Heme-Dependent Siderophore Utilization Promotes Iron-Restricted Growth of the Staphylococcus aureus hemB Small-Colony

Izabela Z Batko1, Ronald S Flannagan1, Veronica Guariglia-Oropeza1

  • 1Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada.

Journal of Bacteriology
|October 4, 2021
PubMed

Insights

Staphylococcus aureus small-colony variants (SCVs) struggle to acquire iron. Hemin aids SCVs in utilizing iron, suggesting heme biosynthesis inhibition as an infection treatment strategy.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Biochemistry

Background:

  • Respiration-deficient Staphylococcus aureus small-colony variants (SCVs) are linked to persistent infections.
  • The iron acquisition mechanisms of SCVs remain poorly understood.
  • Iron is a critical nutrient for bacterial survival and virulence.

Purpose of the Study:

  • To investigate how S. aureus SCVs acquire iron.
  • To determine the role of heme biosynthesis in SCV iron metabolism.
  • To explore potential therapeutic strategies targeting SCV iron acquisition.

Main Methods:

  • Creation of a stable hemB mutant (SCV) of S. aureus USA300.
  • Growth assays under iron-limiting and iron-replete conditions.
  • Transcriptome sequencing (RNA-seq) to analyze gene expression.
  • Measurement of intracellular ATP levels.
  • In vivo murine infection models.

Main Results:

  • The hemB SCV mutant showed impaired growth under iron starvation but utilized exogenous hemin.
  • The hemB mutant exhibited defective siderophore-mediated iron acquisition.
  • Hemin availability promoted siderophore utilization by the hemB mutant, even under iron restriction.
  • In vivo studies confirmed hemin's role in supporting SCV growth and iron acquisition.

Conclusions:

  • Hemin serves as both an iron source and a facilitator of siderophore-iron complex utilization for S. aureus SCVs.
  • Perturbing heme biosynthesis or utilization could be a strategy to combat SCV infections.
  • Understanding SCV iron acquisition is crucial for developing effective treatments against persistent S. aureus infections.

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