TABLE 1.
Quantification of neuronal MV infection and lymphocyte infiltration in neonate and adult micea
| Days p.i. | Site | Neonates (5 to 6 days)
|
Adults (45 to 60 days)
|
||||
|---|---|---|---|---|---|---|---|
| MV | CD4+ | CD8+ | MV | CD4+ | CD8+ | ||
| 3 | Parenchyma | ++ | + | − | − | ++ | + |
| Meninges and ventricles | − | ++ | − | − | ++ | + | |
| 6 | Parenchyma | +++ | ++ | + | − | +++ | +++ |
| Meninges and ventricles | − | ++ | + | − | +++ | +++ | |
At least four mice each of neonatal and adult line 18 NSE-CD46+ mice were inoculated i.c. with 3 × 104 PFU MV-Edmonston. After 3 or 6 days postinfection, mice were sacrificed and brains were collected for cryostat sectioning. Frozen brain sections from each mouse were stained as described in Fig. 3 and in Materials and Methods. Positively labeled cells were counted over the entire section, and assigned to a range as follows: −, 0 to 10 cells; +, 11 to 50 cells; ++, 51 to 250 cells; +++, >250 cells. The data shown are average results from multiple levels of at least two brains per group. Similar results were obtained with line 52 transgenic mice.