The phylogenetic study of the T6SS in Pseudomonas putida strains has revealed that T6SSs is widely distributed in P. putida. In fact, 100% of the strains contain T6SS elements and 90% of them present at least one complete cluster. The T6S clusters found in P. putida strains are highly conserved and clad mainly in 3 groups: 1.2 2 and 4B respectively. The in silico analyses revealed that P. putida KT2440 contains three potential T6SSs that we have named K1- (group 4B), K2- and K3-T6SS (both from group 1.2). Each one of these systems contain the complete set of genes to encode the core components necessary to assemble a functional machinery (Tss components), accessory components (Tag proteins) and over eleven effectors including nucleases and pore-forming colicins together with their cognate immunity pairs (Tke1-Tki1, Tke2-Tki2, Tke3-Tki3, …). I have showed using techniques such as bacterial competition assays, secretion assays and heterologous expression of toxins in non-immune bacteria that the K1-T6SS is a potent antibacterial device which secretes toxic effectors including the putative nuclease Tke2. Remarkably, P. putida kills a broad range of bacteria in a K1-T6SS-dependent manner, including resilient phytopathogens such as Agrobacterium tumefaciens, Pseudomonas syringae, Pectobacterium caratovorum and Xanthomonas campestris. Furthermore, this study shows that the protection occurs in vitro but also in planta and that Nicotiana benthamiana leaves are protected from the attack of X. campestris in a T6SS-dependent manner. All these results show a new role for T6SS weapons as a novel mechanism of biological control.