Journal article
Authors list: Weber, M; Weber, F
Publication year: 2014
Pages: 96-102
Journal: Current Opinion in Microbiology
Volume number: 20
ISSN: 1369-5274
eISSN: 1879-0364
DOI Link: https://doi.org/10.1016/j.mib.2014.05.002
Publisher: Elsevier
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 ligands in their genome.
Abstract:
Citation Styles
Harvard Citation style: Weber, M. and Weber, F. (2014) Segmented negative-strand RNA viruses and RIG-I: divide (your genome) and rule, Current Opinion in Microbiology, 20, pp. 96-102. https://doi.org/10.1016/j.mib.2014.05.002
APA Citation style: Weber, M., & Weber, F. (2014). Segmented negative-strand RNA viruses and RIG-I: divide (your genome) and rule. Current Opinion in Microbiology. 20, 96-102. https://doi.org/10.1016/j.mib.2014.05.002