Abstract
Antagonistic systems of bacteria are often tightly regulated. The human gut Bacteroidales harbor three distinct antagonistic type VI secretion systems (T6SS), one of which is present only in Bacteroides fragilis, known as the GA3 T6SS. Although this is the best studied of the three T6SSs, little is known about how it is regulated. The gene upstream of the GA3 T6SS locus encodes a TetR family transcriptional regulator (TetR(GA3)), which we show represses expression of the GA3 T6SS locus. The gene immediately upstream and divergently transcribed from tetR(GA3), designated here as lgs(GA3), encodes a product of the α-oxoamine synthase family of pyridoxal phosphate-dependent enzymes with structural homology to the CqsA autoinducer synthase of the CAI-1 quorum sensing system of Vibrio spp. When lgs(GA3) is deleted, transcription of the GA3 T6SS locus is repressed in a TetR-dependent manner. Strains synthesizing Lgs(GA3) produce a molecule released into the supernatant that likely serves as the TetR(GA3) ligand, overcoming TetR transcriptional repression of the GA3 T6SS. We show that GA3 T6SS-specific immunity genes present on two acquired immunity defense islands are also regulated by Lgs(GA3) coordinating expression of GA3 T6SS antagonism with protection from competitor's GA3 T6SS toxins. Production and firing of the GA3 T6SS and subsequent antagonism occurs in bacteria deleted for lgs(GA3) when growing with bacteria containing this gene or their supernatants or when cocolonizing gnotobiotic mice. These data show that the GA3 T6SS is regulated by a small molecule acting through TetR(GA3) allowing the bacteria to coordinate antagonistic and protective systems.