Abstract

The conjugative plasmid R388 and a number of other plasmids carry an operon, stbABC, adjacent to the origin of conjugative transfer. We investigated the role of the stbA, stbB, and stbC genes. Deletion of stbA affected both conjugation and stability. It led to a 50-fold increase in R388 transfer frequency, as well as to high plasmid loss. In contrast, deletion of stbB abolished conjugation but provoked no change in plasmid stability. Deletion of stbC showed no effect, neither in conjugation nor in stability. Deletion of the entire stb operon had no effect on conjugation, which remained as in the wild-type plasmid, but led to a plasmid loss phenotype similar to that of the R388ΔstbA mutant. We concluded that StbA is required for plasmid stability and that StbA and StbB control conjugation. We next observed the intracellular positioning of R388 DNA molecules and showed that they localize as discrete foci evenly distributed in live Escherichia coli cells. Plasmid instability of the R388ΔΔstbA mutant correlated with aberrant localization of the plasmid DNA molecules as clusters, either at one cell pole, at both poles, or at the cell center. In contrast, plasmid molecules in the R388ΔΔstbB mutant were mostly excluded from the cell poles. Thus, results indicate that defects in both plasmid maintenance and transfer are a consequence of variations in the intracellular positioning of plasmid DNA. We propose that StbA and StbB constitute an atypical plasmid stabilization system that reconciles two modes of plasmid R388 physiology: a maintenance mode (replication and segregation) and a propagation mode (conjugation). The consequences of this novel concept in plasmid physiology will be discussed.

Highlights

  • Transmissible plasmids contribute greatly to the plasticity of bacterial genomes and to the acquisition of genetic traits by host cells through the collective carriage of adaptive genes, including antibiotic resistance and virulence genes, and through the ability to disseminate them by conjugation [1]

  • By using a fluorescent protein to tag plasmid molecules, we found that R388 plasmid foci, most of which contain a single copy of the plasmid, are evenly distributed within E. coli cells

  • Comparative genomics of the stb operon To study the role of the three stb genes in plasmid R388, we first analyzed the stb operon by protein sequence comparison

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Summary

Introduction

Transmissible plasmids contribute greatly to the plasticity of bacterial genomes and to the acquisition of genetic traits by host cells through the collective carriage of adaptive genes, including antibiotic resistance and virulence genes, and through the ability to disseminate them by conjugation [1]. Vertical transmission requires timely controlled replication and faithful assortment (segregation) of sister plasmid copies to daughter cells. Partition (Par) systems ensure efficient distribution of plasmid molecules to each daughter cell during division (for reviews: [2,3,4,5]). They are composed of a cis-acting centromere-like site and two proteins, a nucleotide-binding cytomotive protein and a centromere-binding adaptor protein. The par centromere locus and the Par proteins are encoded by sets of homologous genes in various plasmids, phages, and chromosomes

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