基础干扰素信号传导和干扰素在控制小反刍动物瘟疫病毒感染中的治疗用途。
Basal interferon signaling and therapeutic use of interferons in controlling peste des petits ruminants virus infection.
机构信息
Center for Biomedical Research, Northwest Minzu University, Gansu 730030, PR China.
Center for Biomedical Research, Northwest Minzu University, Gansu 730030, PR China; State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu, PR China.
出版信息
Infect Genet Evol. 2019 Nov;75:103981. doi: 10.1016/j.meegid.2019.103981. Epub 2019 Jul 29.
Peste des petits ruminants virus (PPRV) is a morbillivirus which causes severe disease in ruminants. Since interferons (IFNs) serve as the important defense line against viral infection, we have investigated the roles of types I and III IFNs in PPRV infection in vitro. Upon PPRV infection, IFN-λ3 was strongly induced, while IFN-β and IFN-λ2 were moderately induced at transcriptional level in human embryonic kidney 293 T (HEK293T) cells. Although the transcription of type I and III IFNs were triggered, the production of functional IFN products was not detected. Importantly, the replication of PPRV was strongly inhibited in HEK293T cells treated by the exogenous IFNs (IFN-α-2b, IFN-β and IFN-λ3). Consistently, these IFNs significantly activate a panel of IFN-stimulated genes (ISGs). The inhibition of JAK-STAT pathway by JAK I inhibitor can abrogate the anti-PPRV activity of IFNs. Thus, our study shall contribute to better understanding of the complex PPRV-host interactions and provide rationale for therapeutic development of IFN-based treatment against PPRV infection.
小反刍兽疫病毒(PPRV)是一种副黏病毒,可引起反刍动物的严重疾病。由于干扰素(IFNs)是抵抗病毒感染的重要防线,我们研究了 I 型和 III 型 IFNs 在 PPRV 感染体外的作用。在 PPRV 感染后,人胚肾 293T(HEK293T)细胞中 IFN-λ3 的转录被强烈诱导,而 IFN-β 和 IFN-λ2 的转录被中度诱导。尽管 I 型和 III 型 IFNs 的转录被触发,但未检测到功能性 IFN 产物的产生。重要的是,外源性 IFN(IFN-α-2b、IFN-β 和 IFN-λ3)处理的 HEK293T 细胞中 PPRV 的复制受到强烈抑制。一致地,这些 IFN 显著激活了一组 IFN 刺激基因(ISGs)。JAK 抑制剂 JAK I 抑制剂抑制 JAK-STAT 通路可消除 IFN 对 PPRV 的抗病毒活性。因此,我们的研究将有助于更好地理解 PPRV 与宿主的复杂相互作用,并为基于 IFN 的治疗 PPRV 感染的治疗开发提供依据。