发布: 2017年12月05日第7卷第23期 DOI: 10.21769/BioProtoc.2643 浏览次数: 10429
评审: Emilie BesnardFei XiaoJose Antonio Reyes-Darias
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Jade Jansen [...] Neeltje A. Kootstra
2025年07月20日 1518 阅读
Abstract
Cellular infection with tick-borne flaviviruses (TBFVs) results in activation of the interferon (IFN) signaling pathway and subsequent upregulation of numerous genes termed IFN stimulated genes (ISGs) (Schoggins et al., 2011). Many ISGs function to prevent virus pathogenesis by acting in a broad or specific manner through protein-protein interactions (Duggal and Emerman, 2012). The potency of the IFN signaling response determines the outcome of TBFV infection (Best, 2017; Carletti et al., 2017). Interestingly, data from our lab show that TBFV replication is significantly restricted in cells of the reservoir species Peromyscus leucopus thereby suggesting a potent antiviral response (Izuogu et al., 2017). We assessed the relative contribution of IFN signaling to resistance in P. leucopus by knocking down a major transcription factor in the IFN response pathway. Signal transducer and activator of transcription 1 (STAT1) was specifically targeted in P. leucopus cells by shRNA technology. We further tested the impact of gene knockdown on the ability of cells to respond to IFN and restrict virus replication; the results indicate that when STAT1 expression is altered, P. leucopus cells have a decreased response to IFN stimulation and are significantly more susceptible to TBFV replication.
Keywords: Interferon (干扰素)Background
IFN signaling is the first line of defense against flaviviruses invading a host cell (Robertson et al., 2009; Lazear and Diamond, 2015). Molecular signatures associated with the virus particles are detected by pattern-recognition receptors (PRRs) which then elicit downstream signaling via transcription factors to release type 1 IFNs from the cell (Kawai and Akira, 2011; Loo and Gale, 2011). Further, the IFN response pathway is initiated by binding of IFN-beta (IFN-β) to its cognate receptor and activation of the JAK-STAT signaling cascade (Loo et al., 2008). STAT1 is a major player in the IFN response pathway and functions within a complex to activate the IFN–stimulated response element (ISRE) promoter in the nucleus (Stark et al., 1998). Ultimately, IFN signaling transcriptionally upregulates numerous host genes that act to curtail infection and limit viral pathogenesis (Liu et al., 2011).
TBFVs contribute to the global burden of disease by causing encephalitis or hemorrhagic fevers in infected individuals. There are about 10,000 cases of TBE annually and disease is endemic to Europe and parts of Asia (Suss, 2008). In recent years, TBFVs have shown emerging nature due to their occurrence in previously unreported regions and re-occurrence in areas of eradication (Robertson et al., 2009; Ebel, 2010). The reason for the increased spread is not known, and treatment for clinically-recognized cases is limited to palliative care (Fernandez-Garcia et al., 2009; Lani et al., 2014). While virus infection in humans and other susceptible species can result in deleterious illness, infection of a natural reservoir host P. leucopus remains asymptomatic (Telford et al., 1997; Santos et al., 2016) suggesting that the host could lack relevant proviral factors or express effective antiviral factors. Data from our lab has explored these possibilities and demonstrated that viral restriction in P. leucopus cells is mediated by an antiviral response occurring via the IFN signaling cascade (Izuogu et al., 2017). Our studies involved resolving the sequence of antiviral gene homologs in P. leucopus and targeting components of the IFN response pathway. Specifically, our study first showed that STAT1 expression was consistently higher in P. leucopus cells compared to the susceptible control M. musculus following IFN treatment and virus infection (Izuogu et al., 2017). Based on these data, we further assessed the relative role of STAT1 in virus restriction by specific gene knockdown. This protocol describes the technique used to design shRNA to target STAT1, packaging into lentiviruses and cellular transduction to establish P. leucopus stable cell lines with diminished STAT1 expression. We further provide details of how these cells were assayed for a loss of restriction following infection with a TBFV, Langat virus (LGTV).
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版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Izuogu, A. O. and Taylor, R. T. (2017). Lentiviral Knockdown of Transcription Factor STAT1 in Peromyscus leucopus to Assess Its Role in the Restriction of Tick-borne Flaviviruses. Bio-protocol 7(23): e2643. DOI: 10.21769/BioProtoc.2643.
分类
微生物学 > 微生物-宿主相互作用 > 病毒
免疫学 > 宿主防御 > 鼠
细胞生物学 > 细胞信号传导 > 胞内信号传导
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