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Cell host & microbeJul 2024 DOI:
10.1016/j.chom.2024.07.005

The bacterial defense system MADS interacts with CRISPR-Cas to limit phage infection and escape

Maestri, Alice; Pons, Benoit J; Pursey, Elizabeth; Chong, Charlotte E; Gandon, Sylvain; Custodio, Rafael; Olina, Anna; Agapov, Aleksei; Chisnall, Matthew A W; Grasso, Anita; Paterson, Steve; Szczelkun, Mark D; Baker, Kate S; van Houte, Stineke; Chevallereau, Anne; Westra, Edze R
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Abstract
The constant arms race between bacteria and their parasites has resulted in a large diversity of bacterial defenses, with many bacteria carrying multiple systems. Here, we report the discovery of a phylogenetically widespread defense system, coined methylation-associated defense system (MADS), which is distributed across gram-positive and gram-negative bacteria. MADS interacts with a CRISPR-Cas system in its native host to provide robust and durable resistance against phages. While phages can acquire epigenetic-mediated resistance against MADS, co-existence of MADS and a CRISPR-Cas system limits escape emergence. MADS comprises eight genes with predicted nuclease, ATPase, kinase, and methyltransferase domains, most of which are essential for either self/non-self discrimination, DNA restriction, or both. The complex genetic architecture of MADS and MADS-like systems, relative to other prokaryotic defenses, points toward highly elaborate mechanisms of sensing infections, defense activation, and/or interference.
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