We investigated effects of various DNAs on duck hepatitis B virus replication in uiuo. One-day-old ducks were infected intravenously with DHBV. Various DNAs were then iqjected intravenously, and duck hepatitis B virus levels were followed for up to 20 days after the inoculation. WhenM13 bacteriophage DNA (M13 DNA), heat-denatured Escherichia coli DNA or CPX 174 phage DNA was injected intravenously at a dose of 2.45 mgkg body wt daily for 10 days, a significant decrease of serum duck hepatitis B virus DNA was detected within 10 days. The efficacy was twice that reported with antisense DNA on a weight basis and f a r more than that reported on a molar basis. M13 DNA was superior, on the basis of effective dose, to acyclovir as an anti-duck hepatitis B virus agent. On treatment with M13 DNA, serum 2-5 A synthetase level was increased five to six times, suggesting that the antiviral effect of M13 DNA is at least partly due to induction of endogenous interferon, which in turn induces 2-5 A synthetase. No sigdicant inhibitory effect on replication of duck hepatitis B virus was demonstrated by DNAs obtained from herring testes, herring sperm, salmon testes, human placenta or calf thymus. On discontinuation of M13 DNA iqjection on day 10, duck hepatitis B virus reappeared in the serum at later time points. Digestion of M13 DNA with S1 nuclease resulted in marked reduction of antiviral activity. These results show that M13 DNA, not its digested product, has potent antiviral activity.