ABSTRACT
Type VI secretion systems (T6SSs) can deliver diverse toxic effectors into eukaryotic and bacterial cells. Although much is known about the regulation and assembly of T6SS, the translocation mechanism of effectors into the periplasm and/or cytoplasm of target cells remains elusive. Here we use the Agrobacterium tumefaciens DNase effector Tde1 to unravel the mechanism of translocation from attacker to prey. We demonstrate that Tde1 binds to its adaptor Tap1 through the N-terminus, which harbours continuous copies of GxxxG motifs resembling the glycine zipper structure found in proteins involved in the membrane channel formation. Amino acid substitutions on G39xxxG43 motif does not affect Tde1-Tap1 interaction and secretion but abolish its membrane permeability and translocation of its fluorescent fusion protein into prey cells. The data suggest that G39xxxG43 governs the delivery of Tde1 into target cells by permeabilizing the cytoplasmic membrane. Considering the widespread presence of GxxxG motifs in bacterial effectors and pore-forming toxins, we propose that glycine zipper mediated permeabilization is a conserved mechanism used by bacterial effectors for translocation across target cell membranes.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
The revised manuscript included new data: 1) viable cell counts of growth inhibition assay (Fig. 2A), 2) Quantitative data of microscope data (Fig. 2C, Fig. 4), 3) quantitative data of interabacterial competition (Fig. 5A, 5B), western blotting data of growth inhibition (Fig. S1A and S1B), secretion assay of single glycine-zipper mutants (Fig. 5C), and inclusion of full gel of western blot results (Fig. S3 and S5). We have improved the manuscript by integrating these new results along with revision of the main texts accordingly.