TABLE 1.
Type of cell | d.p.i. | % Infected cellsb | PFU/mlc | PFU/1,000 infected cellsd |
---|---|---|---|---|
Primary CD46+ mouse neuron | 1 | 5 | NDe | 0 |
2 | 5 | 20 | 10 | |
3 | 10 | 20 | 6 | |
Vero | 1 | 80 | ND | 0 |
2 | 100 | 6.0 × 104 | 600 | |
3 | 100 | 3.2 × 105 | 1,600 | |
HeLa | 1 | 50 | 360 | 10 |
2 | 80 | 7.2 × 103 | 130 | |
3 | 100 | 1.6 × 104 | 170 | |
NT2 | 1 | 50 | 54 | 2 |
2 | 85 | 36 | 1 | |
3 | 90 | 156 | 3 | |
Undifferentiated NT2 | 1 | 60 | 40 | 1 |
2 | 75 | 6.4 × 103 | 130 | |
3 | 95 | 9.2 × 103 | 100 |
Cells plated at a density of 1 × 105 to 2 × 105 cells/coverslip were infected 1 day later with MV Edmonston (MOI = 1). Data represent results from at least two separate experiments, each performed in duplicate.
Percent infected cells was determined by immunohistochemical staining of MV antigen.
Supernatants tested for infectious virus by plaque assay.
PFU/1,000 cell values, used to correct for cell division rates in fibroblast cultures (cell counts determined in parallel uninfected cultures) and the proportion of cells infected at the indicated time, were calculated as {[(PFU/ml) × 4 ml]/(number of cells × proportion infected)} × 1,000.
ND, not detected.