Phage defence loci of Streptococcus thermophilus-tip of the anti-phage iceberg?

Kelleher, Philip; Charneco, Guillermo Ortiz; Kampff, Zoe; Diaz-Garrido, Natalia; Bottacini, Francesca; McDonnell, Brian; Lugli, Gabriele A.; Ventura, Marco; Fomenkov, Alexey; Quenee, Pascal; Kulakauskas, Saulius; de Waal, Paul; van Peij, Noel N. M. E.; Cambillau, Christian; Roberts, Richard John; et. al.

Abstract

--- - Bacteria possess (bacterio)phage defence systems to ensure their survival. The thermophilic lactic acid bacterium, Streptococcus thermophilus, which is used in dairy fermentations, harbours multiple CRISPR-Cas and restriction and modification (R/M) systems to protect itself against phage attack, with limited reports on other types of phage-resistance. Here, we describe the systematic identification and functional analysis of the phage resistome of S. thermophilus using a collection of 27 strains as representatives of the species. In addition to CRISPR-Cas and R/M systems, we uncover nine distinct phage-resistance systems including homologues of Kiwa, Gabija, Dodola, defence-associated sirtuins and classical lactococcal/streptococcal abortive infection systems. The genes encoding several of these newly identified S. thermophilus antiphage systems are located in proximity to the genetic determinants of CRISPR-Cas systems thus constituting apparent Phage Defence Islands. Other phage-resistance systems whose encoding genes are not co-located with genes specifying CRISPR-Cas systems may represent anchors to identify additional Defence Islands harbouring, as yet, uncharacterised phage defence systems. We estimate that up to 2.5% of the genetic material of the analysed strains is dedicated to phage defence, highlighting that phage-host antagonism plays an important role in driving the evolution and shaping the composition of dairy streptococcal genomes. - Graphical Abstract

Más información

Título según WOS: ID WOS:001318598000001 Not found in local WOS DB
Título de la Revista: NUCLEIC ACIDS RESEARCH
Volumen: 52
Número: 19
Editorial: OXFORD UNIV PRESS
Fecha de publicación: 2024
Página de inicio: 11853
Página final: 11869
DOI:

10.1093/nar/gkae814

Notas: ISI