http://orcid.org/0000-0002-8011-6219
Figures
Abstract
Trichomonas vaginalis and Tritrichomonas foetus are pathogens that parasitise, respectively, human and bovine urogenital tracts causing disease. Using LC-MS, reference metabolomic profiles were obtained for both species and stable isotope labelling with D-[U-13C6] glucose was used to analyse central carbon metabolism. This facilitated a comparison of the metabolic pathways of T. vaginalis and T. foetus, extending earlier targeted biochemical studies. 43 metabolites, whose identities were confirmed by comparison of their retention times with authentic standards, occurred at more than 3-fold difference in peak intensity between T. vaginalis and T. foetus. 18 metabolites that were removed from or released into the medium during growth also showed more than 3-fold difference between the species. Major differences were observed in cysteine and methionine metabolism in which homocysteine, produced as a bi-product of trans-methylation, is catabolised by methionine γ-lyase in T. vaginalis but converted to cystathionine in T. foetus. Both species synthesise methylthioadenosine by an unusual mechanism, but it is not used as a substrate for methionine recycling. T. vaginalis also produces and exports high levels of S-methylcysteine, whereas only negligible levels were found in T. foetus which maintains significantly higher intracellular levels of cysteine. 13C-labeling confirmed that both cysteine and S-methylcysteine are synthesised by T. vaginalis; S-methylcysteine can be generated by recombinant T. vaginalis cysteine synthase using phosphoserine and methanethiol. T. foetus contained higher levels of ornithine and citrulline than T. vaginalis and exported increased levels of putrescine, suggesting greater flux through the arginine dihydrolase pathway. T. vaginalis produced and exported hydroxy acid derivatives of certain amino acids, particularly 2-hydroxyisocaproic acid derived from leucine, whereas negligible levels of these metabolites occurred in T. foetus.
Citation: Westrop GD, Wang L, Blackburn GJ, Zhang T, Zheng L, Watson DG, et al. (2017) Metabolomic profiling and stable isotope labelling of Trichomonas vaginalis and Tritrichomonas foetus reveal major differences in amino acid metabolism including the production of 2-hydroxyisocaproic acid, cystathionine and S-methylcysteine. PLoS ONE 12(12): e0189072. https://doi.org/10.1371/journal.pone.0189072
Editor: Andrea Motta, National Research Council of Italy, ITALY
Received: August 9, 2017; Accepted: November 17, 2017; Published: December 21, 2017
Copyright: © 2017 Westrop et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Parabasalids are a large and diverse group of flagellated protozoa that lack mitochondria and have an anaerobic metabolism involving specialised organelles called hydrogenosomes [1]. These are adapted mitochondria that produce hydrogen as an end product of pyruvate fermentation. These protozoa have other distinctive structural features, including 3–5 flagella, a complex cytoskeleton and an enlarged golgi apparatus referred to as a parabasal body. The majority of these organisms are commensals of the enteric tract of animals but the group includes several pathogens, the most important being Trichomonas vaginalis and Tritrichomonas foetus that infect the urogenital tract of humans and cattle, respectively [2, 3].
T. vaginalis is the causative agent of trichomoniasis, an exceptionally common sexually transmitted disease of humans. Infection causes inflammation or vaginitis in about 30% of women and without treatment infection can be long lasting. In men, however, T. vaginalis infections are self-clearing and generally asymptomatic. Trichomoniasis is a cofactor in the transmission of HIV [4], the development of prostate cancer [5–7] and in pregnancy is linked to pre-term delivery and low birth weight [8, 9]. Infections can usually be controlled by 5-nitroimidazoles such as metronidazole, although drug resistance is a problem [10]. Trichomoniasis has been identified as a neglected parasitic infection by the CDC (http://www.cdc.gov/parasites/npi/index.html) and targeted for public health action.
T. foetus infections cause trichomoniasis in cattle where the main symptom is inflammation of the genital tract. Infection can cause sterility and in some cases involves the placenta, lungs and lymph nodes of the developing foetus and results in abortion [3]. Although primarily regarded as a bovine parasite, some strains of T. foetus can infect cats where they colonise mucosal surface of the gastro-intestinal tract and cause feline bowel disease [11]. Bovine and feline strains show a high species and organ specificity.
The T. vaginalis genome is exceptionally large and has a highly repetitive structure [12]; 65% of the genome consists of transposable elements and many protein coding genes are replicated to form high copy number gene families. A draft genome sequence of T. foetus strain K was recently published [13], making it possible to determine how closely related these trichomonads are genetically. Initial analysis revealed that 72% of ORFs in the T. foetus genome were similar to T. vaginalis, and 28% were not found in any other organism. In a separate study application of reduced representation genome sequencing revealed that gene mutations were shared between metronidazole resistant strains of T. vaginalis and T. foetus suggesting a common mechanism for development of resistance [14]. It is interesting that T. foetus has an estimated genome size of 161 Mb [13, 15] which is similarly large to the 160 Mb draft genome of T. vaginalis [12]. It also contains 62% repetitive sequences and many repeatedly duplicated genes suggesting that the genome of T. foetus evolved by massive expansion as proposed for T. vaginalis [13, 16]. Thus extreme genome size seems another common feature of T. vaginalis and T. foetus that distinguishes them from many other parabasalid species.
Similarities and differences between the metabolism of the two species, especially concerning their anaerobic energy metabolism, are known from various biochemical studies and have been reviewed extensively [17]. The major end products of glucose metabolism in T. vaginalis are glycerol, lactate and ethanol in the cytoplasm and H2, CO2 and acetate in the hydrogenosome. Alanine is produced from pyruvate as a minor end product but is not excreted. The end products formed in T. foetus are broadly similar but they do not produce lactate with instead succinate representing about 50% of the carbon released as fermentation products. Interesting differences also occur with the advent of metronidazole resistance, with metabolism shifted to lactate production in T. vaginalis but to ethanol in T. foetus [17].
A notable species difference is that T. vaginalis produces methanethiol (CH3SH), 2-ketobutyrate and NH3 by catabolism of methionine using methionine γ-lyase (MGL), although biochemical analysis failed to detect this activity in T. foetus or other trichomonad species [18]. The T. vaginalis MGL has a broad specificity and it has been proposed that H2S released from homocysteine by MGL is used by the cysteine synthase (CS) to produce cysteine from O-phosphoserine [19]. Cysteine is the main intracellular thiol as T. vaginalis and T. foetus do not produce glutathione or have glutathione-dependent enzymes [20].
In general, targeted biochemical analyses such as these have identified and focussed on pathways that differentiate trichomonad parasites from the mammalian host, with possible value for chemotherapeutic exploitation [21, 22] and have also highlighted differences between the species that could be linked to host range and pathogenicity. The advent of metabolomic techniques allowing non-targeted approaches for comparing the metabolomes of species has provided new opportunities for comparative analysis of the two trichomonad species. We recently compared the metabolomes of promastigotes of three Leishmania species and identified differences in amino acid metabolism that could, if also present in the mammalian form of the parasites, play crucial roles in determining the variations in infection [23]. We have now in this study, using the same methodology, compared the metabolites in and released by T. vaginalis and T. foetus. Samples were analysed by LCMS and metabolites were identified from their accurate mass, by comparison of their retention times with those of authentic standards, or by fragmentation analysis. Standard curves were prepared to provide an estimate of the relative concentrations. Labelling by growth of the parasites in media containing D-[U-13C6] glucose was used to confirm that metabolites were synthesised by the parasites and to compare the rates of production of intermediates in central carbon metabolism. In addition, a targeted analysis of T. vaginalis was carried out by comparing extracts of the parasite grown in media variations known to affect sulphur amino acid metabolism.
Our approach provides new information on the function of metabolic enzymes in T. vaginalis, an organism where methods for transfection and genetic manipulation are difficult and currently limited [14, 24].
Materials and methods
Trichomonad strains used in this study
The strains used in this study were Trichomonas vaginalis clone G3 and Tritrichomonas foetus clone F2. T. vaginalis G3 was the strain used for genomic sequencing [12]. T. foetus F2 is a clonal line originally derived in our laboratory from the Pfizer strain [25].
Culture of T. vaginalis and T. foetus
T. vaginalis and T. foetus cells were maintained in 25 ml of MDM medium in sealed tubes with little gaseous phase. Cultures were initiated at a concentration of 1 x 105 cells/ml and sub-cultured after 16 hours growth at 37°C when the cell concentration was 2 to 4 x 106 cells/ml. The composition of MDM, which contains no added cysteine, was: 20 mg/ml Tripticase™ peptone (BD), 5 mg/ml maltose, 1 mg/ml ascorbic acid, 1 mg/ml KCl, 1 mg/ml KHCO3, 1 mg/ml KH2PO4, 0.5 mg/ml K2HPO4, 0.1 mg/ml FeSO4.2H2O, 10% (v/v) heat inactivated Horse Serum (Thermo Fisher Scientific), pH 6.2–6.3.
Preparation of extracts for LC-MS
T. vaginalis and T. foetus were grown in the same media under identical conditions. Extracts were prepared from at least 4 independent cultures (biological replicates). For each replicate, 60 ml MDM in a 25 cm2 tissue culture flask was inoculated with an overnight culture to give a concentration of 105 cells/ml. The lids were sealed and cultures were incubated in an upright position, with very little gaseous phase so that the culture rapidly becomes anaerobic. After growth for 16 hours at 37°C, 40 ml of the culture was transferred to a 50 ml centrifuge tube and quenched rapidly to a temperature of 4°C using a dry-ice ethanol bath, monitoring the temperature continuously with a digital thermometer.
After centrifugation at 1000 x g for 30 min at 4°C, the supernatant medium was transferred to an ice-cold 50 ml centrifuge tube and stored on ice. The cell pellet was resuspended in 40 ml ice-cold PBS and stored on ice while the cell concentration was determined using a haemocytometer. After a second centrifugation, the cells were re-suspended to give a concentration of 2 x 107 cells/ml. 1 ml of the suspension was transferred to an ice-cold 1.5 ml microfuge tube and the cells were pelleted at 2000 x g for 10 min at 4°C. The pellets were mixed with 0.2 ml of extraction buffer (chloroform: methanol: water, 1:3:1) and the metabolites were extracted by shaking at 1000 rpm for 1 h at 4°C. Extracts were cleared by centrifugation at 21,000 x g for 10 min and 0.2 ml was transferred to a glass HPLC vial with a 0.2 ml insert. A blank was prepared by adding 0.2 ml of extraction buffer to an empty microfuge tube and treating in the same way as the samples. Extracts of media samples were prepared by mixing 75 μl of the sample with 0.3 ml of extraction buffer (chloroform:methanol, 1:3), shaking for 1 h at 4°C and clearing the extract by centrifugation at 21,000 x g for 10 min at 4°C. All extracts were stored at -80°C before use.
Measurement of the protein content of cell extracts
A replicate sample containing 2 x 107 cells was prepared from each culture as described above. The washed cell pellet was resuspended in 100 μl of lysis buffer (0.25 M sucrose, 0.25% (v/v) Triton X-100, 10 μM E64, 1 mM phenanthroline, 20 mM pepstatin A, 5 mM PMSF). Cells were lysed by aspiration with a pipette and the extract was cleared by centrifugation at 14,000 x g for 15 min at 4°C. The protein content was determined using the Bio-Rad protein assay (Bio-Rad).
13C labelling of T. vaginalis and T. foetus for LC-MS
MDM contains 5 mg/ml maltose as the main carbon source. In a preliminary experiment, we found that both T. vaginalis and T. foetus grew at similar rate in modified MDM without maltose supplemented with 5 mg/ml glucose. Labelling experiments were carried out using modified MDM containing 5 mg/ml D-[U-13C6] glucose (CK Isotopes). Cells from an overnight culture were washed by centrifugation (1000 x g for 10 mins at 4°C) and resuspension in modified MDM without glucose. 60 ml of modified MDM containing 5 mg/ml D-[U-13C6] glucose was inoculated with washed cells to give a concentration of 105 cells/ml. Extracts for LCMS were prepared after 2 h, 6 h or 16 h growth at 37°C as described above. The medium contained no maltose and 100% of the available glucose was labelled.
LC-MS
The LC-MS platform for metabolic profiling consisted of an Accela 600 HPLC system combined with an Exactive (Orbitrap) mass spectrometer from Thermo Fisher Scientific (Bremen, Germany). Two complementary columns, the zwitterionic ZIC-pHILLIC column (150 mm × 4.6 mm; 3.5 μm, Merck, Germany) and the reversed phase ACE C18-AR column (150 mm × 4.6 mm; 3.5 μm, Hichrom) were used. With both systems, the injection volume was 10 μl and the flow rate was 0.3 ml/min. The ZIC-pHILLIC column was eluted using a gradient of mobile phase A, 20 mM ammonium carbonate pH 9.2, and mobile phase B, acetonitrile (ACN). The concentration of A was increased from 20% to 80% over 30 min and then held at 92% for 5 mins, before equilibrating at 20%. The mobile phases for the reverse phase column were: A, 0.1% (v/v) formic acid in H20; B, 0.1% (v/v) formic acid in ACN. Mobile phase A was decreased from 95% to 10% over 30 min and held at 10% for 5 min. The settings for the mass spectrometer were as described previously [23].
Data processing
Raw data files of metabolite standard solutions were processed using ToxID 2.1 (Thermo Fisher Scientific Inc., Hemel Hempstead, UK) as described previously [23]. After visual evaluation of the extracted ion chromatograms, the retention times of the standards were used to calibrate IDEOM v19 [26]. Raw files of sample metabolites were processed as described previously [23]. Briefly, the data files were converted to mzXML open format using msConvert (ProteoWizard). Chromatograms were extracted using XCMS and stored in PeakML before aligning replicate peaks and combining them using mzMatch.R. After noise filtering and gap filling a CSV file was generated and imported into IDEOM v19 for metabolite identification based on accurate mass (± 3 ppm) and retention time prediction. The lipids and peptides were excluded from the lists of putatively identified metabolites in the biological samples.
Analysis of 13C labelled metabolites
Raw data from LCMS of the 13C-labelled extracts was processed to generate a combined PeakML file as described above. This was further analysed using mzMatch-ISO in R [27, 28], generating a.pdf file containing chromatograms used to check peak-shape and retention time and a tab-delineated file detailing peak height for each isopotologue which was used to calculate percentage labelling.
Metabolite identification
The identities of a subset of metabolites were confirmed by accurate mass and in addition either by matching the sample retention time to that of an authentic standard (± 0.2 min) or by obtaining MS2 spectra as described previously [23]. The confirmed metabolites correspond to the metabolic standards initiative (MSI) level 1. Metabolites putatively identified by accurate mass and predicted retention time correspond to MSI level 2.
Assay for cysteine synthase and S-methylcysteine synthase activity
Recombinant T. vaginalis cysteine synthase (CS) and T. vaginalis methionine γ-lyase type 1 (MGL1) were expressed and purified as described previously [19, 29]. Specific activities using standard assays were 13 μmol/mg CS (with 3 mM sodium sulfide (Na2S) and 50 mM O-phosphoserine (OPS)) and 8 μmol/min/mg MGL (with 3 mM homocysteine). The activity of CS in the production of S-methylcysteine (SMC) from -OPS and sodium methanethiolate (CH3S.Na) was measured in a coupled assay using MGL1 and lactate dehydrogenase (LDH). The reaction was carried out in 1 ml of 200 mM potassium phosphate pH 7.8, 10 mM OPS, 3 mM CH3S.Na, 5 mM 2-ketoglutarate, 0.2 mM NADH, 60 μg MGL1, 25 units LDH (Sigma) and 2 μg CS. The CS activity was measured under the same conditions by substituting the CH3S.Na with 3 mM Na2S. Kinetic analysis of the SMC synthase and CS activities was carried out with a fixed (saturating) concentration of the first substrate and at least 6 different concentrations of the second. Values for Km and Vmax were determined by plotting the data using GraFit 5 (Erithacus Software).
Identification of genes for metabolic enzymes in the draft genome nucleotide sequence of T. foetus
Putative genes for selected metabolic enzymes were identified by tblastn search of the whole genome shotgun contigs (wgs) database, BioProject ID 345179. Model protein sequences were obtained from TrichDB (trichdb.org) for T. vaginalis or KEGG (www.genome.jp/kegg) for other organisms.
Results
We compared the untargeted metabolomic profiles of T. vaginalis and T. foetus to obtain insights into differences in their biochemical pathways and the levels of variances of metabolites that could be associated with differences in host range and pathogenicity. Cell extracts were first analysed by LC-MS using a ZIC-pHILLIC column for the separation step and conditions previously optimised to identify the widest possible range of polar metabolites [23]. Raw data was processed and metabolites identified using IDEOM v19 [26] calibrated with retention times obtained for 240 authentic standards. The data was screened to remove lipids and peptides which cannot be accurately identified under the conditions used. From the pHILLIC column, 86 metabolites were identified by accurate mass and confirmed by comparison of their retention times with those of authentic standards (difference ≤ 0.2 minutes). The identities of another 5 metabolites were confirmed by MS2 analysis. The same extracts were then analysed using a reverse phase (C18AR) column for LC-MS that provided complementary coverage, allowing confirmed identification of 19 additional metabolites including polyamines. The 110 confirmed metabolites were mapped to metabolic pathways for amino acids, carbohydrates, nucleotides, vitamins and co-factors and energy metabolism with 9 metabolites belonging to no known pathway (S1 Table). 18 of these metabolites were found only in cell extracts and 3 metabolites were specific to the media. An additional 225 metabolites from cell extracts were putatively identified on the basis of accurate mass and predicted retention time in IDEOM v19 (S2 Table). 287 metabolites were putatively identified in medium samples (S3 Table).
Overall comparison of T. vaginalis and T. foetus cell extracts
The mean peak intensity values indicating the relative levels of metabolites in the different species were calculated from results for at least 4 biological replicates. As described previously, our method for extract preparation was optimised so that the LC-MS data did not need normalising (23). In addition, we focused mainly on large differences in mean peak intensity (> 3-fold). 43 out of 107 confirmed metabolites from cell extracts of T. vaginalis and T. foetus showed greater than 3-fold differences in peak intensity between species (Table 1). The pattern observed with the different metabolites showing either relatively high or low levels in the two species could not be the result of differences in cell volume. For example T. vaginalis has 88-fold higher levels of D-gluconic acid but 20-fold lower level of succinic acid compared with T.foetus. In addition, the protein content of T. vaginalis cell extracts, an indication of cell volume, was found to be only 1.5-fold higher than T. foetus. The protein content for 2 x 107 cells was 540 ± 90 μg for T. vaginalis and 360 ± 50 μg for T. foetus. This supports our choice of a three-fold change in peak intensity as the threshold for a clear difference between the species. Differences were observed in the levels of nucleotide and amino sugars, hydroxy acid derivatives of amino acids, carboxylic acids, metabolites belonging to pathways for cysteine and methionine metabolism, arginine metabolism, lysine metabolism and in the production of thioethers not previously identified in trichomonads.
Comparison of cell extracts showed that the intracellular amino acid pools of the two species were generally similar, however T. foetus cell extracts contained 5-fold higher levels of lysine whereas T. vaginalis had relatively high levels of the lysine metabolites pipecolate, N6-methyl-lysine, carnitine and N-acetyl-carnitine (Table 1 and S2 Table). Significantly, our results show that T. foetus maintains up to 20-fold higher levels of cysteine, detected as cystine by LCMS following in-situ oxidation. Various aspects of amino acid metabolism were analysed in more detail and the data are presented in the following sub-sections.
Overall comparison of metabolites in media samples
In order to identify metabolites taken up or exported by the parasites, peak intensity levels in complete or uninfected media samples were compared with spent media, the supernatant after cells were removed from cultures by centrifugation (Table 2, S3 Table). 16 confirmed metabolites from T. vaginalis spent media and 6 from T. foetus showed more than 3-fold difference when compared with complete media. Comparisons of these ratios revealed that for 18 metabolites there was greater than 3-fold difference in their rate of uptake or release between the species. T. vaginalis takes up higher levels of nucleosides, phosphoserine and 5-methylthioadenosine but releases hydroxy acids and SMC. Succinate is produced and exported by T. foetus. In addition, T. foetus releases, 2.8 fold higher levels of putrescine, just outside our 3-fold threshold for a clear difference between species. As expected, spent media from cultures of both species show an increase in putrescine and a decrease in spermidine levels compared with uninfected medium (Table 2). Trichomonads can synthesise putrescine but lack S-adenosylmethionine decarboxylase required for conversion to spermidine. They can obtain spermidine from the growth medium and uptake of spermine is known to be coupled to export of putrescine by an antiporter [30]. T. vaginalis is distinct from T. foetus in importing phosphoserine, purines and purine nucleosides, methylthioadenosine and nicotinamide (Table 2).
Amino acids are metabolised to produce 2-hydroxy acids in T. vaginalis but not in T. foetus
2-Hydroxy acids, derived from amino acids by deamination and reduction, were detected in cell extracts of both species, but with markedly higher peak intensities in T. vaginalis. To analyse the situation in greater depth, the concentrations of the most abundant hydroxy acids together with their keto acid and amino acid precursors were determined by constructing calibration curves using authentic standards, as described previously [23]. The T. vaginalis extracts contained 28 nmol/108 cells of 2-hydroxyisocaproic acid (HICA), 7-fold higher than in T. foetus (Table 3). The intracellular pools of the precursors, 2-isocaproic acid and leucine were also higher in T. vaginalis. Levels of HICA in the spent medium reached 21 μM after growth of T. vaginalis for 20 h, 55-fold higher than the concentration in the original growth medium, whereas there was no significant change in the level of HICA in the T. foetus spent medium (Table 4). Utilisation of leucine by T. vaginalis did not result in a change in the concentration of leucine in the media samples which was approximately 500 μM (Table 4). Tryptophan and phenylalanine were metabolised in a similar way with concentrations of indole lactate and phenyl lactate in T. vaginalis extracts of 14.0 and 1.3 nmol/108 cells, respectively (Table 3). These results show that T. vaginalis can catabolise amino acids to produce 2-hydroxy acids at a markedly higher rate than T. foetus. Certain amino acids are used preferentially by T. vaginalis with higher levels of 2-hydroxy acids obtained from leucine and phenylalanine than from tryptophan. 2-hydroxybutanoate derived from threonine, methionine or homocysteine was also detected in T. vaginalis cell extracts (Table 1) and spent media (Table 2). Relatively high peak intensities were obtained for 2-hydroxybutanoate but this metabolite was not quantified with a calibration curve.
Arginine metabolism
The arginine dihydrolase pathway converts arginine to ornithine via citrulline and is present in both species [31]. In addition to providing ornithine for putrescine biosynthesis, the pathway may contribute to energy metabolism [31], producing ATP by substrate level phosphorylation. T. foetus had 5-fold higher levels of citrulline than T. vaginalis and ornithine levels were increased 3-fold (Table 1). Cell extracts of the two species showed similar levels of putrescine but T. foetus exported almost 3-fold more putrescine than T. vaginalis, as indicated by comparison of spent media samples (Table 2). Other derivatives of arginine, including the organic acid 4-guanidinobutanoate and creatinine were found at increased levels (> 5-fold) in T. vaginalis (Table 1). Proline, which can be produced from arginine via ornithine, was present at similar levels in both species although increased amounts (> 4-fold) of the proline metabolite oxoproline were found in T. vaginalis (Table 1).
Glycolysis and central carbon metabolism
The main end products of energy metabolism in T. vaginalis are glycerol, lactate, ethanol, acetate, CO2 and H2 (Fig 1A) [17]. T. foetus differs in not producing lactate but excretes high levels of succinate. Of these metabolites, only succinate was detected by LCMS under the conditions used in this study and as expected, levels were found to be 20-fold higher in T. foetus (Table 1) as well as being excreted (Table 2). Central carbon metabolism in T vaginalis and T. foetus depends primarily on glycolysis because the TCA cycle is not present [17]. Fermentation of pyruvate is extended in the hydrogenosome with ATP production by substrate level phosphorylation (Fig 1B). Levels of glycolytic intermediates showed only minor differences (<2-fold) between the species (S2 Table) so we used stable isotope labelling to investigate whether the two species differ in how they utilise glucose for biosynthesis and energy production. T. vaginalis and T. foetus were grown in medium containing 100% D-[U-13C6] glucose and extracts were prepared after 2 h, 6 h and 20 h growth at 37°C. The change in the percentage of different 13C isotopologues was determined over the time course (Fig 1C) The total levels of each metabolite were calculated as the sum of the peak intensities of all isotopologues and the log2 fold change in metabolite level (T. vaginalis/T. foetus) was plotted for each time-point (Fig 2). A heat map of percentage incorporation after 20 h is also shown in the supplementary data (S1 Fig).
T. vaginalis and T. foetus were grown at 37°C in MDM containing 100% D-[U-13C6] glucose as the only carbohydrate carbon source. Cell extracts were prepared after 2 h, 6 h and 20 h in culture and analysed by LC-MS. (A) Map of glycolysis and central carbon metabolism in T. vaginalis and T. foetus. Reactions found only in T. foetus are shown by dashed lines. T. vaginalis uses pyrophosphate (ppi) dependent enzymes for the steps indicated [32]. Metabolites detected in the 13C labelling experiment are boxed. (B) Map of pyruvate metabolism in the hydrogenosome in T. vaginalis. Dashed lines indicate the NADH dehydrogenase complex I. Metabolites detected in the 13C labelling experiment are boxed. (C) 13C labelling of metabolites in T. vaginalis and T. foetus. Graphs show the percentage of isotopologues with different numbers of 13C carbon atoms.
Total metabolite levels represent the sum of the peak intensities of all isotopologues. Of metabolites detected in 13C-labelled extracts. Graphs show the log2 fold change in total peak intensities after 2 h, 6 h and 20 h growth. Results represent the mean of 3 independent cultures ± SD. Dashed line indicates the threshold for a definite difference between the species (3-fold or log2 1.6-fold change in metabolite level). Positive values represent a relative increase in T. vaginalis, negative values a relative increase. Glucose-6P, glucose-6-phosphate; Triose phosphate, dihydroxyacetone phosphate and glyceraldehyde-3-phosphate; 3-PG, 3-phoglycerate; PEP, phosphoenol pyruvate. * P ≤ 0.001 (Paired T-Test, assuming equal variance).
Even after 20 h growth, equivalent to four generations, 6-carbon labelled (6C) isotopologues of G-6P still represented only 60% of the total in T. vaginalis and 80% in T. foetus (Fig 1C and S1 Fig). Significant levels of 5C, 4C and 3C isotopologues were also detected along with unlabelled G-6P. Similarly, 3C isotopologues of pyruvate formed 50–60% of the total detected after 20 h.
13C labelling of glycolytic intermediates pointed to differences in glycolytic flux between the species. Although the level of incorporation into G6-P was similar, the labelling of downstream intermediates triose phosphate (LC-MS failed to resolve 3-phosphoglycerate and dihydroxy acetone phosphate), phosphoenolpyruvate (PEP) and pyruvate were a little higher in T. foetus than in T. vaginalis (Fig 1C and S1 Fig). Marked differences were seen in the labelling of metabolites of pathways branching off glycolysis. The total level of sn-glycerol-3-phosphate (sn-G-3P) in T. vaginalis at 20 h was more than 5-fold higher than in T. foetus (Table 1 and Fig 2). The rate of labelling of sn-3-GP was also markedly higher in T. vaginalis (Fig 1C and S1 Fig) confirming that it is synthesised via the triose phosphate dihydroxyacetone phosphate (DHAP).
T. vaginalis produces 4-fold higher levels of malate than T. foetus (Table 1). Both organisms showed 3 carbon and 4 carbon labelling of malate, with somewhat higher levels in T. vaginalis (Fig 1C). 3C and 4C labelled isotopologues of succinate in T. foetus represented 46% and 24% of the total at 20 h, respectively (Fig 1C and S1 Fig), whereas the relatively low levels detected in T. vaginalis were unlabelled. In T. vaginalis, malate is produced from PEP as an intermediate in energy metabolism but in T. foetus, this pathway is extended to convert malate to succinate as an end product (Fig 1A) [17]. The 3C and 4C isotopologues of aspartate would have been produced by transamination of labelled oxaloacetate. T. vaginalis showed higher rates of 13C labelling (Fig 1C and S1 Fig), although at 20 h the total levels of aspartate in the two species were similar (Fig 2).
Alanine is produced by transamination of pyruvate catalysed by alanine aminotransferase. 3C labelled alanine increases from 16% of the total at 2 h to 33% at 20 h in T. vaginalis, 5 fold higher than that seen in T. foetus (Fig 1C). Acetyl-CoA is produced in the hydrogenosome from pyruvate by pyruvate:ferredoxin oxidoreductase (Fig 1B). Total levels of acetyl-CoA were significantly higher in T. vaginalis (Fig 2), with 2C isotopologues making up roughly 50% of the total throughout the time course (Fig 1C). A more complex pattern of labelling was seen in T. foetus with 2C isotopologues representing 60% of the total after 2 h growth but with 2C and 7C isotopologues representing 27% and 26% of the total, respectively, after 20 h (Fig 1C). A 2C labelled acetyl group is incorporated into acetyl-CoA from 3C labelled pyruvate, but label can also be incorporated during coenzyme A biosynthesis.
Differences in methionine metabolism
The T. vaginalis genome encodes all the enzymes required to produce homocysteine from methionine but the transsulfuration pathway for conversion of homocysteine to cysteine via cystathionine was not found (Fig 3) [12, 19]. Using calibration curves, extracts of the two species were shown to have similar levels of methionine and SAM but T. foetus contained approximately 5-fold higher levels of SAH (Fig 3). Thiols are readily oxidised in situ during LC-MS and this is most likely the reason why homocysteine was not detected in cell extracts. However, a metabolite identified as a mixed disulfide of homocysteine and cysteine by MS2 was found in T. foetus extracts but not in T. vaginalis, indicating that higher levels of homocysteine are produced in T. foetus. Similarly, T. foetus apparently has a higher intracellular concentration of cysteine, indicated by the detected levels of its oxidised form, the disulfide cystine. In another clear difference between the species, cystathionine was identified in T. foetus (34 nmol/108 cells) but it was almost undetectable in T. vaginalis (2 nmol/108 cells) (Fig 3). Both species produce relatively high levels of methylthioadenosine (MTA) with 120 nmol/108 cells in T. vaginalis and 270 nmol/108 cells in T. foetus. An unusual metabolite, SMC was also detected in T. vaginalis as detailed in subsequent sections.
T. vaginalis and T. foetus were grown for 20 h at 37°C in MDM which contains no added cysteine. Graphs show concentrations of metabolites (nmol/108 cells) calculated from peak intensity values using standard curves. There were no standards available for the mixed disulfide of cysteine and homocysteine (Cys:Hcy disulfide) and its concentration is represented by peak intensity/108 cells. Broken lines indicate the oxidation of sulfur amino acids to form disulfides. Enzymes found in the T. vaginalis genome are: 1, S-adenosylmethionine synthase; 2, S-adenosylmethionine dependent methyltransferase; 3, S-adenosylhomocysteine hydrolase; 4, methionine γ-lyase (MGL); 5, cysteine synthase (CS); 6, 1-aminocyclopropane-1-carboxylic acid (ACC) synthase. CS from T. vaginalis is a multi-functional enzyme with broad specificity, as demonstrated in later sections. * More than 3-fold difference between species. P ≤ 0.001 (Paired T-Test, assuming equal variance).
Labelling of intermediates in nucleotide and methionine metabolism
T. vaginalis and T. foetus were grown in 13C-glucose which was expected to label SAM via ATP (Fig 4A). The oxidative branch of the pentose phosphate pathway is active in T. vaginalis and T. foetus, with both organisms showing similar levels of 13C incorporation into ribose-5-phosphate after 20 h (Fig 4C, S2 Fig). Ribose-5-phosphate is used to synthesise nucleotides as shown by the presence of 5C isotopologues of UTP, GTP and ATP (Fig 4C, S2 Fig). No labelled pyrimidine or purine bases were detected indicating that nucleotides are synthesised by scavenging or recycling pathways with no evidence of de-novo synthesis, as reported for T. vaginalis previously [33, 34]. Higher percentages of C5 labelled nucleotides are seen in T. foetus compared to T. vaginalis, most markedly in GTP, GDP and UTP (S2 Fig). This could be explained by differences in the capacity of the two organisms for uptake unlabelled nucleosides as nucleotide precursors (Table 2).
T. vaginalis and T. foetus were grown at 37°C in MDM containing 100% D-[U-13C6] glucose as the only carbohydrate carbon source. Cell extracts were prepared after 2, 6 and 20 h in culture and analysed by LC-MS. (A) Map showing pathway from glucose to nucleotide and methionine metabolism in T. vaginalis and T. foetus. Reactions found only in T. foetus are shown by dashed lines. Formation of cystathionine from cysteine and homocysteine has not been confirmed. Metabolites detected in the 13C labelling experiment are boxed. (B) Map showing metabolites labelled with 13C via the glycolytic intermediate 3-phosphoglycerate. Metabolites detected in the 13C labelling experiment are boxed. (C) 13C labelling of metabolites in T. vaginalis and T. foetus. Graphs show the percentage of isotopologues with different numbers of 13C carbon atoms, error bars show standard deviation.
Methionine was not labelled by 13C in T. vaginalis or T. foetus (Fig 4C) but 5C isotopologues of SAM and SAH were identified in both species (Fig 4C, S3 Fig). SAM is synthesised from methionine and ATP and then converted to SAH by transmethylation. The higher levels of incorporation in T. foetus are consistent with the relatively high labelling of ATP in this species (Fig 4C, S3 Fig), and do not necessarily indicate an increased rate of synthesis. C5 isotopologues of SAM and SAH were more abundant in T. foetus, again reflecting the relative incorporation of the label in the intracellular pool of ATP (Fig 4C, S3 Fig). High levels of cystathionine were detected in T. foetus and C3-labelled isotopologues increased with time, representing 60% of the total after 20 h growth (Figs 4C and 5). In contrast, the low level of cystathionine detected in T. vaginalis were not labelled (Figs 4C and 5).
Total metabolite levels represent the sum of the peak intensities of all isotopologues of metabolites detected in extracts of 13C labelled cells. Graphs show the log2 fold change in total peak intensities after 2, 6 and 20 h growth. Results represent the mean of 3 independent cultures ± SD. Dashed line indicates the threshold for a definite difference between the species (3-fold or log2 1.6-fold change in metabolite level). Positive values represent a relative increase in T. vaginalis, negative values a relative decrease. Ribose-5P, Ribose-5-phosphate; SAM, S-adenosylmethionine; SAH, S-adenosylhomocysteine; MTA, 5-methylthioadenosine; OPS, O-phosphoserine; SMC, S-methylcysteine. * P ≤ 0.001 (Paired T-Test, assuming equal variance).
Effect of propargylglycine on methionine metabolism in T. vaginalis
T. vaginalis produces MGL, a broad specificity enzyme that hydrolyses methionine, homocysteine and cysteine although biochemical analysis failed to detect this activity in cell extracts of T. foetus [18, 29, 35]. To determine whether the differences in MGL activity could account for the observed differences in methionine metabolism, T. vaginalis cultures were grown in the presence of 5 μM propargylglycine (PAG), a strong inhibitor of the T. vaginalis MGL. This resulted in a marked increase in the levels of methionine, SAM and SAH (Fig 6). The Cys:Hcy mixed disulfide was also detected in PAG-treated cell extracts, showing that more homocysteine was produced as reported previously [20]. Growth of T. vaginalis with 10 mM cysteine also affected methionine metabolism with increased levels of SAM, cystine and the Cys:Hcy mixed disulfide. (Fig 6). Interestingly, T. vaginalis has the capacity to synthesise cystathionine because when grown in medium containing added 10 mM cysteine or when cells are treated with 5 μM PAG, levels of cystathionine in cell extracts increased to 7.2 and 6.5 nmol/108 cells, respectively (Fig 6).
T. vaginalis and T. foetus were grown for 20 h at 37°C in MDM which contains no added cysteine (MDM), MDM with 10 mM cysteine (CYS) or MDM with 5 μM propargylglycine (PAG). Cell extracts were analysed by LC-MS and the ratios of metabolite peak intensities for different growth conditions were determined. The graph show the log2 of the ratios CYS/MDM and PAG/MDM ± SD. The dotted lines indicate a difference in peak intensity ≥ 3 (or log2 1.6).* P ≤ 0.001 (Paired T-Test, assuming equal variance).
Identification of S-methyl-L-cysteine as a metabolite in T. vaginalis but not in T. foetus
One cellular metabolite found in the study was initially identified as homocysteine on the basis of accurate mass (m/z 135.0354). However, its retention time of 11.11 min differed from that of the authentic homocysteine standard (15.98 min). Thus, fragmentation analysis was carried out and this revealed that the metabolite was S-methyl-L-cysteine (SMC), a thioether analogue of methionine in which a methyl group is linked to the sulfur atom of cysteine (S4 Fig). The most abundant fragment (Fragment 1, 119.0161, C4H7O2S) corresponded to loss of the amino group and fragments with much lower peak intensities to loss of the carboxylate group (Fragment 2, 90.0372, C3H8NS) and to loss of the methyl-sulphur and amino groups (Fragment3, 73.0285, C3H5O2). Generation of the latter fragment arises from cleavage of a carbon-sulphur bond in SMC but requires cleavage of a high energy carbon-carbon bond in the SMC isomer homocysteine; this, makes SMC the most likely identification of the parent compound. Moreover, the fragmentation pattern was identical to those seen in MS2 spectra for SMC published on HMBD (http://www.hmdb.ca) and quite distinct from those obtained for homocysteine. Subsequently, we confirmed that an authentic SMC standard had the same retention time as the metabolite identified. SMC is a characteristic of T. vaginalis with only very low levels detected in T. foetus (≥ 200-fold lower peak intensity) (Table 1, Figs 3 and 5).
Using a standard curve, the concentration of SMC found in T. vaginalis extracts was 11.1 nmol/106 cells but the level in T. foetus was only 0.09 nmol/106 cells. SMC was also detected in spent media from T. vaginalis cultures, reaching 2.4 μM after 20 h growth, 20-fold higher than uninfected medium. These results indicate that SMC is produced in T. vaginalis and released into the medium.
Levels of SMC in T. vaginalis are correlated with the levels of CS
T. vaginalis produces several isoforms of a cysteine synthase (CS), an enzyme linked to SMC production in Entamoeba histolytica [36]. To investigate whether CS could also be involved in SMC synthesis in T. vaginalis cells were grown under conditions known to affect the levels of CS expression and enzyme activity [19]. Intracellular SMC levels were found to be 50-fold lower in cells grown in medium containing 10 mM cysteine (Fig 6). Under the same conditions, CS activity was previously shown to be reduced 10-fold [19], thus raising the possibility that the T. vaginalis CS is involved in SMC synthesis. Treatment with 5 μM PAG resulted in a 4-fold reduction in the amount of SMC (Fig 6) even though cysteine synthase activity is increased [19]. However, under these conditions production of CH3SH, required for synthesis of SMC, is markedly reduced by inhibition of MGL.
SMC is produced by CS in vitro
To determine whether the T. vaginalis CS could synthesise SMC, an in vitro assay was developed based on the finding that the SMC is a substrate for T. vaginalis MGL [35]. SMC was quantified in a coupled assay with recombinant T. vaginalis MGL type 1 (TvMGL1) [29] and lactate dehydrogenase (LDH). In this, SMC is catabolised by TvMGL1 to pyruvate, CH3SHand ammonia in the first reaction and pyruvate is reduced to lactate by LDH with oxidation of NADH in the second (Fig 7A). The production of SMC from OPS and CH3S.Na by CS was monitored by measuring the rate of NADH oxidation. After a lag period of about 10 min, a linear rate was maintained for more than 15 min (Fig 7B). SMC synthase activity was proportional to CS concentration in the range 25 to 125 nM. A substrate saturation curve for reactions with a fixed concentration (10 mM) of O-phosphoserine and 0.25–12 mM CH3S.Na exhibited Michaelis Menton kinetics with a Km for CH3S.Na of 4.3 mM (Fig 7C).
Production of SMC from OPS and CH3S.Na by recombinant T. vaginalis CS was determined at 37°C. (A) A coupled assay for SMC synthase. The assay couples SMC production by CS to NADH oxidation using MGL and LDH. The rate of NADH oxidation and hence the rate of SMC production can be quantified by measuring the absorbance at 340 nm. (B) The effect of increasing amounts of CS in a coupled assay for SMC biosynthesis. The reaction contained 10 mM OPS, 3 mM CH3SNa and 0, 1 and 5 μg/ml CS. The graph shows the rate of NADH oxidation which is equivalent to the rate of SMC biosynthesis in the coupled assay. (C) Substrate saturation curve for CH3SNa. Reactions contained 10 mM OPS, 85 nM CS and 0.25–12 mM sodium CH3SNa. A plot of enzyme activity against CH3SNa concentration shows Michaelis-Menten kinetics.
Cysteine is also hydrolysed by MGL so the assay can be used to measure cysteine production by substituting Na2S for CH3SNa. This allowed a comparison of the kinetics of cysteine and SMC production by CS using the same assay (Table 5). The Km for Na2S was found to be 10-fold lower than that for CH3SNa. The catalytic efficiency of the CS reaction with Na2S was 20-fold higher than for synthesis of SMC with CH3S.Na (Table 5).
13C labelling of cysteine, SMC and serine via glyceraldehyde-3-phosphate
Based on measurement of cystine, T. foetus contains higher intracellular concentration of cysteine than T. vaginalis (Fig 5) and higher rates of 13C incorporation from glucose (Fig 4C). In contrast, 13C incorporation from glucose into cystine in T. vaginalis was <10% even after 20 h growth. Similarly, 80% of the SMC detected in T. vaginalis cells after 20 h growth was unlabelled, whereas the very low levels of SMC detected in T. foetus showed high percentage incorporation (Fig 4C). Clear evidence of SMC synthesis in T. vaginalis is shown, however, by the increase in peak intensity of the 3 carbon-labelled isotopologue with time (Fig 8A) and the increasing amounts of SMC released into the growth medium (Fig 8B). Intracellular levels of the 13C isotopologue of OPS, the precursor of cystine and SMC, increased with time (Fig 8C). However labelled OPS represented markedly lower percentage of the total in T. vaginalis (Fig 8C). Levels of OPS in the growth medium decreased 10-fold during the course of the T. vaginalis culture but there was no change in the complete medium control or in the T. foetus spent medium (Fig 8D). Overall, these results indicate that T. vaginalis imports OPS from the medium, reducing the amount that is synthesised from glucose. 13C labelling also revealed that both T. vaginalis and T. foetus can synthesise serine from phosphoserine, even though a search of the T. vaginalis genome database failed to detect a gene for the phosphatase required ([19]. The percentage of 3 carbon labelled serine in T. foetus was 2-fold higher than in T. vaginalis, again consistent with the lower incorporation of label into OPS in the latter.
Cell extracts prepared after 2, 6 and 20 h growth at 37°C in media containing 100% D-[U-13C6] glucose were analysed by LC-MS. Graphs show the mean peak intensities of 3-carbon labelled isotopologues from 3 biological replicates (± SD). (A) 13C labelled SMC in cell extracts; (B) total SMC levels in media samples; (C) 13C labelled OPS in cell extracts; (D), total OPS levels in media samples. Complete, uninfected or complete media control; TvagSPT, spent media sample from T. vaginalis cultures; TfoeSPT, spent media from T. foetus cultures.
Identification of other thioethers including allylcysteine
The T. foetus extracts contained allycysteine, a thioether with a similar structure to SMC in which the cysteine sulphur is linked to a propenyl group rather than a methyl group. Allylcysteine was identified by comparison with an authentic standard in T. foetus extracts (S2 Table) Allylcysteine was barely detectable in T. vaginalis extracts, its sulfoxide derivative, alliin was found at 10-fold higher peak intensity than obtained for T. foetus. The mechanism of allylcysteine production is not known, although in contrast to results obtained with SMC, we detected allylcysteine in medium containing 10 mM cysteine after overnight incubation at 37°C in the absence of cells. This shows that allylcysteine can be formed spontaneously from media components under certain conditions. We conclude that allylcysteine and alliin are unlikely to be true metabolites of the trichomonads and that SMC is the only thioether detected that is synthesised by T. vaginalis.
Genome analysis of T. foetus strain K
A draft sequence of the genome of T. foetus strain K was released while this manuscript was in preparation [13]. We therefore searched the genome for the genes of key enzymes involved in amino acid metabolism (S6 Table). T. vaginalis encodes several isoforms of a highly specific malate dehydrogenase (MDH) and a closely related lactate dehydrogenase (LDH) but T. foetus genome contained only an MDH, consistent with biochemical evidence that the parasite did not produce lactate [17]. An alignment of the T. foetus MDH proteins with the T. vaginalis MDH and LDH is shown in S5 Fig. T. foetus K encodes 3 isoforms of cysteine synthase, and the enzymes required for phosphoserine production from 3-phosphoglycerate but a gene for serine-O-acetyltransferase was not found (S6 Table). T. foetus might therefore synthesise cysteine from H2S and phosphoserine as reported for T. vaginalis [19]. The enzymes of the transsulfuration pathway, including CBS, were absent but unexpectedly, T. foetus appears to contain 4 isoforms of MGL (S6 Table). These T. foetus proteins have 69–72% amino acid identity with the T. vaginalis MGL isoforms and key active site residues required for PLP binding and a cysteine implicated in specificity for methionine are conserved (S6 Fig). This new finding is not consistent with previous biochemical analyses of T. foetus cell extracts [18].
Discussion
Genomic analysis, transcriptomics and proteomics of T. vaginalis have identified potential surface proteins, secretory proteins and peptidases as virulence factors that may be involved in cell adhesion, cytotoxicity and pathogenesis [12, 37–46]. Recent studies have investigated the effect of different growth conditions on gene expression in T. vaginalis [46–48]. This is the first report of the use of metabolomics on trichomonad species, providing reference metabolic profiles of T. vaginalis and T. foetus and demonstrating how this approach can be used to identify new or unusual metabolites, compare species and identify changes in the levels of soluble metabolites occurring under different growth conditions. This study also revealed the effect of propargylglycine, an inhibitor of PLP-dependent enzymes, on the T. vaginalis metabolome.
Central carbon metabolism in T. vaginalis and T. foetus
Glycolytic intermediates were labelled by growing cells for various times in media containing D-[U-13C6] glucose as the only carbohydrate carbon source. Failure to obtain 100% 13C labelling of G-6P suggests that trichomonads can use an alternative source of carbon skeletons for gluconeogenesis such as amino acids. This would also explain the range of different isotopologues of G-6P detected in T. vaginalis, an organism that readily takes up amino acids from the growth media [49]. These studies revealed differences in metabolic fluxes between the species. The level and rates of incorporation into G-6P and triose-P were similar, and labelling of downstream intermediates 3-PG, PEP and pyruvate were only slightly higher in T. foetus than in T. vaginalis. However, marked differences were seen in the labelling of metabolites of pathways branching off glycolysis. The rate of labelling of sn-G-3P via the triose-P DHAP was higher in T. vaginalis. Sn-G-3P is converted to glycerol, an end product of glucose metabolism in both species and it is a precursor of phosphatidic acid in glycerophospholipid biosynthesis. There were also differences in the levels of metabolites produced from PEP including malate, succinate and aspartate.
T. vaginalis encodes a PEP carboxykinase that produces OAA from PEP and CO2. OAA was not detected by LC-MS, but the products of its metabolism were found in extracts of both species. C3 and C4 isotopologues of malate, succinate and aspartate were identified when cells were grown in D-[U-13C6] glucose, with the C4 isotopologues accumulating at later times. OAA is reduced to malate by malate dehydrogenase (MDH) or transaminated to aspartate by aspartate aminotransferase (AAT). Total levels of malate were 5-fold higher in T. vaginalis and percentage 13C labelling was also higher, with C4 species more abundant than in T. foetus. This is no doubt due to the conversion of malate to succinate (via fumarate) which occurs in T. foetus but not in T. vaginalis [17]. T. foetus extracts contained 20-fold higher levels of succinate and the low level of succinate detected in T. vaginalis was not significantly labelled and most likely imported from the media. These results agree with previously published data [17] and validate our methods.
The high levels of incorporation of 13C into aspartate, particularly in T. vaginalis extracts were not expected. In T. vaginalis multiple isoforms of AAT convert OAA and glutamate to aspartate and α-ketoglutarate [12]. However, it is not clear why T. vaginalis produces such high levels of aspartate, with 70% 13C labelled at 20 h, even when aspartate is available in the medium. T. vaginalis produces cytoplasmic and hydrogenosomal isoforms of MDH and AAT that could function in an aspartate:malate shuttle [40]. Antiporters required for transport of reducing equivalents across the hydrogenosomal membranes were not identified although the proteome contains several mitochondrial carrier family (MCF) proteins [40] An active aspartate:malate shuttle would explain the high rate of aspartate synthesis observed in this study. Hydrogenosomes do not have an electron transport system but NADH is required by the hydrogenosomal pyruvate:ferrodoxin oxidoreductase and reduced ferrodoxin is an electron donor for hydrogenase and the oxygen scavenging flavodiiron protein [50].
Cysteine and SMC are produced in T. vaginalis using a bi-functional CS
Cysteine was detected predominantly in its oxidised form by LC-MS. Levels of cystine were 20-fold higher in T. foetus cell extracts than in T. vaginalis indicating that T. foetus maintains higher intracellular cysteine levels. Both organisms lack glutathione and glutathione-dependent enzymes and cysteine is thought to be a major intracellular reductant. 13C-labelling demonstrated that cysteine is synthesised from OPS in both trichomonad species, although the percentage incorporation was low in T. vaginalis, most likely due to its ability to take up unlabelled OPS from the medium. Surprisingly, OPS can be converted to serine in T. vaginalis and T. foetus, even though no homologues of the phosphatase required could be detected in the T. vaginalis genome [19].
We show that T. vaginalis produces SMC, an unusual metabolite that has limited distribution in nature. It is found in the seeds of leguminous plants and was recently detected in the protozoan parasite Entamoeba histolytica [36] which resembles T. vaginalis in lacking mitochondria and having a fermentative metabolism. E. histolytica uses CS to produce SMC, and we found that the T. vaginalis CS can also produce SMC in vitro from CH3SH and OPS. The catalytic efficiency of the T. vaginalis CS with CH3SH was 20-fold lower than with H2S in the production of cysteine whereas the E. histolytica CS showed no preference for either substrate. CH3SH and H2S are produced by MGL and both metabolites have been detected in T. vaginalis [51], although their intracellular concentrations are not known.
E. histolytica is dependent on an exogenous source of cysteine [36] and growth in medium containing 13C3, 15N-serine labelled SMC but not cysteine, indicating that the E. histolytica CS functioned solely as an SMC synthase [36]. In contrast, T. vaginalis grows well in medium without cysteine and levels of CS are regulated by conditions that affect cysteine availability [19]. Metabolomic profiling revealed that SMC levels are affected by the same conditions and both SMC and cysteine incorporated similar levels of 13C. These results suggest that the T. vaginalis CS is a bi-functional enzyme producing both cysteine and SMC. Cysteine is the main intracellular antioxidant in T. foetus whereas T. vaginalis contains both cysteine and SMC. In this study we measured an SMC concentration of 200 μM using LC-MS which compares with a concentration of 600 μM for cysteine [20]. The function of SMC is not known, but recent evidence indicates a role in other species in protection against oxidative stress [52–54] and inflammation [55].
HPLC analysis revealed that the sulfur atom of SMC is oxidised by H2O2 and the SMC-sulfoxide can be reduced by the enzyme methionine sulfoxide reductase (MSRA) in vitro [52]. In an animal model for Parkinson’s disease based on a recombinant Drosophila line expressing human α-synuclein, disease symptoms were reversed either by overexpressing human MSRA in a doubly transgenic line or by feeding with SMC, which is not produced naturally in the fruitfly [52]. It was proposed that the beneficial effects of SMC resulted from its reversible oxidation in an antioxidant system for scavenging free radicals and peroxides. In this system, consisting of SMC, MSRA, thioredoxin and thioredoxin reductase, SMC is oxidised by peroxides to form the SMC sulfoxide and this is reduced by MSRA in a thioredoxin dependent reaction. All the components of this system are found in T. vaginalis [12, 56–58] and it is possible that SMC acts as an antioxidant in T. vaginalis also.
Role of MGL in methionine metabolism in T. vaginalis
In most organisms, including protozoan parasites, methionine is activated to SAM by methionine adenosyltransferase [59]. SAM plays a central role in cell metabolism as a methyl donor for the methylation of nucleic acids, lipids and proteins and as a source of aminopropyl groups for spermidine synthesis. SAH produced as a bi-product of SAM-dependent methyltransferase reactions is converted to homocysteine which is rapidly removed either by re-methylation to methionine or by conversion to cysteine by the transulfuration pathway. In the first, rate limiting step of transsulfuration, homocysteine is condensed with serine to form cystathionine, catalysed by cystathionine β-synthase (CBS). Cysteine is then synthesised by hydrolysis of cystathionine catalysed by cystathionine γ-lyase (CGL).
In mammals, CBS maintains low homocysteine levels, which is thought to be necessary for adequate rates of SAM-dependent methylation [60, 61]. Serum homocysteine levels are increased 10–30 fold in individuals with genetic defects in CBS or in CBS knockout mice resulting in accumulation of SAH. This is because the SAH hydrolase reaction is reversible and the kinetics in vitro favour the synthesis of SAH over its hydrolysis. SAH is a strong product inhibitor of many SAM-dependent methyl transferases and it has been hypothesised that increased homocysteine and SAH levels could induce epigenetic effects due to DNA hypomethylation. Tissue-specific hypomethylation has been linked to CBS knockout mutation in mice [61, 62] although conflicting results were recently reported [63].
The T. vaginalis genome encodes several isoforms of methionine adenosyl transferase and SAH hydrolase (S6 Table) [12]. Only one potential SAM-dependent methyltransferase was found in the genome although earlier, biochemical evidence demonstrated that transmethylation reactions take place in T. vaginalis and T. foetus [64]. The transulfuration pathway was not found in T. vaginalis but this species produces a broad specificity MGL that hydrolyses homocysteine, methionine and cysteine [29, 35].
In this study, the concentration of SAH in cell extracts was higher in T. foetus compared with T. vaginalis. In addition, homocysteine was detected as a mixed disulfide with cysteine in T. foetus extracts with a peak intensity of 1.0 x 105 but was not detected in T. vaginalis, indicating that T. foetus cells have significantly higher levels of homocysteine. Higher levels of homocysteine and SAH would be expected to inhibit SAM-dependent methyltransferases and it is therefore interesting that lower rates of methylation have been reported in T. foetus compared with T. vaginalis [64].
When T. vaginalis was grown in media containing 5 μM propargylglycine, a potent inhibitor of MGL, the concentrations of all metabolites in the trans-methylation pathway were significantly increased, particularly SAH and homocysteine (detected as a mixed dislfide with cysteine). Methionine and homocysteine are hydrolysed by MGL so an increase in their intracellular levels was expected. SAH is a relatively poor substrate of MGL in vitro [35] so the > 100-fold increase in SAH we observed could be linked to the elevated intracellular levels of homocysteine and the resulting shift in the equilibrium of SAH hydrolase reaction towards synthesis of SAH. Thus it appears that one of the functions of MGL is the rapid removal of homocysteine, a function attributed to CBS in other organisms.
We show that T. foetus extracts contained high levels of cystathionine but only very low levels were detected in T. vaginalis grown under the same conditions. This suggests that T. foetus could have a different mechanism for the regulation of homocysteine levels. Cystathionine was labelled in T. foetus when cells were grown with D-[U-13C6] glucose and is therefore synthesised, possibly by a previously unidentified CBS activity using serine and homocysteine or by CS using cysteine and homocysteine, as reported in vitro for the E.coli CysM [65], an orthologue of the T. vaginalis CS [19]. Interestingly, T. vaginalis has the capacity to produce cystathionine when cells are grown in media containing added 10 mM cysteine or when MGL is inhibited by PAG, resulting in elevated intracellular homocysteine levels. We have shown previously that the T. vaginalis CS can produce S-2-hydroxyethyl-L-cysteine and H2S from cysteine and β-mercaptoethanol [19] but the production of cystathionine by the same mechanism was not investigated.
Failure to detect MGL activity in T. foetus or other trichomonad species by biochemical analysis [18] provides a simple explanation for the relatively low levels of SMC and the increased levels of homocysteine found in T. foetus. However, we found that the recently released draft genome sequence for T. foetus strain K [13] encoded 4 copies of a putative MGL. How can the previous biochemical studies and our new metabolomics analysis be reconciled with these predictions based on sequence analysis? It is possible that SMC is produced in T. foetus but is then rapidly converted to another metabolite. For example, cysteine could be formed by de-methylation of SMC. Alternatively, CH3SH produced from methionine could be utilised in alternative reaction. However, a more plausible explanation is that the putative MGL genes of T. foetus encode proteins adapted for another function. Like many PLP-dependent enzymes, MGL shows a range of different activities in vitro. Hydrolysis of methionine to produce 2-ketobutyrate, ammonia and CH3SH is the result of an α, γ elimination reaction and MGL enzymes from different organisms can use cysteine, homocysteine or cystathionine as alternative substrates in the same reaction with varying efficiency [66] Isoforms within a species show differences in substrate specificity as observed in T. vaginalis (29) and E. hystolytica [67] and the specificity of MGL can be altered by mutation of active site residues [29]. Cysteine and substituted serines including O-acetylserine and OPS are hydrolysed in vitro by an alternative α, β elimination reaction and β or γ replacement reactions are also possible. Functional analysis of the MGL from A. thaliana suggested a role in an alternative pathway for cysteine biosynthesis from methionine involving CH3SH [68]. The pathway was not determined but it was proposed that MGL catalysed a replacement reaction involving CH3SH that resulted in the release of H2S that could be used by CS for cysteine biosynthesis. Interestingly, kinetic analysis of the A. thaliana MGL showed that the efficiency of the α, γ -elimination reaction for hydrolysis of methionine was 3-orders of magnitude lower than that for MGLs from other organisms, leading to the suggestion that a replacement reaction is indeed preferred by the A. thaliana MGL [66]. Thus the catalysis of alternative reactions by MGL may be significant in vivo and MGL seems likely to perform different functions in different organisms. In this study we propose that MGL in T. vaginalis is involved in the removal of homocysteine and production of CMC via CH3SH. This study has shown that the same does not appear to be the case for the putative MGL identified in the T. foetus genome. Further investigation, including detailed kinetic analysis of recombinant proteins, is needed to determine the function served by the putative T. foetus MGL. We have shown that cystathionine is produced and exported by T. foetus but was detected only at very low levels in T. vaginalis. Perhaps the putative MGL isoforms of T. foetus produce cystathionine from cysteine and homocysteine by a β-replacement mechanism as reported for the E. coli CysM.
In mammals and many other organisms SAM decarboxylase produces decarboxylated SAM which acts as donor of aminopropyl groups for spermidine synthesis, producing methylthioadenosine (MTA) as a by-product. Trichomonas lacks SAM decarboxylase and does not synthesise spermidine, nevertheless high levels of MTA were identified in the metabolomic profiles of T. vaginalis and T. foetus. Incorporation of 13C confirmed that MTA was produced from SAM by an unusual mechanism. The T. vaginalis genome encodes a homolog of 1-aminocyclopropane-1-carboxylate (ACC) synthase, a plant enzyme that converts SAM to ACC and MTA [69]. As a standard, ACC gave a peak with a retention time of 12.34 but ACC was not found in cell extracts or media samples, suggesting that it is rapidly converted. In plants ACC is the precursor of the ripening hormone ethylene but there is no evidence of ethylene production in these trichomonads. MTA is a precursor in the methionine regeneration pathway in many organisms. Working with T. vaginalis cell extracts, Berger and co-workers identified an aminotransferase required for the last step in the pathway [70]. The aminotransferase converted ketomethiobutyrate to methionine in vitro and showed a strong preference for lysine as an amino donor. However, failure to detect 13C labelled methionine in our study does not support methionine recycling.
2-Hydroxy acids are produced in T. vaginalis using LDH
T. vaginalis converts several amino acids to 2-hydroxy acid derivatives which are exported into the medium whereas only low levels of these metabolites were detected in T. foetus. 2-hydroxy acids are produced by deamination of amino acids to form the corresponding 2-keto acid followed by reduction using an NADH dependent 2-hydroxy acid dehydrogenase. T. vaginalis encodes a branch-chain amino acid aminotransferase that transaminates leucine [71] to form 2-isocaproate. A broad specificity aspartate aminotransferase has activity with aromatic amino acids in vitro including phenylalanine and tryptophan [72], to produce phenylpyruvate and indole-3-pyruvate. In addition, 2-ketobutyrate can be formed from threonine by threonine dehydratase and from methionine or homocysteine by MGL. There is good evidence that these 2-keto-acid derivatives are converted to the corresponding hydroxy acids by a broad specificity LDH. Six isoforms of LDH were resolved from T. vaginalis extracts by isoelectric focussing and two of these showed high activity for ketobutyrate and 2-isocaproate [73].
One of the LDH isoforms, purified as a recombinant protein, has malate dehydrogenase (MDH) activity in addition to LDH activity [74]. This is unusual because 2-hydroxy acid dehydrogenases generally have a high specificity either for oxaloacetate or pyruvate. Based on sequence analysis it was proposed that LDH evolved from cytoplasmic MDH by gene duplication and mutation. The T. vaginalis genomic sequence encodes 10 isoforms of LDH with between 57% and 94% amino acid identity. These most likely have different substrate specificity, accounting for the wide range of hydroxy acids detected. The absence of biochemical evidence for LDH activity in T. foetus explains why only negligible amounts of hydroxy acids are detected in cell and media extracts. A search of the draft genome sequence of T. foetus strain K identified 4 isoforms of a putative MDH containing the conserved ‘specificity’ residue (S5 Fig) [74] but failed to detect any homolog of the T. vaginalis LDH (S6 Table).
Lactate is a major product of energy metabolism in T. vaginalis and the main function of LDH in T. vaginalis is likely to be redox balance. However, T. vaginalis also produces very high levels of HICA suggesting that catabolism of leucine by this route is important to the organism. HICA is produced by lactic acid bacteria and was recently shown to have antimicrobial [75–77] and anti-inflammatory activity [78]. HICA can also improve muscle recovery by inducing an increase in protein synthesis through mTOR signalling [79], which also regulates the innate immune response to bacterial, fungal or parasitic infection. The healthy vaginal microbiome is dominated by H2O2- and lactic acid-producing lactobacillus species forming a biofilm on the cervico/vaginal mucosa that protects against bacterial vaginosis, although not against trichomoniasis. Trichomonas infection alters the microbiome, thereby increasing vaginal pH. It is worth investigating whether HICA or other 2-hydroxy acids produced by T. vaginalis could have a role in colonisation or maintenance of Trichomonas infection by inhibiting the growth of competing genital bacteria or by modulating the innate immune response.
Higher rate of arginine metabolism in T. foetus
T. foetus showed increased levels of citrulline and ornithine in cell extracts and higher levels of putrescine were found in spent media suggesting increased flux through the arginine dihydrolase pathway. Conversion of citrulline to ornithine generates carbamoyl phosphate which is further catabolised to produce ATP by substrate level phosphorylation, so arginine catabolism could increase the ATP producing capacity in the cell. This may represent a significant contribution to energy production because the rate of arginine catabolism, measured by quantifying ammonia production, was found to be comparable to the rate of carbohydrate catabolism [31]. Arginine deiminase (ADI), the first enzyme of the pathway catalysing the formation of urea and citrulline from arginine, was recently found to be located in the hydrogenosome whereas all other enzymes in the pathway are cytoplasmic [80]. The significance of the sub-cellular localisation of ADI is not known but it has been suggested that ammonium ions released by arginine catabolism could be important for maintenance of hydrogenosomal pH [80]. Alternatively, concentration of arginine in the hydrogenosome could result in increased ADI activity and higher flux. Although levels of intermediates in the arginine dihydrolase pathway were lower in T. vaginalis, other products of arginine metabolism such as 4-guanidinobutanoate were present at higher levels, suggesting that deamination or transamination of arginine may be more active in T. vaginalis.
Conclusions
Although the metabolic profiles of T. vaginalis and T. foetus are overall very similar, this study has identified a number of polar metabolites that differ significantly in relative abundance. Our study indicates that MGL efficiently removes homocysteine in T. vaginalis and hence maintains low levels of SAH. This is important because SAH is an inhibitor of SAM-dependent methyltransferases responsible for the methylation of nucleic acids, proteins and lipids. In addition, CH3SH released from methionine by MGL is used by the T. vaginalis CS to produce SMC, and we proposed that this has a role along with cysteine as an intracellular antioxidant. CS has been investigated as a chemotherapeutic target in other organisms [81]. T. vaginalis and T. foetus are microaerophiles, they are exposed to oxygen in their natural environment and antioxidant defence mechanisms are vitally important to protect against oxidative stress. T. foetus does not produce SMC but maintains much higher intracellular levels of cysteine and appears to remove homocysteine by conversion to cystathionine. These trichomonads do not produce reactive oxygen species by aerobic respiration and the low oxygen concentrations mean that they can tolerate relatively high intracellular concentrations of cysteine [20]. The reactivity of cysteine in transition-metal autoxidation may be important in controlling oxygen levels and protecting hydrogenosomal enzymes from inactivation. T. vaginalis and T. foetus have evolved similar mechanisms for redox homeostasis in a low oxygen environment with some species-specific adaptations. It is thought that T. vaginalis acquired MGL by lateral gene transfer and previous biochemical studies failed to detect MGL activity in T. foetus. However, the recently completed draft genome sequence of T. foetus indicates that the parasite contains 4 isoforms of a putative MGL. Further studies are needed to determine the function that these putative MGL perform in T. foetus, but the differences in methionine metabolism between the species observed in this study suggest that it must differ from that of the T. vaginalis enzyme. The broad specificity T. vaginalis LDH was most likely derived from MDH by gene duplication and mutation and we confirm that LDH is not present in the T. foetus genome. In addition to producing lactate as an end product of energy metabolism, we show that T. vaginalis differs from T. foetus in producing markedly higher levels of the 2-hydroxy acid derivatives of certain amino acids. HICA, the hydroxy acid derived from leucine is also produced by lactic acid bacteria and has antibacterial and antibiotic properties. Early in infection, T. vaginalis must compete with the normal vaginal flora for nutrients and survive exposure to H2O2, produced by the endogenous lactobacilli. Huang and co-workers used glucose restriction to model these early conditions and observed an adaptive response that enhanced survival and increased resistance to H2O2 [47]. Under these conditions, RNAseq revealed a significant up-regulation of branch-chain aminotransferase and LDH expression [47] required for production of HICA. Although there was no increase in CS mRNA levels, increased expression of genes for OPS biosynthesis were observed. The Km of CS for OPS is relatively high [19], thus increased phosphoserine availability could result in higher cysteine and SMC levels. Production of SMC and the release of HICA acid and other hydroxy acids by T. vaginalis could be involved in the changes in the vaginal microbiome observed during infection and may be beneficial in promoting the parasite’s survival and proliferation.
Supporting information
S1 Table. Metabolites confirmed by matching retention times with authentic standards or by MS2 analysis.
https://doi.org/10.1371/journal.pone.0189072.s001
(XLSX)
S2 Table. All metabolites identified in cell extracts of T. vaginalis and T. foetus including confirmed metabolites and putative metabolites identified by accurate mass and predicted retention time.
https://doi.org/10.1371/journal.pone.0189072.s002
(XLSX)
S3 Table. All metabolites identified in media samples.
https://doi.org/10.1371/journal.pone.0189072.s003
(XLSX)
S4 Table. Concentration (μmol/108 cells) of amino acids in cell extracts.
https://doi.org/10.1371/journal.pone.0189072.s004
(XLSX)
S5 Table. Concentration (μM) of amino acids in media samples.
https://doi.org/10.1371/journal.pone.0189072.s005
(XLSX)
S6 Table. Genes for cysteine, methionine and 2-hydroxy acid metabolism found in the draft genome of T. foetus and T. vaginalis.
https://doi.org/10.1371/journal.pone.0189072.s006
(XLSX)
S1 Fig. 13C labelling of intermediates in central carbon metabolism in T. vaginalis and T. foetus.
T. vaginalis and T. foetus were grown for 20 h at 37°C in MDM containing 100% D-[U-13C6] glucose as the only carbohydrate carbon source and cell extracts were analysed by LCMS. Heat maps of the percentage of unlabelled metabolites and isotopologues with increasing number of 13C atoms are shown for (A) T. vaginalis and (B) T. foetus. Numbers on the heat map refer to percentage labelling values.
https://doi.org/10.1371/journal.pone.0189072.s007
(TIF)
S2 Fig. 13C labelling of intermediates in nucleotide metabolism in T. vaginalis and T. foetus.
Heat maps of the percentage of unlabelled metabolites and isotopologues with increasing number of 13C atoms are shown for (A) T. vaginalis and (B) T. foetus.
https://doi.org/10.1371/journal.pone.0189072.s008
(TIF)
S3 Fig. 13C labelling of intermediates in methionine metabolism in T. vaginalis and T. foetus.
Heat maps of the percentage of unlabelled metabolites and their isotopologues with increasing numbers of 13C atoms are shown for (A) T. vaginalis and (B) T. foetus.
https://doi.org/10.1371/journal.pone.0189072.s009
(TIF)
S4 Fig. Identification of S-methyl-cysteine in T. vaginalis by MS2.
A metabolite with predicted formula C4H9NO2S was analysed by MS2. The full length molecule was not seen in the mass spectrum. Fragments detected and their predicted formula are shown (A) in the mass spectrum and (B) in the table. The data is consistent with the structure of S-methyl-cysteine (C).
https://doi.org/10.1371/journal.pone.0189072.s010
(TIF)
S5 Fig. Multiple sequence alignment of putative MDH genes from T. foetus.
Four putative isoforms of T. foetus MDH are aligned with MDH (TVAG_253650) and LDH (TVAG_49988). Conserved residues are in white type on a black background. Conservative amino acid differences are in white type on a grey background. The red arrow below the line indicates a residue found to be a major determinant of substrate specificity, this is arginine in T. vaginalis MDH but leucine in T. vaginalis LDH. All isoforms found in T. foetus have a positively charged residues at this position and are therefore predicted to have MDH activity. Black arrows indicate conserved residues involved in substrate binding or enzyme activity.
https://doi.org/10.1371/journal.pone.0189072.s011
(TIF)
S6 Fig. Multiple sequence alignment of putative MGL genes from T. foetus and T. vaginalis.
Sequences obtained by tblastn search of the T. foetus and T. vaginalis genome sequences with the T. vaginalis MGL1 (TVAG_041600) as a query sequence. Conserved residues are in white type on a black background. Conservative amino acid differences are in white type on a grey background. Symbols: ▲, active site residues involved in PLP binding; , cysteine residue implicated in methionine binding.
https://doi.org/10.1371/journal.pone.0189072.s012
(TIF)
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