Bacterial TIR-based immune systems sense phage capsids to initiate defense

Thoeris systems use proteins with Toll/interleukin-1 receptor domains to protect prokaryotes from phage infection through the synthesis of a cyclic adenosine diphosphate ribose signalling molecule, which activates an effector that depletes the host of the essential metabolite NAD<sup>+</sup> to limit viral propagation. How infection is recognized during Thoeris immunity is not known. Here we investigate the staphylococcal Thoeris defense system, ThsA-B1-B2, and found that, upon infection, the major capsid proteins of Siphoviridae phages from serogroup B, but not A, form a complex with ThsB1 and ThsB2 to activate Thoeris defense. Thoeris cyclases from Streptococcus also recognize major capsid proteins. Our results suggest that the accumulation of capsid mutations that enable avoidance of Thoeris recognition may be an important evolutionary force behind the structural diversity of prokaryotic viruses. More broadly, given that some mammalian immune pathways contain Toll/interleukin-1 receptor domains that recognize viral structures, our findings highlight a conserved mechanism of innate antiviral immunity.

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Publication Details

Journal
Nature Microbiology
Published
2025-10-24
DOI
https://doi.org/10.1038/s41564-025-02150-0
Citations
6
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
4.84

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article

Bacterial TIR-based immune systems sense phage capsids to initiate defense

Cameron G. Roberts, Dalton V. Banh, Dinshaw J. Patel, Chloe B. Fishman et al.
6 citations
Nature Microbiology
RNA and protein synthesis mechanisms
4.84
article

Bacterial TIR-based immune systems sense phage capsids to initiate defense

Cameron G. Roberts, Dalton V. Banh, Dinshaw J. Patel, Chloe B. Fishman, Luciano A. Marraffini, Zhiying Zhang
article en
6 citations

Abstract

Thoeris systems use proteins with Toll/interleukin-1 receptor domains to protect prokaryotes from phage infection through the synthesis of a cyclic adenosine diphosphate ribose signalling molecule, which activates an effector that depletes the host of the essential metabolite NAD<sup>+</sup> to limit viral propagation. How infection is recognized during Thoeris immunity is not known. Here we investigate the staphylococcal Thoeris defense system, ThsA-B1-B2, and found that, upon infection, the major capsid proteins of Siphoviridae phages from serogroup B, but not A, form a complex with ThsB1 and ThsB2 to activate Thoeris defense. Thoeris cyclases from Streptococcus also recognize major capsid proteins. Our results suggest that the accumulation of capsid mutations that enable avoidance of Thoeris recognition may be an important evolutionary force behind the structural diversity of prokaryotic viruses. More broadly, given that some mammalian immune pathways contain Toll/interleukin-1 receptor domains that recognize viral structures, our findings highlight a conserved mechanism of innate antiviral immunity.

Nature MicrobiologyVol. 10(11)
Memorial Sloan Kettering Cancer Center (US), Howard Hughes Medical Institute (US), Rockefeller University (US)
National Science Foundation, Memorial Sloan-Kettering Cancer Center, National Institutes of Health, Weill Cornell Medical College
Openalex Percentile: Top 5%
RNA and protein synthesis mechanisms
4.84
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