Cargando…

Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection

BACKGROUND: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, characterized by a prominent accumulation of pathological isoforms of the prion protein (PrP(TSE)) in the brain and lymphoid tissues. Since the publication in the United Kingdom of four apparent vCJD cas...

Descripción completa

Detalles Bibliográficos
Autores principales: Segarra, Christiane, Bougard, Daisy, Moudjou, Mohammed, Laude, Hubert, Béringue, Vincent, Coste, Joliette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722129/
https://www.ncbi.nlm.nih.gov/pubmed/23894513
http://dx.doi.org/10.1371/journal.pone.0069632
_version_ 1782278146679111680
author Segarra, Christiane
Bougard, Daisy
Moudjou, Mohammed
Laude, Hubert
Béringue, Vincent
Coste, Joliette
author_facet Segarra, Christiane
Bougard, Daisy
Moudjou, Mohammed
Laude, Hubert
Béringue, Vincent
Coste, Joliette
author_sort Segarra, Christiane
collection PubMed
description BACKGROUND: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, characterized by a prominent accumulation of pathological isoforms of the prion protein (PrP(TSE)) in the brain and lymphoid tissues. Since the publication in the United Kingdom of four apparent vCJD cases following transfusion of red blood cells and one apparent case following treatment with factor VIII, the presence of vCJD infectivity in the blood seems highly probable. For effective blood testing of vCJD individuals in the preclinical or clinical phase of infection, it is considered necessary that assays detect PrP(TSE) concentrations in the femtomolar range. METHODOLOGY/PRINCIPAL FINDINGS: We have developed a three-step assay that firstly captures PrP(TSE) from infected blood using a plasminogen-coated magnetic-nanobead method prior to its serial amplification via protein misfolding cyclic amplification (PMCA) and specific PrP(TSE) detection by western blot. We achieved a PrP(TSE) capture yield of 95% from scrapie-infected material. We demonstrated the possibility of detecting PrP(TSE) in white blood cells, in buffy coat and in plasma isolated from the blood of scrapie-infected sheep collected at the pre-clinical stage of the disease. The test also allowed the detection of PrP(TSE) in human plasma spiked with a 10(−8) dilution of vCJD-infected brain homogenate corresponding to the level of sensitivity (femtogram) required for the detection of the PrP(TSE) in asymptomatic carriers. The 100% specificity of the test was revealed using a blinded panel comprising 96 human plasma samples. CONCLUSION/SIGNIFICANCE: We have developed a sensitive and specific amplification assay allowing the detection of PrP(TSE) in the plasma and buffy coat fractions of blood collected at the pre-clinical phase of the disease. This assay represents a good candidate as a confirmatory assay for the presence of PrP(TSE) in blood of patients displaying positivity in large scale screening tests.
format Online
Article
Text
id pubmed-3722129
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37221292013-07-26 Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection Segarra, Christiane Bougard, Daisy Moudjou, Mohammed Laude, Hubert Béringue, Vincent Coste, Joliette PLoS One Research Article BACKGROUND: Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, characterized by a prominent accumulation of pathological isoforms of the prion protein (PrP(TSE)) in the brain and lymphoid tissues. Since the publication in the United Kingdom of four apparent vCJD cases following transfusion of red blood cells and one apparent case following treatment with factor VIII, the presence of vCJD infectivity in the blood seems highly probable. For effective blood testing of vCJD individuals in the preclinical or clinical phase of infection, it is considered necessary that assays detect PrP(TSE) concentrations in the femtomolar range. METHODOLOGY/PRINCIPAL FINDINGS: We have developed a three-step assay that firstly captures PrP(TSE) from infected blood using a plasminogen-coated magnetic-nanobead method prior to its serial amplification via protein misfolding cyclic amplification (PMCA) and specific PrP(TSE) detection by western blot. We achieved a PrP(TSE) capture yield of 95% from scrapie-infected material. We demonstrated the possibility of detecting PrP(TSE) in white blood cells, in buffy coat and in plasma isolated from the blood of scrapie-infected sheep collected at the pre-clinical stage of the disease. The test also allowed the detection of PrP(TSE) in human plasma spiked with a 10(−8) dilution of vCJD-infected brain homogenate corresponding to the level of sensitivity (femtogram) required for the detection of the PrP(TSE) in asymptomatic carriers. The 100% specificity of the test was revealed using a blinded panel comprising 96 human plasma samples. CONCLUSION/SIGNIFICANCE: We have developed a sensitive and specific amplification assay allowing the detection of PrP(TSE) in the plasma and buffy coat fractions of blood collected at the pre-clinical phase of the disease. This assay represents a good candidate as a confirmatory assay for the presence of PrP(TSE) in blood of patients displaying positivity in large scale screening tests. Public Library of Science 2013-07-24 /pmc/articles/PMC3722129/ /pubmed/23894513 http://dx.doi.org/10.1371/journal.pone.0069632 Text en © 2013 Segarra et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Segarra, Christiane
Bougard, Daisy
Moudjou, Mohammed
Laude, Hubert
Béringue, Vincent
Coste, Joliette
Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection
title Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection
title_full Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection
title_fullStr Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection
title_full_unstemmed Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection
title_short Plasminogen-Based Capture Combined with Amplification Technology for the Detection of PrP(TSE) in the Pre-Clinical Phase of Infection
title_sort plasminogen-based capture combined with amplification technology for the detection of prp(tse) in the pre-clinical phase of infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722129/
https://www.ncbi.nlm.nih.gov/pubmed/23894513
http://dx.doi.org/10.1371/journal.pone.0069632
work_keys_str_mv AT segarrachristiane plasminogenbasedcapturecombinedwithamplificationtechnologyforthedetectionofprptseinthepreclinicalphaseofinfection
AT bougarddaisy plasminogenbasedcapturecombinedwithamplificationtechnologyforthedetectionofprptseinthepreclinicalphaseofinfection
AT moudjoumohammed plasminogenbasedcapturecombinedwithamplificationtechnologyforthedetectionofprptseinthepreclinicalphaseofinfection
AT laudehubert plasminogenbasedcapturecombinedwithamplificationtechnologyforthedetectionofprptseinthepreclinicalphaseofinfection
AT beringuevincent plasminogenbasedcapturecombinedwithamplificationtechnologyforthedetectionofprptseinthepreclinicalphaseofinfection
AT costejoliette plasminogenbasedcapturecombinedwithamplificationtechnologyforthedetectionofprptseinthepreclinicalphaseofinfection