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The identification of disease-induced biomarkers in the urine of BSE infected cattle

BACKGROUND: The bovine spongiform encephalopathy (BSE) epidemic and the emergence of a new human variant of Creutzfeldt-Jakob Disease (vCJD) have led to profound changes in the production and trade of agricultural goods. The rapid tests currently approved for BSE monitoring in slaughtered cattle are...

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Autores principales: Simon, Sharon LR, Lamoureux, Lise, Plews, Margot, Stobart, Michael, LeMaistre, Jillian, Ziegler, Ute, Graham, Catherine, Czub, Stefanie, Groschup, Martin, Knox, J David
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546380/
https://www.ncbi.nlm.nih.gov/pubmed/18775071
http://dx.doi.org/10.1186/1477-5956-6-23
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author Simon, Sharon LR
Lamoureux, Lise
Plews, Margot
Stobart, Michael
LeMaistre, Jillian
Ziegler, Ute
Graham, Catherine
Czub, Stefanie
Groschup, Martin
Knox, J David
author_facet Simon, Sharon LR
Lamoureux, Lise
Plews, Margot
Stobart, Michael
LeMaistre, Jillian
Ziegler, Ute
Graham, Catherine
Czub, Stefanie
Groschup, Martin
Knox, J David
author_sort Simon, Sharon LR
collection PubMed
description BACKGROUND: The bovine spongiform encephalopathy (BSE) epidemic and the emergence of a new human variant of Creutzfeldt-Jakob Disease (vCJD) have led to profound changes in the production and trade of agricultural goods. The rapid tests currently approved for BSE monitoring in slaughtered cattle are all based on the detection of the disease related isoform of the prion protein, PrP(d), in brain tissue and consequently are only suitable for post-mortem diagnosis. Objectives: In instances such as assessing the health of breeding stock for export purposes where post-mortem testing is not an option, there is a demand for an ante-mortem test based on a matrix or body fluid that would permit easy access and repeated sampling. Urine and urine based analyses would meet these requirements. RESULTS: Two dimensional differential gel eletrophoresis (2D-DIGE) and mass spectrometry analyses were used to identify proteins exhibiting differential abundance in the urine of BSE infected cattle and age matched controls over the course of the disease. Multivariate analyses of protein expression data identified a single protein able to discriminate, with 100% accuracy, control from infected samples. In addition, a subset of proteins were able to predict with 85% ± 13.2 accuracy the time post infection that the samples were collected. CONCLUSION: These results suggest that in principle it is possible to identify biomarkers in urine useful in the diagnosis, prognosis and monitoring of disease progression of transmissible spongiform encephalopathy diseases (TSEs).
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spelling pubmed-25463802008-09-20 The identification of disease-induced biomarkers in the urine of BSE infected cattle Simon, Sharon LR Lamoureux, Lise Plews, Margot Stobart, Michael LeMaistre, Jillian Ziegler, Ute Graham, Catherine Czub, Stefanie Groschup, Martin Knox, J David Proteome Sci Research BACKGROUND: The bovine spongiform encephalopathy (BSE) epidemic and the emergence of a new human variant of Creutzfeldt-Jakob Disease (vCJD) have led to profound changes in the production and trade of agricultural goods. The rapid tests currently approved for BSE monitoring in slaughtered cattle are all based on the detection of the disease related isoform of the prion protein, PrP(d), in brain tissue and consequently are only suitable for post-mortem diagnosis. Objectives: In instances such as assessing the health of breeding stock for export purposes where post-mortem testing is not an option, there is a demand for an ante-mortem test based on a matrix or body fluid that would permit easy access and repeated sampling. Urine and urine based analyses would meet these requirements. RESULTS: Two dimensional differential gel eletrophoresis (2D-DIGE) and mass spectrometry analyses were used to identify proteins exhibiting differential abundance in the urine of BSE infected cattle and age matched controls over the course of the disease. Multivariate analyses of protein expression data identified a single protein able to discriminate, with 100% accuracy, control from infected samples. In addition, a subset of proteins were able to predict with 85% ± 13.2 accuracy the time post infection that the samples were collected. CONCLUSION: These results suggest that in principle it is possible to identify biomarkers in urine useful in the diagnosis, prognosis and monitoring of disease progression of transmissible spongiform encephalopathy diseases (TSEs). BioMed Central 2008-09-05 /pmc/articles/PMC2546380/ /pubmed/18775071 http://dx.doi.org/10.1186/1477-5956-6-23 Text en Copyright © 2008 Simon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Simon, Sharon LR
Lamoureux, Lise
Plews, Margot
Stobart, Michael
LeMaistre, Jillian
Ziegler, Ute
Graham, Catherine
Czub, Stefanie
Groschup, Martin
Knox, J David
The identification of disease-induced biomarkers in the urine of BSE infected cattle
title The identification of disease-induced biomarkers in the urine of BSE infected cattle
title_full The identification of disease-induced biomarkers in the urine of BSE infected cattle
title_fullStr The identification of disease-induced biomarkers in the urine of BSE infected cattle
title_full_unstemmed The identification of disease-induced biomarkers in the urine of BSE infected cattle
title_short The identification of disease-induced biomarkers in the urine of BSE infected cattle
title_sort identification of disease-induced biomarkers in the urine of bse infected cattle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546380/
https://www.ncbi.nlm.nih.gov/pubmed/18775071
http://dx.doi.org/10.1186/1477-5956-6-23
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