Pinto Amelia K, Williams Graham D, Szretter Kristy J, White James P, Proença-Módena José Luiz, Liu Gai, Olejnik Judith, Brien James D, Ebihara Hideki, Mühlberger Elke, Amarasinghe Gaya, Diamond Michael S, Boon Adrianus C M
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA Department of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), Campinas, SP, Brazil.
J Virol. 2015 Sep;89(18):9465-76. doi: 10.1128/JVI.00996-15. Epub 2015 Jul 8.
Interferon-induced protein with tetratricopeptide repeats 1 (IFIT1) is a host protein with reported cell-intrinsic antiviral activity against several RNA viruses. The proposed basis for the activity against negative-sense RNA viruses is the binding to exposed 5'-triphosphates (5'-ppp) on the genome of viral RNA. However, recent studies reported relatively low binding affinities of IFIT1 for 5'-ppp RNA, suggesting that IFIT1 may not interact efficiently with this moiety under physiological conditions. To evaluate the ability of IFIT1 to have an impact on negative-sense RNA viruses, we infected Ifit1(-/-) and wild-type control mice and primary cells with four negative-sense RNA viruses (influenza A virus [IAV], La Crosse virus [LACV], Oropouche virus [OROV], and Ebola virus) corresponding to three distinct families. Unexpectedly, a lack of Ifit1 gene expression did not result in increased infection by any of these viruses in cell culture. Analogously, morbidity, mortality, and viral burdens in tissues were identical between Ifit1(-/-) and control mice after infection with IAV, LACV, or OROV. Finally, deletion of the human IFIT1 protein in A549 cells did not affect IAV replication or infection, and reciprocally, ectopic expression of IFIT1 in HEK293T cells did not inhibit IAV infection. To explain the lack of antiviral activity against IAV, we measured the binding affinity of IFIT1 for RNA oligonucleotides resembling the 5' ends of IAV gene segments. The affinity for 5'-ppp RNA was approximately 10-fold lower than that for non-2'-O-methylated (cap 0) RNA oligonucleotides. Based on this analysis, we conclude that IFIT1 is not a dominant restriction factor against negative-sense RNA viruses.
Negative-sense RNA viruses, including influenza virus and Ebola virus, have been responsible for some of the most deadly outbreaks in recent history. The host interferon response and induction of antiviral genes contribute to the control of infections by these viruses. IFIT1 is highly induced after virus infection and reportedly has antiviral activity against several RNA and DNA viruses. However, its role in restricting infection by negative-sense RNA viruses remains unclear. In this study, we evaluated the ability of IFIT1 to inhibit negative-sense RNA virus replication and pathogenesis both in vitro and in vivo. Detailed cell culture and animal studies demonstrated that IFIT1 is not a dominant restriction factor against three different families of negative-sense RNA viruses.
含四肽重复序列的干扰素诱导蛋白1(IFIT1)是一种宿主蛋白,据报道对多种RNA病毒具有细胞内在抗病毒活性。针对负链RNA病毒的活性的推测基础是与病毒RNA基因组上暴露的5'-三磷酸(5'-ppp)结合。然而,最近的研究报道IFIT1与5'-ppp RNA的结合亲和力相对较低,这表明IFIT1在生理条件下可能无法有效地与该部分相互作用。为了评估IFIT1对负链RNA病毒产生影响的能力,我们用四种负链RNA病毒(甲型流感病毒[IAV]、拉克罗斯病毒[LACV]、奥罗普切病毒[OROV]和埃博拉病毒)感染Ifit1(-/-)和野生型对照小鼠及原代细胞,这四种病毒分属于三个不同的病毒家族。出乎意料的是,在细胞培养中,Ifit1基因表达的缺失并未导致这些病毒中任何一种的感染增加。类似地,在感染IAV、LACV或OROV后,Ifit1(-/-)小鼠和对照小鼠在组织中的发病率、死亡率和病毒载量是相同的。最后,在A549细胞中缺失人IFIT1蛋白不影响IAV复制或感染,反之,在HEK293T细胞中异位表达IFIT1也不抑制IAV感染。为了解释IFIT1对IAV缺乏抗病毒活性的原因,我们测量了IFIT1对类似于IAV基因片段5'端的RNA寡核苷酸的结合亲和力。其对5'-ppp RNA的亲和力比对非2'-O-甲基化(帽0)RNA寡核苷酸的亲和力低约10倍。基于此分析,我们得出结论,IFIT1不是针对负链RNA病毒的主要限制因子。
包括流感病毒和埃博拉病毒在内的负链RNA病毒是近代史上一些最致命疫情的罪魁祸首。宿主干扰素反应和抗病毒基因的诱导有助于控制这些病毒的感染。IFIT1在病毒感染后被高度诱导,据报道对多种RNA和DNA病毒具有抗病毒活性。然而,其在限制负链RNA病毒感染中的作用仍不清楚。在本研究中,我们在体外和体内评估了IFIT1抑制负链RNA病毒复制和发病机制的能力。详细的细胞培养和动物研究表明,IFIT1不是针对三个不同负链RNA病毒家族的主要限制因子。