# SHFL Post-Transcriptionally Restricts Coxsackievirus A16 In Vitro and In Vivo

## TL;DR

This study shows that the SHFL gene helps protect against Coxsackievirus A16 by limiting its spread and tissue damage in cells and mice.

## Contribution

The study identifies SHFL as a novel host factor that restricts Coxsackievirus A16 replication post-transcriptionally.

## Key findings

- SHFL deficiency increases viral production and accelerates replication in rhabdomyosarcoma cells.
- In mice, SHFL loss leads to severe neurological symptoms, high viral loads, and tissue damage.
- SHFL modulates adhesion and MAPK pathways, suggesting its role in antiviral defense.

## Abstract

Coxsackievirus A16 (CVA16), a major etiological agent of hand, foot, and mouth disease, is increasingly contributing to neurological complications, with no vaccines or virus-specific antivirals currently available. To identify CVA16-restricting host factors, we investigated the role of the interferon-stimulated gene shiftless (SHFL), previously implicated in the control of other RNA viruses. Using CRISPR–Cas 9, we generated SHFL knockout rhabdomyosarcoma cells and assessed viral replication, cytopathic effects, and replication stage dynamics. We evaluated disease progression and tissue injury in neonatal mice infected with a mouse-adapted CVA16 strain. SHFL expression was strongly induced during CVA16 infection and was inducible by exogenous interferon-β treatment, and its loss markedly increased infectious virus production, accelerated early replication, and exerted severe cytopathic effects. In vivo, SHFL deficiency led to rapid weight loss, pronounced neurological signs, increased viral burden across multiple tissues, and uniform mortality, together with high viral loads and extensive pathological damage in the central nervous system, lungs, and skeletal muscle. Transcriptomic analyses revealed SHFL-dependent modulation of adhesion- and mitogen-activated protein kinase-related pathways. Overall, our results suggest SHFL as a key determinant of host resistance to CVA16, acting mainly at the post-transcriptional stage to limit viral spread and tissue injury, and highlight SHFL-linked pathways as promising host-directed antiviral targets.