Resumen:
Biofilm formation plays an important role in bacterial
pathogenesis. In Streptococcus pneumoniae, it has been
demonstrated that biofilm development is associated with
nasopharyngeal carriage and otitis media pathogenesis. In the
present work, we studied the contribution of signal transduction
systems to biofilm development of S. pneumoniae. For this
purpose, we constructed knock-out mutants of the 14 twocomponent systems and the unique serine/threonine kinase (StkP)
and its cognate phosphatase (PhpP). Biofilm formation was
evaluated by crystal violet staining of cells growing statically in
polystyrene plates. The ritR and the ciaH mutants showed
significantly less biofilm formation than the wild-type strain. On
the other hand, the php mutant also showed decreased biofilm
formation, while the stkP mutant displayed a wild-type strain
phenotype. These results indicated that RitR, an orphan response
regulator involved in iron metabolism, and CiaH, a histidine kinase,
together with the phosphatase PhpP, are required for biofilm
development. Because it has been recently reported that PhpP can
interact with RitR and positively regulate ritR transcription, we
suggest a connection between PhpP, RitR and iron metabolism for
the control of biofilm development in S. Pneumoniae.