Macrophages release iron into the bloodstream via a membrane-bound iron export protein, ferroportin (FPN). The hepatic iron-regulatory hormone hepcidin controls FPN internalization and degradation in response to bacterial infection. Salmonella typhimurium can invade macrophages and proliferate in the Salmonella-containing vacuole (SCV). Hepcidin is reported to increase the mortality of Salmonella-infected animals by increasing the bacterial load in macrophages. Here we assess the iron levels and find that hepcidin increases iron content in the cytosol but decreases it in the SCV through FPN on the SCV membrane. Loss-of-FPN from the SCV via the action of hepcidin impairs the generation of bactericidal reactive oxygen species (ROS) as the iron content decreases. We conclude that FPN is required to provide sufficient iron to the SCV, where iron serves as a cofactor for the generation of antimicrobial ROS rather than as a nutrient for Salmonella.
In response to infection, mammalian hosts deploy a strategy to withhold iron, an essential trace element for bacterial proliferation1. This process is a central component of innate nutritional immunity controlled by the master iron regulatory hormone hepcidin, which is synthesized primarily in the liver in response to interleukin-6 (IL-6) signaling upon bacterial infection2,3. Hepcidin promotes the degradation of its receptor, the sole known cellular iron exporter ferroportin (FPN), resulting in iron retention by macrophages and reduction of intestinal iron absorption2. This mechanism decreases the serum iron content to about 30% of its normal level, a physiological change known as hypoferremia of infection4, which limits iron availability for extracellular bacteria but also leads to increased iron storage in macrophages of the liver and spleen. Previously, we reported that induction of hepcidin and eventual hypoferremia upon Salmonella infection was mediated by estrogen-related receptor (ERR)γ5. An inverse agonist of ERRγ (GSK5182) ameliorated Salmonella-mediated hypoferremia through reduction of hepcidin expression. Treatment of mice infected with Salmonella with GSK5182 resulted in an ~30% decrease of iron in hepatic macrophages and a 50–100-fold decrease in bacterial cell numbers in the liver and spleen, resulting in increased survival of the mice. This was interpreted as a typical representation of innate nutritional immunity, under the assumption that the iron status in the vacuoles in which Salmonella reside (SCV)6 would be the same as in the macrophage cytosol.
In this study, we used a reporter system to assess iron and reactive oxygen species (ROS) levels in the SCV, and demonstrated that hepcidin affected ROS generation in macrophages by modulating iron levels in the SCV. This effect was dependent on the presence of FPN in the SCV.
FPN associates with the SCV membrane in absence of hepcidin
Salmonella enters epithelial cells and macrophages by micropinocytosis and resides in unique membrane-bound compartments SCV6. Raw264.7 cells were pretreated with FeSO4 to induce FPN expression7 or with hepcidin to induce FPN degradation3 and then infected with Salmonella for 2 h (Fig. 1a). Confocal microscopy confirmed an increase in FPN with FeSO4 treatment and a reduction in FPN with hepcidin treatment. Salmonella were located immediately adjacent to FPN in cells treated with FeSO4, suggesting that FPN is associated with the SCV (see merged images). FPN remained with the SCV even at 12 h after infection in cells treated with FeSO4 (Supplementary Fig. 1). To further verify the above observation, SCV were isolated from phagocytic cells using magnetized bacteria8. Raw264.7 cells were pretreated with hepcidin, and then infected with Salmonella coated with magnetite nanoparticles, which does not alter total FPN levels in the cell (Supplementary Fig. 2). At 2 h post infection (p.i.), the cells were fractionated, and SCV containing magnetized Salmonella were separated on a magnet. Initially, we analyzed the SCV fraction and the supernatant for the expression of the macrophage specific membrane marker, F4/809, and observed that it was only detected in the supernatant fraction, suggesting that the isolated SCV was free of most membrane components (Supplementary Fig. 3). We next probed the SCV for the presence of FPN and Salmonella by confocal microscopy using specific antibodies (Fig. 1b). FPN was detected only in the SCV isolated from PBS-treated cells, most of which appeared to encapsulate Salmonella. Without hepcidin treatment, FPN was detected by western blotting in the supernatant containing cellular debris and in the SCV fraction (Fig. 1c). When cells were pretreated with hepcidin, FPN was not detected in either fraction. Rab5 and MHC I, which are associated with SCV, as well as with the plasma membrane10,11,12, were detected in both fractions regardless of hepcidin treatment. Plasma membrane-bound annexin V13 was observed only in the supernatant fraction. These findings suggested that FPN is localized at or close to the SCV. To compare the effect of hepcidin before and after infection, Raw264.7 cells were infected with Salmonella for 1 h and then treated with hepcidin for an additional 1 h. The fractions obtained from the samples post-treated with hepcidin showed FPN in the SCV but not in the cell membrane fraction contrasting the data obtained in hepcidin pretreated samples. Of note, hepcidin could not cross the plasma membrane to act on FPN in the SCV (Fig. 1d).
SCV undergo modifications directed by proteins encoded by Salmonella Pathogenicity Islands (SPIs). Initially, the SCV associates with markers of early endosomes, such as early embryonic antigen (EEA)1, the transferrin receptor, and Rab5. This is later followed by acquisition of other lysosomal markers, such as lysosome-associated membrane protein (LAMP)1. Thus, we attempted to localize FPN during SCV maturation with these markers using HeLa cells expressing a FPN-GFP fusion protein. HeLa cells were transfected with the fpn-gfp fusion gene construct, and GFP expression was compared with that probed by specific anti-FPN antibody by confocal microscopy. Images of FPN-GFP showed a similar pattern of fluorescence as the images obtained with an anti-FPN antibody, suggesting that the GFP signal represented subcellular FPN localization (Fig. 2a). HeLa cells expressing FPN-GFP were next treated with hepcidin, and the GFP signal was evaluated by live cell imaging (Fig. 2b). Notably, the GFP signal at the cell membrane decreased in a time-dependent manner, and was almost completely abolished by 100–180 min. A GFP signal in the cytosol would represent FPN being processed through the endoplasmic reticulum and the golgi apparatus for transportation to the plasma membrane. We therefore evaluated the co-localization of FPN with EEA1 and Rab5, early SCV markers, and LAMP1, a later SCV marker. FPN-GFP localized immediately adjacent to EEA1 and Rab5 at 1 h p.i. and with LAMP1 at 12 h p.i., as observed by confocal microscopy (Fig. 2c). These were in marked contrast to the images of Salmonella-infected HeLa cells expressing GFP or uninfected HeLa cells expressing FPN-GFP (Supplementary Fig. 4), where GFP signals were not found near the SCV-associated markers. Therefore, it appeared that FPN is associated with the SCV at all stages of maturation.
FPN acts as an iron transporter in the SCV membrane
We then investigated the role of FPN on the physiology of Salmonella within SCV with respect to iron availability. As direct measurement of iron content in the SCV is virtually impossible, a biosensor was utilized. The tandem iroN iroBCDE gene cluster on the Salmonella chromosome is involved in the uptake of catecholate-type siderophore compounds14. These genes are highly induced under iron-limited growth conditions and repressed under iron sufficiency by binding of the Ferric Uptake Regulator (Fur)-Fe2+ repressor complex to operator sites in the cognate promoter region (data not shown). The expression of these genes, therefore, corresponds to changes in the number of iron atoms per bacterial cell. We took advantage of this iron responsiveness to assess iron conditions within the SCV. First, the iron responsiveness of the iroB promoter (iroBp) was verified using Salmonella carrying a reporter plasmid (iroBp fused to lacZ) (Supplementary Fig. 5A). To measure the activity of this promoter in intra-macrophage Salmonella, another gene reporter system was constructed using the unstable GFP variant gfpOVA15. The gfpOVA was cloned downstream of iroBp on a pSC101-based plasmid16 that was introduced into Salmonella. Salmonella expressing gfpOVA were used to monitor iroBp activity with or without an iron chelator by determining the fraction of GFP+ Salmonella (Fig. 3a). Quantification of the proportion of GFP+ Salmonella revealed that iron chelation increased iroBp activity about 20-fold (Supplementary Fig. 5B). The expression of the iroB gene transcript was quantified by qPCR and was also found to increase ~20-fold (Supplementary Fig. 5C). It is noteworthy that the expression of iroB was unaltered in response to other environmental changes such as magnesium concentration or pH shift (Supplementary Fig. 6). Taken together, these data demonstrate that iroBp is iron-responsive and that the fluorescence of Salmonella carrying iroBp-gfpOVA accurately reflected the iroB mRNA expression in an iron level-dependent manner. To determine the critical iron concentration for the modulation of iroB expression, Salmonella were grown in RPMI 1640, a chemically defined medium containing undetectable amounts of iron, supplemented with defined concentrations of FeSO4 (0.005–500 μM), and the iroBp activity was measured (Fig. 3b, c). Of note, Salmonella growth in the presence of increasing amounts of FeSO4 was indistinguishable, as reported previously (Fig. 3b)17. Fluorescence from iroBp-gfpOVA was repressed at iron concentrations between 0.5 and 5 μM in a concentration-dependent manner (Fig. 3c). The level of iroB mRNA determined by qPCR showed the same results (Supplementary Fig. 7). These data demonstrate that the iroBp-gfpOVA construct functioned accurately as an iron biosensor and that Salmonella could grow in the presence of minute (nM) concentrations of iron.
Hepcidin-induced degradation of FPN on the macrophage plasma membrane resulted in an ~30% increase in total cytosolic iron content (Supplementary Fig. 8). Changes in the iron level in the SCV in the presence or absence of FPN were assessed using Salmonella carrying the iroBp-gfpOVA biosensor. Raw264.7 cells cultured under iron overload conditions (0.1 mM FeSO4) or iron-depleted conditions 100 μM of the iron chelator deferoxamin (DFO)18 were infected with Salmonella (MOI, 100), and iroBp activity was determined at 1 h p.i. (Fig. 3d, e). The activity of iroBp, as determined by measuring the fraction of GFP+ Salmonella, increased in iron-depleted cells and decreased in iron-overloaded cells. Similar results were obtained when iroB mRNA levels were measured by qPCR (Supplementary Fig. 9). Most interestingly, depletion of FPN with hepcidin increased iroBp activity to the level observed in DFO-treated cells, suggesting that degradation of FPN reduced iron levels within the SCV in Raw264.7 cells. Upregulation of iroB with hepcidin was time-dependent, peaking at 2 h p.i. (Supplementary Fig. 10A). This indicates that FPN on the SCV acted as an iron transporter to move iron from the cytosol to the SCV, and depletion of FPN therefore resulted in iron-deficient conditions, leading to the activation of iroBp.
Finally, mice were infected with Salmonella carrying the iroBp-gfpOVA biosensor and treated with GSK5182, which abrogates hepcidin expression and consequently allows FPN to be maintained. The iroBp activity of the Salmonella in the splenic macrophages was determined 2.5 days p.i. (Fig. 3f, g). Quantification of GFP+ Salmonella (Fig. 3f) revealed that GSK5182 treatment repressed iroBp-gfpOVA expression by more than twofold (Fig. 3g). Downregulation of iroBp activity by GSK5182 treatment was confirmed by confocal microscopy, by counting the numbers of Salmonella (red) expressing GFP (green). Taken together, these data demonstrate that FPN on the SCV allows sufficient flow of iron into the SCV, resulting in downregulation of iroBp activity. By contrast, in the absence of FPN, the iron concentration in the SCV is reduced and iroBp activity is increased. FPN therefore acts as an iron transporter in the SCV membrane.
Decreased iron in the SCV impairs ROS-dependent killing
In the early stages of Salmonella infection, there is an abrupt increase in superoxide formation known as the oxidative burst, which is catalyzed by a NADPH oxidase enzyme complex, a prototypical hemoprotein complex with heme iron at the active site19,20,21,22. The superoxide is then converted to hydrogen peroxide, which is further converted to other highly reactive hydroxyl radicals by the iron-catalyzed Fenton reaction23,24. Since downregulation of hepcidin by GSK5182 in mice infected with Salmonella conferred on antimicrobial effect5, we investigated whether the hepcidin-FPN axis is involved in ROS generation in macrophages. Hallmarks of ROS-mediated cellular damage include protein carbonylation25 and lipid peroxidation26. These parameters were therefore assessed as means of evaluating ROS generation in the SCV. Raw264.7 cells pretreated with hepcidin or with DFO, which prevents ROS generation by inhibiting the Fenton reaction27, were infected with magnetized Salmonella, and SCV were isolated 1 h p.i. SCV proteins were separated by SDS-PAGE and probed for carbonylated moieties using specific antibodies (Fig. 4a). There was an ~20% reduction in carbonylated proteins in SCV fraction from hepcidin-treated cells and an approximately 35% reduction in DFO-treated cells. Levels of malondialdehyde (MDA), the most abundant aldehyde produced by lipid peroxidation, were also measured by thiobarbituric acid-reactive substances (TBARS) assay (Fig. 4b)26. Hepcidin and DFO reduced MDA levels similarly. These results suggest that hepcidin treatment inhibited ROS generation.
To further verify the effect of hepcidin on ROS generation, Salmonella carrying an episomal katGp-gfpOVA fusion were used as a ROS biosensor16. The katG promoter is activated by the transcription factor OxyR upon exposure to H2O2 in a concentration-dependent manner (Fig. 4c)16,28. Raw264.7 cells pretreated with DFO or hepcidin were subsequently infected, and katGp activity was evaluated at 1 h p.i. The katGp activity in macrophages was determined by quantifying the fraction of GFP+ Salmonella (Fig. 4d, e). Under DFO treatment, which results in low ROS generation, the fraction of GFP+ bacteria was lower than in macrophages treated with PBS. Of note, treatment with hepcidin, which reduces FPN on the SCV, as well as on the plasma membrane, also reduced katGp activity. Similar results were observed when katG mRNA was measured by qPCR (Supplementary Fig. 11). The repressive effect of hepcidin on katGp activity was time-dependent (Supplementary Fig. 10B). Next, mice were infected with Salmonella expressing katGp-gfpOVA and treated with GSK5182, and the fraction of bacteria in the spleen expressing GFP was determined 2.5 days p.i. Confocal microscopy further revealed that GSK5182 treatment, which allows the maintenance of FPN, resulted in an ~10-fold increase in GFP+ Salmonella (Fig. 4f, g). ROS generation by NADPH oxidase and the iron-catalyzed Fenton reaction is therefore modulated by hepcidin, which presumably limits the availability of the iron cofactor in the SCV by modulating the maintenance of FPN.
This model predicts that GSK5182 would not be effective in controlling Salmonella infection in mice deficient in nox2, which lack the gp91 component of NADPH oxidase, the main cellular source of ROS29. To test this hypothesis, wild-type (WT) and nox2−/− mice were orally infected with Salmonella (1 × 108) and treated with GSK5182 or PBS, and the survival of infected animals was determined. In contrast to WT mice, GSK5182 did not have any therapeutic effect in the nox2−/− mice; in fact, nox2−/− mice expired earlier than WT mice (Fig. 5a). The spleens of these mice were examined for FPN expression 2.5 days p.i. (Fig. 5b and Supplementary Fig. 12). FPN was expressed in the spleens of both WT and nox2−/− mice treated with GSK5182. Apparently, GSK5182 abrogated hepcidin activity and allowed FPN to be maintained in splenic macrophages5. The bacterial loads of Salmonella in the spleen were determined by counting colony forming units (Fig. 5c). Consistent with the survival data (Fig. 5a), the bacterial load in WT mice was about half of that in the nox2−/− mice. However, although GSK5182 reduced Salmonella numbers in WT mice, GSK5182 had little effect on the bacterial load in nox2−/− mice. Subsequently, peritoneal macrophages from WT and nox2−/− mice were isolated, pretreated with DFO, FeSO4, or hepcidin, and infected with Salmonella carrying the episomal iroBp-gfpOVA or katGp-gfpOVA biosensors (Fig. 5d). The iroBp activity, which was determined using the fraction of GFP-expressing bacteria as a surrogate, increased in macrophages treated with hepcidin (FPN−; high-iron level) and macrophages treated with DFO (FPN+; low-iron level), and decreased in macrophages pretreated with FeSO4 (FPN+; high-iron level). This was the case in macrophages derived from both WT and nox2−/− mice. By contrast, katGp activity decreased in WT macrophages treated with hepcidin or DFO and increased in WT macrophages treated with FeSO4. Most interestingly, however, katGp activity in the nox2−/− macrophages did not change in response to hepcidin, DFO, or FeSO4, suggesting that hepcidin affected nox2-derived ROS. This finding was further verified using nox2−/− mice. The effect of GSK5182 was tested in WT and nox2−/− mice infected with Salmonella expressing katGp-gfpOVA. The activity of katGp in the spleen was determined by quantifying the fraction of bacteria expressing GFP+ Salmonella at 1.5 day p.i. (Fig. 5e, f). In the absence of GSK5182, 71% of Salmonella expressed GFP in WT mice, while only 15% of Salmonella in nox2−/− mice were GFP+. GSK5182 treatment further enhanced katGp activity in WT mice but not in nox2−/− mice. Taken together, these findings indicate that the anti-Salmonella effect of GSK5182 treatment is dependent on ROS generation, which is affected by the presence or absence of FPN in the SCV.
Finally, WT mice were infected with Salmonella carrying iroBp-gfpOVA or katGp-gfpOVA and treated with GSK5182 or PBS. Whole spleens were isolated 2.5 days p.i. and examined for iroB or katG expression by fluorescence microscopy (Fig. 6a and Supplementary Fig. 13). In PBS-treated mice, in which FPN is degraded, iroB was expressed but katG was not. In GSK5182-treated mice, in which FPN levels are maintained, iroB expression decreased while katG expression increased. These results show that the maintenance of FPN leads to iron-sufficient conditions in the SCV for ROS generation (Fig. 6b).
The initial stages of SCV formation and the composition of the SCV are only poorly understood. The evidence presented in this study suggests that FPN is selectively internalized along with Salmonella in macrophages, and transports iron into the SCV lumen as supported by the functional analyses (Figs. 1 and 3). FPN1 protein was also localized in M. tuberculosis phagosomes after infection of RAW264.7 macrophages30. In this case, however, the FPN1 was suggested to be involved in the export of iron from the phagosome into the cytosol. The Salmonella iron biosensor (iroBp-gfpOVA) was activated at below μM concentrations of iron and was repressed at higher levels. This suggests that iron levels in the SCV fluctuate in the μM range. It must be emphasized here that Salmonella grows normally when iron levels are in the nM range, presumably by producing the catecholate siderophores enterobactin and salmochelin31. The iron released from the hydrolyzed siderophores would then allow the survival and proliferation of intra-macrophage Salmonella. Thus, the concept of ‘nutritional immunity’ in the control of Salmonella must be used with caution, as Salmonella only require a minute quantity of iron for growth and also reside in a separate compartment within the macrophage. Thus, it is the presence or absence of FPN on the SCV membrane that determines iron levels in the SCV lumen: depletion of FPN increased cytosolic iron content but decreased the iron level in the SCV (Fig. 3 and Supplementary Fig. 8).
Generation of ROS is initiated by heme iron of flavocytochrome b558 in NADPH oxidase transferring electrons from NADPH to oxygen which is reduced to superoxide anion23,24,32. It is inferred that this activity of the NADPH oxidase must be functionally correlated with the availability of iron for insertion of heme prosthetic group into the apoprotein. Our results revealed that the iron level in SCV influenced ROS generation rather than Salmonella proliferation: Salmonella survived better in iron-deficient conditions (no FPN) than in iron-sufficient conditions (with FPN) in vivo (Fig. 5). Studies with ROS biosensors revealed that hepcidin, which induces FPN degradation, reduced ROS generation in the SCV, as determined by measurement of oxidation of macromolecules, as well as katGp activity both in vitro and in a murine model (Fig. 4). A similar effect was reported in mice treated with DFO, which increased intracellular replication of Salmonella27. However, iron chelation has inhibitory effects on the replication of intra-macrophage Salmonella in iron starvation models based on another iron chelator, deferasirox33,34,35. We propose here that reduction of the available iron specifically in the SCV attenuates the production of hydroxyl radicals, which accounts for the capacity of these cells to limit intra-macrophage Salmonella growth36 (Supplementary Fig. 14). This model was based on the observation that depletion of FPN with hepcidin reduced iron intake into the SCV, which is needed for generation of antibacterial ROS in the SCV by NADPH oxidase and Fenton reaction (Fig. 4). Consequently, the increased survival of Salmonella-infected wild-type mice treated with GSK5182 was modest (Fig. 5a), possibly because ROS confer a critical antimicrobial effect early during the respiratory burst as Salmonella infect host cells anew37—GSK5182 removes only a part of various antimicrobial defenses in macrophages. It should be noted that iron-dependent ROS generation in SCV under this experimental condition was only ~20% (Fig. 4a, b), which might be sufficient to damage Salmonella without harming the organelles of the host cell. A similar ROS-dependent mechanism could account for the control of infection by intracellular bacteria such as Legionella pneumophila, and Mycobacterium tuberculosis and avium, known to reside in membrane-bound cytoplasmic vacuoles in macrophages38,39,40. In addition, the iron transporter natural resistance-associated macrophage protein 1 (Nramp1) was suggested to be involved in the regulation of iron level in SCV. Thus, mutations at Nramp1 cause susceptibility to infections by several intracellular pathogens, including Salmonella41,42,43. Therefore, we have executed the same set of experiments with peritoneal macrophages isolated from DBA2 mice (Nramp1+/+) to clarify the function of Nramp1 in regards to iron level in SCV. We observed similar patterns of iroB and katG responses; iroB was increased and katG was decreased following hepcidin treatment (Supplementary Fig. 15). Consistently, we have previously observed and reported a similar protective effect of GSK5182 in DBA2 mice5. Taken together, this study provides a mechanism underlying the control of intracellular bacterial infection by ERRγ inverse agonist, GSK5182, although further studies would elucidate the role of Nramp1 in conjunction with FPN in intracellular bacterial infection.
Bacterial strains, plasmids and culture conditions
Salmonella typhimurium SL1344 was used as the WT strain. WT Salmonella and the pkatGp-gfpOVA plasmid were described previously16. The iroB reporter plasmid (piroBp-gfpOVA) was constructed by replacing the katG promoter of the pkatGp-gfpOVA plasmid with the iroB promoter region (−200 to +100) using the Sph1 and Xba1 restriction enzymes. The pFPN-EGFP plasmid was generated by ligating Xba1 and EcoR1 fragments of full-length fpn and pEGFP-N1 (Clontech). Bacterial cultures were grown in Luria broth (LB; Difco Laboratories) containing 1% NaCl (w/v) with vigorous aeration at 37 °C, and, when necessary, ampicillin (Sigma, #A0166) was added at 100 μg/ml, unless otherwise indicated. For solid support medium, Bacto agar (Difco Laboratories) was included at 1.5% (w/v).
Measurement of bacterial growth
Overnight bacterial cultures were diluted 1:100 into fresh LB and cultured for 3 h at 37 °C. The iron chelator 2,2′-bipyridyl (Sigma, #D216305) was added, and bacteria were further cultured to test the impact of iron deprivation on bacterial growth. To examine the effect of iron concentration on bacterial growth, RPMI 1640 (Gibco/Thermo Fisher Scientific, #1785905) was chosen as the culture medium. Overnight cultures were grown in RPMI 1640 medium containing FeSO4 (0.005–500 μM), and then diluted 1:100 into fresh medium containing the same concentration of iron and further incubated at 37 °C. Bacterial growth was measured every hour at an absorbance of 600 nm (A600).
Culture of Raw264.7 macrophages, HeLa cells, and peritoneal macrophages
RAW264.7 and HeLa cell lines were obtained from ATCC Korea and cultured according to the supplier’s recommendation. Primary peritoneal macrophages were isolated from 8-week-old C57BL/6 J mice (Jackson Laboratory) 3 days after elicitation by injection of 3% thioglycollate into the peritoneal cavity (1 ml per mouse). The isolated macrophages were cultured in RPMI 1640 supplemented with 10% fetal bovine serum (FBS) in an incubator with 5% CO244. The macrophages were seeded at 5 × 105 cells per ml for all experiments.
Localization of FPN in HeLa cells upon Salmonella infection
HeLa cells were transiently transfected with pFPN-EGFP using FuGENE HD transfection reagent (Promega, #E2311). Live cell images were taken of HeLa cells expressing FPN-GFP after treatment with hepcidin using the IncucyteS3 Live Cell Analysis System at ×20 magnification (Essen Biosciences, USA). HeLa cells expressing FPN-GFP were stained with the following antibodies to SCV-associated marker proteins up to 12 h after Salmonella infection (MOI, 100): anti-EEA1 (Abcam, #ab18211), anti-Rab5 (Abcam, #ab2900), and anti-LAMP1 (Abcam, #ab24170). Fluorescent signals were imaged with a LSM 880 confocal laser scanning microscopes equipped with VIS and NIR lasers. All captured images were taken using the Airyscan mode supported by the LSM 880 confocal laser scanning microscopy for image optimization (Carl Zeiss).
Measurement of gene expression using biosensors
Fluorescence of bacteria expressing the piroBp-gfpOVA was measured in vitro using SpectraFluor Plus (Tecan, Austria) at an excitation of 470 nm and an emission of 510 nm. To measure the expression of iroB or katG by Salmonella within macrophages, Raw264.7 cells or peritoneal macrophages were infected with Salmonella expressing the piroBp-gfpOVA or pkatGp-gfpOVA, respectively. Infected macrophages were fixed at 1 h p.i. with 4% paraformaldehyde for 10 min at 4 °C. The fixed cells were washed with PBS three times and then treated with ProLong Gold anti-fade reagent with 4′,6-diamidino-2-phenylindole (DAPI; Invitrogen/Thermo Fisher Scientific, #P36935). Salmonella were stained with an anti-Salmonella primary antibody (Abcam, #ab8274) and an AlexaFluor 568-conjugated goat anti-mouse secondary antibody (Invitrogen/Thermo Fisher Scientific, #A11031) (red). The stained cells were imaged on a fluorescence microscope and the expression of iroB or katG was quantified by comparison of the green and red signals in a single image using ImageJ 1.41 (NIH). A total of 1712 images were analyzed.
Isolation of SCV
For isolation of SCV within Raw264.7 cells, magnetite particles (Bangs Laboratories, #BM570) were used. The particles were prepared as described previously13. Briefly, the particles were washed twice with 0.1 M MES buffer [2-(N-morpholino) ethanesulphonic acid, pH 5.2] using a magnetic rack after centrifugation of the stock suspension (1 ml) at 1000×g for 30 s in a fixed-angle centrifuge. The washed particles were then resuspended with 4 mg ml−1 EDAC [1-ethyl-3-(3-dimethylaminopropyl) carbodiimide], and mixed on a rotator (12 r.p.m.) for 15 min at RT. The activated particles were washed twice with PBS (pH 7.4) using magnetic separation. The prepared particles were mixed with 0.5 × 109 live Salmonella and incubated at 37 °C on a rotator (12 r.p.m.) for 30 min. Raw264.7 cells were infected with the magnetized Salmonella at a MOI of 100. After infection, the cells were washed two times with DPBS (Well Gene, #LB001-02) containing phenylmethanesulfonyl fluoride (PMSF) (10 mM; Sigma, #P7626), and then treated with enzyme-free cell dissociation solution (Millipore, #S-004-B) in a 5% CO2 incubator at 37 °C for 2 min. To inactivate the dissociation solution, RPMI containing PMSF (10 mM) was added, and then the detached cells were transferred into a microfuge tube placed on a magnetic rack (Bioneer, MagListo-2, TM-1010). After washing with DPBS containing PMSF, the cells were fragmented with a Dounce homogenizer (Wheaton, #357542), and then with a Polytoron homogenizer (IKA, Ultra-Turrax T 10), and then sonicated (Sonics, Vibra Cell VC505/VC750). Finally, purified SCV were isolated using a magnetic rack. The SCV were analyzed by confocal microscopy or lysed by mixing with RIPA buffer (Bio-solution, #BR002) containing a cocktail of proteinase K and protein phosphatase inhibitors (Thermos, #RB228066, #RA229831) on ice for western blot analysis.
Western blot analysis of FPN
Macrophages pretreated with hepcidin or PBS for 3 h were infected with Salmonella. The SCV were isolated from whole-cell lysates of macrophages as described above, and the remaining fraction (non-SCV fraction: supernatant) was analyzed by western blot. The samples (50 μg) were run on 10% SDS- polyacrylamide gels and transferred to PVDF membranes (Amersham, #10600002). Primary antibodies were diluted 1:3000 in TBST (TBS with 0.2% Tween-20) and incubated for 16 h at 4 °C. The following primary antibodies were used: anti-FPN (Novus Biologicals, #NBP1-21502), anti-Rab5 (Abcam, #ab18211), anti-annexin V (Abcam, #ab14196), and anti-MHC class I (Novus Biologicals, #NB120-15680). After washing with TBST three times, membranes were incubated with a 1:3000 dilution of horseradish peroxidase (HRP)-conjugated anti-rabbit (Thermo Fisher Scientific, #31430) or anti-rat (Thermo Fisher Scientific, #31470) secondary antibodies in TBST for 1 h at RT. After washing, the signals were visualized using chemiluminescence (Pierce, #32106) and the Fusion Solo (Vilaber) imaging system. Uncropped images of blots are shown in Supplementary Fig. 16.
Analysis of ROS-related damage
The level of protein carbonylation was determined using the oxidized protein detection kit (Millipore, #S7150-Kit). The lysed SCV were separated by SDS-PAGE and blotted on PVDF membranes, followed by western blot analysis45,46. In addition, ROS-related lipid peroxidation was estimated by thiobarbituric acid (TBA)-MDA assay using the TBARS assay kit (R&D Systems, #KGE013). The amount of lipid peroxidation in the sample was quantified by measuring TBARS levels at 532 nm using a SpectraFluor Plus instlument26.
Male and female 8-week-old C57BL/6J WT and nox2−/− mice (B6.129S-Cybbtm1Din/J, stock number: 002365) were from the Jackson Laboratory (Bar Harbor, USA). The hepcidin inhibitor GSK5182 was synthesized as described previously5. To investigate the effect of GSK5182, mice were injected with PBS or GSK5182 (40 mg kg−1) intraperitoneally 12 h before Salmonella infection (n = 5 per group). After bacterial infection, mice were injected with PBS or GSK5182 once daily. Mice were infected with 1 × 108 CFU of Salmonella orally or with 1 × 105 CFU of Salmonella i.v. To determine the viable counts of Salmonella, spleens from five mice per group were collected and homogenized in sterile PBS containing 0.05% Tween-20 with a Polytoron homogenizer (IKA, Ultra-Turrax T 10). Salmonella was recovered from the homogenates and quantified by plating on agar. For the survival assay, 20 C57BL/6J WT or nox2−/− mice were infected orally with 1 × 108 Salmonella with or without GSK5182 treatment (n = 10 per group). Survival rates were estimated by the Gehan-Breslow-Wilcoxon test. All animal experiments were approved and performed according to guidline of the Institutional Animal Use and Care Committee of the Chonnam National University (CNU IACUC-H-2016-15). For measurement of the expression of katG or iroB, mice were infected i.v. with 1 × 105 CFU of Salmonella carrying the pkatGp-gfpOVA or piroBp-gfpOVA plasmid, respectively. Gene expression was evaluated by analysis of red and green fluorescence using ImageJ, as described above.
Immunofluorescence staining and confocal microscopy
Raw264.7 cells were grown on sterilized glass cover slips for 12 h. Pretreatments and Salmonella infection were carried out as described above. The cells were then fixed with 4% paraformaldehyde and blocked with 3% bovine serum albumin (BSA) in PBS. The samples were probed with a mouse anti-Salmonella antibody (1:200 in PBS; Abcam, #ab8274) and an AlexaFluor 568-conjugated secondary antibody (1:500 in PBS; Invitrogen/Thermo Fisher Scientific). The nuclei of the macrophages were stained with ProLong Gold anti-fade reagent with DAPI (Invitrogen/Thermo Fisher Scientific, P36935).
For in vivo experiments, the isolated spleens were fixed with 4% paraformaldehyde, embedded in optimal cutting temperature compound (OCT; Tissue-Tek), and frozen. The frozen spleens were sliced into 6-μm-thick sections using a microtome-cryostat. The tissue sections were mounted on aminopropyltriethoxysilane-coated slides. The slides were washed with PBS (pH 7.4) for complete removal of the OCT and incubated with primary antibodies [rabbit anti-mouse FPN (Alpha Diagnostic, #MTP 11-A) and mouse anti-Salmonella antibody (Abcam, #ab8274)] at 1:200 in PBS for 2 days at 4 °C. AlexaFluor 568-conjugated goat anti-mouse and AlexaFluor 488-conjugated goat anti-rabbit were used as secondary antibodies (1:100 in PBS). The samples were also stained with ProLong Gold anti-fade reagent with DAPI to detect nuclei. The stained images were captured with a Zeiss confocal microscope LSM 510 (Zeiss Laboratories) and the representative images were shown unless otherwise mentioned.
Data were analyzed using GraphPad Prism statistical software. The data met assumptions of a normal distribution as determined by statistical software, and variance was estimated using the standard error of the mean (SEM). The two-tailed Student’s t-test was used to analyze differences between two groups. Differences were considered statistically significant at p < 0.05.
The data supporting the findings of the study are available in this article and its Supplementary Information files, or from the corresponding author upon request.
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This work has been supported by the National Research Foundation of Korea grant funded by the Korea government (NRF-2017R1A2A1A17069809). J.-H.J was supported by the Basic Science Research Program (NRF-2017R1A6A3A04006167) and K.S.K by Basic Science Research Program (NRF-2017R1A6A3A11032659). T.-H.L was supported by the R&D grants for KMPC (NRF-2014M3A9D5A01073658). H.-S.C was supported by the National Creative Research Initiatives Grant (20110018305) through the National Research Foundation of Korea (NRF) funded by the Korean government (Ministry of Science, ICT & Future Planning). D.B. was supported by the Swiss National Foundation (310030_156818). M.U.M was funded by the DFG SFB 1036.
The authors declare no competing interests.
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Lim, D., Kim, K.S., Jeong, J. et al. The hepcidin-ferroportin axis controls the iron content of Salmonella-containing vacuoles in macrophages. Nat Commun 9, 2091 (2018). https://doi.org/10.1038/s41467-018-04446-8
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