# Modulation of antiviral genes by African swine fever isolates of diverse virulence

**Authors:** Giulia Franzoni, Lorena Mura, Susanna Zinellu, Pedro J. Sanchez-Cordon, Miriam Pedrera, Silvia Dei Giudici

PMC · DOI: 10.3389/fvets.2025.1591709 · 2025-06-03

## TL;DR

This study explores how two African swine fever virus strains affect antiviral gene expression in pig macrophages, revealing immune evasion strategies.

## Contribution

The study provides new insights into how ASFV strains modulate antiviral genes during infection.

## Key findings

- Both ASFV strains initially activate antiviral defenses in macrophages.
- Progressive viral replication leads to down-regulation of inflammatory genes, especially with the attenuated strain.
- The data highlight immune evasion strategies used by ASFV.

## Abstract

African swine fever virus (ASFV), the aetiological agent of a devastating swine disease, has developed several strategies to replicate in porcine macrophages, its main target cells. In this work, we investigated the expression of 84 antiviral genes in macrophages infected with the virulent strain 26544/OG10 or the attenuated strain NH/P68. Infection with both strains caused an early activation of antiviral defenses, with up-regulation of RNA-sensing molecules and interferon-stimulating genes. However, as viral replication progresses, down-regulation of key inflammatory genes was observed, especially during infection with NH/P68, suggesting an impairment of macrophages' inflammatory response. Data generated provide a better portrait of ASFV immune evasion strategies.

## Linked entities

- **Diseases:** African swine fever (MONDO:0025377)

## Full-text entities

- **Genes:** GATAD2B (GATA zinc finger domain containing 2B) [NCBI Gene 57459] {aka GANDS, MRD18, P66beta, p68}
- **Diseases:** Infection (MESH:D007239), inflammatory (MESH:D007249)
- **Species:** African swine fever virus (no rank) [taxon 10497]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12172545/full.md

---
Source: https://tomesphere.com/paper/PMC12172545