean C.
Hunter, Nora
Houston, E. Fiona
Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
title Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
title_full Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
title_fullStr Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
title_full_unstemmed Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
title_short Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
title_sort development of a sensitive real-time quaking-induced conversion (rt-quic) assay for application in prion-infected blood
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621866/
https://www.ncbi.nlm.nih.gov/pubmed/37917783
http://dx.doi.org/10.1371/journal.pone.0293845
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