mortality/aging
• 36% survival as compared to 63% survival for controls after infection with WNV
|
immune system
N |
• La Crosse virus (LACV) replication is normal
(J:196200)
• no difference in vial burden as compared to controls in spleen, brain, or spinal cord after infection with 102 PFU of West Nile Virus (WNV)
(J:200140)
• no difference in virus specific IgG or IgM at 6, 8, and 10 days after infection
(J:200140)
• no difference in CD8+ T cells in the brain
(J:200140)
|
• fewer activated microglia, particularly in brainstem and cerebral cortex but not in cerebellum after WNV infection
• macrophage and resting microglia numbers are unchanged
|
• 10 fold lower levels of TNF alpha in brain homogenates relative to controls afer WNV infection
|
• increased vulnerability to infection with 102 PFU of West Nile Virus (WNV)
• elevated WNV RNA in the brainstem but not in the cortex
|
• 36% survival as compared to 63% survival for controls after infection with WNV
|
hematopoietic system
N |
• normal hematopoietc cell development after WNV infection
• typical B and T cell maturation profiles
|
• fewer activated microglia, particularly in brainstem and cerebral cortex but not in cerebellum after WNV infection
• macrophage and resting microglia numbers are unchanged
|
homeostasis/metabolism
• 10 fold lower levels of TNF alpha in brain homogenates relative to controls afer WNV infection
|
nervous system
• 100% of controls infected with 103 PFU of LACV develop neurological disease by 3 weeks whereas homozygous mutant mice develop disease at a significantly lower level
• levels of virus RNA are similar to control levels
• no mitochondrial damage, unlike control mice
|
• apoptosis is reduced in neurons from homozygotes infected with La Crosse virus, LACV, relative to controls (in culture)
• delayed neuronal death
|
• increased apoptosis in the brainstem 8-10 days after infection with WNV but not in the cortex, hippocampus, or cerebellum
|
• fewer activated microglia, particularly in brainstem and cerebral cortex but not in cerebellum after WNV infection
• macrophage and resting microglia numbers are unchanged
|
cellular
• apoptosis is reduced in neurons from homozygotes infected with La Crosse virus, LACV, relative to controls (in culture)
• delayed neuronal death
|
• increased apoptosis in the brainstem 8-10 days after infection with WNV but not in the cortex, hippocampus, or cerebellum
|