Skip to main content
. 2007 May 7;51(7):2470–2482. doi: 10.1128/AAC.00069-07

TABLE 1.

Activities of the 3′ CSI PPMO against mosquito-borne flavivirusesa

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
a

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.

b

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.

c

The reduction (n-fold) in viral titer was calculated as follows: viral titer without PPMO treatment/viral titer with PPMO treatment.