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Updated: Oct 18, 2025

Staphylococcus aureus Growth using Human Hemoglobin as an Iron Source
Published on: February 7, 2013
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.
Abstract:
Respiration-deficient Staphylococcus aureus small-colony variants (SCVs) frequently cause persistent infections, which necessitates they acquire iron, yet how SCVs obtain iron remains unknown. To address this, we created a stable hemB mutant from S. aureus USA300 strain LAC. The hemB SCV utilized exogenously supplied hemin but was attenuated for growth under conditions of iron starvation. Transcriptome sequencing (RNA-seq) showed that both wild-type (WT) S. aureus and the hemB mutant sense and respond to iron starvation; however, growth assays show that the hemB mutant is defective for siderophore-mediated iron acquisition. Indeed, the hemB SCV demonstrated limited utilization of endogenous staphyloferrin B or exogenously provided staphyloferrin A, deferoxamine mesylate (Desferal), and epinephrine. Direct measurement of intracellular ATP in hemB and WT S. aureus revealed that both strains can generate comparable levels of ATP during exponential growth, suggesting defects in ATP production cannot account for the inability to efficiently utilize siderophores. Defective siderophore utilization by hemB bacteria was also evident in vivo, as administration of Desferal failed to promote hemB bacterial growth in every organ analyzed except for the kidneys. In support of the hypothesis that S. aureus accesses heme in kidney abscesses, in vitro analyses revealed that increased hemin availability enables hemB bacteria to utilize siderophores for growth when iron availability is restricted. Taken together, our data support the conclusion that hemin is used not only as an iron source itself but also as a nutrient that promotes utilization of siderophore-iron complexes. IMPORTANCE S. aureus small-colony variants (SCVs) are associated with chronic recurrent infection and worsened clinical outcome. SCVs persist within the host despite administration of antibiotics. This study yields insight into how S. aureus SCVs acquire iron, which during infection of a host is a difficult-to-acquire metal nutrient. Under hemin-limited conditions, hemB S. aureus is impaired for siderophore-dependent growth, and in agreement, murine infection indicates that hemin-deficient SCVs meet their nutritional requirement for iron through utilization of hemin. Importantly, we demonstrate that hemB SCVs rely upon hemin as a nutrient to promote siderophore utilization. Therefore, perturbation of heme biosynthesis and/or utilization represents a viable to strategy to mitigate the ability of SCV bacteria to acquire siderophore-bound iron during infection.
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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