This indicates that the adaptive immune response plays an important role in the late stages of DI virus-mediated protection from influenza virus infection

in vivo. To understand how DI virus mediated protection we examined mice for lung consolidation and lung infectivity. Protection conferred by 1.2 μg of active DI virus (Fig. 2a and b) closely reproduced data shown in Fig. 1. Lungs of SCID mice inoculated GDC-0449 molecular weight with A/WSN only or with inactivated DI virus + A/WSN showed signs of consolidation from day 4 onwards, with lungs exhibiting a plum-coloured discoloration of small areas of the lung surface, particularly around the insertion of the bronchi (Fig. 2c). This looked very similar to the lungs of immune-competent IDH tumor mice infected with A/WSN. Consolidation increased rapidly until, by day 6, the majority of the lung surface was discoloured. During this period there was no sign of consolidation in the lungs

of active DI virus-treated, infected mice, but consolidation developed in these animals from day 8. The timing was atypical as the delayed consolidation appeared 3 days before the onset of clinical disease or weight loss instead of 1 to 2 days afterwards seen with the normal acute disease (Table 1). Lung consolidation in active DI virus-treated, virus-infected SCID mice progressed at a similar rate to that in SCID mice given only infectious virus. Consolidation declined in the few active DI virus-treated mice that survived to day 16. On day 2 post-infection

the lung infectivity in SCID mice inoculated with inactivated DI virus + A/WSN was already 10% of the maximum value reached on day 4, while the lung titre in mice receiving active DI virus + A/WSN was 83-fold lower on day 2. Although the infectious load in active DI virus-treated mice increased slowly over the next few days the difference seen with treated with active or inactive DI virus remained at over 10-fold to day 6 post infection. At this ADP ribosylation factor time active DI virus-treated, infected mice appeared perfectly normal, while mice that received inactivated DI virus + A/WSN had had lost nearly 20% body mass and were extremely ill. From days 4 to 8 the infectious load in DI treated-mice rose steadily, and at day 8 there was overt lung consolidation (Fig. 2c). Consolidation, infectious virus load, weight loss and clinical disease all increased thereafter (Fig. 2a–d). Taken together, the data show that active DI virus treatment significantly delayed the production of infectious virus in the lungs of SCID mice compared to those treated with inactive DI virus and this correlated with delays in the lung consolidation and overt clinical disease. There are no reports in the literature for the dynamics of influenza full-length or DI RNA synthesis in the mouse lung.