Bacteria tracking by in vivomagnetic resonance imaging
- Verena Hoerr1,
- Lorena Tuchscherr2,
- Jana Hüve†3, 5,
- Nadine Nippe†4,
- Karin Loser4,
- Nataliya Glyvuk5,
- Yaroslav Tsytsyura5,
- Michael Holtkamp6,
- Cord Sunderkötter4,
- Uwe Karst6,
- Jürgen Klingauf3, 5,
- Georg Peters2,
- Bettina Löffler2 and
- Cornelius Faber1Email author
© Hoerr et al.; licensee BioMed Central Ltd. 2013
Received: 1 February 2013
Accepted: 22 May 2013
Published: 28 May 2013
Different non-invasive real-time imaging techniques have been developed over the last decades to study bacterial pathogenic mechanisms in mouse models by following infections over a time course. In vivo investigations of bacterial infections previously relied mostly on bioluminescence imaging (BLI), which is able to localize metabolically active bacteria, but provides no data on the status of the involved organs in the infected host organism. In this study we established an in vivo imaging platform by magnetic resonance imaging (MRI) for tracking bacteria in mouse models of infection to study infection biology of clinically relevant bacteria.
We have developed a method to label Gram-positive and Gram-negative bacteria with iron oxide nano particles and detected and pursued these with MRI. The key step for successful labeling was to manipulate the bacterial surface charge by producing electro-competent cells enabling charge interactions between the iron particles and the cell wall. Different particle sizes and coatings were tested for their ability to attach to the cell wall and possible labeling mechanisms were elaborated by comparing Gram-positive and -negative bacterial characteristics. With 5-nm citrate-coated particles an iron load of 0.015 ± 0.002 pg Fe/bacterial cell was achieved for Staphylococcus aureus. In both a subcutaneous and a systemic infection model induced by iron-labeled S. aureus bacteria, high resolution MR images allowed for bacterial tracking and provided information on the morphology of organs and the inflammatory response.
Labeled with iron oxide particles, in vivo detection of small S. aureus colonies in infection models is feasible by MRI and provides a versatile tool to follow bacterial infections in vivo. The established cell labeling strategy can easily be transferred to other bacterial species and thus provides a conceptual advance in the field of molecular MRI.
KeywordsBacterial cell labeling Bacteria tracking Infectious diseases Mouse models of infection Cellular and molecular MRI
Bacterial infections remain one of the major challenges to human societies around the world. In particular, the emergence of multiple antibiotic resistant bacteria, which are difficult to treat and which can spread locally and systemically in different organs within the infected host, requires novel approaches for rapid diagnosis and efficient treatment [1–3]. Also, a deeper understanding of pathogen biology as well as of the complex host-pathogen interactions between bacteria and host tissues are urgently required to improve antimicrobial strategies. Staphylococcus aureus is a clinically highly relevant human pathogen, which has the potential to infect almost every organ leading to a number of diverse infections , such as skin and wound infections, pneumonia, endocarditis and osteomyelitis [5, 6]. S. aureus induces a strong immune response either via a plethora of toxins and superantigens , complement activation, or by activation of the inflammasome and the related sterile injury danger signal pathways. Yet, the dynamics of dissemination and the exact bacterial strategies to establish metastasizing infections in different organs are largely unknown.
For research on dissemination dynamics in the entire host organism, murine models of bacterial infections are pivotal. Non-invasive in vivo imaging techniques, such as magnetic resonance imaging (MRI), computed tomography (CT), fluorescence/bioluminescence imaging (BLI) or positron emission tomography (PET), have been employed to visualize infections over the time course [8–12]. Although different strategies for specific detection of bacteria have been developed [13–15], most imaging studies target host factors  or detect immune cells . Due to its high spatial resolution and excellent soft tissue contrast, especially MRI is a versatile method to image inflammatory processes upon bacterial infections non-invasively. While native MRI provides diagnostic information on tissue structures and the inflammatory status , detection of distinct cellular populations requires labeling with a suitable contrast agent, such as iron oxide particles [19, 20]. Cell labeling and tracking experiments are commonly performed either by labeling immune cells in vitro and regrafting them or by systemic application of iron oxide particles which are then phagocytosed by macrophages . By using negative iron contrast immunological reactions and bacteria-induced inflammatory dissemination have already been investigated in animal models of Staphylococcus aureus[22–26], Toxoplasma gondii, Mycobacterium tuberculosis or LPS-induced sepsis conditions [29, 30]. However, only BLI so far was capable of visualizing bacteria directly. This technique exploits detection of light emitted from luminescent proteins in transgenic and metabolically active bacteria. Owing to this unique property, BLI has become the most important and wide spread modality of detecting bacteria in vivo. Here, we propose a complementary imaging modality based on MRI that requires the application of pre-treated bacteria, but which is also suitable for metabolically inactive or anaerobic pathogens and which provides detailed information about the bacterial localization in tissue. While native MRI provides diagnostic information on tissue structures and the inflammatory status, detection of distinct cellular populations requires labeling with a suitable contrast agent. We have used bimodal iron oxide nano particles (IONPs) to detect bacteria and have monitored dissemination in mouse models of local and systemic S. aureus infection. While for eukaryotic cells a variety of labeling protocols for cell imaging have been established, bacteria require specific labeling procedures that account for the presence of the bacterial cell wall. We have implemented a protocol that affords stable labeling of S. aureus cells with rhodamine-labeled 5-nm citrate-coated IONPs.
Results and discussion
Larger particles or particles with other surface properties did not result in a homogeneous labeling of the cells, as shown by fluorescence microscopy (Figure 1D, Additional file 1). All studied 100-nm IONPs, independent from coating and surface charge, formed large particle aggregates which were attached to sporadic cells (see Additional file 1). When electro-competent S. aureus bacteria were incubated with 5-nm particles, only particles with citrate-coating led to a uniform iron labeling, while amine-coated particles labeled the cell suspension very inhomogeneously and resulted in scattered red fluorescent bacteria (Figure 1C, D). In contrast, for Gram-negative E. coli bacteria good labeling results were achieved both for citrate- and amine-coated IONPs leading to a labeling efficiency of 0.024 ± 0.003 pg/cell and 0.060 ± 0.004 pg/cell respectively (see Additional file 2).
It is known that electro-competent cells have a weakened cell wall with pores in the structure [36, 37] and a much more homogeneous distribution of positively and negatively charged ions on the peptidoglycan matrix, providing an enlarged surface for interactions between charged iron particles and the cell wall. In Gram-positive S. aureus bacteria the cell wall mainly consists of a thick peptidoglycan layer giving rise to a positive net charge which may explain the high labeling efficiency when citrate-coated iron particles were used. In contrast, in Gram-negative E. coli bacteria the negatively charged lipopolysaccharide outer membrane leaf , which envelopes the cell, may explain the good labeling results for amine-coated IONPs.
Most iron oxide particles have the formula Fe23+O3Fe2+O, embedding the bi- and trivalent iron ions in a crystalline structure, which is chemically protected by molecular coatings. In our labeling procedure the iron particles are attached to the cell wall instead of being incorporated by the bacteria. This approach avoids bactericidal iron ions entering the bacteria, which may otherwise lead to toxic effects as described for iron complexes .
One of the most important types of immune cells recognizing invading bacteria in vivo, are macrophages. Therefore, we investigated in in vitro experiments whether bacteria carrying iron particles can still induce phagocytotic responses of macrophages. After adding iron-labeled bacteria to a suspension of murine macrophages, live microscopy showed that macrophages immediately started phagocytizing the labeled bacteria (Figure 2B, Additional file 3). These data show that iron labeling does not abrogate phagocytosis.
In vivomouse models
The particular strength of MRI for bacterial detection lies in its independence from metabolic activity and oxygenic environment, making it possible to also follow intracellular metabolically inactive S. aureus, such as the clinically highly relevant small colony variants [43, 44]. For many bacterial pathogens and particularly for S. aureus, the intracellular persistence is increasingly recognized as an important infection and immune evasion strategy that causes chronic and therapy-refractory infections . It has been demonstrated that S. aureus can invade and survive in different cell types, including professional phagocytes . The use of iron labeled bacteria allowed us to track the surviving bacterial population in macrophages. Iron of digested bacteria is also distributed by immune cells over the time course, but these give rise to a different MRI pattern. Macrophage labeling by i.v. injection of IONPs 2 h and 5 h post infection resulted in a circumferential dark pattern at the border of the inflammation (Figure 4C) without clear hypointensities that indicated bacterial colonies. Histologically, large, not circumscribed areas of distributed iron were detected in zones of intense macrophage invasion (Figure 4P, Q). By contrast, after infection with iron labeled bacteria only sparely distributed single macrophages were labeled with Prussian blue (Figure 4R).
In conclusion, we have established a novel modality for in vivo detection and tracking of bacteria, which is complementary to BLI. With the application of pre-labeled bacteria, the method is limited to use in animal models, as is BLI. The great advantage of MRI is the simultaneous imaging of morphology, organ compartments and immune response together with the data on bacterial tracking. Additionally, MRI detection is also applicable to metabolically less active as well as anaerobic bacteria and not subject to limited penetration depth. Therefore, we are confident that this modality greatly enhances the diagnostic and analytical options in fundamental and translational research on bacterial infections.
Bacteria and growth conditions
Experiments were performed with the two S. aureus bacterial strains, 6850 (ATCC 53657)  and SH1000  which is a derivate of strain 8325–4 with restored rsbUþ-gene. As a Gram-negative strain E. coli K12 was used.
Bacteria were cultured in Mueller-Hinton (MH, S. aureus) or Luria Bertani (LB, E. coli) medium overnight at 37°C with shaking at 160 rpm and were subsequently used to prepare electro-competent cells or to perform in vitro assays.
The cell concentration was determined by measuring the OD578 (optical density at 578 nm) spectroscopically and by counting the colony forming units (CFU). A bacterial sample was serially diluted and a known volume was plated on blood agar. The bacterial concentration was obtained by counting the number of colonies that had formed.
Electro-competent S. aureus and E. coli bacteria were made according to the manufacturer’s protocol suggested for each microorganism  and were frozen in 10% glycerol in a concentration of 109 to 1010 cells/ml.
To label bacteria, either electro-competent or naïve cells were used. A total of 50 μl of the cell suspension was incubated with 2 μl of iron oxide particles in 950 μl MH or LB medium for 1 h at 37°C and 160 rpm. The following IONPs were used: VSOP-rhodamine 5 nm and VSOP-link-rhodamine 5 nm (Very Small Iron Oxide Particles, both Ferropharm AG, Teltow, Germany), screenMAG 100 nm (diethylamine ethyl, phosphatidyl-cholin and poly(maleic acid-co-olefin), polysaccharide, all Chemicell, Berlin, Germany). VSOP particles consist of a 5 nm maghemit core and hold an iron concentration of approximately 2.2 × 10-19 g/per particle. Prior to use, cell suspensions were centrifuged at 5,000 rpm for 10 minutes to remove culture media as well as excessive IONPs and pellets were washed once with phosphate-buffered saline (PBS) and were resuspended in PBS. Labeling efficiency was visualized by fluorescence microscopy and bacteria were additionally labeled with Syto 9 (Invitrogen, Darmstadt, Germany) for co-registration according to molecular probes standard protocols.
Lysostaphin protection assay
The invasiveness of S. aureus with or without iron labeling in endothelial cells was performed by lysostaphin protection assay. Two days prior to the assay 1 ml HUVEC (2 × 105 cells/ml) was plated in 12-well plates in M199 medium (PAA Laboratories GmbH, Cölbe, Germany) and was stimulated with live bacteria. Bacteria from frozen stock suspensions were washed once with PBS and adjusted to a cell concentration of 5 × 108 cells/ml in MH medium and were incubated for 1 h at 37°C and 160 rpm. When the assay was performed with iron-labeled bacteria, freshly prepared cultures according to the labeling protocol were used directly. Bacteria were harvested, washed once and resuspended in PBS. A total of 100 μl of the bacterial suspensions were added to each well. After an invasion period of 3 h, HUVEC were washed with PBS, the culture medium was replaced by M199 plus 10% FCS (fetal calf serum) and the HUVEC were incubated with lysostaphin (20 μg/ml) for 30 minutes at 37°C in order to remove extracellular staphylococci. The cells were washed with PBS and intracellular bacteria were released by incubation in 1 ml of H2O for 30 minutes at 37°C. Samples were diluted in PBS and plated on blood agar plates to determine the number of recovered CFUs. The assay was performed with a positive (Cowan I) and a negative control (TM300). The invasiveness of the laboratory strain Cowan I was set as 100%.
Cell death assays
Analysis of cell death was performed by measuring the proportion of hypodiploid nuclei as described in Haslinger-Löffler et al. . Briefly, HUVEC plated in 12-well plates were incubated for 3 h with 20 μl of 5 × 108 CFU/ml S. aureus bacteria per well. Incubation with lysostaphin for 30 minutes followed. After the removal of extracellular staphylococci, HUVEC were washed with PBS and full medium was added. After 20 h the cell death was determined and cells were stained with the DNA-dye propidium iodide and analyzed with a FACS Calibur flow cytometer (Becton Dickinson, Heidelberg, Germany).
Growth curve assay
In a 500 ml flask, 50 ml of bacterial staphylococcal cell suspension with an initial cell concentration of OD 0.5 was incubated for 7 h at 37°C and 160 rpm in MH medium. Every hour a sample was taken to measure OD and CFU counts/ml.
Bacteria recovered from infected tissue
Approximately 0.1 g infected skin tissue was collected and homogenized in 2 ml PBS. An aliquot of 100 μl was plated on blood agar over night and the CFUs harvested and suspended in 1 ml PBS. The iron concentration of the cell suspension was subsequently measured by atomic spectrometry. To determine the iron concentration per cell the measured iron content was corrected by an iron baseline. Since iron is an important nutrient in agar plates, it is taken up during cell growth. As a baseline a defined number of S. aureus bacteria were cultured on blood agar plates, harvested, suspended in 1 ml PBS and measured by atomic spectrometry.
The number of iron labeled bacteria in infected tissue was determined with the aid of magnetic separation. For this purpose, 1 ml tissue sample was placed in a magnetic field for five minutes, washed twice with PBS, diluted with 1 ml PBS and plated for CFU count. CFU counts of iron-labeled and unlabeled bacteria were analyzed by a Mann–Whitney-Test.
Labeled bacteria suspensions were added with 0.1% agarose and sealed by a second coverslip. Fluorescence images were obtained with a commercial 4Pi microscope (TCS 4Pi microscope type A, Leica Microsystems GmbH, Wetzlar, Germany) employing oil immersion lenses (×100, numerical aperture 1.46). The TCS 4Pi is a confocal laser scanning microscope of type TCS SP2 incorporating single as well as two-photon excitation, photon-counting by avalanche photodiodes, and a 4Pi attachment. Because of these features the microscope could be employed in the confocal mode with upright or inverted beam path and single- or two-photon excitation, or as a two-photon excitation 4Pi microscope. The images were taken in the confocal mode of the microscope. Due to the spherical shape of the S. aureus bacteria the 4Pi mode brings no significant gain in resolution. In a 4Pi image, every pixel has attached an interference function in z direction. If we take a picture of a sphere, these functions strongly overlap and cause blurring. Single-photon excitation wavelengths of 476 and 561 nm was used, yielding best case resolutions of 166 nm and 196 nm, respectively, in both x and y direction. The beam expander was set to 6. Fluorescence originating from the sample was passed through a filter cube (short-pass 700 nm, beam splitter 560 nm, band-pass 500 to 550 nm, and band-pass 607 to 683 nm), and its intensity was measured by photon-counting avalanche photodiodes (PerkinElmer, Waltham, MA, USA). The detection pinhole was set to 1 Airy unit. Images of the cells were recorded with a pixel size between 12 × 12 nm2 and 42 × 42 nm2. Raw images were linearly brightened, rescaled and linearly filtered by a subresolution mask using the image processing program ImageJ (Wayne Rasband, US National Institutes of Health, ).
Live cell microscopy
Bone marrow-derived macrophages (BMDMs) were differentiated in vitro from bone marrow as previously described . BMDMs were transferred to fibronectin-coated LabTek chamber slides and incubated for at least 12 h to achieve adherence. After that, live bacteria were added (MOI 50) and life cell imaging was performed using an inverted fluorescence microscope (Zeizz Axio Observer Z1; Carl Zeiss MicroImaging GmbH, Jena, Germany; 40× objective magnification).
For histopathology, cryo and paraffin sections of lymph node and skin tissue were prepared and Gram-positive bacteria were stained with crystal violet/iodine and Prussian blue according to standard protocols. Macrophages were stained with hematoxylin and eosin. Bacteria and macrophages were visualized using a light microscope (Zeiss Axioskop, Goettingen, Germany; 100×, 40×, 20× 10× objective magnification).
For immunohistology, paraffin embedded sections of infected skin tissue (5 μm) were prepared on slides and blocked with 2% BSA. Macrophages and S. aureus bacteria were stained according to standard protocols using an appropriate dilution of a monoclonal rat anti-mouse F4/80 antibody (clone BM8, purchased from Biolegend, Fell, Germany) or a polyclonal rabbit anti-S. aureus IgG (Abcam, Cambridge, UK) followed by incubation with AlexaFluor 568-conjugated anti-rat and AlexaFluor 488-conjugated anti-rabbit secondary antibodies (both purchased from Invitrogen, Karlsruhe, Germany). Nuclei were counterstained using 0.1 μg/ml 4′,6-diamidino-2-phenylindole (DAPI). Macrophages and S. aureus bacteria were visualized by fluorescence microscopy using an Olympus BX63 microscope and the CellSens Software (Olympus, Münster, Germany). Immunofluorescence staining is depicted in an original magnification of 100×.
Mice were sacrificed and intravenously perfused with modified Karnovsky’s fixative consisting of 2.5% glutaraldehyde, 2% paraformaldehyde in PBS. After fixation of the infected organ or tissue, samples were dissected and placed in fresh fixative and kept overnight at 4°C. Subsequently, tissue was washed three times with 0.1 M cacodylat buffer for 5 to 10 minutes, cut into pieces ≤1 mm and post-fixed with 2% osmium tetroxide at room temperature for 1 h. The samples were extensively washed with 0.1 M cacodylat buffer and stained with 1.5% uranyl acetate for 1 h during dehydration in an ethanol series. In the last dehydration step after pure ethanol pure acetone was used. Tissue samples were then embedded in Epon 812. Ultrathin sections (<60 nm) were collected on Formvar coated copper grids and viewed with a Phillips CM 10 or Zeiss Libra 120 (Zeiss, Oberkochen, Germany) electron microscope.
Iron-labeled bacteria samples were embedded in 1% agarose and then fixed for more than 24 h using the same fixative as for the animal tissues. Subsequent preparation steps were performed as described above.
In case of iron enhancement so called Perl’s reaction was used in between the primary fixation of the samples with aldehyde mixture and post-fixation with osmium. The procedure was performed as described in Parmley et al. .
Gallium standard solution (c = 1.000 mg/l) in the highest quality available was purchased from Fluka Chemie GmbH (Buchs, Switzerland). Total reflection X-ray fluorescence analysis (TXRF) was carried out on a S2-PICOFOX instrument (Bruker AXS, Berlin, Germany) with an air-cooled molybdenum anode for X-ray generation. The excitation settings were 50 kV and 750 mA and quartz glass disks were used as sample carriers. As internal standard, gallium with a concentration of 10 mg/l was applied. Aliquots of the samples were mixed with the same volume of the 10 mg/l gallium standard solution, placed on the sample carriers and evaporated to dryness. The analysis was performed by signal integration over 1.000 seconds. For the determination, the peaks of iron (Kα1 = 6.3921 keV) and gallium (Kα1 = 9.251 keV), as internal standard, were used. Quantification was performed by the Bruker Spectra software (version 126.96.36.199) and based on the known concentration of the internal gallium standard.
Magnetic resonance imaging (MRI)
Images were acquired at 9.4 T on a Bruker BioSpec 94/20 (Ettlingen, Germany).
In vivo measurements
The subcutaneous lesions of infected mice were measured with a 1 T/m gradient system and a 35 mm volume coil using FLASH and UTE sequences with the following parameters (FLASH: TR: 1,500 ms, TE: 6 ms, FA: 30°, FOV: 3.20 × 3.20 cm, MTX: 256 × 256; UTE: TR: 100 ms, TE: 314 μs, FA: 20 deg, FOV: 3.20 × 3.20 cm, MTX: 256 × 256). For lymph node imaging a 0.7 T/m gradient system and a surface coil was used and images were acquired by a TurboRARE sequence (TR: 4.5 ms, TE: 9.3 μs, FOV: 4.50 × 2.50 cm, MTX: 512 × 312).
In vitro measurements
A total of 500 μl of iron-labeled S. aureus suspensions in a concentration of OD 0.5 were washed with PBS and suspended in 500 μl of a 0.5% agarose solution. T1 and T2 measurements were performed using a 0.7 T/m gradient system and a 72 mm volume coil by using the following pulse sequences: RAREVTR: TE: 10 ms, 30 ms, 50 ms, 70 ms, 90 ms, 110 ms, 130 ms; TR: 5,500 ms, 3,000 ms, 1,500 ms, 800 ms, 400 ms, 200 ms; average: 1; slice thickness: 1.5 mm; MTX: 128 × 128; RARE factor: 2; FOV: 23 mm × 40 mm. MSME: TE: 11 ms, 22 ms, 33 ms, 44 ms, 55 ms, 66 ms, 77 ms, 88 ms, 99 ms, 110 ms, 121 ms, 132 ms, 143 ms, 154 ms, 165 ms, 176 ms, 187 ms, 198 ms, 209 ms, 220 ms, 231 ms, 242 ms, 253 ms, 264 ms, 275 ms, 286 ms, 297 ms, 308 ms, 319 ms, 330 ms; TR: 2,500 ms; average: 1; slice thickness: 1.5 mm; MTX: 256 × 256; FOV: 23 mm × 40 mm.
Female C57BL/6 wild-type mice 8- to 12-weeks old were purchased from Harlan-Winkelmann (Borchen, Germany) and kept one week at the animal facility of the Translational Research Imaging Center, Muenster, Germany, before the beginning of the experiments. All animal studies were performed with the approval of the State Review Board of North Rhine-Westphalia, Germany (TVA-Nr. 87–51.04.2001.A003, TVA-Nr. 8.87-50.10.36.08.194).
The infection was induced in the left flank of C57BL/6 mice by subcutaneous injection of 100 μl of either iron-labeled or unlabeled S. aureus suspensions (1 × 108 CFU/ml in PBS). N = 6 mice were used to assess the fraction of iron-labeled bacteria 24 h post infection.
Systemic lymph node infection
Mice were inoculated subcutaneously with 2 × 107 CFU of iron-labeled or unlabeled S. aureus bacteria, by injecting 50 μl of the cell suspensions (4 × 108 cells/ml in PBS) into the left hind footpad as described previously by Nippe et al. . Control animals injected with the same amount of PBS or PBS-based iron suspension showed no significant swelling reaction. For each group of infected mice four or five mice were used. Footpad swelling was measured daily with a micrometric caliper, and specific footpad swelling was assessed by subtracting the diameter of injected (left) from non-injected (right) footpad. Lymph node swelling and bacterial distribution was observed by MRI. Mice were sacrificed by CO2 asphyxiation after the MRI measurements and lymph nodes were either used for histology, electron microscopy or CFU counts. Colonies were counted after incubation of homogenized tissue overnight at 37°C.
Two hours and five hours post infection, mice were injected i.v. with 100 μl of 5-nm IONP (VSOP, Ferropharm AG, Teltow, Germany) suspensions (300 μmol/kg body weight).
Bone marrow-derived macrophages
Colony forming unit
Fetal Calf Serum
Fast Low-Angle Shot
Field of view
Human Umbilical Vascular Endothelial Cell
Iron oxide nano particle
Magnetic resonance imaging
Multi Slice Multi Echo
Phosphate buffered saline
Positron emission tomography
Rapid Acquisition with Refocused Echoes
Total reflection X-ray Fluorescence
Longitudinal relaxation time
Transverse relaxation time
Ultra-short echo time.
This work was supported by the German Research Foundation (SFB TR34, Z3 and C12 projects; SFB 1009, Z2 project), the interdisciplinary center for clinical research (IZKF) Münster (core unit SAMRI and project Löf2/030/10), the Bundesministerium für Bildung und Forschung (SkinStaph 01Kl1009A) and the Cells in Motion (CiM) Cluster of Excellence. The authors thank Brigitte Schuhen, Katrin Broschwig, Florian Breuer, Daniela Jeising und Kornelia Parusel for technical support.
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