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2023年6月，中國天津大學生命科學學院;天津市生物大分子結構功能與應用重點實驗室研究所;天津大學環境科學與工程學院(School of Life Sciences, Tianjin University, Tianjin, China；Institute of Tianjin Key Laboratory of Function and Application of Biological Macromolecular Structures, Tianjin, China；School of Environmental Science and Engineering, Tianjin University, Tianjin, China) Jun Kang老師研究團隊在《MICROBIOL SPECTR》上發表論文：
“Enterovirus D68 VP3 Targets the Interferon Regulatory Factor 7 To Inhibit Type I Interferon Response"
“腸病毒D68 VP3靶向干擾素調節因子7抑制I型干擾素應答"
Abstract：
Enterovirus D68 (EV-D68) is a globally emerging pathogen causing severe respiratory illnesses mainly in children. The protease from EV-D68 could impair type I interferon (IFN-I) production. However, the role of the EV-D68 structural protein in antagonizing host antiviral responses remains largely unknown. We showed that the EV-D68 structural protein VP3 interacted with IFN regulatory factor 7 (IRF7), and this interaction suppressed the phosphorylation and nuclear translocation of IRF7 and then repressed the transcription of IFN. Furthermore, VP3 inhibited the TNF receptor associated factor 6 (TRAF6)-induced ubiquitination of IRF7 by competitive interaction with IRF7. IRF7Δ305-503 showed much weaker interaction ability to VP3, and VP3Δ41-50 performed weaker interaction ability with IRF7. The VP3 from enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) was also found to interact with the IRF7 protein. These results indicate that the enterovirus structural protein VP3 plays a pivotal role in subverting host innate immune responses and may be a potential target for antiviral drug research. IMPORTANCE EV-D68 is a globally emerging pathogen that causes severe respiratory illnesses. Here, we report that EV-D68 inhibits innate immune responses by targeting IRF7. Further investigations revealed that the structural protein VP3 inhibited the TRAF6-induced ubiquitination of IRF7 by competitive interaction with IRF7. These results indicate that the control of IRF7 by VP3 may be a mechanism by which EV-D68 represses IFN-I production.
摘要：
腸病毒D68 (EV-D68)是一種全球新發病原體，主要在兒童中引起嚴重呼吸道疾病。EV-D68的蛋白酶可以抑制I型干擾素(IFN-I)的產生。然而，EV-D68結構蛋白在拮抗宿主抗病毒反應中的作用在很大程度上仍然未知。研究人員發現EV-D68結構蛋白VP3與IFN調控因子7 (IRF7)相互作用，抑制IRF7的磷酸化和核易位，進而抑制IFN的轉錄。此外，VP3通過與IRF7的競爭性相互作用抑制TNF受體相關因子6 (TRAF6)誘導的IRF7泛素化。IRF7Δ305-503與VP3的互作能力弱得多，VP3Δ41-50與IRF7的互作能力弱得多。來自腸病毒A71 (EV-A71)和柯薩奇病毒A16 (CV-A16)的VP3也被發現與IRF7蛋白相互作用。這些結果表明，腸道病毒結構蛋白VP3在破壞宿主先天免疫應答中起著關鍵作用，可能是抗病毒的藥物研究的潛在靶點。EV-D68是一種全球新發病原體，可引起嚴重呼吸道疾病。在這里，研究人員報道EV-D68通過靶向IRF7抑制先天免疫反應。進一步研究發現，結構蛋白VP3通過與IRF7的競爭相互作用抑制traf6誘導的IRF7泛素化。這些結果表明VP3對IRF7的控制可能是EV-D68抑制IFN-I產生的機制之一。
該論文中，對HEK293T、橫紋肌肉瘤(RD)和HeLa細胞及其經過脂質體轉染細胞的體外培養是使用Ausbian特級胎牛血清完成的。
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