Summary
The soil‐borne bacterium
Ralstonia solanacearum
invades the roots and colonizes the intercellular spaces and then the xylem. The expression of
lecM
, encoding a lectin LecM, is induced by an OmpR family response regulator HrpG in
R. solanacearum
strain OE1‐1. LecM contributes to the attachment of strain OE1‐1 to the host cells of intercellular spaces. OE1‐1 produces methyl 3‐hydroxymyristate (3‐OH MAME) through a methyltransferase (PhcB) and extracellularly secretes the chemical as a quorum sensing (QS) signal, which activates QS. The expression of
lecM
is also induced by the PhcA virulence regulator functioning through QS, and the resulting LecM is implicated in the QS‐dependent production of major exopolysaccharide EPS I and the aggregation of OE1‐1 cells. To investigate the function of LecM in QS, we analysed the transcriptome of
R. solanacearum
strains generated by RNA sequencing technology. In the
lecM
mutant, the expression of positively QS‐regulated genes and negatively QS‐regulated genes was down‐regulated (by >90%) and up‐regulated (by ~60%), respectively. However,
phcB
and
phcA
in the
lecM
mutant were expressed at levels similar to those in strain OE1‐1. The
lecM
mutant produced significantly less ralfuranone and exhibited a significantly greater swimming motility, which were positively and negatively regulated by QS, respectively. In addition, the extracellular 3‐OH MAME content of the
lecM
mutant was significantly lower than that of OE1‐1. The application of 3‐OH MAME more strongly increased EPS I production in the
phcB
‐deleted mutant and strain OE1‐1 than in the
lecM
mutant. Thus, the QS‐dependent production of LecM contributes to the QS signalling pathway.