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Two cGAS-like receptors induce antiviral immunity in Drosophila

  • Andreas Holleufer
  • , Kasper Grønbjerg Winther
  • , Hans Henrik Gad
  • , Xianlong Ai
  • , Yuqiang Chen
  • , Lihua Li
  • , Ziming Wei
  • , Huimin Deng
  • , Jiyong Liu
  • , Ninna Ahlmann Frederiksen
  • , Bine Simonsen
  • , Line Lykke Andersen
  • , Karin Kleigrewe
  • , Louise Dalskov
  • , Andreas Pichlmair
  • , Hua Cai
  • , Jean Luc Imler
  • , Rune Hartmann
  • Aarhus University
  • Universite de Strasbourg
  • The Third Affiliated Hospital of Guangzhou Medical University
  • Technical University of Munich
  • German Center for Infection Research (DZIF)

Research output: Contribution to journalArticlepeer-review

125 Scopus citations

Abstract

In mammals, cyclic GMP–AMP (cGAMP) synthase (cGAS) produces the cyclic dinucleotide 2′3′-cGAMP in response to cytosolic DNA and this triggers an antiviral immune response. cGAS belongs to a large family of cGAS/DncV-like nucleotidyltransferases that is present in both prokaryotes1 and eukaryotes2–5. In bacteria, these enzymes synthesize a range of cyclic oligonucleotides and have recently emerged as important regulators of phage infections6–8. Here we identify two cGAS-like receptors (cGLRs) in the insect Drosophila melanogaster. We show that cGLR1 and cGLR2 activate Sting- and NF-κB-dependent antiviral immunity in response to infection with RNA or DNA viruses. cGLR1 is activated by double-stranded RNA to produce the cyclic dinucleotide 3′2′-cGAMP, whereas cGLR2 produces a combination of 2′3′-cGAMP and 3′2′-cGAMP in response to an as-yet-unidentified stimulus. Our data establish cGAS as the founding member of a family of receptors that sense different types of nucleic acids and trigger immunity through the production of cyclic dinucleotides beyond 2′3′-cGAMP.

Original languageEnglish
Pages (from-to)114-118
Number of pages5
JournalNature
Volume597
Issue number7874
DOIs
StatePublished - 2 Sep 2021

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