Fujian Key Laboratory of Traditional Chinese Veterinary Medicine and Animal Health (Fujian Agriculture And Forestry University), Fuzhou 350002, PR China; University Key Laboratory for Integrated Chinese Traditional and Western Veterinary Medicine and Animal Healthcare in Fujian Province, Fuzhou 350002, PR China.
Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Sciences, Fuzhou 350003, PR China.
Vet Microbiol. 2023 Mar;278:109660. doi: 10.1016/j.vetmic.2023.109660. Epub 2023 Jan 13.
The pro- and inflammatory cytokines fail to effectively inhibit FAdV-4, which has always puzzled us. In the current study, the data determined that the mRNA levels of interferons were significantly enhanced in the livers and LMH cells from 24 h to 72 h post FAdV-4 infection. But the viral load of FAdV-4 was still significantly increased, which meant that FAdV-4 evaded innate immune response. We additionally revealed that the protein levels not mRNA levels of PKR were degraded in host cell at 48 h post FAdV-4 infection. Moreover, the results of over expression and silent expression of PKR revealed that PKR could inhibit FAdV-4 proliferation. These results indicated that FAdV-4 degraded the protein levels of PKR to evade innate immune response. We also found that the protein degradation levels of PKR induced by FAdV-4 were recovery in LHM cells after treatment with proteasome inhibitor MG132, and ubiquitin-specific proteases inhibitor DUB-IN-1. Furthermore, our current data presented that FAdV-4 52/55 K protein directly interacted with PKR and degraded it determined by Co-immunoprecipitation and immunofluorescence. We also determined that 52/55 K protein triggered PKR degradation, and the degradation of PKR could be recovery in LHM cells after treatment with MG132, or DUB-IN-1, respectively. Finally, our data demonstrated that 52/55 K protein was a ubiquitylase that could directly degrade PKR protein in host cells via the ubiquitin-proteasome pathway. Therefore, the current study firstly revealed that FAdV-4 52/55 K protein played the key role in triggering PKR degradation by ubiquitin-proteasome system pathway to escape from innate immunity response.
促炎细胞因子和抗炎细胞因子不能有效抑制 FAdV-4,这一直让我们感到困惑。在本研究中,数据确定在 FAdV-4 感染后 24-72 小时,肝脏和 LMH 细胞中的干扰素 mRNA 水平显著增强。但是 FAdV-4 的病毒载量仍显著增加,这意味着 FAdV-4 逃避了先天免疫反应。我们还发现,在 FAdV-4 感染后 48 小时,宿主细胞中 PKR 的蛋白水平而非 mRNA 水平降解。此外,PKR 的过表达和沉默表达的结果表明,PKR 可以抑制 FAdV-4 的增殖。这些结果表明,FAdV-4 通过降解 PKR 的蛋白水平来逃避先天免疫反应。我们还发现,在用蛋白酶体抑制剂 MG132 和泛素特异性蛋白酶抑制剂 DUB-IN-1 处理后,FAdV-4 诱导的 PKR 蛋白降解水平在 LHM 细胞中恢复。此外,我们目前的数据表明,FAdV-4 的 52/55 K 蛋白直接与 PKR 相互作用,并通过免疫共沉淀和免疫荧光确定其降解。我们还确定 52/55 K 蛋白触发了 PKR 的降解,并且在 LHM 细胞中用 MG132 或 DUB-IN-1 处理后,PKR 的降解可以恢复。最后,我们的数据表明,52/55 K 蛋白是一种泛素连接酶,可以通过宿主细胞中的泛素-蛋白酶体途径直接降解 PKR 蛋白。因此,本研究首次表明,FAdV-4 的 52/55 K 蛋白通过泛素-蛋白酶体系统途径在触发 PKR 降解中起关键作用,从而逃避先天免疫反应。