Viral Targeting of Importin Alpha-Mediated Nuclear Import to Block Innate Immunity

被引:1
|
作者
Vogel, Olivia A. [1 ]
Forwood, Jade K. [2 ]
Leung, Daisy W. [3 ]
Amarasinghe, Gaya K. [4 ]
Basler, Christopher F. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY 10029 USA
[2] Charles Sturt Univ, Sch Dent & Med Sci, Wagga Wagga, NSW 2678, Australia
[3] Washington Univ, Dept Internal Med, Sch Med St Louis, St. Louis, MO 63110 USA
[4] Washington Univ, Dept Pathol & Immunol, Sch Med St Louis, St. Louis, MO 63110 USA
关键词
African swine fever virus; coronavirus; Ebola virus; flavivirus; hantavirus; hepatitis B virus; human immunodeficiency virus-1; importin alpha; immune evasion; innate immunity; interferon; vaccinia virus; RESPIRATORY SYNDROME CORONAVIRUS; NF-KAPPA-B; DOUBLE-STRANDED-RNA; NLS-BINDING-SITE; EBOLA-VIRUS; INTERFERON-ALPHA; IFN-GAMMA; LOCALIZATION SEQUENCES; TRANSCRIPTION FACTOR; KARYOPHERIN ALPHA-1;
D O I
10.3390/cells13010071
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cellular nucleocytoplasmic trafficking is mediated by the importin family of nuclear transport proteins. The well-characterized importin alpha (IMPA) and importin beta (IMPB) nuclear import pathway plays a crucial role in the innate immune response to viral infection by mediating the nuclear import of transcription factors such as IRF3, NF kappa B, and STAT1. The nuclear transport of these transcription factors ultimately leads to the upregulation of a wide range of antiviral genes, including IFN and IFN-stimulated genes (ISGs). To replicate efficiently in cells, viruses have developed mechanisms to block these signaling pathways. One strategy to evade host innate immune responses involves blocking the nuclear import of host antiviral transcription factors. By binding IMPA proteins, these viral proteins prevent the nuclear transport of key transcription factors and suppress the induction of antiviral gene expression. In this review, we describe examples of proteins encoded by viruses from several different families that utilize such a competitive inhibition strategy to suppress the induction of antiviral gene expression.
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页数:17
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