Abstract
It was recently shown that bacteria use, apart from CRISPR–Cas and restriction systems, a considerable diversity of phage resistance systems1–4, but it is largely unknown how phages cope with this multilayered bacterial immunity. Here we analysed groups of closely related Bacillus phages that showed differential sensitivity to bacterial defence systems, and discovered four distinct families of anti-defence proteins that inhibit the Gabija, Thoeris and Hachiman systems. We show that these proteins Gad1, Gad2, Tad2 and Had1 efficiently cancel the defensive activity when co-expressed with the respective defence system or introduced into phage genomes. Homologues of these anti-defence proteins are found in hundreds of phages that infect taxonomically diverse bacterial species. We show that the anti-Gabija protein Gad1 blocks the ability of the Gabija defence complex to cleave phage-derived DNA. Our data further reveal that the anti-Thoeris protein Tad2 is a ‘sponge’ that sequesters the immune signalling molecules produced by Thoeris TIR-domain proteins in response to phage infection. Our results demonstrate that phages encode an arsenal of anti-defence proteins that can disable a variety of bacterial defence mechanisms.
Original language | English |
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Pages (from-to) | 352-359 |
Number of pages | 8 |
Journal | Nature |
Volume | 625 |
Issue number | 7994 |
Early online date | 22 Nov 2023 |
DOIs | |
Publication status | Published - 11 Jan 2024 |
Bibliographical note
We thank the members of the laboratory of R.S. for comments on the manuscript and discussion; Y. Peleg and S. Albeck for assistance with protein expression; Y. Fridmann-Sirkis for help with surface plasmon resonance analysis; and H. Keren-Shaul and D. Pilzer for help with PacBio sequencing. R.S. was supported, in part, by the European Research Council (grant no. ERC-AdG GA 101018520), the Israel Science Foundation (MAPATS grant 2720/22), the Deutsche Forschungsgemeinschaft (SPP 2330, Grant 464312965), the Ernest and Bonnie Beutler Research Program of Excellence in Genomic Medicine, and the Knell Family Center for Microbiology. E.Y. is supported by the Clore Scholars Program, and, in part, by the Israeli Council for Higher Education via the Weizmann Data Science Research Center. P.J.K. was supported, in part, by the Pew Biomedical Scholars programme and The Mathers Foundation. S.J.H. is supported through a Cancer Research Institute Irvington Postdoctoral Fellowship (number CRI3996). X-ray data were collected at the Northeastern Collaborative Access Team beamlines 24-ID-C and 24-ID-E (P30 GM124165), and used a Pilatus detector (S10RR029205), an Eiger detector (S10OD021527) and the Argonne National Laboratory Advanced Photon Source (DE-AC02-06CH11357), and at beamline 8.2.1 of the Advanced Light Source, a US Department of Energy Office of Science User Facility under contract number DE-AC02-05CH11231 and supported in part by the Howard Hughes Medical Institute, the ALS-ENABLE programme and the NIGMS grant P30 GM124169-01.Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
All Science Journal Classification (ASJC) codes
- General