Key result
Co-infection with defective interfering genomes resulted in a 100-fold decrease in wild-type poliovirus titers, driven by competition for limiting cellular resources and viral capsid proteins.
Why the study?
The interactions between viral variants determine the fitness of RNA virus populations and the outcome of infection, requiring investigation into the effects of defective interfering genomes on wild-type poliovirus replication.
Defective interfering genomes effectively inhibit wild-type poliovirus production through competition for replication resources and encapsidation, as demonstrated by experimental and mathematical models.
Hypothesis-generating for defective interfering genomes as antivirals; leaves open translation to human poliovirus therapy.
1 Abstract During replication, RNA viruses accumulate genome alterations, such as mutations and deletions. The interactions between individual variants can determine the fitness of the virus population and, thus, the outcome of infection. To investigate the effects of defective interfering genomes (DI) on wild-type (WT) poliovirus replication, we developed an ordinary differential equation model. We experimentally determined virus and DI replication during co-infection, and use these data to infer model parameters. Our model predicts, and our experimental measurements confirm, that DI replication and encapsidation are the most important determinants for the outcome of the competition. WT replication inversely correlates with DI replication. Our model predicts that genome replication and effective DI genome encapsidation are critical to effectively inhibit WT production, but an equilibrium can be established which enables WT to replicate, albeit to reduce levels.
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Shirogane et al. (2021) studied Poliovirus infection. Defective interfering (DI) genome co-infection vs. Wild-type poliovirus single infection was evaluated on Wild-type virus production (infectious titers). Co-infection with defective interfering genomes resulted in a 100-fold decrease in wild-type poliovirus titers, driven by competition for limiting cellular resources and viral capsid proteins.
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