Cell Host & MicrobeMicrobiologyPeer-reviewed journal article
YprA family helicases provide the missing link between diverse prokaryotic immune systems
Ryan T. BelliD, Thomas Gaudin, Yi WuiD, Sofya K. GarushyantsiD, Harutyun SahakyaniD, Kira S. MakarovaiD, Yuri I. WolfiD, Simon A. JacksoniD, Franklin L. NóbregaiD, Chase L. BeiseliD, Eugene V. KooniniD
Abstract
Bacteria and archaea possess an enormous variety of antivirus immune systems that often share homologous proteins and domains, some of which contribute to diverse defense strategies. YprA family helicases are central to widespread defense systems DISARM, Dpd, and Druantia. Here, through comprehensive phylogenetic and structural prediction analysis of the YprA family, we identify several major, previously unrecognized clades, with unique signatures of domain architecture and associations with other genes. Each YprA family clade defines a distinct class of defense systems, which we denote ARMADA (disARM-related Antiviral Defense Array), BRIGADE (Base hypermodification and Restriction Involving Genes encoding ARMADA-like and Dpd-like Effectors), or TALON (TOTE-like and ARMADA-Like Operon with Nuclease). In addition to the YprA-like helicase, ARMADA systems share two more proteins with DISARM. However, ARMADA YprA homologs are most similar to those of Druantia, suggesting ARMADA is a missing link connecting DISARM and Druantia. We show experimentally that ARMADA protects bacteria against a broad range of phages via a direct, non-abortive mechanism. We also discovered multiple families of satellite phage-like mobile genetic elements that often carry both ARMADA and Druantia Type III systems and show that these can provide synergistic resistance against diverse phages.
- organism: bacteria (other)
- research focus: host-pathogen & immune response
- approach: comparative / phylogenetic analysis
- Citations
- 9
- FWCI
- 24.66
- Field percentile
- top 1%
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