Key result
Recombinant MLB astroviruses with deletions in the 3' end of the capsid-coding region were strongly attenuated in iPSC-derived neuronal cultures despite wild-type-like growth in permissive cells.
Why the study?
Detection of neurotropic astroviruses has increased dramatically, with MLB genogroup astroviruses causing gastroenteritis and severe neurological complications in vulnerable populations.
This is the authors' abstract. We don't add key points for this paper.
During the last decade, the detection of neurotropic astroviruses has increased dramatically. The MLB genogroup of astroviruses represents a genetically distinct group of zoonotic astroviruses associated with gastroenteritis and severe neurological complications in young children, the immunocompromised and the elderly. Using different virus evolution approaches, we identified dispensable regions in the 3′ end of the capsid-coding region responsible for attenuation of MLB astroviruses in susceptible cell lines. To create recombinant viruses with identified deletions, MLB reverse genetics and replicon systems were developed. Recombinant truncated MLB viruses had wild type-like or enhanced growth and replication properties in permissive cells but were strongly attenuated in iPSC-derived neuronal cultures confirming the location of neurotropism determinants. This approach can be used for the development of vaccine candidates using attenuated astroviruses that infect humans, livestock animals and poultry.
Identification of dispensable regions in the 3' end of the capsid-coding region responsible for attenuation of MLB astroviruses provides a platform for developing vaccine candidates.
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Ali et al. (2022) studied Neurotropic human astrovirus infection. Recombinant MLB astroviruses with 3' deletions vs. Wild-type recombinant MLB astroviruses was evaluated on Viral replication and infectivity in iPSC-derived neuronal cultures. Recombinant MLB astroviruses with deletions in the 3' end of the capsid-coding region were strongly attenuated in iPSC-derived neuronal cultures despite wild-type-like growth in permissive cells.
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