Strengthening Phage Resistance of Streptococcus thermophilus by Leveraging Complementary Defense Systems

Abstract

CRISPR-Cas and restriction-modification systems represent the core defense arsenal in Streptococcus thermophilus to block lytic phages, but their effectiveness is compromised by phages encoding anti-CRISPR proteins (ACRs) and other counter-defense strategies. Here, we explored the resistome of 263 S. thermophilus strains to uncover other anti-phage systems. The defense landscape of S. thermophilus was enriched by 21 accessory defense systems, 13 of which had not been previously investigated in this species. Experimental validation of 17 systems with 14 phages showed varying anti-phage levels, uncovering intra-genus specificities among the five viral genera infecting S. thermophilus. Interestingly, the resistance levels were even higher when some defense systems (Dodola and PD-Lambda-1) were expressed from a low-copy plasmid or when integrated into the chromosome. We also observed a synergistic effect when combining Gabija with CRISPR-Cas, underscoring the potential of these additional defense systems for developing more robust industrial S. thermophilus strains, particularly against ACR-encoding phages.