Fensterl Volker, Wetzel Jaime L, Sen Ganes C
Department of Molecular Genetics, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Department of Molecular Genetics, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA
J Virol. 2014 Sep;88(18):10303-11. doi: 10.1128/JVI.01341-14. Epub 2014 Jul 2.
The interferon system provides the first line of host defense against virus infection. Mouse pathogenesis studies have revealed the importance of specific interferon-induced proteins in providing protection against specific viruses. We have previously reported that one such protein, Ifit2, protects neurons of the central nervous system from intranasal infection by the neurotropic rhabdovirus, vesicular stomatitis virus (VSV). Here, we demonstrate that Ifit2 protects the peripheral nervous system from VSV infection as well. In Ifit2(-/-) mice, VSV, injected subcutaneously into the footpad, entered the proximal lymph node, where it replicated and infected the nodal nerve endings. The infection spread to the sciatic nerve, the spinal cord, and the brain, causing paralysis. In contrast, in the wild-type mice, although VSV replicated equally well in the lymph node, infection of the sciatic nerve and the rest of the nervous system was impaired, thus preventing paralysis. Ifit2 protected only the nervous system from VSV infection; other tissues were well protected even in Ifit2(-/-) mice. These results indicate that Ifit2 is the interferon-induced protein that prevents VSV infection of neurons of both the peripheral and the central nervous systems, thus inhibiting the consequent neuropathy, but it is dispensable for protecting the cells of other tissues from VSV infection.
Although viral infection is quite common, the immune system effectively protects us from viral diseases. A major part of this protection is mediated by interferon, the antiviral cytokine secreted by virus-infected cells. To empower the neighboring uninfected cells in combating the oncoming infection, interferon induces the synthesis of more than 200 new proteins, many of which have antiviral activities. The virus studied here, vesicular stomatitis virus (VSV), like its relative, rabies virus, can cause neuropathy in mice if it enters the peripheral nervous system through skin lesions; however, interferon can protect neurons from VSV infection. We have identified a specific interferon-induced protein, Ifit2, as the protein that protects neurons from VSV infection. Surprisingly, Ifit2 was not needed to protect other cell types from VSV. Our results indicate that the effector antiviral proteins of the interferon system have highly specialized functions.
干扰素系统是宿主抵御病毒感染的第一道防线。小鼠发病机制研究揭示了特定干扰素诱导蛋白在抵御特定病毒方面的重要性。我们之前报道过,一种这样的蛋白Ifit2可保护中枢神经系统的神经元免受嗜神经性弹状病毒——水疱性口炎病毒(VSV)的鼻内感染。在此,我们证明Ifit2也能保护外周神经系统免受VSV感染。在Ifit2基因敲除小鼠中,皮下注射到足垫的VSV进入近端淋巴结,在那里复制并感染淋巴结神经末梢。感染扩散到坐骨神经、脊髓和大脑,导致麻痹。相比之下,在野生型小鼠中,尽管VSV在淋巴结中复制情况相同,但坐骨神经和神经系统其他部分的感染受到抑制,从而预防了麻痹。Ifit2仅保护神经系统免受VSV感染;即使在Ifit2基因敲除小鼠中,其他组织也受到良好保护。这些结果表明,Ifit2是一种干扰素诱导蛋白,可防止VSV感染外周和中枢神经系统的神经元,从而抑制随之而来的神经病变,但它对于保护其他组织细胞免受VSV感染是可有可无的。
尽管病毒感染很常见,但免疫系统有效地保护我们免受病毒疾病侵害。这种保护的主要部分由干扰素介导,干扰素是病毒感染细胞分泌的抗病毒细胞因子。为了使邻近未感染细胞有能力对抗即将到来的感染,干扰素诱导合成200多种新蛋白,其中许多具有抗病毒活性。这里研究的病毒水疱性口炎病毒(VSV)与其亲属狂犬病病毒一样,如果通过皮肤损伤进入外周神经系统,可在小鼠中引起神经病变;然而,干扰素可保护神经元免受VSV感染。我们已确定一种特定的干扰素诱导蛋白Ifit2是保护神经元免受VSV感染的蛋白。令人惊讶的是,保护其他细胞类型免受VSV感染不需要Ifit2。我们的结果表明,干扰素系统的效应抗病毒蛋白具有高度专业化的功能。