College of Veterinary Medicine, Yunnan Agricultural University, Kunming 650201, China.
College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China.
Int J Mol Sci. 2024 Jan 30;25(3):1681. doi: 10.3390/ijms25031681.
Hydropericardium hepatitis syndrome (HHS) is primarily caused by fowl adenovirus serotype 4 (FAdV-4), causing high mortality in chickens. Although vaccination strategies against FAdV-4 have been adopted, HHS still occurs sporadically. Furthermore, no effective drugs are available for controlling FAdV-4 infection. However, type I and III interferon (IFN) are crucial therapeutic agents against viral infection. The following experiments were conducted to investigate the inhibitory effect of chicken IFN against FadV-4. We expressed recombinant chicken type I IFN-α (ChIFN-α) and type III IFN-λ (ChIFN-λ) in and systemically investigated their antiviral activity against FAdV-4 infection in Leghorn male hepatocellular (LMH) cells. ChIFN-α and ChIFN-λ dose dependently inhibited FAdV-4 replication in LMH cells. Compared with ChIFN-λ, ChIFN-α more significantly inhibited viral genome transcription but less significantly suppressed FAdV-4 release. ChIFN-α- and ChIFN-λ-induced IFN-stimulated gene (ISG) expression, such as , , , , , , , and , in LMH cells; however, ChIFN-α induced a stronger expression level than ChIFN-λ. Thus, our data revealed that ChIFN-α and ChIFN-λ might trigger different ISG expression levels, inhibiting FAdV-4 replication via different steps of the FAdV-4 lifecycle, which furthers the potential applications of IFN antiviral drugs in chickens.
包涵体肝炎综合征(HHS)主要由禽腺病毒血清型 4(FAdV-4)引起,可导致鸡高死亡率。尽管已采用针对 FAdV-4 的疫苗接种策略,但 HHS 仍会零星发生。此外,目前尚无有效药物可用于控制 FAdV-4 感染。然而,I 型和 III 型干扰素(IFN)是对抗病毒感染的重要治疗药物。进行以下实验以研究鸡 IFN 对 FadV-4 的抑制作用。我们在 和系统中表达了重组鸡 I 型 IFN-α(ChIFN-α)和 III 型 IFN-λ(ChIFN-λ),并系统地研究了它们在莱航雄性肝细胞(LMH)细胞中对 FAdV-4 感染的抗病毒活性。ChIFN-α和 ChIFN-λ 呈剂量依赖性抑制 LMH 细胞中的 FAdV-4 复制。与 ChIFN-λ 相比,ChIFN-α更显著地抑制病毒基因组转录,但较少抑制 FAdV-4 释放。ChIFN-α和 ChIFN-λ 诱导 IFN 刺激基因(ISG)在 LMH 细胞中的表达,如 、 、 、 、 、 、 和 ;然而,ChIFN-α诱导的表达水平强于 ChIFN-λ。因此,我们的数据表明 ChIFN-α 和 ChIFN-λ 可能通过不同的 FAdV-4 生命周期步骤触发不同的 ISG 表达水平,从而抑制 FAdV-4 的复制,这进一步推动了 IFN 抗病毒药物在鸡中的潜在应用。