Viral unmasking of cellular 5S rRNA pseudogene transcripts induces RIG-I-mediated immunity.

Nat Immunol 2018 Jan 27;19(1):53-62. Epub 2017 Nov 27.

Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA.

The sensor RIG-I detects double-stranded RNA derived from RNA viruses. Although RIG-I is also known to have a role in the antiviral response to DNA viruses, physiological RNA species recognized by RIG-I during infection with a DNA virus are largely unknown. Using next-generation RNA sequencing (RNAseq), we found that host-derived RNAs, most prominently 5S ribosomal RNA pseudogene 141 (RNA5SP141), bound to RIG-I during infection with herpes simplex virus 1 (HSV-1). Infection with HSV-1 induced relocalization of RNA5SP141 from the nucleus to the cytoplasm, and virus-induced shutoff of host protein synthesis downregulated the abundance of RNA5SP141-interacting proteins, which allowed RNA5SP141 to bind RIG-I and induce the expression of type I interferons. Silencing of RNA5SP141 strongly dampened the antiviral response to HSV-1 and the related virus Epstein-Barr virus (EBV), as well as influenza A virus (IAV). Our findings reveal that antiviral immunity can be triggered by host RNAs that are unshielded following depletion of their respective binding proteins by the virus.

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http://dx.doi.org/10.1038/s41590-017-0005-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815369PMC
January 2018
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