Regulation of IDO Activity by Oxygen Supply: Inhibitory Effects on Antimicrobial and Immunoregulatory Functions

Tryptophan is an essential amino acid for human beings as well as for some microorganisms. In human cells the interferon-γ (IFN-γ) inducible enzyme indoleamine 2,3-dioxygenase (IDO) reduces local tryptophan levels and is therefore able to mediate broad-spectrum effector functions: IDO activity restricts the growth of various clinically relevant pathogens such as bacteria, parasites and viruses. On the other hand, it has been observed that IDO has immunoregulatory functions as it efficiently controls the activation and survival of T-cells. Although these important effects have been analysed in much detail, they have been observed in vitro using cells cultured in the presence of 20% O2 (normoxia). Such high oxygen concentrations are not present in vivo especially within infected and inflamed tissues. We therefore analysed IDO-mediated effects under lower oxygen concentrations in vitro and observed that the function of IDO is substantially impaired in tumour cells as well as in native cells. Hypoxia led to reduced IDO expression and as a result to reduced production of kynurenine, the downstream product of tryptophan degradation. Consequently, effector functions of IDO were abrogated under hypoxic conditions: in different human cell lines such as tumour cells (glioblastoma, HeLa) but also in native cells (human foreskin fibroblasts; HFF) IDO lost the capacity to inhibit the growth of bacteria (Staphylococcus aureus), parasites (Toxoplasma gondii) or viruses (herpes simplex virus type 1). Additionally, IDO could no longer efficiently control the proliferation of T-cells that have been co-cultured with IDO expressing HFF cells in vitro. In conclusion, the potent antimicrobial as well as immunoregulatory functions of IDO were substantially impaired under hypoxic conditions that pathophysiologically occurs in vivo.


Introduction
Human hosts are permanently confronted with a variety of pathogens that have the potency to infect every niche within the body. Therefore, efficient defense strategies of the host as well as immune escape mechanisms of different pathogens are constantly in the scope of research. One major antimicrobial effector mechanism is the tryptophan-degrading enzyme indoleamine 2,3-dioxygenase (IDO), which can be induced in many human cell types, including myeloid cells, fibroblasts, epithelial cells and tumour cells upon stimulation with the pro-inflammatory cytokine interferon-c (IFN-c) by JAK-STAT signalling. IDO belongs to the family of heme enzymes that catalize the oxidative cleavage of tryptophan and this IDO-mediated local tryptophan depletion limits the growth of various pathogens including bacteria (e.g. Staphylococci, Streptococci, Enterococci), viruses (e.g. herpes simplex virus, measles virus) and parasites (e.g. Toxoplasma, Neospora) [1]. Hence, IDO is an important molecule of the innate immune response that is directed against a broad range of pathogens. In addition, IDO has been shown to influence the adaptive immune response as well. In this context IDO acts immunoregulatory, not only by depleting local tryptophan levels and therefore modulating T-cell responses, but also by producing immunorelevant, T-cell inhibitory metabolites and by enzymatic and non-enzymatic mechanisms resulting in tolerance [2][3][4][5].
Although these divergent roles of IDO have been investigated in much detail, most of the results have been obtained by in vitro studies. For this purpose different freshly isolated IDO-expressing cells or cell lines have been incubated in a regular humidified incubator at 37uC and under 21% O 2 corresponding to the oxygen content in the air. Even though this normoxic air is inhaled, in vivo oxygen concentrations are much lower. Physiolog-ical oxygen levels lie for the most part between 3 to 5% O 2 and rarely exceed 12% O 2 , even in well-vascularized tissues [6]. In pathologically altered tissues like infected or cancerous organs oxygen contents drop even to levels below 1% and tissue foci are therefore referred to as ''hypoxic environment'' [7,8]. Host cells have to adapt to these low oxygen conditions and must optimize their cell energetics and homeostasis, especially since many common pathogens proliferate readily in hypoxic environments where they additionally deprive infected cells of O 2 [9].
Up to now IDO-mediated effects under hypoxic conditions were only analysed in an infection model with intracellular bacteria. In 2010 Roth et al. described that the IFN-c-mediated antichlamydial properties were abrogated under low oxygen concentrations in human fallopian tube cells due to disturbances in JAK-STAT signalling. As the activity of the IFN-c-induced IDO enzyme was also diminished the cells were unable to limit the growth of Chlamydia trachomatis [10].
In this work we focussed on the effect of hypoxia on the IDOmediated defense against a broader range of pathogens. We found that the expression and activity of IDO was impaired by hypoxia in different tumour cells (86HG39 and HeLa cells) and native cells (HFF cells) and that the tryptophan-dependent growth-inhibition of three prototypic pathogens in these cells was compromised, resulting in an unhindered proliferation of extracellular bacteria (Staphylococcus aureus), the intracellular parasite Toxoplasma gondii and herpes simplex virus type 1. Additionally, we examined the role of oxygen on the function of IDO in the regulation of T-cell responses. IDO was no longer able to inhibit the proliferation of activated T-cells under hypoxia. Therefore, IDO-mediated effector functions depend on the environmental oxygen supply and we discuss cellular advantages and disadvantages that result from insufficient IDO activation.

IDO Activity and Expression are Reduced Under Hypoxic Conditions
In order to disclose an impact of the local oxygen concentration on the enzyme activity of indoleamine 2,3-dioxygenase (IDO) the capacity of tumour and native cell lines to degrade tryptophan was analysed in vitro. Therefore IDO expression in human glioblastoma cells (86HG39), HeLa cells and human foreskin fibroblasts (HFF) was induced by treatment with IFN-c (500 U/mL) and cells were incubated for 72 h under normoxic conditions (20% O 2 ), intermediate oxygen conditions (10% O 2 ) or under hypoxic conditions (1% O 2 ), respectively. The enzyme activity of IDO was then determined by measuring the formation of the product kynurenine in the cell culture supernatants. As shown in figure 1 no kynurenine was detected in the supernatants of unstimulated cells but all cell lines produced kynurenine after stimulation with IFN-c under normoxic conditions. This production of kynurenine was not impaired under intermediate oxygen conditions (10% O 2 ) but it was significantly reduced under hypoxia (1% O 2 ) ( Fig. 1 A-C).
Since the reduction of kynurenine could result from a reduced IDO enzyme activity or from a reduced IDO expression we next analysed IDO protein levels in the different cell lines after a 24 h stimulation period with IFN-c (0, 30, 300, 500 U/mL) under normoxia (20% O 2 ) or hypoxia (1% O 2 ) by Western Blotting. As expected, IDO protein was found after the stimulation with IFN-c dose-dependently in all analysed cells. However, IDO protein levels were decreased upon hypoxia in all groups, suggesting that not only IDO activity but also IDO protein biosynthesis was diminished ( Fig. 1D-F). Highly decreased IDO protein levels were especially detected under low stimulation conditions (30 U/mL IFN-c) in tumour cells and in all HFF cell groups, where more than 60% of the protein was absent under hypoxia (Fig 1G-I).
Reduced IDO expression levels under low oxygen conditions can be a consequence of an impaired activation of the JAK-STAT signalling pathway [10]. In order to find out whether JAK-STAT signalling was also compromised by hypoxia in the analysed tumour and native cell models the amount of STAT1 protein was determined via immunoblotting. Under normoxic conditions the stimulation with IFN-c-induced JAK-STAT signalling in all cells could be detected by the presence of phosphorylated STAT1 (pSTAT1). In contrast, pSTAT1 was nearly absent in tumour cells and was drastically reduced in HFF cells under hypoxia (Fig. 1D-F and 1J-L) indicating that JAK-STAT signalling was also affected in the in vitro models.
To elucidate a possible influence of hypoxia on JAK2 we analysed the effectivity of the JAK2 inhibitor BSK805 on IFN-cinduced IDO activity of HFF. As shown in figure 2A the addition of BSK805 to IFN-c stimulated HFF reduces IDO activity. However the inhibitory effect was comparable under hypoxia and normoxia and reached 60-75% of the respective positive control. As shown in figure 1D-F the protein levels determined by the measurement of b-actin is slightly reduced in all probes from cells cultured under hypoxia. Therefore we excluded a potentially enhanced IDO degradation by the use of the proteasome inhibitor MG-132 and the sumoylation inhibitors Anancardic Acid or Ginkgolic Acid. As shown in figure 2B the addition of these inhibitors to IFN-c stimulated HFF did not result in an enhancement of IDO activity in cells stimulated under hypoxia. We therefore conclude that enhanced protein degradation is not responsible for the observed IDO inhibition under hypoxic conditions. JAK-STAT signalling is essential for the regulation of a broad palette of interferon-induced proteins [11]. We were therefore interested whether hypoxia also influences other IFN-c induced and JAK-STAT dependent molecules and checked exemplarily the expression of HLA-DR, a cell surface receptor of the major histocompatibility complex (MHC) class II. For this purpose, HeLa cells were pre-stimulated with IFN-c for three days, stained with DAPI and antibodies against human HLA-DR and analysed via FACS. Under normoxic conditions HeLa cells expressed HLA-DR after stimulation with IFN-c as expected. In contrast, hypoxic incubation clearly decreased the expression of HLA-DR ( Fig. 3A) demonstrating that hypoxia can indeed effectively interfere with the regulation of interferon-induced effector molecules as well.
Since not only IDO but also pSTAT1 and HLA-DR levels were decreased under hypoxic conditions, hypoxia-induced cell death had to be excluded. Cell survival was confirmed by several observations. First, there was only a slight difference in the protein levels of b-actin in normoxia-and hypoxia-cultivated cells in the Western Blot analysis (Fig. 1D-F). Second, cell viability assays based on alamarBlue reagent detected that both normoxia-and hypoxia-treated cells (24 h-72 h) had a comparable reducing power of resazurin which is a cell health indicator (Fig. 3B-D). Third, FACS analysis revealed that the bulk of cells survived at least the 72 h stimulation phase, not only under normoxia, but also under hypoxia and even under anoxia, whereas PFA fixed cells served as positive control for cell death (Fig. 3E). Fourth, IDO activity was restored in reoxygenated cells. Therefore, HeLa cells were stimulated with IFN-c (500 U/mL) and incubated for an initial 72 h hypoxic phase, followed by a 48 h normoxic phase. Figure 3F shows that the cells efficiently produced kynurenine after reoxygenation and therefore confirms cell survival during the hypoxic phase.  Together these data indicate that the reduced IDO expression and activity were due to impairment in the activation of IFN-c dependent JAK-STAT signalling by low oxygen conditions in tumour cells as well as in native cells but not the result of hypoxiainduced cell death.

Antimicrobial Function of IDO is Abrogated Under Hypoxia
Next, we investigated whether hypoxia abolishes functional effects of IDO in vitro. Since IDO is well-known for its antimicrobial properties the IDO-mediated antibacterial, antiparasitic and antiviral functions within hypoxic environment are of particular interest. In different in vitro infection models it could be shown that an IFN-c induced IDO activity was sufficient to control the growth of different microorganisms within tumour and native human cells [1]. Figure 4 shows the result of experiments using HFF cells that were infected with Staphylococcus aureus, Toxoplasma gondii and herpes simplex virus type I, since fibroblasts are physiologically important for their infection. Additionally, these native cells stop proliferating when confluency is reached; therefore, they do not overgrow pathogen-infected cells and the proliferation of pathogens is well detectable. It was tested whether IFN-c-induced IDO activity in the cells was able to inhibit the growth of these pathogens under normoxia (20% O 2 ), intermediate oxygen conditions (5-10% O 2 ) or hypoxia (1-3% O 2 ).
The facultative anaerobic bacterium Staphylococcus aureus was able to grow in cell culture supernatants of unstimulated cells irrespective of the prevailing oxygen concentration that were used during the stimulation period. As expected bacterial growth was inhibited by IFN-c pre-stimulated cells that had been incubated under normoxia. The lower oxygen concentration of 1% O 2 allowed growth of Staphylococci not only in supernatants of unstimulated cells but also in supernatants of IFN-c pre-stimulated cells indicating that the reduced IDO activity had abolished antibacterial effects (Fig. 4A). To reveal the magnitude of the IFNc-induced antibacterial effect, bacterial growth was determined by measuring colony forming units. Figure 4B indicates that under normoxia IFN-c has a more then tenfold higher antibacterial activity. Comparable results were obtained for 86HG39 cells or HeLa cells (data not shown). Figure 4C shows that the intracellular parasite Toxoplasma gondii proliferated well in HFF cells and, as expected, Toxoplasma growth was inhibited by IFN-c pre-stimulation. Moreover, a detailed study revealed that this significant growth inhibition was detected when the cells were cultured in the presence of 20% O 2 , 10% O 2 and 5% O 2 , indicating that normoxic or intermediate oxygen conditions were needed for an efficient defense against Toxoplasma. In contrast, oxygen levels below 3% O 2 were not sufficient for parasite growth inhibition. The addition of Ltryptophan to IFN-c-stimulated cells together with the parasites rescued Toxoplasma growth in all groups displaying that IDO-mediated tryptophan degradation was the underlying antiparasitic mechanism.
In a last set of experiments we also found out that the replication of herpes simplex virus type 1 (HSV1) was significantly inhibited in IFN-c pre-stimulated HFF cells. Again, this inhibition of replication could only be detected when the cells were incubated under normoxic but not under hypoxic conditions (Fig. 4D).
In summary, the IFN-c-induced IDO-mediated antibacterial, antiparasitic and antiviral defense was lost in human cells incubated under hypoxic oxygen conditions, demonstrating that hypoxia negatively influences the immune response in all analysed cell lines.

Immunoregulatory Function of Indoleamine 2,3dioxygenase is Abrogated Under Low Oxygen Concentrations
Beside its antimicrobial potency, IDO also provides immunosuppressive functions by modulating T-cell responses. As hypoxia physiologically occurs at sites of infection, T-cells frequently encounter these hypoxic regions during inflammatory processes. Therefore we were interested in the influence of hypoxia on IDOmediated T-cell regulation. We analysed IDO-mediated T-cell regulation in the absence or presence of oxygen in an experimental setting resembling the physiological situation, without usage of synthetic IFN-c. Therefore PBMC and HFF cells were cocultivated for 72 h either under normoxia (20% O 2 ) or hypoxia (1% O 2 ). The T-cells did not proliferate unless they were activated with a monoclonal anti-CD3 antibody (data not shown). When the T-cells in the culture system were activated with OKT3 they produced IFN-c which in turn induced IDO activity in the HFF cells. Figure 5A indicates that the T-cells proliferated in the absence or presence of oxygen; however the number of cocultured HFF cells affected this proliferation. With increasing HFF cells in the culture system a lower proliferation rate of T-cells was detected. Importantly, this inhibitory effect was only observed under normoxia, not under hypoxia. The involvement of IDO was confirmed by additional tryptophan in the culture system, which abrogated the effect (Fig. 5B).
In summary, the hypoxia-dependent inhibition of IDO is paralleled by an enhanced T-cell proliferation since the growth of T-cells is not controlled by tryptophan starvation.

Discussion
We investigated the expression and activity of the tryptophandegrading enzyme IDO in the presence of different oxygen amounts in vitro. Under normoxic (20% O 2 ) and physiologic (10% O 2 ) oxygen conditions, IDO was expressed in IFN-c-stimulated human tumour cells and fibroblasts. IDO efficiently degraded tryptophan to kynurenine which could be detected in cell culture supernatants. However, in contrast IFN-c-activated human cells did not express IDO protein and did not produce kynurenine when they were cultured under hypoxic conditions (1% O 2 ). This was in line with the findings of Roth et al. and Herbert et al. who also observed decreased IDO protein levels and a diminished IDO activity in hypoxia-treated human fallopian tube cells and monocyte-derived endothelial-like cells [10,12]. Herbert et al. detected a significant reduction of IDO protein (up to 5-fold) and decrease in IDO activity (up to 100 fold) under hypoxia which was similar to our data with human tumour cells and fibroblasts (Fig. 1). The reduced IDO expression under hypoxia has been shown to result from impairment in JAK-STAT signalling [10]. We therefore evaluated JAK-STAT signalling in the different human cell lines by measurement of phosphorylated STAT1 (pSTAT1) protein amounts and found that a stimulation of the cells with IFN-c under hypoxia resulted indeed in a reduced expression of pSTAT1. Thus, downregulation of IDO expression in human tumour cells and fibroblasts was likewise suggested to be caused by a hypoxia-induced blockade in JAK-STAT signalling. Additional experiments with JAK2 inhibitors and inhibitors of protein degradation showed no specific influence on IDO activity induced under hypoxic conditions (Fig. 2).
We proved cell survival under hypoxic conditions in vitro by cell viability assays and re-oxygenation studies (Fig. 3). The latter showed that IDO activity recovered when cells were incubated in normoxia for 48 h subsequent to a 72 h hypoxia treatment. Such a recovery of IDO protein and enzyme activity by reoxygenation was also observed by others [12].
The cellular response to a hypoxic environment is dependent on the hypoxia-inducible factor (HIF) protein complex. This central regulator can be activated in all mammalian cells by hypoxia where it regulates the expression of more than 100 genes included in metabolism, angiogenesis, vascular tone, cell differentiation and apoptosis [13]. The HIF complex is comprised of the constitutively expressed HIF1b subunit (also called AhR nuclear translocator; ARNT) which binds to one of two inducible a-subunits HIF1a or HIF2a [14]. Interestingly, ARNT also dimerizes with the ligandactivated aryl hydrocarbon receptor (AhR), a helix-loop-helix transcription factor that regulates cell growth, differentiation and immunological responses [15,16]. Recently it has been shown that kynurenine, the downstream product of IDO-mediated tryptophan degradation is an endogenous ligand of AhR [5]. Given the fact that hypoxia reduces kynurenine levels by inhibiting IDO it could be possible that lower kynurenine amounts fail to activate the AhR which therefore does not translocate into the nucleus and cannot dimerize with the constitutively expressed ARNT. By this way unbound ARNT protein could be used for HIF1a binding, facilitating the cellular response to hypoxia. In this model a reduced kynurenine production by IDO would be beneficial for the cells as it enables them to adapt to the hypoxic environment.
IDO is not the only antimicrobial effector mechanism that is inhibited by hypoxia. The activities of the inducible nitric oxide synthase (iNOS or NOS2) and the phagocyte NADPH oxidase (PHOX) were impaired under hypoxic conditions as well [6]. Both enzymes are involved in the defense against bacteria in mice as iNOS-or PHOX-deficient mice had an increased susceptibility to Staphylococcus aureus (S. aureus) infections [17,18]. Furthermore, it has been published that hypoxia inhibited mitochondrial antibacterial effector functions active against S. aureus and Escherichia coli by impairing the respiratory chain in murine macrophages [6].
However, hypoxia not only negatively but also positively influences specialized antimicrobial effector mechanisms. For example macrophages have revealed an enhanced phagocytosis and bacterial killing under hypoxia due to HIF1a activation and also the apoptosis rate of neutrophils has been diminished in a HIF1a-dependent way leading to a prolonged inflammatory response [19,20]. Additionally, low oxygen concentrations have been shown to increase the production of the antimicrobial peptide cathelicidin within murine blood leukocytes and, although its activity was diminished by hypoxia, iNOS has been upregulated HIF1a-dependently [21,22].
In this work we examined the consequence of a reduced IFN-cinduced IDO expression under hypoxia on two different IDO effector functions in vitro. We thereby focussed not on specialized immune cells but on human fibroblasts and tumour cells that also get into contact with pathogens in vivo and are able to express IDO endogenously.
The first set of data describes that the human non-immune cells were no longer able to control the growth of three different pathogens prototypic for an infection with extracellular bacteria, intracellular parasites or viral infection (Fig. 4). S. aureus was used as model for an extracellular bacterium that causes not only skin infections but also a variety of organ-specific infections and sepsis. Animal in vivo studies have shown that systemic hypoxia inhibited the clearance of S. aureus in lung and skin infections [23,24]. This was to some extend pinpointed to an enhanced biofilm production by the bacteria as resistance mechanism to a hypoxic environment that occurs for example in the lung of patients with cystic fibrosis [25]. Our present study now demonstrates that also an impairment of IDO could be responsible for these detrimental effects of S. aureus (Fig. 4A) and of other tryptophan-auxotroph bacteria in vivo. Nevertheless, observational cohort studies have demonstrated that an enhanced IDO activity, as detected by an increased kynurenine to tryptophan ratio in plasma, is a deleterious host response in human sepsis. A high IDO activity has been associated with decreased microvascular reactivity and T cell lymphopenia and its role as independent predictor of severe disease and case fatality has been discussed [26,27]. Given these facts a regulation of IDO activity by hypoxia could serve as protective mechanism for the host, especially since IDO-derived bioactive tryptophan metabolites have been fatal for T cell survival, depleting overall thymocyte counts in vitro and in vivo [28].
Toxoplasma gondii (T. gondii) is an obligate intracellular parasite that chronically persists in healthy human beings. The infection with T. gondii is mostly asymptomatic; however it can cause lifethreatening encephalitis, myocarditis or pneumonia in immunocompromised patients [29]. Interestingly, T. gondii infection of fibroblasts resulted in an up-regulation of HIF1a causing several changes in the host cell gene expression profile, thus allowing the intracellular survival of the pathogen [30,31]. Such interplay of pathogen survival and hypoxia needs further examination in the future especially with respect to the diminished IDO-mediated antiparasitic capacities that refer to occur during hypoxic phases (Fig. 4B). Again, a reduced IDO activity could be beneficial in the case of hypoxic inflammation that is present e.g. in necrotic tissue in the centre of brain abscesses, whereas IDO activity could still mediate a protective antiparasitic effect at the border between healthy tissue and the abscess [32]. Herpes simplex virus type 1 (HSV1) was used as model for a viral infection. HSV1 infections lead to life-long persistence within the immunocompetent host but can also cause life-threatening pneumonia or encephalitis within immunocompromised patients [33,34]. It has been shown that HSV1 replication was increased as response to low oxygen concentrations in vitro and that human herpes-virus 8 was reactivated under hypoxia [35,36]. Whether this was due to a diminished IDO-mediated antiviral capacity needs to be elucidated. In fact, our data indicate that hypoxia results in an inhibition of IDO activity that allows viral growth also in IFN-c activated human fibroblasts (Fig. 4C).
The second part of the data demonstrates that the immunoregulatory function of IDO was likewise affected in human fibroblasts by hypoxia (Fig. 5). IDO-mediated tryptophan depletion inhibited T cell proliferation in supernatants of IFN-c prestimulated fibroblasts or in the presence of fibroblasts in costimulation assays. However, this regulatory effect on T cells was abrogated by hypoxia. Several studies have indicated that T cells underwent hypoxia-mediated and HIF-dependent cell death and therefore may only play a minor role in hypoxic tissues [13]. For example, T cells from HIF1a-deficient mice released significantly more tumor necrosis factor and IFN-c after T cell receptor activation than wildtype T cells and mice showed an enhanced survival rate in a sepsis model [37]. Additionally also the T cell differentiation was controlled by hypoxia. Clambey et al. have found a robust HIF1a-dependent induction of FoxP3 and therefore an enhanced abundance of regulatory T cells under hypoxia in vitro and in vivo [38]. All these accumulating data give the hint that T cell responses are tightly regulated under hypoxic conditions, probably in order to avoid an ''over-inflammation'' to limit deleterious effects of inflammatory hypoxia and that in this context further analysis must be done to reveal a role of the IDO enzyme.
In conclusion our data show that an IFN-c-induced IDO activity was inhibited under hypoxic conditions in vitro. Therefore IDO-mediated effector functions were lost and human tumour cells and fibroblasts were no longer able to constrain bacterial, parasitic and viral growth in the cells or in the presence of the cells. Additionally the IDO-mediated regulation of T cell proliferation was abrogated by hypoxia. Since an overwhelming IDO activity can have detrimental effects in host cells, an adjustment of IDO activity by hypoxia could serve as cellular or systemic protective mechanism.

Ethics Statement
This study obtained ethics approval from the ethics committee of the Medical Faculty of the Heinrich-Heine University Düsseldorf (study no. 3838). Human PBMC were generated from the blood of healthy individuals after informed and written consent.
Peripheral blood mononuclear cells (PBMC) were prepared from heparinised blood of healthy donors after density gradient centrifugation.
Hypoxic growth was carried out using a HERAcell 150 i CO 2 incubator (ThermoFisher Scientific, Langenselbold, Germany) or, for Western Blot analysis, in an Invivo200 hypoxia chamber (Ruskinn) with attached flasks of nitrogen, CO 2 and compressed air [40].

Kynurenine Assay
Supernatants harvested from unstimulated or stimulated cells were analysed for their kynurenine content, using Ehrlich reagent as described before [41]. As a standard we diluted kynurenine (Sigma-Aldrich, Deisenhofen, Germany) in culture medium. For the calculation of the kynurenine content in the supernatant, linear regression and GraphPad Prism software were used.

Determination of Bacterial Growth
For the infection experiments tryptophan-auxotroph Staphylococcus aureus, obtained from routine diagnostic specimens was used [45]. S. aureus was grown on brain heart infusion agar (Difco, Hamburg, Germany), containing 5% sheep blood and incubated at 37uC in 5% CO 2 -enriched atmosphere. For infection experiments, a 24 h old single bacterial colony was picked and resuspended in tryptophan-free RPMI 1640 (Gibco, Grand Island, USA). Bacteria were serially diluted in the same medium and 10 ml were added to 200 ml of conditioned medium corresponding to 10-100 CFU. After incubation for 16-24 h, bacterial growth was monitored using a microplate photometer (SLT Labinstruments, Crailsheim, Germany) by measuring the optical density at 620 nm. In additional experiments the CFU were determined. Therefore, the bacteria-containing cell culture media were serially diluted in PBS and 10 ml of each dilution was cultivated on Columbia blood agar plates. After 18 h resulting colonies were counted.

Determination of Toxoplasma Growth
After pre-stimulation for 72 h at 37uC, HFF cells were infected with 2610 4 toxoplasma tachyzoites per well. Toxoplasma gondii growth was measured by the 3 H-uracil incorporation method [46]. 48 h after infection, 0.33 mCi 3 H-uracil were added and after additional 24 h host cells and toxoplasma were lysed by freeze thawing. 3 H-uracil incorporation was measured using liquid scintillation spectrometry (1205 Betaplate, PerkinElmer, Jugesheim, Germany).

Determination of Viral Replication
Infection experiments with herpes simplex virus type 1 were conducted as before [47]. In brief, pre-stimulated HFF cells were infected with 1.45610 5 HSV-1 copies (equal to a TCID 50 of about 1610 2 /well) and viral replication was monitored. Therefore a plasmid containing the amplified region was used as a standard. The amplification was carried out using an iCycler and analysed with iCycler iQ Version 3.0a (Bio-Rad, München, Germany).

T Cell Proliferation Assays
T-cell immunoregulation by IDO was determined via two assays.
In the co-stimulation assay 0-10000 HFF cells and 1.5610 5 PBMC were incubated together in one well for 72 h. IFN-c was produced by activated T-cells that were stimulated with the anti-CD3 antibody OKT3. The IFN-c-dependent IDO induction in HFF lead to a degradation of tryptophan. The T-cell proliferation in the presence or absence of supplemented tryptophan was determined by adding [ 3 H] thymidine for 24 h and measurement via liquid scintillation spectrometry.

FACS Analysis
1610 6 HeLa cells/flask were stimulated with IFN-c (0, 100 U/ mL) under normoxic (20% O 2 ), hypoxic (1% O 2 ) or anoxic conditions in tryptophan-supplemented (100 mg/mL) IMDM cell culture medium for 72 h. Correct IDO induction was determined by measurement of kynurenine in the culture supernatants. Then the cells were harvested, centrifuged and resuspended in FACS buffer (PBS containing 2% FCS and 2 mM EDTA) or the respective antibody (mouse-anti-human HLA-DR no. 559866 or Isotype APC mouse IgG2ak no. 555576, BD Biosciences, Heidelberg, Germany). After incubation for 60 min at RT in the dark, the samples were again centrifuged and the cells resuspended in FACS buffer and charged 1:1000 with DAPI (Roche Diagnostics GmbH, Mannheim, Germany). As positive control for cell death, cells were harvested and additionally treated for 45 min with PFA [4%].

Cell Viability Assay
Cell survival under normoxia (20% O 2 ) or hypoxia (1% O 2 ) was evaluated via alamarBlue cell viability reagent (Invitrogen, Karlsruhe, Germany). For the experiment different numbers of HFF, HeLa or 86HG39 cells (1610 3 -3610 4 ) were incubated for the given time periods (24 h, 48 h or 72 h) in IMDM cell culture medium containing 5% FCS. Then 20 ml alamarBlue reagent was added to the cells. The resazurin within the alamarBlue is reduced to resofurin in living cells which is red in colour and can be determined by the absorbance at OD 570 nm vs. OD 600 nm .

Statistical Analysis
All experiments were done in duplicates (virus growth) or triplicates (all other experiments) and data are given as mean +/2 SEM of a minimum of three independent experiments. For statistical analysis the unpaired t-test was used and significant differences were marked with asterisks (* = p,0.05; ** = p,0.01; *** = p,0.001). The analysis was performed with GraphPad Prism software.