Transcriptome profiling of a Sinorhizobium meliloti fadD mutant reveals the role of rhizobactin 1021biosynthesis and regulation genes in the control of swarming
Artículo académico
Background: Swarming is a multicellular phenomenom characterized by the coordinated and rapid movement of
bacteria across semisolid surfaces. In Sinorhizobium meliloti this type of motility has been described in a fadD
mutant. To gain insights into the mechanisms underlying the process of swarming in rhizobia, we compared the
transcriptome of a S. meliloti fadD mutant grown under swarming inducing conditions (semisolid medium) to
those of cells grown under non-swarming conditions (broth and solid medium).
Results: More than a thousand genes were identified as differentially expressed in response to growth on agar
surfaces including genes for several metabolic activities, iron uptake, chemotaxis, motility and stress-related genes.
Under swarming-specific conditions, the most remarkable response was the up-regulation of iron-related genes.
We demonstrate that the pSymA plasmid and specifically genes required for the biosynthesis of the siderophore
rhizobactin 1021 are essential for swarming of a S. meliloti wild-type strain but not in a fadD mutant. Moreover,
high iron conditions inhibit swarming of the wild-type strain but not in mutants lacking either the iron limitation
response regulator RirA or FadD.
Conclusions: The present work represents the first transcriptomic study of rhizobium growth on surfaces including
swarming inducing conditions. The results have revealed major changes in the physiology of S. meliloti cells grown
on a surface relative to liquid cultures. Moreover, analysis of genes responding to swarming inducing conditions
led to the demonstration that iron and genes involved in rhizobactin 1021 synthesis play a role in the surface
motility shown by S. meliloti which can be circumvented in a fadD mutant. This work opens a way to the
identification of new traits and regulatory networks involved in swarming by rhizobia.
