mortality/aging
• infection of mice with VSV or mouse-adapted influenza induces greater lethality than in similarly treated wild-type mice
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immune system
N |
• mice exhibit normal immune systems in the absence of viral infection
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• mouse embryonic fibroblasts infected with vesicular stomatitis virus (VSV) exhibit increased apoptosis and viral replication compared to similarly treated wild-type cells
(J:63671)
• infection of mice with VSV induces respiratory distress, paralytic disease, and premature lethality unlike in wild-type mice
(J:63671)
• however, pre-treatment with IFNalpha/beta or gamma restores protection against virally induced apoptosis
(J:63671)
• mouse embryonic fibroblasts exhibit increased susceptibility to RNA virus replication compared with wild-type cells
(J:167126)
|
• mice infected with mouse-adapted influenza exhibit increased apoptosis in the lungs and lethality compared with similarly treated wild-type mice
• replication of mouse-adapted influenza in mouse embryonic fibroblasts is increased compared to in similarly treated wild-type mice
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cellular
• mouse embryonic fibroblasts are resistant to double-strand RNA-induced apoptosis unlike wild-type cells
|
• mouse embryonic fibroblasts infected with vesicular stomatitis virus exhibit increased apoptosis compared to similarly treated wild-type cells
• however, pre-treatment with IFNalpha/beta or gamma restores protection against virally induced apoptosis
|