Abstract

Members of the Rhizobiaceae, often carry multiple secondary replicons in addition to the primary chromosome with compatible repABC-based replication systems. Unlike secondary chromosomes and chromids, repABC-based megaplasmids and plasmids can undergo copy number fluctuations and are capable of conjugative transfer in response to environmental signals. Several Agrobacterium tumefaciens lineages harbor three secondary repABC-based replicons, including a secondary chromosome (often linear), the Ti (tumor-inducing) plasmid and the At megaplasmid. The Ti plasmid is required for virulence and encodes a conjugative transfer (tra) system that is strictly regulated by a subset of plant-tumor released opines and a well-described acyl-homoserine lactone (AHL)-based quorum-sensing mechanism. The At plasmids are generally not required for virulence, but carry genes that enhance rhizosphere survival, and these plasmids are often conjugatively proficient. We report that the At megaplasmid of the octopine-type strain A. tumefaciens 15955 encodes a quorum-controlled conjugation system that directly interacts with the paralogous quorum sensing system on the co-resident Ti plasmid. Both the pAt15955 and pTi15955 plasmids carry homologs of a TraI-type AHL synthase, a TraR-type AHL-responsive transcription activator, and a TraM-type anti-activator. The traI genes from both pTi15955 and pAt15955 can direct production of the inducing AHL (3-octanoyl-L-homoserine lactone) and together contribute to the overall AHL pool. The TraR protein encoded on each plasmid activates AHL-responsive transcription of target tra gene promoters. The pAt15955 TraR can cross-activate tra genes on the Ti plasmid as strongly as its cognate tra genes, whereas the pTi15955 TraR is preferentially biased toward its own tra genes. Putative tra box elements are located upstream of target promoters, and comparing between plasmids, they are in similar locations and share an inverted repeat structure, but have distinct consensus sequences. The two AHL quorum sensing systems have a combinatorial effect on conjugative transfer of both plasmids. Overall, the interactions described here have implications for the horizontal transfer and evolutionary stability of both plasmids and, in a broad sense, are consistent with other repABC systems that often have multiple quorum-sensing controlled secondary replicons.

Highlights

  • Many members of the Alphaproteobacteria (APB) group contain large secondary replicons, in addition to the primary chromosomal replicon with the majority of core genes

  • In addition to proper coordination with the cell cycle, tight regulation of copy number and horizontal gene transfer of large secondary replicons serves to limit the costs associated with DNA replication and horizontal transfer

  • The opine-dependent quorum sensing system is wellcharacterized in Agrobacterium species harboring the wide host range octopine-type and nopaline-type Ti plasmids, with prototypes pTiR10 and pTiC58, respectively (Gordon and Christie, 2014)

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Summary

Introduction

Many members of the Alphaproteobacteria (APB) group contain large secondary replicons, in addition to the primary chromosomal replicon with the majority of core genes. Several APB, notably within the Family Rhizobiaceae, harbor multiple large secondary replicons that are stably maintained by compatible repABC systems These plasmids have extensive systems for their retention and proliferation, including copy number control, efficient partitioning with the chromosomes, and conjugative transfer (Pinto et al, 2012). A. tumefaciens causes the plant neoplastic disease crown gall, by driving cross-kingdom horizontal gene transfer to host plants, delivering a segment of the Ti plasmid called the T-DNA, into host cells (Chilton et al, 1977) This process is strictly regulated by plant-released signals via the VirAVirG two-component system (Winans, 1991) which activates virulence (vir) gene expression including the VirB Type IV secretion system (T4SS) that delivers the T-DNA to plant cells (Christie, 2001). The Ti plasmid encodes a LuxI-type AHL synthase called

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