坏死性下垂
猴痘
病毒学
生物
牛痘
干扰素
程序性细胞死亡
先天免疫系统
病毒
病毒复制
细胞凋亡
免疫系统
基因
免疫学
遗传学
重组DNA
作者
Jacqueline Williams,James C. Bonner,Karen V. Kibler,Bertram L. Jacobs
标识
DOI:10.1007/978-3-031-57165-7_8
摘要
Poxviruses are notorious for having acquired/evolved numerous genes to counteract host innate immunity. Chordopoxviruses have acquired/evolved at least three different inhibitors of host necroptotic death: E3, which blocks ZBP1-dependent necroptotic cell death, and vIRD and vMLKL that inhibit necroptosis downstream of initial cell death signaling. While this suggests the importance of the necroptotic cell death pathway in inhibiting chordopoxvirus replication, several chordopoxviruses have lost one or more of these inhibitory functions. Monkeypox/mpox virus (MPXV) hasMonkeypox/mpox virus lost a portion of the N-terminus of its E3 homologue. The N-terminus of the vaccinia virus E3 homologue serves to inhibit activation of the interferon-inducible antiviral protein, ZBP1. This likely makes MPXV unique among the orthopoxvirusesOrthopoxviruses in being sensitive to interferonInterferon (IFN) treatment in many mammals, including humans, which encode a complete necroptotic cell death pathway. Thus, IFN sensitivity may be the Achille's Heel for viruses like MPXV that cannot fully inhibit IFN-inducible, ZBP1-dependent antiviral pathways.
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