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Status |
Public on May 01, 2011 |
Title |
Coxsackievirus B3 (CVB3) infection of AJ, B10.A, CSS3 and B6.chr3AJ (heart tissue day 4) |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
The pathogenesis of viral myocarditis is a multifactorial process involving host genetics, viral genetics and the environment in which they interact. Here, we used a model of infection with Coxsackievirus B3 to characterize the contribution of host genetics to viral myocarditis. We determined heart CVB3 load in mice from a classical intercross between progenitors A/J (H2a) and B10.A-H2a (B10.A) of different genetic backgrounds but with a common H2 haplotype. Here we compare whole genome expression patterns in infected and uninfected A/J and B10.A mice in order to determine which gene expression programs are common or distinct to each strain.
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Overall design |
Total RNA obtained from hearts of 3 AJ, 3 B10.A(H2a), 3 CSS3 and 3 B6.chr3AJ that were infected or uninfected with CVB3(CG) at 400pfu/g and collected at day 4 post infection.
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Contributor(s) |
Vidal S, Wiltshire S |
Citation(s) |
21525387 |
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Submission date |
Dec 15, 2009 |
Last update date |
Jan 16, 2019 |
Contact name |
Sean A Wiltshire |
Organization name |
McGill University
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Department |
Human Genetics
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Lab |
Silvia Vidal
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Street address |
3649 Sir william Osler, Rm 356
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City |
Montreal |
ZIP/Postal code |
H3G 0B1 |
Country |
Canada |
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Platforms (1) |
GPL6887 |
Illumina MouseWG-6 v2.0 expression beadchip |
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Samples (24)
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Relations |
BioProject |
PRJNA122413 |