Picornaviruses perturb nucleocytoplasmic trafficking by targeting FG-nucleoporins via proteolytic degradation or phosphorylation to enhance viral replication and prevent host immune responses.
Picornaviruses utilize distinct mechanisms to disrupt host nucleocytoplasmic trafficking, facilitating viral replication and evading innate immune responses.
Picornaviruses are positive-stranded RNA viruses. Even though replication and translation of their genome take place in the cytoplasm, these viruses evolved different strategies to disturb nucleocytoplasmic trafficking of host proteins and RNA. The major targets of picornavirus are the phenylalanine-glycine (FG)-nucleoporins, which form a mesh in the central channel of the nuclear pore complex through which protein cargos and karyopherins are actively transported in both directions. Interestingly, while enteroviruses use the proteolytic activity of their 2A protein to degrade FG-nucleoporins, cardioviruses act by triggering phosphorylation of these proteins by cellular kinases. By targeting the nuclear pore complex, picornaviruses recruit nuclear proteins to the cytoplasm, where they increase viral genome translation and replication; they affect nuclear translocation of cytoplasmic proteins such as transcription factors that induce innate immune responses and retain host mRNA in the nucleus thereby preventing cell emergency responses and likely making the ribosomal machinery available for translation of viral RNAs.
Lizcano-Perret et al. (Wed,) conducted a review in Picornavirus infection. Picornaviruses was evaluated. Picornaviruses perturb nucleocytoplasmic trafficking by targeting FG-nucleoporins via proteolytic degradation or phosphorylation to enhance viral replication and prevent host immune responses.
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