Segmented negative-strand RNA viruses and RIG-I: divide (your genome) and rule

被引:21
作者
Weber, Michaela [1 ]
Weber, Friedemann [1 ]
机构
[1] Univ Marburg, Inst Virol, D-35043 Marburg, Germany
关键词
FACTOR-KAPPA-B; INTERFERON INDUCTION; TRANSCRIPTION FACTOR; ANTIVIRAL RESPONSES; BETA INTERFERON; NSS PROTEIN; ML PROTEIN; VIRAL-RNA; ACTIVATION; RECOGNITION;
D O I
10.1016/j.mib.2014.05.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The group of negative-stranded RNA viruses (NSVs) with a segmented genome comprises pathogens like influenza virus (eight segments), Rift Valley fever virus and Hantavirus (three segments), or Lassa virus (two segments). Partitioning the genome allows rapid evolution of new strains by reassortment. Each segment carries a short double-stranded (ds) 'panhandle' structure which serves as promoter. Similar dsRNA structures, however, represent the optimal ligand for RIG-I, a cytoplasmic pathogen sensor of the antiviral interferon response. Thus, segmenting a virus genome can entail an increased RIG-I sensitivity. Here, we outline the astonishingly diverse and efficient strategies by which segmented NSVs are compensating for the elevated number of RIG-I Iigands in their genome.
引用
收藏
页码:96 / 102
页数:7
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