A toxin-antitoxin system provides phage defense via DNA damage and repair

Widespread in bacteria and archaea, toxin-antitoxin (TA) systems have been recently demonstrated to function in phage defense. Here we characterize the anti-phage function of a type IV TA system, ShosTA. Using structural and biochemical approaches, we show that ShosT couples phosphoribosyltransferase and pyrophosphatase activities to disrupt purine metabolism, resulting in DNA duplication, cell filamentation and ultimate cell death. ShosA binds DNA and likely recruits other proteins to facilitate DNA homologous recombination to antagonize ShosT's toxicity. We identify Gp0.7 of T7 phage as a trigger for ShosTA system via shutting off the protein synthesis, and the C-terminus-mediated intrinsic instability of ShosA releases the toxicity of the existing ShosT proteins. Collectively, our results provide a novel toxin-antitoxin mechanism for anti-phage immunity and shed light on the triggering of this TA system.

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Publication Details

Journal
Nature Communications
Published
2025-04-01
DOI
https://doi.org/10.1038/s41467-025-58540-9
Citations
4
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
6.87

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article

A toxin-antitoxin system provides phage defense via DNA damage and repair

Hai-Rong Pu, Dongmei Tang, Yamei Yu, Aiping Tong et al.
4 citations
Nature Communications
Bacteriophages and microbial interactions
6.87
article

A toxin-antitoxin system provides phage defense via DNA damage and repair

Hai-Rong Pu, Dongmei Tang, Yamei Yu, Aiping Tong, Lunzhi Dai, Yuxin Chen, Qiang Chen, Xinjun Zhao
article en
4 citations

Abstract

Widespread in bacteria and archaea, toxin-antitoxin (TA) systems have been recently demonstrated to function in phage defense. Here we characterize the anti-phage function of a type IV TA system, ShosTA. Using structural and biochemical approaches, we show that ShosT couples phosphoribosyltransferase and pyrophosphatase activities to disrupt purine metabolism, resulting in DNA duplication, cell filamentation and ultimate cell death. ShosA binds DNA and likely recruits other proteins to facilitate DNA homologous recombination to antagonize ShosT's toxicity. We identify Gp0.7 of T7 phage as a trigger for ShosTA system via shutting off the protein synthesis, and the C-terminus-mediated intrinsic instability of ShosA releases the toxicity of the existing ShosT proteins. Collectively, our results provide a novel toxin-antitoxin mechanism for anti-phage immunity and shed light on the triggering of this TA system.

Nature CommunicationsVol. 16(1)
Sichuan University (CN), West China Medical Center of Sichuan University (CN), State Key Laboratory of Biotherapy
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Sichuan University, Natural Science Foundation of Sichuan Province, West China Hospital, Sichuan University
Openalex Percentile: Top 4%
Bacteriophages and microbial interactions
6.87
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A toxin-antitoxin system provides phage defense via DNA damage and repair — Hai-Rong Pu, Dongmei Tang, et al. · Nature Communications (2025) | TGRS Research Map | TGRS