Single-stranded DNA derived from M13 phage was evaluated for antiviral
activity in mice infected with vaccinia virus. M13 DNA at a dose as l
ow as 16.7 mg/kg was effective in reducing the number of tail lesions
caused by vaccinia virus by more than 90%. A single administration of
M13 DNA 1 day before infection was sufficient to reduce significantly
the number of tail lesions caused by vaccinia virus. Denatured eukaryo
tic nucleic acids such as calf thymus DNA and human placenta DNA were
not effective. A mixture of nucleotides prepared according to the nucl
eotides composition of M13 DNA was also ineffective. Within 4 h after
the administration of M13 DNA, the serum interferon (IFN, predominantl
y type beta) titer rose from undetectable levels to as much as approxi
mately 700 IU/ml. IFN was delectable for up to 12 h after the administ
ration of M13 DNA. IFN titers as high as 1050 IU/ml were detected in v
itro when M13 DNA was added to spleen cultures. We conclude that at le
ast part of the antiviral activity of M13 DNA can be explained on the
basis of IFN induction.