TABLE 1.
Capsid used for trans-encapsidationa | Virus recovered from transfection (PFU/ml [expt 1b]) | Relative efficiency of trans-encapsidation (%)c
|
||
---|---|---|---|---|
Expt 1 | Expt 2 | Expt 3 | ||
Poliovirus | 4 × 108 | 100 | 100 | 100 |
Coxsackievirus B3 | 2 × 108 | 6.1 | 3.7 | n.d. |
HRV14d | 1 × 107 | 0.23 | n.d. | 1.2 |
Mengovirus | 7 × 107 | 0.06 | n.d. | 0.6 |
HAV | Negative | Negative | n.d. | n.d. |
Viral capsids were produced following transfection with the corresponding viral cDNA constructs described in Materials and Methods.
Experiment 1 is the experiment represented in Fig. 7.
Relative efficiency was calculated by arbitrarily setting poliovirus trans-encapsidation at 100%, based on luciferase activity after infection. Values represent the percentage of luciferase activity resulting from infection of trans-encapsidated replicon. n.d., not done.
Plaque assay mixture for HRV14 was incubated at 34°C.