TABLE 1.
Virus | Targeted sequenceb | Viral titer (PFU/ml) after treatment with:
|
3′ CSI PPMO-mediated reduction (n-fold)c | Viral titer (PFU/ml) after treatment with scramble PPMO | Scramble PPMO-mediated reduction (n-fold)c | |
---|---|---|---|---|---|---|
No PPMO | 3′ CSI PPMO | |||||
WNV | AACAGCATATTGACACCTGGGA | 5.8 × 108 | 5.9 × 103 | 98,300 | 4.1 × 108 | 1.4 |
JEV | AACAGCATATTGACACCTGGGA | 2.8 × 107 | 1.4 × 103 | 20,000 | 2.0 × 107 | 1.4 |
SLEV | AACAGCATATTGACACCTGGGA | 5.5 × 106 | 4.5 × 103 | 1,200 | 4.2 × 106 | 1.3 |
DENV-2 | AACAGCATATTGAC-GCTGGGA | 6.1 × 106 | 6.0 × 105 | 10 | 1.9 × 107 | 0.3 |
YFV | GGGACCATATTGACGCCAGGGA | 1.7 × 107 | 6.1 × 106 | 3 | 4.6 × 106 | 3.7 |
Vero cells were infected with the indicated virus (MOI of 0.1), treated with a redesigned 3′ CSI PPMO (7.5 μM), and assayed for viral titers at 40 to 42 h postinfection.
Sequences from various mosquito-borne flaviviruses targeted by the 3′ CSI PPMO. Nucleotide changes relative to the WNV sequence are underlined, and a nucleotide deletion is indicated by a hyphen. Sequences were derived from GenBank entries with accession numbers AF404756, NC_001437, CQ897117, U87411, and U17066 for WNV, JEV, SLEV, DENV-2, and YFV viruses, respectively.
The reduction (n-fold) in viral titer was calculated as follows: viral titer without PPMO treatment/viral titer with PPMO treatment.