Staphylococcus aureus exhibits heterogeneous siderophore production within the vertebrate host

Siderophores, iron-scavenging small molecules, are fundamental to bacterial nutrient metal acquisition and enable pathogens to overcome challenges imposed by nutritional immunity. Multimodal imaging mass spectrometry allows visualization of host−pathogen iron competition, by mapping siderophores within infected tissue. We have observed heterogeneous distributions of Staphylococcus aureus siderophores across infectious foci, challenging the paradigm that the vertebrate host is a uniformly iron-depleted environment to invading microbes.

Siderophores, iron-scavenging small molecules, are fundamental to bacterial nutrient metal acquisition and enable pathogens to overcome challenges imposed by nutritional immunity. Multimodal imaging mass spectrometry allows visualization of host−pathogen iron competition, by mapping siderophores within infected tissue. We have observed heterogeneous distributions of Staphylococcus aureus siderophores across infectious foci, challenging the paradigm that the vertebrate host is a uniformly iron-depleted environment to invading microbes. siderophore | metallophore | mulitmodal molecular imaging | infectious disease | nutritional immunity M etals are required by organisms to carry out metabolic processes (1). During infection, host metalloproteins sequester nutrient metals to prevent microbial colonization, a process termed nutritional immunity (2,3). Bacteria have evolved sophisticated metal acquisition strategies, including the use of siderophores (4,5). Siderophores are secondary metabolites (<1 kDa) characterized by a high binding affinity for iron (Fe) (dissociation constant [K d ] > 10 −30 M) (5,6). Staphylococcus aureus is an opportunistic pathogen that utilizes siderophores for Fe acquisition, and siderophore production is required for maximum virulence (5,7).
One hallmark of S. aureus infection is the formation of tissue abscesses (8). Abscess architecture consists of staphylococcal abscess communities (SACs) segregated from host tissue by layers of necrotic and healthy innate immune cells (Fig. 1A) (9). In Fe-limiting environments, transcriptional repression of the S. aureus ferric uptake regulator (Fur) regulon is ceased, and bacteria increase expression of Fe acquisition machinery (5). Known mechanisms of staphylococcal Fe acquisition include heme uptake, inorganic Fe transport, and secretion of the siderophores staphyloferrin A (SA) and staphyloferrin B (SB) (10,11). Emerging literature suggests that abscesses exhibit molecular heterogeneity, and, therefore, SACs elaborate differential gene expression, questioning the spatial and temporal importance of siderophores (12). However, the distribution of bacterial siderophores within vertebrate tissue has not been visualized. We sought to revisit the paradigm that bacteria are uniformly Festarved during vertebrate colonization, by mapping siderophore distributions in infected tissues using high-performance matrixassisted laser desorption/ionization Fourier transform ion cyclotron resonance imaging mass spectrometry (MALDI FT-ICR IMS) (2,5,(12)(13)(14)(15)(16)(17)(18)(19).
Mice were infected with wild-type S. aureus, and tissue was harvested 7 d post infection (DPI) and frozen on dry ice (20). Tissues were sectioned serially for hematoxylin/eosin (H&E) staining, MALDI IMS, and 56 Fe analysis using laser ablationinductively coupled plasma (LA-ICP) IMS ( Fig. 1 A- (Fig. 1 B and C). Tentative molecular identifications are based on accurate mass measurements. The SA molecular assignment was validated by MALDI IMS of mice infected with a S. aureus mutant genetically inactivated for SA production (Δsfa) (21). Methods, supplemental information, and raw data can be found at https://doi.org/10.6084/ m9.figshare.9617633.v4.
Both siderophores localize to infection sites and expand beyond the perimeter of the SACs, highlighting the metabolic effort of S. aureus to acquire Fe ( Fig. 1 A-C). Differences in siderophore production can be observed across abscesses. Comparing the 2 siderophore distributions, SA has increased prevalence at most infection sites. However, some foci show higher relative abundances of SB, suggesting differential Fe starvation at these sites. Notably, little to no siderophore is detected within some abscesses. Attempts to detect ferric SA and ferric SB were unsuccessful. It is possible that the complex is not stable due to the high basicity of the MALDI matrix or does not survive the MALDI process. Alternatively, but less likely, ferric SA and ferric SB are present but at low abundance and not detectable. Fe is largely excluded from infection sites (Fig. 1D). However, some pixels show colocalization of Fe to SACs (Fig. 1D, arrows), presumably highlighting successful acquisition of the metal.
To further investigate host−pathogen Fe competition, heart, liver, and kidney lesions were compared using a multimodal approach integrating IMS, H&E staining, and fluorescence microscopy. Mice were infected with S. aureus P isdA gfp, where green fluorescent protein (GFP) expression is driven by the Furregulated isdA promoter (12). After 10 DPI, tissues presented with abscesses (Fig. 2). Fluorescence micrographs of GFP expression allow for a MALDI IMS-compatible technique to visualize SAC responses to host Fe sequestration (Fig. 2). Fig. 2 shows siderophores colocalizing with GFP expression. Comparing H&E stains to Fe distributions, some SACs colocalize with Fe, while others do not. This observation supports nutritional heterogeneity of SACs and suggests differential molecular responses. Siderophores are produced by S. aureus across necrotic abscesses in all tissues examined. In the heart abscess, SA extends beyond the abscess, highlighting SA diffusion (Fig. 2B). Siderophore distributions localize to GFP expression. Fe distributions within the liver and kidney lesions (Fig. 2 A and C) localize to GFP absence and lessened siderophore signals. These data highlight differential siderophore production across abscesses from liver, heart, and kidney tissues.
These results provide insight into staphylococcal metal acquisition during infection and emphasize the capabilities of IMS to investigate host−microbe interactions. While it is accepted that siderophores play a role in pathogenesis, it is less clear why bacteria produce multiple distinct siderophores. In addition to Fe, glucose represses SA production, and heme affects SB production (7,22,23). Furthermore, SA and SB differentially impact infection outcomes in murine models (5,7,21,22). These results suggest a niche-specific role for each siderophore, rather than functional redundancy. Differential distributions of these siderophores may be explained by molecular heterogeneity within the abscess. Use of spatial molecular technologies such as MALDI IMS reveals siderophore distributions in tissue, and, when combined with multimodality integration, enables an unprecedented view of the struggle for metal between host and pathogen. The ability to image bacterial metabolites within tissue has the potential to be broadly applicable to infection biology, microbiome studies, and clinical microbiology.