Bacterial defences interact synergistically by disrupting phage cooperation

Summary The constant arms race between bacteria and their phages has resulted in a large diversity of bacterial defence systems1,2, with many bacteria carrying several systems3,4. In response, phages often carry counter-defence genes5–9. If and how bacterial defence mechanisms interact to protect against phages with counter-defence genes remains unclear. Here, we report the existence of a novel defence system, coined MADS (Methylation Associated Defence System), which is located in a strongly conserved genomic defence hotspot inPseudomonas aeruginosaand distributed across Gram-positive and Gram-negative bacteria. We find that the natural co-existence of MADS and a Type IE CRISPR-Cas adaptive immune system in the genome ofP. aeruginosaSMC4386 provides synergistic levels of protection against phage DMS3, which carries an anti-CRISPR (acr) gene. Previous work has demonstrated that Acr-phages need to cooperate to overcome CRISPR immunity, with a first sacrificial phage causing host immunosuppression to enable successful secondary phage infections10,11. Modelling and experiments show that the co-existence of MADS and CRISPR-Cas provides strong and durable protection against Acr-phages by disrupting their cooperation and limiting the spread of mutants that overcome MADS. These data reveal that combining bacterial defences can robustly neutralise phage with counter-defence genes, even if each defence on its own can be readily by-passed, which is key to understanding how selection acts on defence combinations and their coevolutionary consequences..

Medienart:

Preprint

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

bioRxiv.org - (2023) vom: 04. Apr. Zur Gesamtaufnahme - year:2023

Sprache:

Englisch

Beteiligte Personen:

Maestri, Alice [VerfasserIn]
Pursey, Elizabeth [VerfasserIn]
Chong, Charlotte [VerfasserIn]
Pons, Benoit J. [VerfasserIn]
Gandon, Sylvain [VerfasserIn]
Custodio, Rafael [VerfasserIn]
Chisnall, Matthew [VerfasserIn]
Grasso, Anita [VerfasserIn]
Paterson, Steve [VerfasserIn]
Baker, Kate [VerfasserIn]
Houte, Stineke van [VerfasserIn]
Chevallereau, Anne [VerfasserIn]
Westra, Edze R. [VerfasserIn]

Links:

Volltext [kostenfrei]

Themen:

570
Biology

doi:

10.1101/2023.03.30.534895

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

XBI039127362