|Home | About | Journals | Submit | Contact Us | Français|
Ergosterol biosynthesis and homeostasis in the parasitic protozoan Trypanosoma brucei was analyzed by RNAi silencing and inhibition of sterol C24β-methyltransferase (TbSMT) and sterol 14α-demethylase [TbSDM (TbCYP51)] to explore the functions of sterols in T. brucei growth. Inhibition of the amount or activity of these enzymes depletes ergosterol from cells at <6 fg/cell for procyclic form (PCF) cells or <0.01 fg/cell for bloodstream form (BSF) cells and reduces infectivity in a mouse model of infection. Silencing of TbSMT expression by RNAi in PCF or BSF in combination with 25-azalanosterol (AZA) inhibited parasite growth and this inhibition was restored completely by adding synergistic cholesterol (7.8 μM from lipid-depleted media) with small amounts of ergosterol (1.2 μM) to the medium. These observations are consistent with the proposed requirement for ergosterol as a signaling factor to spark cell proliferation while imported cholesterol or the endogenously formed cholesta-5,7,24-trienol act as bulk membrane components. To test the potential chemotherapeutic importance of disrupting ergosterol biosynthesis using pairs of mechanism-based inhibitors that block two enzymes in the post-squalene segment, parasites were treated with AZA and itraconazole at 1 μM each (ED50 values) resulting in parasite death. Taken together, our results demonstrate that the ergosterol pathway is a prime drug target for intervention in T. brucei infection.
Trypanosomes carried by the tsetse fly are responsible for African sleeping sickness, a serious health risk in Sub-Saharan Africa which is spreading in travelers to Europe and the United States (1–3). Sterol biosynthesis is an extremely important area of biochemical difference between these protozoan parasites and their animal hosts that might be exploited in the development of new chemotherapeutic leads. Therefore, it is notable that Trypanosoma brucei operates a phyla-specific ergosterol biosynthesis pathway distinct from other Kinetoplastids or fungi, and produce a sterol metabolome that is different from animals (Fig. 1) (4–6). The uniqueness of ergosterol biosynthesis and homeostasis in T. brucei resides primarily in formation of a 24β-methyl group in the sterol side chain structure catalyzed by sterol C24-methyl transferase (TbSMT) and in the amount of final product, ergosterol, utilized in growth support. Detailed studies of metabolism using 13C- and 2H-labeled intermediates supported by mechanistic analysis of the cloned TbSMT reveal that the introduction of the C24β-methyl group in the sterol side chain proceeds in T. brucei by a methylation-deprotonation Δ25(27)-olefin pathway, which likely diverged from the methylation-deprotonation Δ24(28)-olefin pathway yielding fungal ergosterol very early in the evolution of eukaryotes (6–8).
T. brucei encounters diverse environments during its life cycle, with the different stages taking on very different sterol compositions. Despite having an intact ergosterol biosynthesis pathway in the procyclic forms (PCFs), the bloodstream forms (BSFs) are generally considered to lack ergosterol biosynthesis and to be auxotrophic for sterol (9–13). At this stage, cells satisfy their sterol requirements through dietary supplementation of cholesterol via lipoproteins in full-growth medium (FGM) present in the blood meal (10, 11). Consequently, the existence of a sterol uptake process which permits the formation of BSF membranes containing exclusively cholesterol could provide resistance to a range of antifungal drugs, e.g., amphotericin B, that function typically in membranes formed by ergosterol (14, 15). However, all the genes for ergosterol biosynthesis have been found recently to be expressed in BSF (16, 17) and inhibitors of the post-squalene portion of ergosterol biosynthesis can inhibit growth of BSFs (4, 18–20); therefore, the ability for BSFs to grow as an ergosterol-depleted protozoan with dietary cholesterol as an ergosterol surrogate remains enigmatic.
In nature, sterols are chiefly used as structural components of membranes (21, 22). Mammalian cell membranes are considered to be more flexible than fungal or protozoan cell membranes (23), and the chemodiversity in sterol biosynthesis may contribute to their architectural suitability (24). However, there is growing evidence that the sterol requirements for membrane structures across kingdoms are rather broad and can be met by several closely related compounds. Thus, cholesterol can be shown to replace ergosterol in yeast membranes and phytosterols can be shown to replace cholesterol in animal membranes (25–28). On the other hand, functional diversity of sterols is reported to exist, with emphasis on the variation in sterol side chain structures which contribute to the regulatory role that sterols per se may play, apart from modulating the bulk physical properties of the membrane. For yeast, the “regulatory role” of ergosterol, also referred to as sparking (29), is to provide direct integration of a chemical switch into membrane domains to signal cell proliferation and possibly affect cell shape (29–31). The phenomenon by which ergosterol can play dual roles in yeast has been defined as sterol synergism (26) and the two kinds of function, bulk and sparking, can be distinguished quantitatively from each other by differing sensitivities to the 24β-methyl group of the sterol’s structure (31).
Given the possibility that BSFs generate ergosterol in small amounts to promote growth and accessibility of very few therapeutic drugs, with many produced over 30 years ago, and toxicity issues (32, 33), we examined the concentration dependence of ergosterol in T. brucei growth and evaluated the potential use of targeted enzymes of ergosterol biosynthesis for future therapies. Here we demonstrate that quantitative differences in the ergosterol content of PCFs or BSFs of different infective types contribute to variations in the growth response. Additionally, by examination of the knockdown of TbSMT and TbSDM (sterol 14α-demethylase) gene expression together with inhibitor treatment of PCFs and BSFs cultured in vitro or in vivo using infected mice, we show that C24-sterol methylation and ergosterol are the sine qua non of sparking trypanosome proliferation.
Sterol compounds, referenced to the retention time of cholesterol in capillary GC at 13.8 min, or somewhat longer depending on whether the column length was clipped due to age, and HPLC at 17 or 22 min, depending on the particle size of the stationary phase of 3 and 5 μm, respectively, were quantified by integration of the detector signal (flame ionization detector in GC and UV at 210 nm in HPLC, from 10 to 30 min). Products were routinely identified by their retention times in GC and electron-impact spectrum with those of reference samples. For the identification of select products, preparative HPLC was carried out on large amounts of cell pellet using a Phenomenex analytical Luna C18-column 5 μm particle size (eluted with methanol at 20°C at 1 ml/min) linked to a diode array detector which provided UV spectra at 210 and 282 nm; fractionation was followed by GC-MS (ZB-5 capillary column of 30 m) using a Hewlet-Packard LS 6500 gas chromatograph interfaced to a Hewlet-Packard 5973 mass spectrometer.
Cholesterol and ergosterol were recrystallized from commercial samples and lanosterol was purified by HPLC from a mixture of compounds in the commercial lanosterol sample purchased from Sigma (1). The [methyl-3H3]AdoMet (10–15 Ci-mmol), which was diluted to 10 μCi/μmol for the activity assays, was purchased from Perkin Elmer. Itraconazole (ITC) was purchased from Sigma. The 25-azalanosterol (AZA) and 25-thialanosterol sulfonium salts were prepared as previously reported (34, 35).
T. brucei strains 427 and 328 PCF cells were grown in SDM-79 medium supplemented with 10% heat-inactivated FBS (Atlanta Biologicals), referred to as the FGM at 27°C. The T. brucei 427 (29-13) cell line, resistant to hygromycin (Invitrogen) and neomycin (G418) (Invitrogen), expressing the tetracycline repressor (TetR) gene and T7RNA polymerase, were grown in the same medium containing appropriate antibiotics (hygromycin, 50 μg/ml; G418, 15 μg/ml) (36, 37). BSF cells were maintained in HMI-9 medium supplemented with 10% heat-inactivated FBS (Atlanta Biologicals) and 10% Serum Plus (SAFC Biosciences), which is a FGM. The T. brucei 427 single marker cell line, resistant to G418 and expressing the TetR gene and T7RNA polymerase, was grown in the same medium containing G418 (2.5 μg/ml). For preparation of lipid-depleted medium (LDM), PCFs in SDM-79 medium were supplemented with 10% heat-inactivated lipid-free FBS (Sigma-Aldrich). For a low-cholesterol medium, the BSF cells were grown in HMI-9 medium containing 10% lipid-free heat-inactivated FBS (Sigma-Aldrich). For growth curves, SMT and SDM RNAi engineered cells were diluted into FGM or LDM, induced by RNAi by the addition of doxycycline (DOX) (1 μg/ml final), and cell density monitored for another 4–6 days. Typically, procyclic cells were inoculated at 2–3 × 106 cells/ml and BSF cells inoculated at 1 × 105 cells/ml in medium containing antibiotic and cultured for 6–8 days. Cell densities were maintained in the range of 0.5–1 × 107 cells/ml for the PCF and 0.1–1 × 106 cells/ml for the BSF by reinoculation in fresh medium. Cells were harvested by centrifugation. TbSMT inhibitors and ITC were added to PCF or BSF cells from stock solutions in dimethyl sulphoxide, such that the organic solvent was less than 1% (v/v) of total culture volume. Five different concentrations of each compound were tested in triplicate between 0 (control) and 10 μM; the 50% growth inhibition reported as the IC50 relative to the growth of control. Cell densities were determined using a Neubauer hemocytometer counter. The cumulative cell number was plotted versus time of growth.
Human epithelial cells (HEK 293T) were purchased from ATCC (Manassas, VA). HEK cells were cultured at 37°C in a humidified 5% CO2 incubator in DMEM (Invitrogen, Carlsbad, CA) supplemented with 10% FBS. Cell viability was checked by trypan blue dye exclusion as described (38, 39). A set of subspecies of T. brucei trypomastigotes, T. brucei brucei (strains 328-114 and 427), T. brucei rhodesiense (Etatl.2S), and T. brucei gambiense (LiTatl.3), were cultured as described above (40).
Total RNA was isolated from T. brucei PCF and BSF SMT RNAi and SDM RNAi cell lines grown in the presence and absence of DOX using Trizol reagent (Invitrogen) and Northern blot analysis was performed as described (41). Total RNA (5–10 μg) was loaded per lane and the blot was probed with 32P-labeled DNA probe corresponding to the same SMT sequence corresponding to the SMT RNAi.
Initially, the steady-state kinetic parameters, Km and Vmax, were established using lysate of Escherichia coli (8). Zymosterol concentration was varied from 5 to 150 μM and [3H3-methyl]S-adenosyl-l-methionine (SAM) concentration was fixed at 100 μM and the assay was performed under initial velocity conditions on soluble protein. The resulting kinetics for zymosterol conversion to ergosta-8,25(27)-dienol were calculated by fitting the liquid scintillation data to the Michaelis-Menten equation using the Enzyme Kinetic Module from SigmaPlot (42). The Km and Vmax values generated for zymosterol against cloned TbSMT for experiments performed herein were essentially the same as those reported in (8). Inhibitor dissociation constants of 25-thialanosterol sulfonium salt and lanosterol for TbSMT were based on steady-state experiments for assays performed in triplicate at varied zymosterol concentrations from 5 to 100 μM and [3H3-methyl]SAM fixed at 100 mM in the presence of inhibitor varied in the amount from 5 to 75 nM (25-thialanosterol sulflonium salt) or from 10 to 150 μM (lanosterol), while the data for AZA was previously reported in (8). Minimal variation was detected in the experimentally determined kinetic constants with standard errors of 2–10% between trials.
T. brucei cell pellets were saponified directly in 10% KOH in 80% aqueous methanol at the reflux temperature for 1 h, which yielded total sterol (free plus esterified sterols). The neutral lipids obtained by dilution with water and extraction with hexane (Fisher) after the saponification were analyzed by GC (3% SE-30 pack column operated isothermally at 245°C). Total sterols in the nonsaponifiable lipid fraction were purified on an Agilent 1100 series HPLC system coupled to a diode array detector. The total sterols were loaded onto a C18 reversed phase analytical column (Phenomenex, 4 μm) eluted isocratically with methanol at a flow rate of 1 ml/min. The standard for HPLC data was cholesterol, and the rates of movement are given relative to cholesterol (αc). HPLC fractions in the sterol region of the chromatogram (αc 0.5–2.0) were collected and analyzed by GC-MS with a Hewlett-Packard LS 6500 gas chromatograph at 70 eV. GC was performed using an Agilent ZB-5 column (30 m × 25 μm in diameter). Cholesterol was the standard for determination of the relative retention time (RRTc). Quantitation of the amounts of unlabeled sterols was accomplished by GC with a standard curve for cholesterol. To several cell pellets undergoing the saponification process, a known amount of 5α-cholestane was added as an internal standard.
To prepare the construct for TbSMT double stranded RNA expression, the 588 bp fragment of the coding region was PCR amplified from T. brucei genomic DNA by using high-fidelity pfu polymerase (Stratagen). Sense and antisense primers containing the restriction sites for BamH1 and HindIII at the 5′ ends were TbSMTFor 5′agtcggatcctgtgaatggcgatgtgaatgc3′ and TbSMTRev 5′agtcaagcttcatacaggtccgtcaaacaccac3′, respectively. The amplified product was cloned into the BamH1/HindIII sites of a tetracycline-inducible dual-promoter plasmid vector, p2T7Ti-177 (43). The construct for TbSMT RNAi was verified by sequencing. The purified plasmid DNA was linearized by NotI and transfected into T. brucei 427 29-13 PCF and the single marker 427 BSF cells expressing T7 polymerase and TetR proteins according to standard protocol (37). Transfectants were selected by phleomycin (2.5 μg/ml). Similar approaches were used to generate the TbSDM RNAi cell line.
Sixteen male Balb/C mice (10–12 weeks old) were divided into two groups of eight mice in each group. Mice were pretreated for 5 days and continued throughout the experiment with either DOX (50 mg/kg body weight/day) in 5% sucrose water (SMT RNAi group) or 5% sucrose water alone (control group) via oral gavages. DOX is the water soluble and bio-available form of tetracycline, which induces the expression of RNAi in vivo but does not itself affect the infection process. Each mouse was then infected with 1 × 104 T. brucei BSF SMT RNAi cells by intraperitoneal injection. Parasitemia was measured each day in tail-vein blood from mice until the parasite count reached within the range of 4–8 × 108/ml. At this point mice were euthanized according to the Institutional Animal Care guidelines. Mice were also monitored daily for general appearance, behavior, and weight loss. If a mouse showed obvious distress and >20% weight loss, the mouse was euthanized. The protocols involving mice were approved by the Institutional Care and Use Committee of the Meharry Medical College.
There were three groups of mice and each group had six mice: group I, control, treated with vesicle; group II, treated with aza-lano; and group III, treated with thia-lano. Mice were infected with BSF (104 parasites/mouse) by ip injection. Inhibitors were adminstered (50 mg/kg each, ip) after 2 h of injection of parasites and on each day post infection. The parasitemia level was monitored by counting cell numbers (bloodstream trypanosomes) in blood each day after infection. Mice were euthanized when the blood parasitemia level reached 4–8 × 108/ml.
Growth of wild-type PCF strain 427 in FGM, which provides 678 μM (262 μg/ml) cholesterol (4), followed a logarithmic course with a doubling time of 12 h and yielded cell densities at 6 days of 1–3 × 107 per ml. When these cells were extracted, the GC-MS analysis of the neutral lipid fraction showed the presence of cholesterol and a set of endogenously formed 24-desalkyl (mostly cholesta-5,7,24-trienol) and 24-alkyl sterols (mostly ergosta-5,7,25(27)-trienol) in approximate 50:50 ratio (Table 1). Ergosterol in GC at RRTc 1.11 was determined to be in trace amounts. However, this compound was barely detectable by GC-MS analysis (supplementary Figs. 1–5, supplementary Table 1) because it chromatographs underneath the cholesta-5,7,24-trienol peak at RRTc 1.10, which dominates the neutral lipid fraction. Ergosterol in the neutral lipid fraction could be quantified accurately by HPLC-UV scanning at 282 nm, which is the λmax for the absorption band of the Δ5,7-diene system. Using a combination of GC-MS and HPLC-UV scanning, the amount of total sterol in the cells was estimated to be 163 fg/cell (±10 fg/cell) and the amount of ergosterol was approximately 6 fg/cell (±1 fg/cell) or 3.5% of the total sterol; co-metabolite analysis and determination of the ergosterol content of T. brucei strain 328 indicated these cells produce a similar sterol profile to strain 427.
A different situation was obtained when the serum lipoproteins were removed from the media, i.e., LDM, which provides approximately 7.8 μM (3 μg/ml) cholesterol [(4) reports the amount of cholesterol in lipid depleted medium and we converted that amount to μM.]. In this case, the total sterol was approximately the same as for cells cultured in FGM at 145 fg/cell (±10 fg/cell), while the cellular cholesterol was minor (21% total sterol); the sterol mixture was mostly cholesta-5,7,24-trienol and ergosta-5,7,25(27)-trienol (supplementary Table 1) and cells grew to a lower density at 6 days of 4–5 × 106 cells per ml. Coincidently, the amount of cellular ergosterol was drastically reduced to a level of approximately 0.9 fg/cell (±0.1 fg/cell) or 0.6% total sterol.
Subsequent experiments showed, however, that the concentration of ergosterol in BSF could be even much lower than in the PCF, making routine GC-MS analysis problematic for quantification of this compound. To generate a more exacting analysis, we repeated our previous efforts at sterol analysis of cultured cells by harvesting much larger cell pellets of the previously studied T. brucei brucei strain 427. In addition, we cultured large amounts of strain T. brucei brucei 328 and two related subspecies, T. brucei rhodesiense and T. brucei gambiense, of cell numbers that ranged from 3 × 109 to 7 × 1010. When strain T. brucei brucei 427 was extracted, GC-MS analysis of the neutral lipids showed a mixture of cholesterol and a set of phytosterols of dietary origin, which eluted from 16 to 18 min (Fig. 2A), in agreement with previous studies (4). The sterol profile of strain 427 was similar to that of the other strains and subspecies examined with the amount of total sterol estimated to be 150 fg/cell (±10 fg/cell).
The neutral lipid fractions of T. brucei brucei (strains 427 and 328), T. brucei gambiense, and T. brucei rhodesiense were chromatographed by HPLC. The total sterols in the combined fractions (αc 0.5–0.95) from semi-preparative HPLC (Luna C18 column) were injected in 100 μl aliquots into an analytical HPLC (Prodigy column) affording trace amounts of ergosterol. HPLC-UV scanning showed ergosterol was present in all the cells (Fig. 2B). The identity of the recovered material was confirmed by GC-MS analysis as ergosterol (RRTc 1.10; M+ at m/z 396, which agreed with an authentic specimen). HPLC-UV scanning of the ergosterol in BSF cultured in FGM showed 0.01 fg/cell (±0.01 fg/cell), and in cells cultured in LDM showed five to ten times less ergosterol at 0.005–0.001 fg/cell (±0.01 fg/cell).
To assess the importance of ergosterol biosynthesis enzymes for the parasite’s metabolism, we first downregulated TbSMT and TbSDM gene expression by RNA silencing in PCF. In the absence of DOX, the resulting RNAi cell lines grew in a manner similar to the wild-type trypanosome cell line, with cell densities at day 7 yielding 8 × 106 cells/ml or 1–3 × 106 cells/ml in FGM and LDM, respectively (Fig. 3A, B). However, in the presence of DOX, growth was significantly reduced with cell densities at day 7 yielding 2–3 × 106/ml or below in FGM and LDM, respectively, or in LDM, TbSDM RNAi plus DOX lines did not grow at all. Northern blot analysis showed that TbSMT and TbSDM transcript levels were undetectable within 1–2 days of DOX pressure (Fig. 3C, D), proving silencing of the genes of ergosterol biosynthesis, as expected. The effect of the RNAi on cell growth was more pronounced on later days because of the gradual loss of these gene products by cell division and product turnover. The amount of total sterol, 161 fg/cell (±10 fg/cell), in engineered cells in FGM without DOX was similar to wild-type cells, while with DOX induction, the amount of sterol in the cell increased to 220 fg/cell (±15 fg/cell). Ergosterol was evident at near trace levels of 0.1–0.3 fg/cell, as judged by routine GC-MS analysis using the SIM mode selecting for ions at m/z 396, 381, and 363 (Fig. 3E inset). GC-MS analysis showed that the major endogenously formed sterols of TbSMT and TbSDM knockdown parasites were cholesta-8,24-dienol (RRTc, 1.06; M+ at m/z 384), cholesta-7,24-dienol (RRTc, 1.15; M+ at m/z 384), cholesta-5,7,24-trienol (RRTc, 1.10; M+ at m/z 382), lanosterol (RRTc, 1.31; M+ at m/z 426), 31-norlanosterol (RRTc, 1.15; M+ at m/z 412), 14α-methylzymosterol (RRTc, 1.07; M+ at m/z 398), 14α-methyl ergosta-8,25(27)-dienol (RRTc, 1.14; M+ at m/z 412), and 4α,14α-diemethyl ergosta-8,25(27)-dienol (RRTc, 1.24; M+ at m/z 426) (Fig. 3F; supplementary Figs. 4, 5; Table 1). The accumulation of endogenously formed 14α-methyl sterols, which might be considered as toxic intermediates, was not particularly pronounced in the DOX-induced RNAi lines. DOX-induced TbSMT and TbSDM RNAi lines produced minor amounts of endogenously formed sterol, while cholesterol from the media was the major cellular sterol (Table 1). Together, our results show that the ergosterol biosynthesis pathway remains similar to wild-type cells following reduction of TbSMT or TbSDM by RNAi. Thus an incomplete inhibition of growth in DOX-induced RNAi cell lines, despite the decrease in ergosterol biosynthesis, can be understood, as downregulation or inhibition of the target enzymes is not quite complete and the reduced ergosterol level is still sufficient to maintain an adequate amount of signal molecule to spark growth.
To further examine the importance of TbSMT and TbSDM enzymes in PCF growth in a manner complementary to RNAi silencing, we exposed wild-type cells to increasing concentrations of AZA, 25-thialanosterol sulfonium salt, or ITC, drugs which should inhibit these enzymes for mechanistic reasons (supplementary Fig. 6) (4, 44). Cell growth of wild-type PCF in FGM at day 6 was inhibited in a dose-dependent manner of ED50 values from 1 to 3 μM; there was no significant difference in the ED50 values for cells cultured in LDM (Fig. 3G). The dose causing a 50% cell growth inhibition at ED50 <10 μM being proposed as a threshold to consider a compound as a potential anti-sleeping sickness drug (45). When the PCF cells were exposed to AZA, 25-thialanosterol sulfonium salt, or ITC, the sterol mixture of treated cells was the same as reported previously for the TbSMT and TbSDM RNAi cell lines, but in different proportions depending on the concentration of inhibitor added to the media (Fig. 3G; supplementary Table 1). Cells treated with the inhibitors in FGM grow in a similar manner to treated cells in LDM (supplementary Fig. 7) and accumulate cholesterol proportional to the degree of inhibition imposed on the target enzyme; at the ED50 drug concentration, cholesterol represents approximately 50% of the total sterol, while at the ED90 drug concentration, cholesterol represents approximately 90% total sterol. The amount of total sterol in these cells ranged from 145 fg/cell at ED50 to 160 fg/cell at the ED90, which is similar to control. Ergosterol could not be detected in any of the treated cells in routine GC-MS analyses.
In fully developed cultures at the IC99 value, cells can survive for several days, as these cells were shown to contain a full complement of endogenously formed sterols of cholesterol to 24-deasalkyl sterol:24-alkyl sterol [mostly ergosta-5,7,25(27)-trienol] in a ratio of 66:33:1 (AZA) and 40:57:3 (25-thialanosterol sulfonium salt), and to contain significantly more total sterol than controls at approximately 302 fg/cell (±15 fg/cell). These observations show that the inability of potent inhibitors of TbSMT to be toxic to PCF at high drug concentrations could result from a feedback response that signals upregulation of ergosterol biosynthesis enzymes to overcome the effect of the inhibitor. As the response of the cells to inhibitors of TbSMT and TbSDM failed to lead to cell death, the unexpected results just recorded at the ED99 drug concentration prompted us to examine the effects of combining two drugs on growth by cells kept in FGM or LDM. When AZA was combined with ITC at approximately the ED50 values of 1 μM, minimal growth was observed for cells cultured in FGM, but in LDM a no growth response was observed with cell fragments apparent microscopically showing cell death (Fig. 3G, supplementary Fig. 8). Although cholesterol available from the serum could provide a buffering capacity in membranes to counter the potentially toxic 14α-methyl sterol intermediates (46, 47), cells died in LDM, nonetheless, when the media was supplemented with a combination of the two drugs (Fig. 3G). The foregoing results imply that the reason why PCFs are responsive to ergosterol biosynthesis inhibitors is that small amounts of ergosterol are required for essential cell functions, rather than that they accumulate unusual sterols which may perturb membrane structures.
Kinetic studies were carried out to investigate the interaction of TbSMT and the test drugs. Previously, the TbSMT was cloned and the optimal substrate for activity shown as zymosterol (Km = 47 μM, kcat = 0.6 min−1) affording a catalytic competence (Vmax/Km) of 0.13 (8). The enzyme is known to be a tetramer and catalyze an irreversible reaction with SAM binding first (48). The substrate-based inhibitors examined with TbSMT were reversible transition state analogs in which the protonated or salt form of the molecule mimicked the carbonium ion intermediate in the C24-methylation reaction. Thus, Ki values for AZA and 25-thialanosterol sulfonium salt determined over the concentration range of 25–75 nm with TbSMT were 39 nM (noncompetitive against zymosterol) and 86 nM (noncompetitive against zymosterol), respectively, while the Ki value for lanosterol examined over the concentration range of 15–150 μM was 126 μM (competitive against zymosterol) (supplementary Fig. 9). The Ki/Km values of 39 nm/47 μM = 0.008 and 86 nM/47μM = 0.018 for AZA and 25-thialanosterol sulfonium salt, respectively, compared with the Ki/Km value of 126 μM/47 μM = 2.6 for lanosterol indicate that the test compounds are potent transition state analogs of TbSMT catalysis, which interrupt the C24-methylation reaction as shown for the fungal SMT (49–51).
The TbSDM was also cloned and characterized previously (6), and the optimal substrate was shown as 31-norlanosterol (Km = 9 μM and kcat = 4 min−1) with a catalytic competence of 0.43. Azole drugs have been shown to be tight binding inhibitors of the TbSDM (6). We have not examined ITC against the isolated TbSDM; however, a similar azole (ketoconazole) was found to generate a Kd of approximately 4 μM against the cloned TbSDM (51). The accumulation of specific 24-desalkyl sterol and 14α-methyl sterols coupled to the suppression of growth from the test inhibitors agrees with the substrate specificities of the target enzymes.
All the test drugs demonstrated a clear dose-dependent inhibitory effect on BSF cells cultured in FGM (supplementary Figs. 8, 11) with ED50 values that ranged from 1 to 3 μM, while they failed to inhibit cultured HEK cells at greater than or equal to 50 μM (Table 1) (45). Thus, the relative trypanocidal activity for each compound affording a therapeutic index <25 (ED50 against the mammalian cell line/ED50 against the parasite) is similar to the action of commercial drugs used to treat first- or second-stage sleeping sickness, such as suramin, ED50 of 0.4 μM and nifurtimox and eflornithine combination therapy of 5 μM (52). In view of successes with azoles to treat Chagas disease (53, 54) and our observations with combinations of AZA and ITC to kill PCF cells, we tested the possibility of drug synergism as an approach to inhibit BSF growth. Thus, by combining AZA at ED50 with ITC at ED50, BSF growth in LDM led to cell death or to marked growth inhibition in FGM (supplementary Fig. 10).
In a first attempt to test whether there is an ergosterol-dependent disease process linked to T. brucei infections, we examined the response of mice infected with BSF cells engineered for RNAi-mediated depletion of TbSMT or infected with wild-type BSF and treated with inhibitors of TbSMT. Preliminary studies showed DOX-induced knockdown of TbSMT in BSF failed to prevent growth, although cells cultured in LDM grew to a lower population density than cells cultured in FGM (Fig. 4, for PCF cultures in FGM see supplementary Fig. 11). Northern blot analysis of total RNA showed that induction of RNAi was effectively complete by day 4 (Fig. 4B). GC-MS analysis of cells harvested between 3 and 5 days showed cholesterol as the major cellular sterol (<99%) in agreement with wild-type controls (4).
Next, we tested mice infected with T. brucei strain 427 engineered with DOX-inducible TbSMT RNAi and treated mice with a wild-type strain with AZA or 25-thialanosterol sulfonium salt. To assess the virulence of TbSMT RNAi cells, Balb/C mice (eight per group) were either left untreated (uninduced control) or treated with DOX in their drinking water to induce TbSMT RNAi. Mice were then infected intraperitoneally with 1 × 104 freshly prepared BSF TbSMT RNAi trypanosomes. The uninduced control infection resulted in a mean-time-to-death of 8–9 days. However, when TbSMT RNAi was induced in the DOX-treated mice, there was protection against death that extended their life for another 4–11 days. Northern blot analysis of BSF isolated from day 13 infected mice clearly indicated the TbSMT gene was transcribed at a level approximately one-sixth that recorded for procyclic cells cultured on FGM (Fig. 4C). In a separate study with mice, the animals were infected with BSF and 5 mg/kg of inhibitor at one dose per day to conserve drug. As with the knockdown TbSMT lines, survival was extended for at least 2 days (Fig. 4D). The survival results from the two experiments complement each other and show that C24-methylation of the ergosterol side chain is functionally important for full virulence in mice.
To determine whether the absence of ergosterol production is responsible for the growth phenotype observed using ergosterol biosynthesis inhibitors, we developed conditions in which the background of ergosterol could be brought to insignificant levels by culturing the TbSMT RNAi cell line in LDM with AZA, affording continued synthesis of cholesta-5,7,24-trieno,l while growth was restricted to less than 1.5 × 105 cells/ml by day 2 and 4.5 × 105 cells/ml by day 6 (Fig. 4E). Figure 4E shows the growth response of BSF cultured in LDM supplemented with a fixed concentration of AZA at IC90, a synergistic mixture of 7.8 μM cholesterol (3 μg/ml from the serum lipids) and varied concentrations of ergosterol, which ranged from 0.12 μM to 12 μM [at 0 μg/ml, 0.12 μM; 0.05 μg/ml (1:60 ergosterol/cholesterol), 1.2 μM; 0.5 μg/ml (1:7 ergosterol/cholesterol), 12 μM; and 5.0 μg/ml (3/5 ergosterol/cholesterol)]. At 0.12 μM ergosterol, cells did not grow. However, at 1.2 μM ergosterol, giving 1:7 ratio of ergosterol to cholesterol, the growth was completely rescued. Neither the doubling time nor the yield was affected by further supplementation of ergosterol at 12 μM. To determine whether a 14-methyl sterol intermediate could replace ergosterol and spark growth of PCF or BSF, lanosterol was added at increasing concentrations from 0.1 μM to 12 μM to the LDM media supplemented with AZA. In these experiments, lanosterol failed to spark growth, such that the RNAi cell lines continued to show a no growth response after a 6 day incubation period. These results show that ergosterol with a 24β-methyl group is necessary for cell viability and proliferation in small amounts, so long as another Δ5-sterol with a 24-H atom, such as cholesterol, is present in large amounts.
The sensitivity of trypanosomatid protozoa to regulation of ergosterol biosynthesis by gene silencing and inhibitors offers a unique opportunity for understanding ergosterol biology, drug target identification, and the subsequent development of new anti-parasite agents. In the present work, we explored the little understood multiple functions of sterols in parasite growth by analyzing the sterol composition of PCF and BSF cells and correlating this information to growth responses resulting from the knockdown of TbSMT and TbSDM gene expression and blocking TbSMT and TbSDM action involved with ergosterol biosynthesis. This approach showed that PCF and BSF can live with variable, albeit minute, amounts of ergosterol, as long as prevalent cholesterol is available from the host to serve as the architectural component of membranes. We were able to pinpoint the vastly different natural concentrations of ergosterol associated with growth of PCF and BSF cultured in FGM as 6 fg/cell or 0.01 fg/cell, respectively. In contrast, the overall sterol composition of these cells remain fairly constant at 150 fg/cell, and cholesterol can contribute from 50 to <99% of the total sterol, depending on culture conditions. Notably, alterations in cholesterol environment by changing the FGM to LDM media, which mirrors cholesterol availability in human blood and insects, respectively (24, 55), can decrease ergosterol biosynthesis in cells and suppress growth rates of PCF or BSF. The most logical explanation for this association involves a stage-specific relationship between the biosynthetic renewal of ergosterol and cell proliferation.
Ergosterol, at near hormonal levels in cells, has been implicated as a signal molecule of variant nonpathogenic microorganisms (26). By virtue of the RNAi silencing and inhibitors designed specifically to prevent TbSMT and TbSDM catalysis, it has been possible to block complete metabolism of lanosterol to ergosterol, which results in high cholesterol import, while there is only minor accumulation of intermediates under normal metabolic conditions. In contrast, Perez-Moreno et al. (56) failed to observe any antiprolierative effects of 22,26-azasterol on the procyclic parental line of T. brucei or of induced (+DOX) or noninduced (−DOX) after 6 days of TbSMT interference or detected any ergosterol in these cells. Our results demonstrate that the virtually complete replacement of endogenously formed sterols by cholesterol is not compatible with cell growth unless small amounts of ergosterol are available to spark cell proliferation. In the present experiments, the quantities of sterol supplied to the media found necessary to rescue PCF or BSF cultures that were devoid of ergosterol were similar to other microorganisms auxotrophic for sterol. Additionally, the minimal synergistic mixture of ergosterol and cholesterol in a 1:7 ratio used to promote growth is similar to the combination of ergosterol and cholesterol provided to GL7 yeast to spark its growth (26). The results show a commonality in ergosterol function across kingdoms distinct from the bulk membrane role. The failure of earlier workers to find ergosterol in BSF (55) probably has its origins in the experimental difficulties in the methods one uses in recognizing ergosterol from its isomers or detecting ergosterol as a trace component eluting underneath cholesta-5,7,24-trienol in GC-MS analysis.
In the case of parasitic diseases, there are very few validated enzyme targets. The only drug for which there is a well-defined molecular target is eflornithine, an analog of ornithine which blocks spermidine synthesis and the formation of trypanothione through irreversible inhibition of ornithine decarboxylase; administered with nifurtimox, the combination therapy has enjoyed rapid implementation (52). Based on previous successes with substrate analogs containing nitrogen or sulfur on the lateral sterol side chain proving them to be potent antifungal agents (5, 49–51), we studied two of them, AZA and 25-thialanosterol sulfonium salt, as reversible tight-binding inhibitors of TbSMT. When these compounds were examined for effects on cell growth, ergosterol biosynthesis, and inhibition of the cloned TbSMT, it became evident that TbSMT is crucial for life support and is assayable and druggable, and that these trypanocidal agents may exhibit a limited drug resistance when used synergistically with another mechanism-based inhibitor which can block at a different step in the late-stages of ergosterol biosynthesis. It is interesting that as the concentration of the AZA is increased to ED99, rather than forcing an accumulation of harmful intermediates that cause cells to die, they continued to live due to a compensatory upregulation in ergosterol biosynthesis. However, when AZA was combined with itraconzaole at their ED50, cell proliferation stopped and cells died. The total dependence of inhibitor-treated cells on ergosterol for sparking cell proliferation is thus understandable and can be reconciled with all experimental observations, by their depletion of ergosterol production, and may turn out to be useful in the design of a new generation of irreversible suicide substrates targeted to impair essential sterol functions in trypanosomes (8, 57). All things considered, due to the limits of monotherapies, greater emphasis should be placed on orally administered analogs of TbSMT catalysis in combination with specific azoles, which together might be effective in smaller amounts and have less deleterious effects on the host than the drugs presently in use.
This work was supported, in whole or in part, by National Science Foundation Grant MCB-0929212 (to W.D.N.), National Institutes of Health Grants AI080580 and MD007593 (to F.V.) and GM081146 (to M.C.), and the Belgian National Fund for Scientific Research (FRSM) and the Interuniversity Attraction Poles Programme-Belgian Policy (to B.V.).
[S]The online version of this article (available at http://www.jlr.org) contains supplementary data in the form of eleven figures and two tables.