mortality/aging
• decreased lethality is observed in mice challenged with influenza A virus or VSV
• mice infected with VSV by an intracerebal route have longer mean survival times (2.7 days vs. 1.5)
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• no lethality is observed in mice challenged with Thogoto virus while all the littermate controls died
• mice infected with influenza A virus by an intracerebal route have longer mean survival times (6.0 days vs. 3.9)
• mice infected with pneumotropic influenza A virus have increased rates of survival (33.3% vs 0%) for wild-type controls
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immune system
• supernatant of embryonic fibroblasts infected with VSV contains 10-40 fold less infectious particles 25 hours after infection
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• decreased lethality is observed in mice challenged with influenza A virus or VSV
• mice infected with VSV by an intracerebal route have longer mean survival times (2.7 days vs. 1.5)
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• no lethality is observed in mice challenged with Thogoto virus while all the littermate controls died
• mice infected with influenza A virus by an intracerebal route have longer mean survival times (6.0 days vs. 3.9)
• mice infected with pneumotropic influenza A virus have increased rates of survival (33.3% vs 0%) for wild-type controls
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• supernatant of embryonic fibroblasts infected with influenza A virus contains 10-40 fold less infectious particles 25 hours after infection
• supernatant of embryonic fibroblasts infected with Thogoto virus contains no infectious particles 3 days after infection
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