Protein phosphorylation plays a key role in Mycobacterium tuberculosis (Mtb) physiology and pathogenesis. We have previously shown that a secreted protein tyrosine phosphatase, PtpA, is essential for Mtb inhibition of host macrophage acidification and maturation, and is a substrate of the protein tyrosine kinase, PtkA, encoded in the same operon. In this study, we constructed a ∆ptkA deletion mutant in Mtb and found that the mutant exhibited impaired intracellular survival in the THP-1 macrophage infection model, correlated with the strain’s inability to inhibit macrophage phagosome acidification. By contrast, the mutant displayed increased resistance to oxidative stress in vitro. Proteomic and transcriptional analyses revealed upregulation of ptpA, and increased secretion of TrxB2, in the ΔptkA mutant. Kinase and protein-protein interaction studies demonstrated that TrxB2 is a substrate of PtkA phosphorylation. Taken together these studies establish a central role for the ptkA-ptpA operon in Mtb pathogenesis.
The etiological agent of tuberculosis (TB), Mycobacterium tuberculosis (Mtb), remains one of the most devastating infectious agents in the world. One-third of the world’s population is exposed to Mtb, resulting in nearly two million deaths annually1. The emergence of extensively drug-resistant (XDR) strains and co-infection with HIV has exacerbated the global burden of TB2. Therefore, there is an urgent need for the development of novel therapeutics against the deadly disease.
Mtb primarily infects alveolar macrophages, the first line of defense against microbial invasion in the lung. Macrophages engulf the bacteria into phagosomes which acidify and mature by remodeling the membrane and luminal contents3. Antimicrobial molecules such as acidic hydrolases are delivered to the compartment, and interaction with the endosomal network ultimately leads to phagosome-lysosome fusion and elimination of the foreign particle4. However, Mtb blocks phagosome maturation and prevents the phagosome from acquiring antimicrobial properties, enabling its survival within the hostile environment of the macrophage5,6,7,8.
Mtb utilizes multiple mechanisms to protect itself from the host antimicrobial assault. The Mtb cell wall glycolipid ManLAM co-operates with the secreted acid phosphatase SapM to block phagosome fusion with late endosomes. Both prevent phagosomal accumulation of phosphatidylinositol 3-phosphate (PI3P), which mediates the recruitment of membrane trafficking proteins such as the early endosomal antigen, EEA19,10. Mtb is resistant to host-generated reactive oxygen and nitrogen species; ROS and RNS are adsorbed in its thick cell wall and inactivated by detoxification enzymes or antioxidants, such as catalase (KatG)11, peroxidase and the peroxynitrite reductase complex (AhpC, AhpD, DlaT and Lpd)12, the thioredoxin system13, and mycothiol14.
Mtb has evolved systems to sense the stages of engulfment within macrophages and activate bacterial systems to block host defense pathways15,16,17. Mtb possesses a wide repertoire of signal transduction systems, including eleven “two-component” systems, eleven eukaryotic-like serine/threonine protein kinases (PknA-PknL), two protein tyrosine phosphatases (PtpA and PtpB), and the newly identified protein tyrosine kinase, PtkA8,18,19,20,21,22. These signaling proteins play key roles in bacterial adaptation and response to host defense mechanisms. In particular, PtpA, a secreted protein essential for Mtb pathogenesis, interacts with the host vacuolar-H+-ATPase complex to block its trafficking to the mycobacterial phagosome, thereby preventing phagosome acidification and ultimately phagosome-lysosome fusion15,20. PtkA, encoded within the same operon as ptpA, phosphorylates PtpA19, thereby enhancing PtpA phosphatase activity23. This suggests that PtkA and PtpA may act cooperatively to provide a function essential for Mtb pathogenesis.
In this work, we constructed a deletion mutant of ptkA to assess its role in Mtb physiology. The ΔptkA strain was found to have impaired intracellular survival within the THP-1 macrophage infection model, and failed to inhibit phagosome acidification. However, the ΔptkA mutant strain also displayed enhanced resistance against oxidative stress in vitro. We therefore used a global proteomics approach to compare ΔptkA and its parental wild type (WT) strain when exposed to oxidative stress. Additionally, given that PtpA is secreted, we compared the secretomes of ΔptkA and its parental strain. We discovered that thioredoxin reductase TrxB2, an important protein in the defense against oxidative stress, is secreted by Mtb and its secretion is up-regulated in the ΔptkA mutant strain. Through kinase assays and protein-protein interaction studies, we discovered that TrxB2 is a substrate of PtkA phosphorylation.
Construction of a ptkA knockout mutant in Mtb
To assess the role of PtkA in Mtb physiology, we constructed an Mtb mutant with a deletion of the gene encoding the PtkA tyrosine kinase by specialized phage transduction24. Genomic DNA isolated from the parental WT strain and the ∆ptkA mutant strain were subjected to Southern hybridization analysis to confirm that the gene encoding PtkA was replaced with the hygromycin resistance cassette as outlined in Fig. 1a and b. Whole genome sequencing confirmed successful replacement of the ptkA gene as designed without interruption of the rest of the genes within the ptkA operon25.
Intracellular survival in THP-1 macrophages
Since ptkA and ptpA are present in the same polycistronic operon, and PtpA is known to be essential for Mtb pathogenesis15,20,26 as well as being the phosphorylation substrate of PtkA19,23, we hypothesized that PtkA might also be required for Mtb intracellular growth within human macrophages. To test our hypothesis, we investigated the ability of the mutant strain to survive in the human THP-1 macrophage infection model. Indeed, the ΔptkA strain was found to be attenuated within the macrophage, whereas the parental and the complemented strains were able to establish a stable infection after 3 days (Fig. 2a). At 6 days after infection, the mutant strain showed more than a log reduction in CFU compared to the WT strain. While the parental and complemented strains entered growth phase within the macrophage, the ΔptkA strain was continuously cleared, establishing the importance of PtkA for Mtb growth within macrophages.
Inhibition of the macrophage’s phagosomal acidification
In the case of the ΔptpA mutant, impaired intracellular survival results from its inability to inhibit phagosome acidification20. To investigate whether this was the case with the ΔptkA mutant, we examined phagosomal pH in THP-1 macrophages infected with the ΔptkA mutant and compared it to its parental WT strain. We used fluorescence-activated cell sorting (FACS) to analyze the pH of Mtb-containing phagosomes. Parental and mutant strains were dually labeled with the pH-sensitive pHrodo fluorescent dye and the pH-insensitive Alexa Fluor 488. The ΔptpA strain, shown earlier to be incapable of inhibiting phagosome acidification, was used as a control. As seen in Fig. 2b–d and Table 1, overlaid FACS histograms showed an increase in the mean pHrodo fluorescence intensity for phagosomes harboring the ΔptkA strain (corresponding to pH 5.40), as compared to those containing the WT strain (corresponding to pH 6.64). This increase is similar to that observed for the ΔptpA strain (corresponding to pH 5.46), indicating that the ΔptkA strain failed to block phagosome acidification.
Increased cellular expression of ptpA and PtpA
As the ΔptkA and ΔptpA strains demonstrated similar phenotypes in the macrophage infection, and because ptkA is the first gene in the ptpA operon, we checked whether ptkA deletion could have resulted in the loss of ptpA expression. Using quantitative real-time PCR (qPCR), we found that ptpA transcription was not disrupted but rather upregulated in the ΔptkA mutant compared to WT Mtb (Fig. 3a). Western analysis confirmed increased levels of PtpA protein in the ΔptkA mutant compared to WT (Fig. 3b, 2nd panel). PtkA and the unrelated protein, DosR, were used as controls to confirm knockout of PtkA in the mutant and equal loading, respectively (Fig. 3b, 1st and 4th panels). Our iTRAQ experiment (below) also identified increased intracellular levels of both PtpA and Rv2235 (encoded in the same operon as ptkA and ptpA) in the ΔptkA mutant. Complementation, however, did not restore WT levels of ptpA (Fig. 3a) or PtpA (Fig. 3b). Analysis of the genomic sequence of the ΔptkA mutant suggests that upregulation of ptpA may be due to the introduction of a putative promoter sequence downstream of the hygromycin cassette25. Nevertheless, complementation did restore the macrophage infection phenotypes observed in the ΔptkA mutant (Fig. 2). Therefore, while not ideal, the overexpression of ptpA in the mutant was a fortuitous, though accidental control, indicating that the similarity between the ΔptkA and ΔptpA strains is not due to loss of ptpA expression in the ΔptkA mutant, but that PtkA is independently essential for Mtb pathogenesis.
Resistance to oxidative stress in liquid cultures
To further characterize the ΔptkA strain, we examined whether the deletion of the ptkA gene affected the growth of Mtb in vitro. The growth of the mutant with its parental and the complemented strains in various conditions was compared. No differences in growth rate were observed between the ΔptkA mutant and its parental strain when grown as rolling or static cultures in 7H9-ADS or Sauton’s medium (Fig. 4a and b). As PtkA was shown to be phosphorylated by Ser/Thr protein kinases specifically under peroxide treatment27, and to mimic in vivo oxidative stress conditions, we tested the growth of the ΔptkA mutant exposed to peroxides. Surprisingly, ΔptkA growth, as measured by OD600 and colony forming units, was more resistant to sub-lethal and lethal concentrations of hydrogen peroxide (Fig. 4c,d,g and h) and cumene hydroperoxide (Fig. 4e,f,i, and j). Sensitivity to these oxidizing agents was suppressed by complementation of the ΔptkA mutant with the WT gene, thus confirming that the mutated allele made the strain more resistant to oxidative stress in vitro. This in vitro phenotype appears to be in stark contrast to the mutant’s impaired intracellular survival.
Proteomic analysis of the ΔptkA mutant
To gain insight into potential regulation mediated by PtkA, we compared the protein expression profiles of ΔptkA and WT Mtb with and without H2O2 treatment using the quantitative mass spectrometry proteomics approach, iTRAQ. We were able to identify and compare the levels of up to 1163 cellular proteins using a cutoff of 95% confidence in the identification of peptides. The ratios of individual protein levels ranged from 0.269 to 4.099 for untreated samples, and from 0.235 to 4.878 for H2O2-treated samples (Supplementary Data 1). Using an arbitrary cut-off of 1.5-fold change, 10 proteins were up-regulated and 8 proteins were down-regulated in untreated samples, while 11 were up-regulated and 21 down-regulated in treated samples. Graphical analysis of a plot of treated vs untreated ΔptkA/WT ratios revealed that the largest subset of differentially expressed proteins mapped to the lower right quadrant, corresponding to a 1.4-fold decrease in ΔptkA /WT ratios upon treatment with H2O2 (Fig. 5A, blue circles). This subgroup of 49 proteins was enriched for proteins related to the ESX type VII secretion systems and ribosome or ribosome-modifying proteins based on DAVID (Database for Annotation, Visualization and Integrated Discovery) gene ontology analysis. Further inspection also identified several proteins encoded in the zinc uptake regulator (Zur) regulon (Table 2). In addition to this subgroup, a lone protein involved in pyrimidine biosynthesis, PyrE, was found highly upregulated in the ΔptkA mutant only upon treatment with H2O2 (Fig. 5A). Additionally, as noted above, the intracellular levels of PtpA and Rv2235 were highly upregulated in the ΔptkA mutant independent of H2O2 treatment (Fig. 5A).
As the PtkA substrate, PtpA, is secreted, and Mtb secretes anti-oxidative defense enzymes, including a superoxide (SodA) and a catalase (KatG), we compared the culture filtrate proteins (CFPs) of ΔptkA and WT. iTRAQ analysis of CFPs revealed 877 proteins identified with 95% confidence. Of these, 29 proteins were found to be increased by at least 2-fold in the ΔptkA mutant, while 12 proteins decreased, with levels ranging from 0.153 to 10.784 (Supplementary Data 1). CFP levels were plotted against the corresponding cellular protein levels of Mtb grown in Sauton’s media and shown in Fig. 5B. Of note, the thioredoxin reductase TrxB2 was found to be 3.2-fold higher in protein abundance in the culture filtrate of the ΔptkA strain. Since the thioredoxin system participates in the detoxification of ROI13 and therefore may account for the enhanced resistance to oxidative stress observed in the ΔptkA mutant, we decided to further investigate the link between PtkA and TrxB2.
TrxB2 expression and phosphorylation
The increased secretion level of TrxB2 was confirmed by Western blot analysis of CFPs (Fig. 3c, upper panel). The absence of Mtb autolysis during culturing was confirmed by Western blot analysis of the harvested CFPs with antibodies against the cytosolic DosR protein (Fig. 3c, lower panel). However, both expression of the trxB2 gene (Fig. 3a) as well as the intracellular protein levels of TrxB2 (Fig. 3b) revealed no difference in the ΔptkA mutant compared to WT and complement strains.
Given that PtpA is secreted and is a substrate of PtkA19, we tested the possibility that TrxB2, being secreted and dysregulated in the ΔptkA mutant, may also serve as a substrate for PtkA. Indeed, in vitro kinase assays demonstrated that PtkA phosphorylated TrxB2 in a dose- and time-dependent manner (Fig. 6a,b). Phosphoamino acid analysis of the phosphorylated TrxB2 protein further revealed that PtkA phosphorylated TrxB2 on tyrosine, consistent with PtkA’s tyrosine kinase activity (Fig. 6c). We further performed site-directed mutagenesis to examine which Tyr residue in TrxB2 was phosphorylated. Mutation of Tyr32 significantly reduced phosphorylation of TrxB2, indicating that Tyr32 is targeted by PtkA for phorphorylation (Fig. 6d).
To further verify the kinase-substrate interaction in a cellular model, PtkA and TrxB2 were subjected to the mycobacterial protein fragment complementation assay28. Co-expression of TrxB2-F3 with PtkA-F1,2 resulted in reconstitution of mDHFR activity, as evidenced by growth of M. smegmatis on media supplemented with trimethoprim, confirming PtkA interaction with TrxB2 (Fig. 6e). The interaction between PtkA and TrxB2 was found to be similar to that of PtkA and PtpA, based on comparable M. smegamatis growth in the presence of trimethoprim.
Tyr phosphorylation in mycobacteria has long been a subject of interest29. Our results19, along with studies from others30,31, have demonstrated Tyr kinase activity in Mtb. However, the physiological function of Tyr phosphorylation in Mtb has not been explored. We have previously shown that PtkA represents a novel prokaryotic protein Tyr kinase19,32. PtkA was also proposed to play a key role in Mtb pathogenesis21,32 based on its substrate, PtpA, being essential for preventing phagosome acidification and maturation15,20. Here, we examined the role of PtkA in Mtb pathophysiology and pathogenesis by generating a mutant Mtb strain with a deletion of the ptkA gene. The ΔptkA mutant was impaired in intracellular survival within the THP-1 macrophage infection model and is consistent with the mutant’s failure to inhibit phagosomal acidification. These results match the phenotype of the ΔptpA deletion mutant15,20 suggesting that PtkA inhibition of phagosomal acidification may be mediated via PtpA function, either through PtkA phosphorylation of PtpA, which enhances PtpA phosphatase activity23, and/or via PtkA-dependent PtpA secretion. Further experiments are needed to test this hypothesis.
While ptkA was needed for intracellular survival, the lack of ptkA enhanced the mutant stain’s resistance to oxidative stress in vitro. Proteomic analyses identified the thioredoxin reductase, TrxB2, to have increased secretion in the ΔptkA mutant. While the exact mechanism of this upregulation was not identified and may be a result of increased expression of PtpA and/or Rv2235 as complementation of the ptkA mutant did not restore WT levels, we found that PtkA is able to bind and phosphorylate TrxB2 on tyrosine. Additionally, we demonstrated that TrxB2 is secreted, which has not been reported previously to our knowledge. Secretion of TrxB2 is consistent with the finding that TrxC, the thioredoxin substrate of TrxB2, is secreted33,34,35,36, as we also observed (Supplementary Data 1).
While it is tempting to speculate that increased secretion of TrxB2 is responsible for the mutant’s increased resistance to oxidative stress, the fact that TrxB2 secretion was also upregulated in the complement, while complementation restored the WT sensitivity to oxidative stress suggests an alternative mechanism is at play. Furthermore, the relatively modest 3.2-fold increased secretion of TrxB2, is unlikely to be able to result in the up-to 2-log enhanced growth/survival of the ΔptkA mutant in lethal concentrations of oxidative stress (Fig. 4). Other variations in protein levels identified in the iTRAQ experiment, such as the decrease in ribosomal proteins and rRNA methyltransferases observed in the ΔptkA mutant (Table 2), may lead to a slower metabolism and thus increased resistance to oxidative stress. Alternatively, in S. aureus, the methylation status of rRNA has been shown to affect resistance to oxidative stress37. However, we did not establish a direct role for PtkA in this downregulation which may be an indirect downstream effect of the oxidative stress.
A second cluster of enriched proteins that were identified to be dysregulated in the ΔptkA mutant when exposed to H2O2 belong to the ESX type 7 secretion systems (Table 2). Interestingly, each of these proteins are predicted to be secreted by either the ESX-3 or ESX-5 secretion systems38. Consistent with this finding, the structural components of the ESX secretion systems that were identified in our iTRAQ analysis showed little to no difference in protein levels between WT and mutant (Supplementary Data 1). Given that the two identified substrates of PtkA, PtpA19 and TrxB2 (this study), are secreted, and that the dysregulated ESX proteins are secretion proteins, suggests that PtkA may play a role in secretion.
The ESX-5 secretion system has been described to be involved in nutrient uptake39, while the ESX-3 system is necessary for iron and zinc homeostasis40. Interestingly both the identified ribosomal proteins and the ESX-3 proteins are encoded in the zur regulon which responds to zinc levels41. Disruption of metalloregulatory proteins can result in a change to intrabacterial redox state42 and may contribute to the mutant’s resistance to oxidative stress, as over-exposure to metal ions could render them highly toxic through interference with the functioning of macromolecules and the generation of free radicals43.
While the ΔptkA mutant demonstrated enhanced resistance to oxidative stress, this resistance was not sufficient to compensate for or overcome the mutant’s inability to block phagosomal acidification in the macrophage infection model, and the failure to grow and survive within the macrophage. Additionally, Mehra et al.44 discovered that the EsxG-EsxH complex, secreted by the ESX-3 system, interacts and interferes with the endosomal sorting complex required for transport (ESCRT), demonstrating a direct role for ESX-3 in the arrest of phagosome maturation. In this regard, the downregulation of EsxH identified in the ΔptkA mutant could also potentially lead to the failure in blocking phagosome-lysosome fusion during macrophage infection and explain the impaired intracellular survival phenotype observed for the ΔptkA strain. Further experiments are needed to test this hypothesis.
To conclude, our studies established a central role for PtkA in macrophage infection by Mtb and correlated the enzyme activity to phosphorylation and secretion of TrxB2 and PtpA.
Strains, media and conditions
Mtb H37Rv and their derivative strains were grown on Middlebrook 7H10 agar (BD Diagnostic Systems, Mississauga, ON, Canada) supplemented with 10% (v/v) OADC (oleic acid, albumin, dextrose and catalase solution). For liquid cultures, Mtb strains were grown in Middlebrook 7H9 broth (BD Diagnostic Systems) supplemented with 10% (v/v) OADC or ADS (albumin, dextrose and NaCl solution) and 0.05% (v/v) Tween-80 (Sigma-Aldrich) or Sauton’s media supplemented with 0.05% (v/v) Tween-80 at 37 °C standing or rolling in incubator. Escherichia coli strains were cultured in Luria-Bertani (LB) broth. The concentrations of antibiotics used were 75 μg/ml hygromycin and 20 μg/ml kanamycin for mycobacterial strains, and 150 μg/ml hygromycin and 40 μg/ml kanamycin for E. coli.
Construction of ΔptkA deletion mutant
Construction of the ΔptkA deletion mutant was performed according to the specialized transduction with conditionally replicating mycobacteriophage method described previously24. Briefly, 1000-bp of the upstream and downstream flanking regions of the ptkA gene were PCR-amplified from genomic DNA of Mtb H37Rv. Subsequently, the upstream and downstream flanks were digested with the indicated restriction enzymes, and ligated with Van91I-digested p0004-SacB vector containing the γδres-sacB-hyg-γδres cassette comprising of the sacB gene and hygromycin resistance gene flanked by res-sites of the γδ-resolvase. The resulting knockout plasmids were then linearized with PacI and cloned and packaged into the temperature-sensitive phage phAE159, as previously described24, yielding knockout phages which were propagated in M. smegmatis at 30 °C. The mycobacteriophages harboring the knockout constructs were harvested and used for allelic exchange with specialized transduction as reported previously. Mtb H37Rv cultures were grown to an OD600 of 0.8–1.0, washed with 7H9-glycerol-ADS and resuspended in buffer before mixing with the mycobacteriophages at a multiplicity of infection of 10:1 (mycobacteriophage: mycobacteria), and the mixture was incubated at 37 °C overnight. The cells were pelleted and resuspended in 7H9-glycerol-ADS and plated in three 7H10-glycerol-OADC plates with 50 μg/mL of hygromycin and incubated at 37 °C to select for gene deletion and replacement by the γδres-sacB-hyg-γδres cassette. Putative ΔptkA clones were screened by PCR using two pairs of oligonucleotides targeting the hygromycin gene and region flanking the hygromycin cassette. Based on the PCR analysis, two isolates were chosen for Southern hybridization analysis. Genomic DNAs isolated from the parental WT and the two isolates of the ΔptkA strain were subjected to Digoxigenin (DIG)-based Southern hybridization analysis to confirm ptkA deletion.
Complementation of ΔptkA strain
For complementation of ΔptkA, the DNA sequence encoding WT PtkA under the control of the native promoter was cloned into the pKP186 integrative vector. The ΔptkA strain was co-transformed with the resulting plasmid and pBSint, a non-replicating plasmid that provides integrase in trans but is subsequently lost from the cells, thereby reducing the chances of integrase-mediated excision of the complementing DNA. Transformants were selected on 7H10 agar with 10% OADC and 50 μg/mL kanamycin.
Hydrogen peroxide sensitivity assay
Mtb cultures at OD600 = 0.15 in 7H9 media supplemented with 0.05% (v/v) Tween-80 and ADS or Sauton’s media supplemented with 0.05% (v/v) Tween-80 were exposed to a single dose of H2O2 (0 mM–4 mM) in vitro. Bacterial growth (OD600) and colony forming unit (CFU) were monitored every 24 hours after addition of stress. Three independent experiments were conducted for each H2O2 concentration.
Infection of THP-1
Infection of THP-1 macrophages was performed using human serum-opsonized Mtb at a multiplicity of infection (MOI) of 10:1 or 1:1 (Bacteria: Macrophage). For Mtb intracellular survival studies, infected macrophages were harvested at defined time points, lysed with 0.025% SDS, serial diluted, and plated on 7H10 agar medium supplemented with OADC and appropriate antibiotics. The plates were incubated at 37 °C for 2 weeks until colonies could be counted.
Measurement of phagosomal pH in THP-1 macrophages infected with Mtb
Phagosomal pH measurement was performed as described previously20. Briefly, THP-1 macrophages were seeded on 6 well plates (1.0 × 106) with 40 ng/ml PMA. Mtb strains were first labeled with 20 M pHrodo succinimidyl ester (SE) (Invitrogen) at 37 °C for one hour. The bacteria were washed with 7H9 supplemented with 0.05% Tween-80 three times before being labeled with 25 g/mL Alexa Fluor 488 carboxylic acid SE (Invitrogen). The bacteria were then washed and opsonized with human serum. The THP-1 macrophages were subsequently infected with the labeled Mtb at a MOI of 10:1 for 2 hours at 37 °C with 5% CO2. Non-internalized bacteria were washed away, and the infection was carried out for another 2 hours at 37 °C with 5% CO2. For pH calibration, the infected cells were incubated in 10 mM phosphate-citrate buffer with pre-determined pH (5.0–8.0) (Fig. S1A and S1B). The cells were then washed, scraped off the plate and fixed with 2.5% paraformaldehyde. The fixed cells were then analyzed with FACS on FACSCalibur (BD Bioscience) and the FlowJo 8.7 software. Color compensation was performed to prevent signal overlapping. Mean fluorescence intensities of pHrodo and Alexa Fluor 488 were used to calculate phagosomal pH.
Protein preparation for proteomics analysis
Mtb H37Rv and their derivative strains were grown in Middlebrook 7H9 broth (BD Diagnostic Systems) supplemented with 10% (v/v) OADC or ADS and 0.05% (v/v) Tween-80 (Sigma-Aldrich) to an OD600 = 0.6. The cultures were washed with 7H9 or Sauton’s media and inoculated into fresh 7H9-ADS or Sauton’s media supplemented with 0.05% (v/v) Tween-80. Sauton’s media was used when culture filtrate proteins were analyzed. 2 mM H2O2 was added when appropriate, and the cultures were grown at 37 °C rolling in incubator until OD600 = 1.0. The culture filtrate proteins were harvested by centrifuging the Mtb cultures to obtain the spent culture supernatant. The supernatant was filtered through a 0.22 μm syringe filter unit (Corning) before removal from BSL-3 laboratory. The filtered supernatant was then concentrated with a stirred cell concentrator (EMD Millipore) fitted with YM-3 membrane (3 kDa-cutoff). Cytosolic fractions were extracted by lysing Mtb through bead-beating. The lysate was centrifuged, and the supernatant was filtered through a 0.22 μm syringe filter unit before removal from BSL-3 laboratory.
iTRAQ (isobaric tags for relative and absolute quantitation)
Protein concentrations were determined using a bicinchonic acid protein assay (Sigma). Samples (85 µg of each) were precipitated overnight in acetone at 4 °C followed by resolubilization in 0.5 M triethylammoniumbicarbonate, 0.2% SDS. Proteins were reduced with tris-(2-carboxyethyl)phosphine and alkylated with methyl methanethiosulfonate Proteins were then “in-solution” digested with trypsin (Promega) and labeled with the appropriate iTRAQ label. iTRAQ labeled peptides were then combined and separated by strong cation exchange HPLC. HPLC fractions containing peptides were then reduced in volume by speed-vac and analyzed by LC-MS/MS. The length of the reverse gradient used was 2 hours per HPLC fraction. Samples were analyzed by reversed phase nanoflow (300 nL/min) HPLC with nano-electrospray ionization using a LTQ-Orbitrap mass spectrometer (LTQ-Orbitrap Velos, Thermo-Fisher) operated in positive ion mode. All data was analyzed using Proteome Discoverer v1.3 (Thermo-Fisher) and MASCOT v2.3 (Matrix Science). Raw data files were searched against the Uniprot-SwissProt database with “All Species” filter and Mycobacterium tuberculosis complex species only.
RNA extraction and real-time quantitative PCR
WT Mtb and ΔptkA Mtb strains were grown in rolling cultures at 37 °C in Sauton’s medium. Bacteria were harvested at OD~1.0 and RNAs were extracted using FastRNA Pro Blue kit (MP Biomedicals). Cells were lysed in the presence of glass beads in a FastPrep ribolyzer (MP Biomedicals) according to manufacturer’s instructions. Post lysis, RNA extraction was performed with chloroform, and after ethanol precipitation, RNA was dissolved in nuclease-free water. Purified RNA was treated with RNase-free Turbo DNase (Ambion) according to the supplier’s instructions in order to digest contaminating DNA and the Illustra RNAspin minikit (GE Healthcare) was used for the subsequent cleanup procedures. Removal of DNA was confirmed by performing PCR using an aliquot of the DNase-treated RNA as a template. Reverse transcription reactions were carried out in 20-μl volumes containing 2 μg RNA, random primers, and the buffer and enzyme components of the EasyScript cDNA Synthesis kit (ABM) according to the supplied protocol. Real-time PCR analysis was carried out on the Step One Real Time PCR system (Life Technologies). Each qPCR reaction contained 2X FastStart SYBR green master mix (Roche), 15ng cDNA and 0.3 μM of each primer. Control reactions without reverse transcriptase were also included with each run to confirm the absence of genomic DNA contamination. Expression level was normalized to the constitutively expressed sigA gene.
Western blot analysis
Western blot analyses were performed according to standard protocols. Briefly, 26–30 µg of cellular extracts and CFP of the indicated Mtb strains were resolved by SDS-PAGE and transferred onto a nitrocellulose membrane (Bio-Rad). The blots were blocked with 2% milk proteins in TBS-T and probed with affinity purified rabbit polyclonal (YenZym Antibodies, LLC) anti-PtkA (1:50000), anti-PtpA (1:500), anti-TrxB2 (1:50000), or anti-DosR (1:2500) and incubated overnight at 4 °C. For detection, Alexa Fluor 680 goat anti-rabbit (ThermoFisher) antibody was used as the secondary detection reagent (1:10,000), and detection was done using an Odyssey Infrared CLx Imager (LI-COR Biosciences). Brightness and contrast were adjusted and applied to entire images using Adobe Photoshop CS5.1. Full-length images are shown in Supplementary Fig. 1.
In vitro kinase assay
Kinase assays were carried out using [γ-32P]ATP as the phosphate donor according to published protocols45 with some modifications. The in vitro kinase reactions contained 20 mM Tris-HCl, pH = 7.5, 1 mM MnCl2, 0.1 mM MgCl2 and 1 mM DTT. Proteins (1.3–1.4 µM of PtkA and 1.2 µM of TrxB2 for the time-dependent assay and 3.4 µM of TrxB2 for the single amino acid point mutation kinase assay) were separated by SDS/PAGE (12%) supplemented with 8 M urea, and silver-stained. The 32P-radioactively labeled protein bands were detected using a PhosphorImager SI (Molecular Dynamics). Brightness and contrast were adjusted and applied to entire autoradiography images using Adobe Photoshop CS5.1. Full-length images are shown in Supplementary Fig. 2. Densitometric analysis of TrxB2 phosphorylation in Fig. 6d using Adobe Photophop CS5.1 is shown in Supplementary Fig. 3.
Phosphoamino acid analysis
Recombinant PtkA was incubated with [γ-32P]ATP in the kinase buffer described above. The sample was hydrolyzed with 6 N HCl at 110 °C for 1 hour and separated on a cellulose TLC plate by ascending chromatography45. For TrxB2 phosphorylation by PtkA, the reaction was stopped with sample buffer, loaded into SDS-PAGE (12%) containing 8 M urea, and subjected to electrophoresis. The gel was electroblotted on to an Immobilon PVDF membrane46. Phosphorylated proteins bound to the membrane were detected by autoradiography using a PhosphorImager apparatus. The 32P-labelled protein band corresponding to the migration of TrxB2 was excised from the membrane and hydrolyzed following the same procedure as described above. After hydrolysis, samples were separated on ascending TLC chromatography. After migration, radioactive amino acids were detected by autoradiography. Brightness and contrast were adjusted and applied to entire autoradiography images using Adobe Photoshop CS5.1. Phosphoserine, phosphothreonine and phosphotyrosine standards (Sigma) were separated on cellulose TLC plate in parallel and visualized by staining with ninhydrin.
Mycobacterial protein fragment complementation assay
The mycobacterial protein fragment complementation assay was performed as described28. The genes of interest were PCR-amplified and cloned into pUAB100 (expressing mDHFR fragment F1,2) or pUAB200 (expressing mDHFR fragment F3). M. smegmatis was co-transformed with both plasmids, and the co-transformants were selected on 7H11 agar plates with 25 μg/mL kanamycin and 50 μg/mL hygromycin and tested for growth over 3–4 days on 7H11 kanamycin/hygromycin plates supplemented with 20 μg/mL trimethoprim.
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D.W. and W.L. contributed equally to this study. We thank the British Columbia Centre for Disease Control for providing access to a Containment Level 3 facility. This study was Funded by the Canadian Institute of Health Research (CIHR) operating grant # MOP-106622 (Y. A-G). We would like to thank Sara Dalkilic for her careful editing of the manuscript.
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