Abstract

Unlike nucleobase modifications in canonical restriction-modification systems, DNA phosphorothioate (PT) epigenetic modification occurs in the DNA sugar-phosphate backbone when the nonbridging oxygen is replaced by sulfur in a double-stranded (ds) or single-stranded (ss) manner governed by DndABCDE or SspABCD, respectively. SspABCD coupled with SspE constitutes a defense barrier in which SspE depends on sequence-specific PT modifications to exert its antiphage activity. Here, we identified a new type of ssDNA PT-based SspABCD-SspFGH defense system capable of providing protection against phages through a mode of action different from that of SspABCD-SspE. We provide further evidence that SspFGH damages non-PT-modified DNA and exerts antiphage activity by suppressing phage DNA replication. Despite their different defense mechanisms, SspFGH and SspE are compatible and pair simultaneously with one SspABCD module, greatly enhancing the protection against phages. Together with the observation that the sspBCD-sspFGH cassette is widely distributed in bacterial genomes, this study highlights the diversity of PT-based defense barriers and expands our knowledge of the arsenal of phage defense mechanisms.IMPORTANCE We recently found that SspABCD, catalyzing single-stranded (ss) DNA phosphorothioate (PT) modification, coupled with SspE provides protection against phage infection. SspE performs both PT-simulated NTPase and DNA-nicking nuclease activities to damage phage DNA, rendering SspA-E a PT-sensing defense system. To our surprise, ssDNA PT modification can also pair with a newly identified 3-gene sspFGH cassette to fend off phage infection with a different mode of action from that of SspE. Interestingly, both SspFGH and SspE can pair with the same SspABCD module for antiphage defense, and their combination provides Escherichia coli JM109 with additive phage resistance up to 105-fold compared to that for either barrier alone. This agrees with our observation that SspFGH and SspE coexist in 36 bacterial genomes, highlighting the diversity of the gene contents and molecular mechanisms of PT-based defense systems.

Highlights

  • Unlike nucleobase modifications in canonical restriction-modification systems, DNA phosphorothioate (PT) epigenetic modification occurs in the DNA sugar-phosphate backbone when the nonbridging oxygen is replaced by sulfur in a double-stranded or single-stranded manner governed by DndABCDE or SspABCD, respectively

  • Together with the detection of PT-linked d(CPSC) dinucleotides by liquid chromatography-coupled tandem quadrupole mass spectrometry (LC-MS/MS) in JM109, the results demonstrated that IscS and SspBCD in FF-93 confer DNA PT modification at 59-CPSCA-39 consensus sequences capable of stimulating the antiphage defense of SspE from 3234/ A

  • Based on our previous results showing that solitary DNA PT modification catalyzed by DndABCDE has evolved additional functions, such as the epigenetic control of gene expression, maintenance of cellular redox homeostasis, and environmental fitness [20, 25], we propose that PTs catalyzed by solitary SspBCD systems might act as versatile participants in multiple cellular processes resembling that of dsDNA PTs governed by solitary DndABCDE modules

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Summary

Introduction

Unlike nucleobase modifications in canonical restriction-modification systems, DNA phosphorothioate (PT) epigenetic modification occurs in the DNA sugar-phosphate backbone when the nonbridging oxygen is replaced by sulfur in a double-stranded (ds) or single-stranded (ss) manner governed by DndABCDE or SspABCD, respectively. SsDNA PT modification can pair with a newly identified 3-gene sspFGH cassette to fend off phage infection with a different mode of action from that of SspE Both SspFGH and SspE can pair with the same SspABCD module for antiphage defense, and their combination provides Escherichia coli JM109 with additive phage resistance up to 105-fold compared to that for either barrier alone. The functional similarities between DndA and SspA as cysteine desulfurases and between DndC and SspD as ATP pyrophosphatases lead to the prediction that the DndABCDE and SspABCD machineries share the initial sulfur mobilization pathway but follow divergent DNA target selection steps [12] This divergence is considered to occur due to SspB, a DNA-nicking nuclease whose nicking activity has been demonstrated to be essential to ssDNA PT formation but has not yet been found for DndABCDE proteins [12]

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