Guangdong Provincial Key Laboratory of Agro-animal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou 510642, China.
Key Lab of Chicken Genetics, Breeding and Reproduction, Ministry of Agriculture, Guangzhou 510642, China.
Viruses. 2019 May 30;11(6):498. doi: 10.3390/v11060498.
The avian leukosis virus subgroup J (ALV-J) belongs to the chicken retrovirus that causes enormous economic losses in the poultry industry. Interferon-stimulated genes (ISGs) are critical for controlling virus infections. Here, we identified 897 type I ISGs induced by interferon-α (IFN-α) in chicken peripheral blood mononuclear cell (PBMC) by RNA-Seq. In addition, we further identified 152 potential anti-ALV-J chicken type I ISGs. Among these potential anti-ALV-J ISGs, chicken cholesterol 25-hydroxylase () was selected for further antiviral mechanism studies in chicken embryo fibroblast cell lines (DF1). The gene is located on chromosome 6 and clustered in a distinct group with mammals in the phylogenetic tree. The core promoter region of was located within -75/-1 sequence. We found that was induced by chicken IFN-α and ALV-J in DF1 cells. The overexpression of significantly inhibited ALV-J replication in DF1 cells at 48 h post infection (hpi). In addition, ALV-J replication was significantly enhanced in the chCH25H- knockout DF1 cells. Furthermore, we demonstrated that restricted ALV-J infection through the production of 25-hydroxycholesterol (25HC), rather than type I and II interferon. Our results identified 152 potential anti-ALV-J chicken type I ISGs and revealed that 25HC, the product of , could be used as a natural antiviral agent to control ALV-J infection.
禽白血病病毒 J 亚群(ALV-J)属于鸡反转录病毒,会给家禽业造成巨大的经济损失。干扰素刺激基因(ISGs)对于控制病毒感染至关重要。本研究通过 RNA-Seq 鉴定了干扰素-α(IFN-α)诱导鸡外周血单核细胞(PBMC)中 897 种 I 型 ISGs。此外,我们进一步鉴定了 152 种潜在的抗 ALV-J 鸡 I 型 ISGs。在这些潜在的抗 ALV-JISGs 中,鸡胆固醇 25-羟化酶()被选为进一步研究在鸡胚成纤维细胞系(DF1)中抗 ALV-J 的抗病毒机制的候选基因。基因位于第 6 号染色体上,在系统发育树中与哺乳动物 聚类在一起形成一个独特的群组。的核心启动子区域位于-75/-1 序列内。我们发现 可被鸡 IFN-α和 ALV-J 诱导,在感染后 48 小时(hpi)在 DF1 细胞中显著抑制 ALV-J 复制。此外,在 chCH25H-敲除的 DF1 细胞中,ALV-J 复制显著增强。此外,我们证明通过产生 25-羟胆固醇(25HC),而不是 I 型和 II 型干扰素,来限制 ALV-J 的感染。我们的研究结果鉴定了 152 种潜在的抗 ALV-J 鸡 I 型 ISGs,并揭示了 25HC(的产物)可用作控制 ALV-J 感染的天然抗病毒剂。