Linking Virulence and Iron Limitation Response in Staphylococcus aureus: The sRNA IsrR Is Involved in SaeRS Activation

The Gram-positive opportunistic pathogen Staphylococcus
aureus colonizes ∼30% of the human population
but also causes various diseases. Precise regulation of genes involved
in virulence and metabolic functions is required to adapt to changing
host conditions, such as severe restriction of iron availability.
In addition to the global regulator Fur (ferric uptake regulator),
the iron limitation response of S. aureus is shaped by the recently identified sRNA IsrR (iron sparing response
regulator). IsrR mediates an iron sparing response by inhibiting the
synthesis of nonessential iron-containing proteins, which are in particular
involved in the central metabolism. In addition, we demonstrate that isrR expression is positively associated with α-hemolysin
levels and the hemolysis activity of S. aureus HG001. To investigate the influence of IsrR on virulence factor
production, we performed a mass spectrometry-based secretome analysis
of isrR-expressing and nonexpressing strains under
iron-limited and iron-sufficient conditions. The SaeR regulon was
positively influenced by the presence of IsrR, and IsrR is likely
involved in the activation of the Sae system. Additionally, IsrR also
positively affected the protein levels of the isdABCDEFGH-encoded heme uptake system (e.g., IsdB). Taken together, IsrR establishes
a link between the iron limitation response and the virulence in S. aureus.