| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2010: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
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| Research Abstract |
Mouse hepatitis virus (MHV) is a member of the coronavirus family. Spike (S) protein, composed of virion projections, is responsible for binding to a receptor and also for the cell entry mechanism of MHV. Soluble receptor-resistant mutant 7 (srr7) isolated from the highly neuropathogenic JHM strain of MHV, cl-2, shows slightly reduced virulence compared to its maternal virus, inducing spongiotic degeneration at 48 hours post-inoculation (pi) with viral antigens-expression in the periventricular areas.During the course of infection with srr7, small spongiotic lesions appear at 2 days pi,and these spread out to form spongiform encephalopathy by 8 to 10 days pi. In thisstudy, we noted that the neurovirulence of srr7 increases with a shorter incubationperiod, and, in some cases, exhibits infectivity of neurons, similar to the observation incl-2 infection. Through the re-cloning of srr7, we obtained several mutants with singleor double substitutions of amino acids in the S protein rei on. All of these mutantviruses exhibited major MHV receptor (MHVR)-independent infectivity due to themutation of the S-coding region, which was examined by in vitro expression of thegenes. Each mutant virus showed different pattern of invasion into the brainparenchyma, provably due to the difference in the affinity to extracellular matrixemerged after the infection in the brain, which provides a new paradigm to elucidatethe mechanisms of spongiotic degeneration in the brain.
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