Staphylococcus aureus RNAIII coordinately represses the synthesis of virulence factors and the transcription regulator Rot by an antisense mechanism

  1. Sandrine Boisset1,5,
  2. Thomas Geissmann2,5,
  3. Eric Huntzinger2,5,
  4. Pierre Fechter2,
  5. Nadia Bendridi1,
  6. Maria Possedko2,
  7. Clément Chevalier2,
  8. Anne Catherine Helfer2,
  9. Yvonne Benito1,
  10. Alain Jacquier3,
  11. Christine Gaspin4,
  12. François Vandenesch1, and
  13. Pascale Romby2,6
  1. 1 Institut National pour la Recherche Médicale (INSERM) E0230, Université Lyon 1, Centre National de Référence des Staphylocoques, Faculté Laennec, Lyon, F-69008, France;
  2. 2 Architecture et Réactivité de l’ARN, Université Louis Pasteur, Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Moléculaire et Cellulaire (IBMC), F-67084 Strasbourg, France;
  3. 3 Unité de Génétique des Interactions Macromoléculaires, URA 2171-Centre National de la Recherche Scientifique, Institut Pasteur, F-75724 Paris, France;
  4. 4 Unité de Biométrie et Intelligence Artificielle, Institut de National de la Recherche Agronomique (INRA)-UR875 Chemin de Borde-Rouge, F-31326 Castanet-Tolosan, France
  1. 5 These authors contributed equally to this work.

Abstract

RNAIII is the intracellular effector of the quorum-sensing system in Staphylococcus aureus. It is one of the largest regulatory RNAs (514 nucleotides long) that are known to control the expression of a large number of virulence genes. Here, we show that the 3′ domain of RNAIII coordinately represses at the post-transcriptional level, the expression of mRNAs that encode a class of virulence factors that act early in the infection process. We demonstrate that the 3′ domain acts primarily as an antisense RNA and rapidly anneals to these mRNAs, forming long RNA duplexes. The interaction between RNAIII and the mRNAs results in repression of translation initiation and triggers endoribonuclease III hydrolysis. These processes are followed by rapid depletion of the mRNA pool. In addition, we show that RNAIII and its 3′ domain mediate translational repression of rot mRNA through a limited number of base pairings involving two loop–loop interactions. Since Rot is a transcriptional regulatory protein, we proposed that RNAIII indirectly acts on many downstream genes, resulting in the activation of the synthesis of several exoproteins. These data emphasize the multitude of regulatory steps affected by RNAIII and its 3′ domain in establishing a network of S. aureus virulence factors.

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