J Gen Virol Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 85 (2004), 3459-3471; DOI 10.1099/vir.0.80110-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary material
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Booth, S.
Right arrow Articles by Somorjai, R. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Booth, S.
Right arrow Articles by Somorjai, R. L.
Agricola
Right arrow Articles by Booth, S.
Right arrow Articles by Somorjai, R. L.
© 2004 Society for General Microbiology

Identification of central nervous system genes involved in the host response to the scrapie agent during preclinical and clinical infection

Stephanie Booth1, Christopher Bowman2, Richard Baumgartner2, Garrett Sorensen1, Catherine Robertson1, Michael Coulthart1, Clark Phillipson1 and Rajmund L. Somorjai2

1 Division of Host Genetics and Prion Diseases, National Microbiology Laboratory, Health Canada, Winnipeg, MB, Canada R3E 3R2
2 Institute for Biodiagnostics, National Research Council Canada, Winnipeg, MB, Canada R3B 1Y6

Correspondence
Stephanie Booth
Stephanie_Booth{at}hc-sc.gc.ca

Genes that are expressed differentially in the central nervous system of mice during infection with mouse-adapted scrapie agents were identified in this study. cDNA microarrays were used to examine gene-expression profiles at early, middle (preclinical) and late (clinical) time points after inoculation. A number of genes that showed significant changes in expression during the clinical stage of disease were identified. Of these, 138 were upregulated and 20 were downregulated. A smaller number of genes showed differential expression at the early and middle stages of the disease time course. These genes are interesting, as they may reflect biological processes that are involved in the molecular pathogenesis of the prion agent. At present, little is known about the early events in the disease process that trigger neurodegeneration. Perhaps most interestingly, one group of genes that exhibited decreased expression in all tested stages of the disease was identified in this study. This cluster included four transcripts representing haematopoietic system-related genes, which suggests that the haematopoietic system is involved in the disease process from an early stage.

Raw data and a hyperlinked version of Table 1 are available as supplementary material in JGV Online.




This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
G. P. Sawiris, K. G. Becker, E. J. Elliott, R. Moulden, and R. G. Rohwer
Molecular analysis of bovine spongiform encephalopathy infection by cDNA arrays
J. Gen. Virol., April 1, 2007; 88(4): 1356 - 1362.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
S. Saha, P. Sugumar, P. Bhandari, and P. N. Rangarajan
Identification of Japanese encephalitis virus-inducible genes in mouse brain and characterization of GARG39/IFIT2 as a microtubule-associated protein.
J. Gen. Virol., November 1, 2006; 87(Pt 11): 3285 - 3289.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
S. Saha, S. Murthy, and P. N. Rangarajan
Identification and characterization of a virus-inducible non-coding RNA in mouse brain
J. Gen. Virol., July 1, 2006; 87(7): 1991 - 1995.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2004 by the Society for General Microbiology.