Crosstalk between three CRISPR-Cas types enables primed type VI-A adaptation in Listeria seeligeri
- PMID: 40829593
- PMCID: PMC12370272
- DOI: 10.1016/j.chom.2025.05.020
Crosstalk between three CRISPR-Cas types enables primed type VI-A adaptation in Listeria seeligeri
Abstract
CRISPR-Cas systems confer adaptive immunity to their prokaryotic hosts through the process of adaptation, where sequences are captured from foreign nucleic acids and integrated as spacers in the CRISPR array, thereby enabling crRNA-guided interference against new threats. While the Cas1-2 integrase is critical for adaptation, it is absent from many CRISPR-Cas loci, rendering the mechanism of spacer acquisition unclear for these systems. In this study, we show that the RNA-targeting type VI-A CRISPR system of Listeria seeligeri acquires spacers from DNA substrates through the action of a promiscuous Cas1-2 integrase encoded by a co-occurring type II-C system, in a transcription-independent manner. We further demonstrate that the type II-C integration complex is strongly stimulated by preexisting spacers in a third CRISPR system (type I-B), which imperfectly match phage targets and prime type VI-A adaptation. Altogether, our results reveal an unprecedented degree of communication among CRISPR-Cas loci encoded by a single organism.
Keywords: CRISPR; Cas13; bacteriophage; primed adaptation; spacer acquisition.
Copyright © 2025 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests A.J.M. is a co-founder and advisor of Profluent Bio.
Update of
-
Crosstalk between three CRISPR-Cas types enables primed type VI-A adaptation in Listeria seeligeri.bioRxiv [Preprint]. 2024 Oct 26:2024.10.25.620265. doi: 10.1101/2024.10.25.620265. bioRxiv. 2024. Update in: Cell Host Microbe. 2025 Sep 10;33(9):1550-1560.e4. doi: 10.1016/j.chom.2025.05.020. PMID: 39484522 Free PMC article. Updated. Preprint.
References
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources