Thakur Naveen, Chakraborty Poushali, Tufariello JoAnn M, Basler Christopher F
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
mBio. 2025 Jun 25:e0107125. doi: 10.1128/mbio.01071-25.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) non-structural protein 14 (Nsp14) possesses an N-terminal exonuclease (ExoN) domain that provides a proofreading function for the viral RNA-dependent RNA polymerase and a C-terminal N7-methyltransferase (N7-MTase) domain that methylates viral mRNA caps. Nsp14 also modulates host functions. This includes the activation of NF-κB and downregulation of interferon alpha/beta receptor 1 (IFNAR1). Here, we demonstrate that Nsp14 exerts broader effects, activating not only NF-κB responses but also extracellular-signal-regulated kinase (ERK), p38, and Jun amino-terminal kinase (JNK) mitogen-activated protein kinase (MAPK) signaling, promoting cytokine production. Furthermore, Nsp14 downregulates not only IFNAR1 but also IFN-γ receptor 1 (IFNGR1), impairing cellular responses to both IFNα and IFNγ. IFNAR1 and IFNGR1 downregulation is via a lysosomal pathway and occurs in SARS-CoV-2-infected cells. Analysis of a panel of Nsp14 mutants reveals a consistent pattern. Mutants that disable ExoN function remain largely active, whereas N7-MTase mutations impair both pro-inflammatory pathway activation and IFN receptor downregulation. Innate immune modulating functions also require the presence of both the ExoN and N7-MTase domains, likely reflecting that the ExoN domain must be present to enable N7-MTase activity. We further identify multi-functional host protein Tollip as an Nsp14 interactor. Interaction requires the phosphoinositide-binding C2 domain of Tollip and sequences C-terminal to the C2 domain. Full-length Tollip or regions encompassing the Nsp14 interaction domain are sufficient to counteract both Nsp14-mediated and Nsp14-independent activation of NF-κB. Knockdown of Tollip partially reverses IFNAR1 and IFNGR1 downregulation in SARS-CoV-2-infected cells, suggesting the relevance of Nsp14-Tollip interaction for Nsp14 innate immune evasion functions.IMPORTANCESevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) non-structural protein 14 (Nsp14) both activates NF-κB, which promotes virus replication and inflammation, and downregulates interferon alpha/beta receptor 1 (IFNAR1), which can render infected cells resistant to the antiviral effects of IFN-α/β. Our study demonstrates that Nsp14 also activates MAPK signaling and downregulates IFN-γ receptor 1 (IFNGR1), causing broader impacts than previously recognized. Data from a panel of Nsp14 mutants suggest that a common underlying effect of Nsp14 may be responsible for its multiple innate immune activities. We further describe a novel interaction between Nsp14 and Tollip, a selective autophagy receptor. We show that Tollip expression downregulates Nsp14 activation of NF-κB and that Tollip knockdown reverses IFNAR1 and IFNGR1 downregulation in SARS-CoV-2 infection, suggesting that Tollip functions as a regulator of Nsp14 innate immune modulation.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)非结构蛋白14(Nsp14)具有一个N端核酸外切酶(ExoN)结构域,该结构域为病毒RNA依赖性RNA聚合酶提供校对功能,以及一个C端N7-甲基转移酶(N7-MTase)结构域,该结构域可甲基化病毒mRNA的帽结构。Nsp14还可调节宿主功能。这包括激活核因子κB(NF-κB)以及下调干扰素α/β受体1(IFNAR1)。在此,我们证明Nsp14具有更广泛的作用,不仅激活NF-κB反应,还激活细胞外信号调节激酶(ERK)、p38和Jun氨基末端激酶(JNK)丝裂原活化蛋白激酶(MAPK)信号通路,促进细胞因子的产生。此外,Nsp14不仅下调IFNAR1,还下调干扰素γ受体1(IFNGR1),损害细胞对IFNα和IFNγ的反应。IFNAR1和IFNGR1的下调是通过溶酶体途径发生的,并且发生在SARS-CoV-2感染的细胞中。对一组Nsp14突变体的分析揭示了一种一致的模式。使ExoN功能丧失的突变体在很大程度上仍保持活性,而N7-MTase突变则损害促炎途径的激活和IFN受体的下调。天然免疫调节功能也需要ExoN和N7-MTase结构域同时存在,这可能反映出必须存在ExoN结构域才能使N7-MTase发挥活性。我们进一步鉴定出多功能宿主蛋白Toll相互作用蛋白(Tollip)是Nsp14的相互作用分子。相互作用需要Tollip的磷酸肌醇结合C2结构域以及C2结构域C端的序列。全长Tollip或包含Nsp14相互作用结构域的区域足以抵消Nsp14介导的和Nsp14非依赖性的NF-κB激活。敲低Tollip可部分逆转SARS-CoV-2感染细胞中IFNAR1和IFNGR1的下调,这表明Nsp14-Tollip相互作用与Nsp14的天然免疫逃避功能相关。
重要性
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)非结构蛋白14(Nsp14)既激活促进病毒复制和炎症的NF-κB,又下调可使感染细胞对IFN-α/β的抗病毒作用产生抗性的干扰素α/β受体1(IFNAR1)。我们的研究表明,Nsp14还激活MAPK信号通路并下调干扰素γ受体1(IFNGR1),其影响比之前认识到的更为广泛。一组Nsp14突变体的数据表明,Nsp14的多种天然免疫活性可能存在共同的潜在作用机制。我们进一步描述了Nsp14与选择性自噬受体Toll相互作用蛋白(Tollip)之间的新型相互作用。我们表明,Tollip的表达下调Nsp14对NF-κB的激活,并且敲低Tollip可逆转SARS-CoV-2感染中IFNAR1和IFNGR1的下调,这表明Tollip作为Nsp14天然免疫调节的调节剂发挥作用。