Key result
The high-fidelity 3D-G64S poliovirus mutant demonstrated significantly reduced pathogenesis and viral fitness compared to wild-type virus under selective pressure in a mouse model.
Why the study?
Does increased fidelity reduce poliovirus fitness and virulence under selective pressure in mice?
Does increased fidelity reduce poliovirus fitness and virulence under selective pressure in mice?
p-value: p=<0.05
Increased fidelity of the viral polymerase reduces poliovirus fitness under selective pressure, explaining its reduced pathogenicity in vivo.
Supports fidelity mutations for poliovirus attenuation in mice; leaves open translation to human vaccines or therapies.
RNA viruses have high error rates, and the resulting quasispecies may aid survival of the virus population in the presence of selective pressure. Therefore, it has been theorized that RNA viruses require high error rates for survival, and that a virus with high fidelity would be less able to cope in complex environments. We previously isolated and characterized poliovirus with a mutation in the viral polymerase, 3D-G64S, which confers resistance to mutagenic nucleotide analogs via increased fidelity. The 3D-G64S virus was less pathogenic than wild-type virus in poliovirus-receptor transgenic mice, even though only slight growth defects were observed in tissue culture. To determine whether the high-fidelity phenotype of the 3D-G64S virus could decrease its fitness under a defined selective pressure, we compared growth of the 3D-G64S virus and 3D wild-type virus in the context of a revertible attenuating point mutation, 2C-F28S. Even with a 10-fold input advantage, the 3D-G64S virus was unable to compete with 3D wild-type virus in the context of the revertible attenuating mutation; however, in the context of a non-revertible version of the 2C-F28S attenuating mutation, 3D-G64S virus matched the replication of 3D wild-type virus. Therefore, the 3D-G64S high-fidelity phenotype reduced viral fitness under a defined selective pressure, making it likely that the reduced spread in murine tissue could be caused by the increased fidelity of the viral polymerase.
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Pfeiffer et al. (2005) studied Poliovirus infection. 3D-G64S high-fidelity mutant poliovirus vs. Wild-type poliovirus was evaluated on Time to first symptoms (weakness and paralysis of the inoculated limb) (p=<0.05). The high-fidelity 3D-G64S poliovirus mutant demonstrated significantly reduced pathogenesis and viral fitness compared to wild-type virus under selective pressure in a mouse model.
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