Key result
Co-infection of RAW cells with two wild-type murine norovirus isolates generated a viable homologous recombinant virus with distinct biological properties from the parental viruses.
Provides the first experimental evidence that murine norovirus undergoes homologous recombination, generating viruses with distinct biological properties.
Recombinants with distinct traits arise in murine norovirus co-infection; leaves open role in human strain diversity and evolution.
Based on sequencing data, norovirus (NoV) recombinants have been described, but no experimental evidence of recombination in NoVs has been documented. Using the murine norovirus (MNV) model, we investigated the occurrence of genetic recombination between two co-infecting wild-type MNV isolates in RAW cells. The design of a PCR-based genotyping tool allowed accurate discrimination between the parental genomes and the detection of a viable recombinant MNV (Rec MNV) in the progeny viruses. Genetic analysis of Rec MNV identified a homologous-recombination event located at the ORF1-ORF2 overlap. Rec MNV exhibited distinct growth curves and produced smaller plaques than the wild-type MNV in RAW cells. Here, we demonstrate experimentally that MNV undergoes homologous recombination at the previously described recombination hot spot for NoVs, suggesting that the MNV model might be suitable for in vitro studies of NoV recombination. Moreover, the results show that exchange of genetic material between NoVs can generate viruses with distinct biological properties from the parental viruses.
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Mathijs et al. (2010) studied Murine norovirus (MNV) infection. Co-infection with two wild-type MNV isolates vs. Parental wild-type MNV was evaluated on Occurrence of genetic recombination and generation of viable recombinant MNV. Co-infection of RAW cells with two wild-type murine norovirus isolates generated a viable homologous recombinant virus with distinct biological properties from the parental viruses.
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