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bioRxiv · 10.1101/2020.12.15.422598

Co-Dependent and Interdigitated: Dual Quorum Sensing Systems Regulate Conjugative Transfer of the Ti Plasmid and the At Megaplasmid in Agrobacterium tumefaciens 15955

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. 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 homologues 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 preferentially biased towards 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. CONTRIBUTION TO THE FIELDMany bacteria harbor multiple types of plasmids, and in a fraction of these the plasmids encode independent conjugative transfer systems. In the plant pathogen Agrobacterium tumefaciens, conjugation of the virulence plasmid, called the Ti (tumor-inducing) plasmid, is regulated by plant released signals called opines, and by a well characterized quorum sensing mechanism also encoded on the plasmid. The co-resident At megaplasmid also has its own conjugative transfer system. In certain lineages of A. tumefaciens the At plasmid carries a discrete quorum sensing system. This study aimed to determine the extent to which these plasmid-borne quorum sensing systems overlap to co-regulate conjugative transfer of both plasmids. Co-resident plasmids can impact each other, and the host bacterium at multiple levels, and for the Ti plasmid and At plasmid, we find that each plasmid clearly can influence the conjugative transfer systems of the other plasmid. The findings reported also shed light on how bacteria with multiple quorum sensing pathways have evolved to integrate these systems, in this case to control horizontal gene transfer of two different plasmids. Overall, the interactions described here have broader implications for the horizontal transfer and evolutionary stability of co-resident plasmids, and the degree to which their regulatory systems are coordinated.

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BibTeXRIS

Barton, I. S., Eagan, J. L., Nieves-Otero, P. A., Reynolds, I. P., Patt, T. G., Fuqua, C.. 2020-12-15. Co-Dependent and Interdigitated: Dual Quorum Sensing Systems Regulate Conjugative Transfer of the Ti Plasmid and the At Megaplasmid in Agrobacterium tumefaciens 15955. https://doi.org/10.1101/2020.12.15.422598

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