Abstract

Type VI secretion systems (T6SS) function to deliver lethal payloads into target cells. Many studies have shown that protection against a single, lethal T6SS effector protein requires a cognate antidote immunity protein, both of which are often encoded together in a two-gene operon. The T6SS and an effector-immunity pair is sufficient for both killing and immunity. HereIn this paper we describe a T6SS effector operon that differs from conventional effector-immunity pairs in that eight genes are necessary for lethal effector function, yet can be countered by a single immunity protein. In this study, we investigated the role that the PefE T6SS immunity protein plays in recognition between two strains harboring nearly identical effector operons. Interestingly, despite containing seven of eight identical effector proteins, the less conserved immunity proteins only provided protection against their native effectors, suggesting that specificity and recognition could be dependent on variation within an immunity protein and one effector gene product. The variable effector gene product, PefD, is encoded upstream from pefE, and displays toxic activity that can be countered by PefE independent of T6SS-activity. Interestingly, while the entire pef operon was necessary to exert toxic activity via the T6SS in P. mirabilis, production of PefD and PefE alone was unable to exert this effector activity. Chimeric PefE proteins constructed from two P. mirabilis strains were used to localize immunity function to three amino acids. A promiscuous immunity protein was created using site-directed mutagenesis to change these residues from one variant to another. These findings support the notion that subtle differences between conserved effectors are sufficient for T6SS-mediated kin discrimination and that PefD requires additional factors to function as a T6SS-dependent effector.

Highlights

  • The type VI secretion system (T6SS) functions upon cell contact with a target cell to deliver a payload of effectors through a contractile puncturing device [1,2,3,4]

  • A non-canonical T6SS effector operon discrimination of self during the multicellular swarming behavior of Proteus mirabilis requires the lethal action of the T6SS, T6SS-dependent effectors, and immunity proteins

  • We propose that subtle sequence variation in the effector operons contribute to self and non-self recognition in these bacteria

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Summary

Introduction

The type VI secretion system (T6SS) functions upon cell contact with a target cell to deliver a payload of effectors through a contractile puncturing device [1,2,3,4]. We and others have shown that multicellular behavior exhibited by Proteus mirabilis is linked to T6S and enables discrimination during cellcell contact to eliminate non-self bacteria from the population [10, 11]. Based on these findings, we hypothesize that the T6SS must provide an advantage for P. mirabilis to discriminate, recognize, and kill competitors that would otherwise interfere with or benefit from their cooperative behavior. Kin discrimination has recently been established in multicellular Bacillus subtilis swarming populations as a mechanism to exclude non-kin from colonizing an ecological niche [12]

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