YprA-family helicases provide the missing link between diverse prokaryotic immune systems

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Authors: Ryan T. Bell, Thomas Gaudin, Yi Wu, Sofya K. Garushyants, Harutyun Sahakyan, Kira S. Makarova, Yuri I. Wolf, Simon A. Jackson, Franklin L. Nóbrega, Chase L. Beisel, Eugene V. Koonin
Cited by: 5
References: 48

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.

Fields of Study & Subjects

Vibrio bacteria research studies Escherichia coli research studies Enterobacteriaceae and Cronobacter Research

Publication details

Journal / source
Cell Host & Microbe
Publisher
Elsevier BV
Volume
34
Issue
7
Pages
1430–1444.e3
Publication date
11 June 2026
Language
EN