Iron sources utilized by M. tuberculosis

In order to establish a solid basis for identifying genetic requirements for iron utilization by Mtb, we first wanted to establish which iron sources Mtb can utilize. In particular, we aimed to examine the proposed utilization of transferrin and lactoferrin as iron sources [34,35] which is in contrast to our previous result [23]. To this end, we utilized the mbtD deletion mutant ML1600 which does not produce mycobactins and carboxymycobactins [12,23]. We measured growth of the avirulent parent strain Mtb mc²6230 (H37Rv ΔRD1, ΔpanCD; S1 Table) and of Mtb ML1600 in self-made low-iron Middlebrook 7H9 medium using 20 μM ammonium ferric citrate (control), 10 μM human holo-transferrin, 10 μM human holo-lactoferrin, 5 μM human hemoglobin, 20 μM hemin, 0.2 μM mycobactin and 0.2 μM carboxymycobactin as sole iron sources, respectively. These experiments clearly showed that Mtb utilizes iron from mycobactin, carboxymycobactin, hemin and hemoglobin consistent with previous results [23,24,27,36]. In contrast, iron salts, transferrin and lactoferrin were only used in the presence of siderophores (Fig 1). This result is consistent with previous studies establishing that Mtb siderophores can solubilize iron from transferrin or lactoferrin [37,38] indicating that Mtb does not produce a specific transferrin or lactoferrin uptake system under those growth conditions.

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Fig 1. Growth of wild-type M. tuberculosis and of the ΔmbtD mutant with different iron sources.

Growth of wild-type Mtb mc²6230 (A) and the ΔmbtD::hyg^r mutant (B) in self-made low-iron 7H9 medium supplemented with: 20 μM ammonium ferric citrate; 10 μM human holo-transferrin; 10 μM human holo-lactoferrin; 5 μM human hemoglobin; 20 μM hemin; 0.2 μM mycobactin (MBT) and 0.2 μM carboxymycobactin (cMBT), respectively. The Mtb strains were grown in self-made low-iron 7H9 medium for 5 days to deplete intracellular iron before growth analysis. The initial OD₆₀₀ of all the cultures was 0.01. Error bars represent standard deviations from the mean results of biological triplicates.

https://doi.org/10.1371/journal.ppat.1008337.g001

Construction and characterization of Mtb transposon libraries grown with different iron sources

To reveal the genetic requirements for iron utilization by Mtb we constructed transposon libraries of Mtb ΔmbtD (ML1600) using a modified himar1-based transposon [39]. The Mtb transposon library was grown on self-made low-iron 7H9 agar plates containing 0.5% bovine albumin and 0.01% tyloxapol supplemented with the following iron sources: (i) 500 ng/mL (~0.64 μM) Fe-cMBT; (ii) 250 ng/mL (~0.275 μM) Fe-MBT (“high” MBT); (iii) 50 ng/mL (~0.055 μM) Fe-MBT (“low” MBT); (iv) 20 μM hemin; (v) 5 μM hemoglobin and (vi) 20 μM hemin plus 250 ng/mL Fe-MBT, respectively (Fig 2A). Three independent libraries were generated in Mtb ML1600 grown in media containing 250 ng/mL Fe-MBT and 20 μM hemin, respectively. Two independent libraries were generated for each of the other iron conditions. Thus, a total of 14 independent libraries, each containing approximately 200,000 transposon mutants, were obtained. Then, the chromosomal DNA was extracted from each pool, digested using the restriction enzyme HinP1I, ligated to asymmetric adapters using a previously described method with modifications [39,40]. The transposon-chromosome junctions were amplified using PCR and subjected to Illumina sequencing (Fig 2B). An average of 8.5 million unique transposon-chromosome junction sequencing reads covered ~ 74% of the TA dinucleotide sites in the chromosome in each individual library (S5 Table), corresponding to approximately one insertion every 80 base pairs on average (Fig 2C). The high saturation of transposon insertions in our libraries also enabled us to assess the essentiality of the 1,312 small ORFs (≤ 9 TA sites), in contrast to earlier TnSeq studies of Mtb, in which small genes with fewer than 9 TA dinucleotide sites were not well-classified [39,41]. Only 75 to 90 small ORFs had no insertions. The classification of most of those genes (70–90) as essential across all iron conditions is similar to the results of a previous high density (84%) transposon library, which defined 92 small genes as essential after accounting for the presence of non-permissive TA sites [42].

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Fig 2. Construction of M. tuberculosis transposon libraries.

(A) The Mtb transposon mutagenesis library was generated from the siderophore-deficient mutant ML1600 (ΔmbtD::hyg^r). The library was cultured on low iron 7H9/ADS agar plates supplemented with (i) 500 ng/mL Fe-cMBT; (ii) 250 ng/mL Fe-MBT (high concentration); (iii) 50 ng/mL Fe-MBT (low concentration); (iv) 20 μM hemin; (v) 5 μM hemoglobin and (vi) 20 μM hemin plus 250 ng/mL Fe-MBT, respectively. The library DNA was isolated from the plates after three weeks. (B) Library building protocol. Genomic DNA pool was digested by HinP1I to generate GC-tails, allowing to the ligation of GC-tailed adapters which compose of short 3’ blocked and long oligonucleotides. The 3’ end of the shorter oligo was blocked (*) by C6-TFA-amino modification so that it could not be extended during amplification. The transposon-chromosome junctions were selectively amplified using primers (S2 Table) that recognize the end of the transposon and the 5’ end of the long adapter oligo. These primers contain all requisite sequences to permit direct multiplex sequencing of amplicons on an Illumina NextSeq 500 platform. (C) Transposon-chromosome junctions from high density mutant libraries were identified by deep sequencing. The six concentric circles in different colors represent the six libraries corresponding to (A). From the outer to the inner, they are (i) cMBT; (ii) high MBT; (iii) low MBT; (iv) hemin; (v) hemoglobin and (vi) hemin plus high MBT, respectively. The number of normalized sequence reads corresponding to each insertion site is represented as one color bars mapped onto the circular chromosome of M. tuberculosis H37Rv. Black contour represents the GC content of the chromosome (G+C content higher or lower than 50% are represented as contours outside or inside the ring, respectively). The genomic deletion regions such as ΔRD1, ΔpanCD and ΔmbtD are indicated in black. The genomic regions such as esx-3, irtA/B, mmpL5 and rv2047c are indicated in red. Nucleotide positions are indicated (million bases). Plots were generated using Circos 0.69–5 [43].

https://doi.org/10.1371/journal.ppat.1008337.g002

The genetic requirements for Mtb to utilize iron from siderophores and heme are drastically different

The intolerance of a gene to transposon (Tn) insertions reflects its importance under a given growth condition. This genetic requirement can be quantitatively assessed by the statistical analysis of the location and frequency of Tn insertions across a gene. Here, we used this quantitative information to determine the essentiality of genomic regions of Mtb when grown with different iron sources. First, we determined which genes exhibited statistically significant differences in Tn insertion counts across different iron sources using ANOVA. We identified 165 genes which exhibited a statistically significant number of insertions under at least one of the tested iron conditions, after correction for false discovery rates (adjusted P values < 0.05; S6 Table). The largest groups of varying genes were involved in intermediary metabolism and respiration, lipid metabolism, cell wall associated and conserved hypothetical proteins (Fig 3A). Hierarchical cluster analysis revealed iron utilization profiles that are specific for each of the six iron conditions (Fig 3B and S1 Fig). The genes required for utilization of hemin and hemoglobin as iron sources are very similar (Fig 3B, 3C and S1 Fig). This is consistent with our previous finding that hemoglobin and heme acquisition pathways overlap [36]. In the presence of hemin or hemoglobin as the sole iron source, Mtb exhibits increased requirements for genes involved in lipid metabolism, PDIM biosynthesis, ESX-3 secretion system, leucine biosynthesis, and decreased requirements for genes involved in heme/porphyrin biosynthesis, glycine metabolism, inorganic phosphate transporters, RND efflux pumps and Mce4 family proteins (Fig 3B and S1 Fig). Interestingly, Mtb exhibits nearly opposite genetic requirements in the presence of siderophores as the sole iron source (Fig 3B, 3C and S1 Fig).

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Fig 3. TnSeq analysis of the M. tuberculosis transposon libraries.

A subset of 165 varying genes were identified by ANOVA. The mean normalized insertion count is calculated for each gene in each of the 6 conditions. Then a log-fold-change is calculated for each condition relative to the mean count across all the conditions. (A) The 165 varying genes were categorized by different physiological functions as annotated in TubercuList [44]. (B) Heatmap with 84 selected genes (See full heatmap in S1 Fig) showing variability in transposon insertion counts across iron-supplementation conditions. The color 'red' means the counts in one condition are lower than the other conditions on average, suggesting a greater requirement for that gene in that condition, and 'blue' means insertion counts are higher than average, suggesting it is less required. The dendrogram shows the hierarchical clustering of the conditions (columns) using complete-linkage clustering. Gene insertion count profiles (rows) are also clustered using the hclust package in R, and gene pathway associations are indicated. (C) Correlation plot between each pair of iron-supplementation conditions. The correlation coefficients between pairs of conditions are calculated between vectors of log-fold-changes for the varying genes. The size of each circle indicates the magnitude of the correlation, and the color indicates the sign, as shown by the scale. (D) Volcano plot of resampling analysis between hemin and high MBT conditions. TnSeq-FC- and false discovery rate-adjusted P values (q values) from the resampling test are plotted for each genetic locus. Loci meeting the significance threshold of a q value of <0.05 are colored. The genes with increased log-fold-change or decreased minus log-fold-change are predicted to have more essentiality in utilizing mycobactin or hemin, respectively. Selected mutants are indicated by name.

https://doi.org/10.1371/journal.ppat.1008337.g003

To further distinguish the iron utilization profiles in Mtb between siderophore and heme, we used a permutation test on insertion counts (resampling analysis in Transit [45]) and found that 64 and 54 genes are involved in utilization of MBT and heme, respectively, by comparing the number of transposon insertions in each gene in medium with high mycobactin concentrations (250 ng/mL) versus hemin (Fig 3D, S7 Table). In the presence of high MBT concentrations, Mtb exhibited significantly stronger requirements for genes encoding the RND efflux pumps MmpL5/MmpS5 and MmpL11, the heme/porphyrin biosynthesis enzymes (except HemD), the ABC transporters IrtA/IrtB, MurI (peptidoglycan biosynthesis), the pyruvate/phosphate dikinase PpdK, the polyketide synthase Pks12, MmaA4 (mycolic acid modification) and proteins of unknown functions such as Rv2047c and Rv0455c (Fig 3D, S7 Table). By contrast, in the presence of hemin, Mtb had significantly stronger requirements for the putative secretory lipase Rv1592c, the sensor-transducer protein BlaR, the zinc-responsive transcriptional repressors Zur and SmtB, PPE37, the dehydrogenase Rv1432, the iron-sulfur-binding reductase Rv0338c, the ESX-3 component MycP3, the hemolysin-like protein Rv1085c, Gpm1 (carbon and amino acids metabolism), and the electron transfer flavoprotein FixAB (Fig 3D, S7 Table). Taken together, our TnSeq experiments revealed the distinct iron-source dependent genetic requirements by Mtb.

Siderophore utilization by M. tuberculosis

To classify the contribution of Mtb genes to the utilization of different iron sources by Mtb, we used a Hidden Markov Model (HMM) which defines four different states of essentiality: essential (ES), growth defect (GD), non-essential (NE), and growth advantage (GA) [42]. Our study identified 428 genes which are essential or required for optimal growth (GD) of Mtb and shared among the five conditions with a single iron source (Fig 4), suggesting that these genes are generally required by Mtb and not involved in iron-specific processes. Indeed, almost all of these shared genes (96.5%) were previously identified as essential or required for optimal growth by Mtb in enriched Middlebrook medium replete with iron salts [42].

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Fig 4. Quantitative classification of the requirement of genes by M. tuberculosis for growth under different iron conditions.

Venn diagram of Mtb genes with ‘essential’ or ‘growth defect’ states from five iron conditions: cMBT (500 ng/mL), high MBT (250 ng/mL), low MBT (50 ng/mL), hemin (Hm) (20 μM) and hemoglobin (Hb) (5 μM). The number of overlapping genes in their respective zones is indicated.

https://doi.org/10.1371/journal.ppat.1008337.g004

The ESX-3 secretion system was previously shown to be required for siderophore-mediated iron acquisition in mycobacteria [17,19]. As anticipated, most genes of the esx-3 operon were classified by HMM analysis as ‘essential’ or ‘growth-defect’ for Mtb growing with cMBT (500 ng/mL) or low concentrations of MBT (50 ng/mL) (S8 Table, Fig 5A). Interestingly, significantly more insertions were observed in the ppe4 gene when Mtb was grown with high concentrations of MBT (250 ng/mL) (Fig 5A and S8 Table). Thus, ppe4 was classified as non-essential in medium with high MBT, in contrast to Mtb grown with cMBT (500 ng/mL) or low concentrations of MBT (50 ng/mL). These results are consistent with previous experiments which show that neither the Δesx-3 mutant nor the Δpe5-ppe4 mutant grew on 7H10 plates with low concentrations of MBT (2 to 20 ng/mL), but that they were rescued by high concentrations of MBT (200 ng/mL) [19]. Surprisingly, the esx-3 operon was also assessed to be essential for Mtb grown with hemin or hemoglobin as the sole iron source (Fig 5A, S8 Table). No insertions were observed in any of the esx-3 genes except for ppe4 (Fig 5A). The ppe4 gene tolerated insertions in the 3’ end when Mtb was grown with heme or hemoglobin, while the 5’ end of ppe4 appeared to be essential for Mtb under all conditions (Fig 5A, Table 1). These findings are consistent with previous observations that hemin does not support growth of either the Δesx-3 or the Δpe5-ppe4 mutant on 7H10 plates, unless 0.05% Tween 80 was included [19]. In addition, ppe3 and ppe20 mutants had significantly reduced fitness at high concentrations of MBT or with cMBT (Fig 3B, S7 Table). In conclusion, these results indicated that PPE4 is the most important PPE protein of Mtb for iron utilization.

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Fig 5. M. tuberculosis genomic regions involved in siderophore utilization.

The distribution of the transposon insertions in Mtb genomic regions including esx-3 operon (A); rv0455c gene, mmpS5-mmpL5 operon, irtA-irtB operon (B); and pks12-rv2047c operon (C). The iron conditions are marked with different colors. The y-axis (0, 10, 20) represents the counts of the Tn-insertions and x-axis represents the genomic position (bp). Potential TA dinucleotide insertions sites are indicated. Regions containing genes of interest are highlighted by red boxes. Plots were generated using MochiView 1.46 [46].

https://doi.org/10.1371/journal.ppat.1008337.g005

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Table 1. Genes with differential importance in iron utilization by Mycobacterium tuberculosis.

45 genes selected from the 165 varying genes which were assessed by HMM analysis as either essential (ES), “essential domain” (ESD) or “growth defect” (GD) under different iron conditions. The 21 genes which were classified as essential or “growth defect” under all iron conditions (S6 Table) were excluded from this list. cMBT: carboxymycobactin, MBT: mycobactin at high or low concentrations, hemin (Hm), hemoglobin (Hb) and hemin plus mycobactin (Hm/MBT). NE: non-essential.

https://doi.org/10.1371/journal.ppat.1008337.t001

Siderophore poisoning of Mtb

MmpS4 and MmpS5 are the only proteins known to be required for siderophore secretion by Mtb [12]. Our TnSeq analysis indicated that mmpS4 (rv0451c, 15 TA sites) was essential under all conditions containing single iron sources (S3A Fig, S8 Table). The important role of MmpS4 is consistent with our previous finding that MmpS4 can substitute for MmpS5 in siderophore secretion but not vice versa [12], indicating that mmpS4 is essential for siderophore secretion under these conditions. However, the Mtb mmpS4 deletion mutant did not show a growth defect in vitro [12]. These divergent results might reflect the differences between experiments with pooled transposon mutants in the TnSeq experiments and isogenic mutants grown individually [12]. The essentiality for MmpS4 by Mtb grown with hemin and hemoglobin as iron sources is unexpected (S3A Fig, S8 Table) and indicates an unknown metabolic role of MmpS4 in addition to siderophore secretion.

Our TnSeq analysis also showed no transposon insertions in mmpS5 (rv0677c, 6 TA sites) in the presence of 250 ng/mL MBT (“high”) (Fig 5B, S8 Table). In contrast to mmpS4, mmpS5 is not essential for Mtb grown with heme or hemoglobin as sole iron sources (S3A Fig, S8 Table). The mmpL5 gene (rv0676c, 32 TA sites) is located in the same operon as mmpS5 and the encoded proteins were proposed to interact [12]. Indeed, the TnSeq results for mmpL5 mimicked the results for mmpS5: In the presence of 250 ng/mL MBT the mmpL5 gene had almost no transposon insertions, but most of the 32 TA sites had insertions in the presence of heme and hemoglobin as sole iron sources (Fig 5B, S8 Table). Importantly, hemin did not rescue the Mtb mutants with Tn insertions in mmpS5 or mmpL5 in the presence of 250 ng/mL MBT, in contrast to genes involved in siderophore uptake such as ppe4 (Fig 5A). This is likely due to the previously observed toxicity of mycobactin and carboxymycobactin for Mtb mutants defective in siderophore secretion regardless of the presence of other iron sources in the medium [13]. Interestingly, the irtA and irtB genes encoding the siderophore importer IrtAB showed a similar pattern of transposon insertions (Fig 5B). IrtA and irtB were classified as ‘growth defect’, but not as essential, at high concentrations of MBT (Table 1), indicating that there might be alternative transporters for siderophore uptake. This conclusion is consistent with the previous growth assays in which irtA and irtB mutants had growth defects in iron-deficient medium but not in iron-replete medium [10]. Although irtA and irtB were found to be not essential in the presence of hemin or hemoglobin, adding high concentrations of MBT in the presence of hemin significantly reduced the fitness of Mtb mutants with insertions in irtA and irtB indicating that blocking siderophore uptake across the inner membrane is also toxic for Mtb, possibly by increased siderophore accumulation in the periplasm (Figs 3B and 5B, S7 Table).

We identified two other genes which showed the siderophore poisoning phenotype: rv0455c and rv2047c (Fig 5B and 5C). To examine experimentally whether siderophores are indeed toxic for Mtb mutants lacking these genes TnSeq analysis is indeed capable of identifying genes with a similar phenotype as mmpS5 and mmpL5, we constructed an isogenic rv2047c deletion mutant in Mtb mc²6230 (H37Rv ΔRD1 ΔpanCD) using the vector pML3605 (S4 Table). While the parent strain Mtb mc²6230 and the Δrv2047c deletion mutant showed similar growth rates in 7H9 medium (without ADS) containing 0.01% Tyloxapol, the addition of 1 μM MBT completely inhibited growth of the Δrv2047c mutant (Fig 6). The growth of the Δrv2047c mutant was only modestly reduced in the presence of 1 μM cMBT. This observation is consistent with our previous finding that MBT is much more toxic for siderophore secretion-defective mutants compared to cMBT [13]. Growth of the Δrv2047c mutant was fully restored by expressing the rv2047c gene using a chromosomal expression vector pML4211 integrated at the L5 attB site (S4 Table). These results demonstrated that rv2047c is essential for Mtb to grow in the presence of exogenous high concentrations of MBT, further validating our TnSeq analysis.

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Fig 6. Growth of the M. tuberculosis Δrv2047c mutant.

Growth of Mtb mc²6230 (as WT), Δrv2047c (ML2256) and the complementation Δrv2047c mutant (ML2257) in 7H9 Middlebrook medium (A) supplemented with 1 μM carboxymycobactin (B) and 1 μM mycobactin (C), respectively. The initial OD₆₀₀ of all the cultures is 0.01. Error bars represent standard deviations from the mean results of biological triplicates.

https://doi.org/10.1371/journal.ppat.1008337.g006

Roles of the MmpL4/MmpS4 and MmpL5/MmpS5 efflux systems in siderophore-mediated iron utilization by M. tuberculosis

The small membrane proteins MmpS are encoded in the same operon as their associated large transmembrane proteins MmpL [47]. This association, and the interaction of the MmpS4 protein with MmpL4 [12], has led to the assumption that the MmpS and their MmpL counterparts are involved in the same functions [48]. This appears to be true for mmpS5 and mmpL5, as Mtb has identical requirements for these genes for growth on different iron sources (Fig 3B and 3D, S7 Table). Surprisingly, mmpL4 was not required by Mtb for utilization of any iron source, in stark contrast to mmpS4, which was essential under all conditions containing a single iron source (S3A Fig, S8 Table). To further examine the roles of the mmpL4 and mmpL5 genes in iron utilization by Mtb, we determined the growth of the isogenic Mtb mutants lacking either one or both of these genes (S1 Table). The ΔmmpL4/L5 double mutant (Mtb ML2302) did not grow at all in low-iron 7H9 medium, while both single mutants, Mtb ML2300 (ΔmmpL4) and Mtb ML2301 (ΔmmpL5) grew like the parent Mtb strain (Fig 7A). As expected, the mycobactin biosynthesis mutant Mtb ΔmbtD [23] and the siderophore secretion-defective mutant Mtb ΔmmpS4/S5 [12] did not grow in low-iron 7H9 medium (Fig 7A). All mutants with a growth defect in low-iron 7H9 medium were rescued at least partially with 10 μM hemin (Fig 7B). By contrast, adding 1 μM cMBT and 1 μM MBT as the sole iron sources rescued only the mycobactin biosynthesis mutant ΔmbtD, as expected [23], while growth of the ΔmmpS4/S5 and the ΔmmpL4/L5 double mutants was completely suppressed (Fig 7C and 7D). The phenotypes of the double mutants are identical, indicating that the mmpL4 and mmpL5 genes are involved in siderophore secretion as described for mmpS4 and mmpS5 [12]. Thus, the complete growth inhibition of the ΔmmpL4/L5 double mutant is likely due to self-poisoning by intracellular accumulation of siderophores, as shown for the Mtb ΔmmpS4/S5 mutant [13]. Taken together, these results indicated that MmpL4, together with MmpL5, is required for siderophore secretion in Mtb, and that MmpL5 plays a major role in this process.

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Fig 7. Growth of the M. tuberculosis mmpL4 and mmpL5 mutants under different iron conditions.

Growth curves of Mtb strains including Mtb mc²6230 (as WT), ΔmmpL4 (ML2300), ΔmmpL5 (ML2301), ΔmmpL4/L5 (ML2302), ΔmmpS4/S5 (ML859) and ΔmbtD (ML1600) in low-iron 7H9 medium (A) supplemented with 10 μM hemin (B), 1 μM carboxymycobactin (C) and 1 μM mycobactin (D), respectively. The Mtb strains were grown in self-made low-iron 7H9 medium for 5–7 days to deplete intracellular iron before growth assays. The initial OD₆₀₀ of all the cultures is 0.01. Error bars represent standard deviations from the mean results of biological triplicates.

https://doi.org/10.1371/journal.ppat.1008337.g007

Heme and hemoglobin utilization by M. tuberculosis

The nearly opposite requirement for genes depending on whether Mtb utilized iron from heme or hemoglobin versus siderophore (Fig 3B and 3D) indicated that there is little, if any, overlap between these iron acquisition pathways. Transposon insertions in 31 genes were uniquely required by Mtb to grow with hemin and hemoglobin as iron sources, but not with siderophores (Fig 4, S9 Table). Among those genes, we found that Mtb exhibits significantly stronger requirements for ppe37 and rv1085c encoding a hemolysin-like protein (Figs 3D and 8A; S7 and S9 Tables). The growth defect of Mtb mutants with insertions in ppe37 is consistent with previous findings that PPE37 is involved in heme utilization in the Mtb Erdman strain [27]. However, the requirement for Rv1085c for growth of Mtb in vitro in the absence of erythrocytes indicates that the molecular function of Rv1085c is probably different from that of hemolysins [49]. The TnSeq analysis also identified blaR (rv1845c), zur and smtB as essential for Mtb to utilize heme or hemoglobin as iron sources (Figs 3D and 8A; S7 and S9 Table, Table 1), indicating that gene activation is a necessary component in this process. To examine this question experimentally, we focused on SmtB and Zur, two transcriptional regulators, which are encoded in the same operon and have been shown to be involved in zinc uptake [50]. To this end we deleted the smtB-zur operon in the avirulent Mtb mc²6206 strain (ΔpanCD ΔleuCD) to obtain Mtb ML2277 (ΔsmtB-zur) (S1 Table, S5 Fig). Mtb ML2277 was complemented with chromosomal expression vectors for the zur and smtB genes and for the smtB-zur operon, respectively. Integration of these vectors into the L5 attB site created the Δzur single mutant ML2278 (ML2277::smtB), the ΔsmtB single mutant ML2279 (ML2277::zur), and the fully complemented strain ML2280 (ML2277::smtB-zur) (S5 Fig, S1 Table). The parent Mtb mc²6206 strain, the fully complemented double mutant and the Mtb strain lacking only zur had no or only a minor growth defect in low iron or replete iron 7H9 medium, while the strain lacking smtB and the ΔsmtB-zur double mutant had a general growth defect independent of the iron concentration as shown in Figs 8B and S6. Collectively, these results suggested that SmtB and Zur are not required for utilization of Fe³⁺ ions. Growth of the strain lacking only zur was significantly reduced in the presence of 20 μM hemin as the sole iron source in contrast to iron-replete or iron-deficient conditions, while the strain lacking SmtB had a similar growth defect compared to the parent strain in media with low iron and with hemin (Fig 8B and 8C and S6 Fig). These results indicated that Mtb requires Zur but not SmtB for hemin utilization. No growth of the ΔsmtB-zur double mutant was observed in medium with hemoglobin as the sole iron sources (Fig 8D). Interestingly, only expression of both smtB and zur enhanced growth of the ΔsmtB-zur double mutant, indicating that both regulators are essential for Mtb to grow with hemoglobin as the sole iron source (Fig 8D).

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Fig 8. M. tuberculosis genes involved in heme and hemoglobin utilization.

(A) The distribution of the transposon insertions in Mtb genomic regions including rv1085c, ppe37 and smtB-zur operon. The iron conditions are marked with different colors. The y-axis (0, 10, 20) represents the counts of the Tn-insertions and x-axis represents the genomic position (bp). Potential TA dinucleotide insertions sites are indicated. Regions containing genes of interest are highlighted by red boxes. Plots were generated using MochiView. (B-D) Growth assays of wild-type Mtb mc²6206, ΔsmtB-zur deletion mutant (ML2277), smtB complementation strain (ML2278), zur complementation strain (ML2279), and smtB-zur complementation strain (ML2280) under low-iron 7H9 medium containing 10 μM 2,2’-dipyridyl (DIP) (B) supplemented with 20 μM hemin (C) and 5 μM hemoglobin (D), respectively. The Mtb strains were grown in self-made low-iron 7H9 medium for 7 days to deplete intracellular iron before growth assays. The initial OD₆₀₀ of all the cultures is 0.01. Error bars represent standard deviations from the mean results of biological triplicates.

https://doi.org/10.1371/journal.ppat.1008337.g008

Siderophore utilization

Among the 69 genes predicted to be required for Mtb for cMBT and/or MBT utilization were irtA, irtB and mmpS5 which were previously shown to be involved in carboxymycobactin uptake [10] and siderophore secretion [12] validating the TnSeq analysis. In a previous TnSeq study using a saturated transposon library, 27 of these genes (S9 Table) were identified as essential for growth of Mtb in rich 7H9 or 7H10 Middlebrook media supplemented with oleic acid, albumin, dextrose and catalase [42]. Interestingly, none of these genes are required when Mtb utilizes heme or hemoglobin as an iron source. These genes encode proteins with functions in intermediary metabolism such as NadC (NAD⁺ biosynthesis) or OtsB2 (trehalose metabolism), in protein degradation such as PrcA and PrcB (proteasome) or in cell wall biosynthesis such as MurI (glutamate racemase) (S9 Table), indicating that the iron source has a surprisingly strong influence on Mtb physiology well beyond the proteins directly involved in acquisition of these iron sources. One example is the hem genes which are required for porphyrin biosynthesis and were only found to be essential when siderophores were used as iron sources (Fig 4, S8 Table). This is consistent with previous TnSeq studies which used standard Mtb growth medium containing iron salts which do not contain heme [39,42,51] because Mtb cannot utilize iron salts without siderophores [13]. Importantly, the porphyrin biosynthesis genes are not essential when Mtb grows with hemin as the sole iron source indicating that Mtb is capable of utilizing protoporphyrin IX after iron is removed from heme and that genes involved in porphyrin biosynthesis are conditionally essential for Mtb in vitro growth.

The siderophore-dependent self-poisoning phenotype

An interesting observation was that a few Mtb genes such as mmpS5, mmpL5, rv2047c and rv0455c were essential for growth in medium with high concentrations of MBT in the presence of hemin, although the same genes were not required for growth in medium with hemin or hemoglobin alone. This phenotype cannot be explained by the dependency of Mtb growth on a particular iron source since hemin can rescue mutants with defects in siderophore utilization and vice versa [23,26,36]. This phenotype, however, mimics the self-poisoning phenotype observed for the ΔmmpS4/ΔmmpS5 siderophore secretion mutant [13] and for the ΔmmpL4/ΔmmpL5 in this study. Indeed, growth experiments confirmed that MBT is toxic for an isogenic rv2047c deletion mutant of Mtb, demonstrating that TnSeq experiments are a valuable tool to identify the siderophore-dependent self-poisoning phenotype in Mtb. The rv2047c gene encodes a protein with two predicted domains, an N-terminal NAD⁺-dependent epimerase domain and a C-terminal phosphoenolpyruvate-utilizing domain. The rv2047c gene is located in an operon with pks12 which encodes a polyketide synthetase required for the biosynthesis of mannosyl-β-1-phosphomycoketides, also called mycoketides or MPMs [52]. Interestingly, Mtb also exhibited a strong requirement for pks12 in the presence of MBT (Figs 3B, 3D and 4) indicating that Rv2047c might be involved in mycoketide biosynthesis. However, it is unclear whether the role of Rv2047c in the siderophore-dependent self-poisoning phenotype is direct or indirect. It is possible that disruption of mycoketide biosynthesis compromises the outer membrane permeability barrier and enables uncontrolled and possibly poisonous influx of MBT into Mtb. Alternatively, mycoketides might be required for the function of the siderophore secretion system.

Transposon insertions into the rv0455c gene also showed a pattern consistent with siderophore poisoning (Fig 5B). The encoded Rv0455c protein contains a predicted N-terminal Sec-secretion peptide and was found in Mtb culture filtrates [53]. It is possible that Rv0455c transports MBT to the extracellular medium in Mtb. However, an indirect role of Rv0455c in siderophore secretion cannot be excluded. Thus, further genetic and biochemical experiments are needed to reveal the molecular function of Rv0455c.

Roles of the MmpL4 and MmpL5 efflux pumps in siderophore secretion

The mmpL5 gene showed a concentration-dependent essentiality in the TnSeq experiments: It was classified as “growth defect” in the presence of low concentrations of MBT (50 ng/mL) and as essential in the presence of high concentrations of MBT (250 ng/mL) (Fig 3B and 3D; S8 Table). The isogenic ΔmmpL5 deletion mutant showed a growth defect in liquid medium with 1 μM MBT as the sole iron source (Fig 7D), but no growth defect with 1 μM cMBT (Fig 7C). The stronger phenotype of Mtb siderophore secretion mutants in the TnSeq experiments in the presence of MBT versus cMBT is consistent with the six-fold increased toxicity of MBT over cMBT for the ΔmmpS4/S5 mutant [13]. This might be due to the increased toxicity of the more hydrophobic MBTs due to their membrane association. This phenotype of mmpL5 mutants is in contrast to the mmpL4 gene which was classified as non-essential in the TnSeq experiments. This classification was confirmed by the absence of any growth defect of the isogenic ΔmmpL4 mutant (Fig 7D). The increased importance of mmpL5 compared to mmpL4 is consistent with the approximately 7-fold higher transcription level of mmpL5 during in vitro growth of Mtb [54] and the importance of MmpL5 in efflux of bedaquline, clofazimine and azoles compared to other MmpL proteins [55,56,57]. It is important to note that some of the results obtained by TnSeq are in apparent contradiction with results from growth experiments with isogenic Mtb mutants. E.g. the mmpS4 and mmpS5 single deletion mutants did not show any growth defect in low iron media [12], while the TnSeq results showed that MmpS4 is essential under all iron conditions examined in this study. However, in the TnSeq study we used the siderophore-deficient mbtD deletion mutant which prevented Mtb from utilizing iron salts as an iron source, whereas the isogenic mutants mmpS4 and mmpS5 single deletion mutants were grown in medium with iron salts [12]. When MBT was used as an iron source the mmpL5 deletion mutant had a significant growth defect (Fig 7D) consistent with the importance of MmpL5 in the TnSeq results (Fig 5B).

Does MmpL11 have a role in siderophore secretion?

Considering the proposed function of MmpL11 in heme uptake [24,58], it was surprising that the TnSeq data showed a significantly higher requirement for mmpL11 in the presence of MBT by Mtb compared to hemin or hemoglobin (Figs 3B, 3D and 4; S3B Fig). Interestingly, mmpL11 showed a transposon insertion pattern indicative of the siderophore-dependent self-poisoning phenotype (S3B Fig). The simplest explanation for this phenotype is that MmpL11 directly secretes siderophores similar to the related MmpL4 and MmpL5 efflux pumps. However, the ΔmmpL4/L5 mutant did not grow at all in liquid medium indicating that MmpL4 and MmpL5 are sufficient for siderophore secretion in Mtb (Fig 7C and 7D). Alternatively, the known activity of MmpL11 in transport of surface lipids such as mycolic acid wax esters and long-chain triacylglycerols in Mtb and M. smegmatis [59,60] might indirectly influence the activity of the siderophore secretion systems of Mtb by lipid-protein interactions. Further investigation is clearly needed to clarify the role of MmpL11 in iron utilization by Mtb.

Why do mbt genes not show a phenotype in TnSeq experiments?

Siderophore biosynthesis in Mtb is dispensable in the presence of either exogenous siderophores or heme [23,24]. The mbt genes encode enzymes required for siderophore biosynthesis [7,61] and were, as expected, not essential in our study using the Mtb ΔmbtD mutant with a defect in mycobactin synthesis [23]. Surprisingly, however, almost all mbt genes were classified as ‘non-essential’ in highly saturated transposon libraries on standard 7H10 medium containing copious amounts of iron salts [42]. The apparent permissiveness of mbt genes in TnSeq experiments is in conflict with the observation that Mtb cannot utilize iron salts and grow without siderophores [13] and with several reports demonstrating that the genetic or chemical inactivation of mycobactin biosynthesis results in severe growth defects of Mtb in medium with iron salts [23]. We reasoned that transposon insertions into mbt genes do not result in growth defects of Mtb in TnSeq experiments because mbt mutants are cross-complemented by the many other clones with unaffected mycobactin biosynthesis in the pool of transposon mutants. Thus, the mbt genes should be included in the list of essential genes for utilization of iron salts and serve as a reminder of potential pitfalls of TnSeq experiments.

Heme and hemoglobin utilization by Mtb

Most of the genes which are predicted by our TnSeq analysis to be required for optimal growth or are essential for heme utilization by Mtb are also required for optimal growth or are essential for hemoglobin utilization (Fig 4). This is consistent with our previous observation that both pathways appear to converge on the cell surface of Mtb [26]. However, the TnSeq analysis did not identify any gene required for this pathway such as the ppe36 and dpp genes [26,36]. This might be a consequence of a second, previously unrecognized pathway for heme utilization which depends on albumin. Serum albumin binds heme with high affinity [62,63] and enables heme uptake independent of the ppe36 and dpp genes, although these genes are essential for growth of Mtb in medium with heme or hemoglobin as sole iron sources in the absence of albumin [36]. Since Mtb was grown on agar plates containing albumin in our TnSeq experiments, albumin-dependent heme uptake might explain the lack of requirement for the ppe36 and dpp genes. By contrast, ppe37 which was identified in Mtb Erdman as required for heme utilization in the presence of albumin [27] was classified as “growth defect” in our TnSeq experiments. These divergent results might be caused also by significant strain differences between the Mtb H37Rv derivative ML1600 (ΔRD1 ΔpanCD ΔmbtD::hyg^R) used in our study (S1 Table) and the Mtb Erdman strain used in the previous study [27]. This hypothesis is supported by recent results demonstrating the deletion of ppe37 in the H37Rv derivative Mtb mc²6206 did not show any growth defect with heme as the sole iron source [36]. In this regard, it is noteworthy that transposon mutants with insertions in the genes encoding the heme oxygenase MhuD (Rv3592) which liberates iron by cleavage of the tetrapyrrole ring [64] and the heme-binding protein Rv0203 [65] did not show reduced fitness in the medium with hemin or hemoglobin (S8 Table). It is possible that the lack of phenotypes for some of these genes in the TnSeq experiments is caused by functional redundancy in Mtb or inter-strain complementation. However, strain-specific growth requirements or differences in growth conditions might also explain some of these divergent results.

The HMM analysis classified four genes encoding proteins of unknown functions as essential for utilization of hemin (rv2016, rv3673c) and hemoglobin (rv0199, rv2420c) (Fig 4, S8 Table). A detailed look into the insertion counts in the other biological replicates revealed that the rv0199, rv2016, and rv2420c genes still had a significant number of transposon insertions which suggesting that they are not truly essential under these conditions. However, the rv3673c gene had zero insertions indicating that it might indeed be involved in heme utilization by Mtb. The rv3673c gene was not essential when Mtb was grown on plates with siderophores. This classification is consistent with a previous TnSeq analysis when Mtb was grown in medium with iron salts [42]. Rv3673c is predicted to be a membrane-anchored thioredoxin-like protein. Further experiments with an isogenic mutant are needed to examine whether Rv3673c indeed plays a role in heme utilization by Mtb.

Does heme poisoning exist in Mtb?

Considering the toxicity of excess heme for bacteria [66,67], we questioned whether our TnSeq analysis would also reveal genes with a heme poisoning pattern similar to that observed for siderophore poisoning, i.e. genes which are not essential in medium with cMBT or MBT, but essential or required for optimal growth in medium with hemin and with hemin+MBT. Indeed, we identified seven genes with such a pattern: rv0338c, rv0489, rv0542c, rv0548c, rv1122, rv3028c and rv3029c. However, none of these genes encoded transport proteins. In particular we did not see such a phenotype for the efflux pump MmpL11 which was shown to be involved in heme utilization by Mtb [24]. Furthermore, Mtb grows very efficiently at hemin concentrations as high as 100 μM [19] indicating that Mtb is highly resistant to the toxic effects of heme in contrast to other bacterial pathogens such as Staphylococcus aureus which is strongly inhibited at 10 μM hemin [68]. Thus, it is questionable whether a heme poisoning effect exists in Mtb, i.e. protein-mediated uptake and intracellular accumulation of heme to toxic concentrations as it was shown for siderophores [13].

Regulation of heme utilization by Mtb

The regulator protein Zur (Rv2359) was identified in our study as essential for utilization of heme by Mtb in the comprehensive TnSeq analysis and in growth experiments using an isogenic Δzur mutant. The dimeric Zur protein binds two Zn(II) ions per monomer [69]. Zn-binding by Zur is required to repress transcription of 32 genes in Mtb [50]. A straightforward explanation would be that Zur is an activator of genes required for heme utilization. However, no genes had lower transcription levels in a previous microarray analysis of an Mtb zur mutant compared with the wt strain indicating that Zur acts as a repressor [50]. It is conceivable that Zur represses a repressor gene which controls genes required for heme utilization. However, the only regulator gene under control of Zur appears to be rv0232 [50] which encodes a TetR-like repressor which is not known to activate genes. The surprising essentiality of the esx-3 operon for heme utilization by Mtb as shown in this study and the strong induction of the esx-3 operon in the Mtb zur mutant [50] provide an alternative mechanism for the regulatory role of Zur in heme utilization. It is possible that the uncontrolled uptake of large quantities of heme mediated by the constitutively produced ESX-3 system in the absence of Zur is toxic for Mtb. The toxicity of excess heme is well documented in other bacteria [66,67,70,71] and might also require Mtb to synthesize PDIM and other lipids to “harden” the outer membrane as observed in our study (Fig 3B) and thereby prevent the uncontrolled diffusion of the hydrophobic heme molecules into the cell. The apparent attempt of Mtb to control heme uptake on a transcriptional level is reminiscent of the important role of IdeR, the iron-dependent repressor of many genes involved in iron uptake and storage in Mtb [32,72] to prevent toxicity of free iron [1,4]. Obviously, further experiments are required to examine this hypothesis and to understand the role of the ESX-3 system and of the other genes of unknown functions revealed by this study in iron uptake from siderophores and heme.

Conclusions

During much of the infection cycle Mtb resides inside host cells, mainly in macrophages but also in neutrophils [73]. Intracellular Mtb has access to iron from both heme- and non-heme proteins [74]. The available iron source is heavily shifted to heme in macrophages which recycle iron from damaged or senescent erythrocytes, mainly in the spleen [75]. During a chronic infection Mtb is localized in lung granulomas which contain extracellular bacteria [76,77]. A recent analysis of necrotic human granulomas revealed an abundance of host iron-sequestering proteins and iron-restricting factors, establishing an iron-deprived environment for Mtb [33]. This proteomic analysis also indicated that iron from both heme- and non-heme proteins is available to Mtb. Pulmonary tuberculosis is characterized by extensive tissue damage and airway bleeding, resulting in hemoglobin as the prevalent iron source. Thus, during most stages of infection Mtb has access to heme and non-heme iron sources. The much higher efficiency of siderophore-mediated uptake of iron ions indicates that this is the default pathway primarily used by Mtb [13]. However, when heme becomes the major iron sources, Mtb switches from utilization of iron ions to heme. This switch appears to be mainly regulated by Zur and SmtB with an important role of the ESX-3 system and is accompanied by a metabolic shift involving more than 160 genes. Further studies are required to understand how this regulatory process is coordinated to enable Mtb to adapt to the iron sources available at different stages during infection.

Bacterial strains, media, and growth conditions

All the strains used in this study are listed in S1 Table. The transposon mutant library was generated from Mtb ΔmbtD::hyg^r (ML1600) [23] which derived from avirulent Mtb strain mc²6230 (H37Rv ΔRD1 ΔpanCD) [78]. For genetic manipulations, Mtb mc²6230 derived strains were grown in Middlebrook 7H9 broth (Difco) supplemented with 10% ADS (50 g/L bovine albumin, 20 g/L dextrose, 8.5 g/L NaCl), 0.5% glycerol, 24 μg/mL pantothenate, 0.2% casamino acids and 0.01% tyloxapol. All transposon libraries were grown on self-made low-iron 7H9 Noble Agar (Difco) plates (supplemented with 10% ADS, 0.5% glycerol, 24 μg/mL pantothenate, 0.2% casamino acids, 0.01% tyloxapol, 20 μM 2,2’-dipyridyl (DIP) and 30 μg/mL kanamycin) with different iron sources: (i) 500 ng/mL Fe-cMBT; (ii) 250 ng/mL Fe-MBT (high concentration); (iii) 50 ng/mL Fe-MBT (low concentration); (iv) 20 μM hemin; (v) 5 μM hemoglobin and (vi) 20 μM hemin plus 250 ng/ml Fe-MBT, respectively. The siderophores cMBT and MBT were purified from Mycobacterium bovis BCG and Mycobacterium smegmatis, respectively, by chromatography and were provided by Dr. Colin Ratledge [79]. All Mtb plates were cultured at 37 ^oC for 21 days. Avirulent Mtb mc²6206 and its derivative strains were grown in Middlebrook liquid 7H9 or solid 7H10 medium supplemented with 0.5% glycerol, 10% ADS, 0.2% casamino acids, 24 μg/mL pantothenate and 50 μg/mL L-leucine. Escherichia coli DH5α was grown in LB medium containing appropriate antibiotics at 37 ^oC with shaking at 200 rpm. The following antibiotics were used when required: kanamycin (Kan) at 30 μg/mL for mycobacteria or E. coli, and hygromycin (Hyg) at 200 μg/mL for E. coli, and 50 μg/mL for mycobacteria.

Growth of Mtb strains in media with different iron sources

Mtb mc²6230 (as wt) and ΔmbtD::hyg^r (ML1600) were pre-grown in 7H9/hemin medium (Supplements: 0.5% glycerol, 24 μg/mL pantothenate, 0.2% casamino acids, 0.01% tyloxapol) until an OD₆₀₀ of 1.0 was reached. Then, the cells were iron-depleted in self-made low-iron 7H9 medium containing the supplements (less than 0.1 μM Fe³⁺ as determined by ICP-MS) for 5–7 days. The iron-depleted cells were inoculated into 10 mL of low-iron 7H9 medium (containing the supplements) at an initial OD₆₀₀ of 0.01 with different iron sources: 20 μM ammonium ferric citrate; 10 μM human holo-transferrin; 10 μM human holo-lactoferrin; 5 μM human hemoglobin; 20 μM hemin; 0.2 μM Fe-MBT; 0.2 μM Fe-cMBT, respectively. The OD₆₀₀ of the cultures were determined every 24 hrs. All experiments were done in triplicate.

Transposon mutagenesis

The Mtb ΔmbtD::hyg^r (ML1600) strain was mutagenized by using himar1-based transposon as previously described with some modifications [39,40]. A total of 4.0×10¹¹ Mtb cells were harvested at OD₆₀₀ of 1.0 to 1.2. Cells were washed twice with MP buffer [50 mM Tris-Cl pH 7.5, 150 mM NaCl, 10 mM MgSO₄, 2 mM CaCl₂] and then infected with the ΦMycoMarT7 phage at an MOI of 20 at 37 ^oC for 4 hrs. Subsequently, the infected Mtb cells were washed twice with 10% glycerol and then cultured in self-made low-iron 7H9/ADS medium at 37 ^oC for 24 hrs. The recovered cells were spread on self-made low-iron 7H9/ADS Noble agar plates containing the six iron sources as described above and 30 μg/mL kanamycin. Three independent libraries were generated for each of high Fe-MBT and hemin condition and two independent libraries were generated for each of the other four iron conditions. All plates were cultured at 37 ^oC for 21 days. 14 independent libraries each containing ~200,000 transposon mutants were obtained.

Preparation of chromosome-transposon junctions DNA for sequencing

Genomic DNA isolation, partial restriction digestion, ligation to asymmetric adapters, and transposon amplification were performed as previously described with modifications [39,40]. 12.5 μg library DNA was partially digested by HinP1I (NEB). Fragments from 150 to 700 bp were purified from a 1.2% agarose gel using the Qiaquick gel purification kit (Qiagen). 2 μg HinP1I-digested DNA was ligated with 8 μM adapter DNA (S2 Table) by T4 DNA ligase at 16 ^oC overnight and the ligation products were purified using the Qiaquick PCR purification kit. The transposon-chromosomal junctions were selectively amplified twice by PCR. The first amplification was performed by the short transposon-specific PCR primers (S2 Table) with the PCR conditions: 96 ^oC for 5 min; 20 cycles of 96 ^oC for 1 min, 58 ^oC for 1 min, 72 ^oC for 45 sec, and 72 ^oC for 2 min by LA-taq DNA polymerase (Takara). The PCR fragments from 200 to 600 bp were purified from a 2% agarose gel. The second amplification was performed using the hemi-nested PCR primers (S2 Table) with the following conditions: 96 ^oC for 5 min; 20 cycles of 96 ^oC for 1 min, 58 ^oC for 1 min, 72 ^oC for 30 sec, and 72 ^oC for 2 min by LA-taq DNA polymerase. The PCR fragments from 250 to 450 bp were purified from a 2% agarose gel for Illumina sequencing. The libraries were subjected to 150-bp paired-end sequencing on the NextSeq 500 platform and raw sequence data were exported to fastq files for TPP processing.

Processing of the TnSeq sequencing data

Raw reads were mapped to TA sites in the reference strain H37Rv (NC_000962.2) and read counts were reduced to unique template counts using a customized version of the TPP tool from version 2.0.2 of TRANSIT [45]: we modified the ADAPTER2 and three constant regions to match the sequences used in our protocol (Hendrickson RC, v2.0.2_zhang. 2019 Oct 4. In: GitHub [Internet]. Forked TRANSIT repository. Available from https://github.com/rusalkaguy/transit/tree/v2.0.2_zhang). The resulting .wig files containing the unique template counts were then processed with version 3.0.0 of TRANSIT [45] for statistical analyses. Template counts at each TA site were normalized by the TTR (total trimmed read count) method to adjust for differences in total counts between datasets [45].

TnSeq analysis

The ANOVA (analysis of variance) method was used on the 14 independent datasets (S5 Table) grouped into the 6 iron conditions to determine which genes exhibit statistically significant variability (log₂ fold-change, LTnSeq-FC) of the normalized Tn insertion counts across multiple conditions (using f_oneway in the scipy python package). P-values were adjusted for multiple comparisons using the Benjamini-Hochberg procedure. 165 genes (≥ 3 TA sites) were identified (q values < 0.05).

The resampling analysis of TRANSIT (version 3.0.0) platform was performed on the triplicate samples (S5 Table) of high MBT and hemin conditions to compare the mutant frequency for each gene between the two conditions based on a permutation test as previously described [45]. The significant differences between the sum of the normalized read counts between the high MBT and hemin conditions were evaluated by comparison to a null distribution derived by random permutation of the observed counts at TA sites. P-values were adjusted for multiple comparisons by the Benjamini-Hochberg procedure to control the false-discovery rate at < 0.05. Positive LTnSeq-FC or negative LTnSeq-FC values indicate an increased genetic requirement for utilizing MBT or hemin, respectively. The genes unrelated to either MBT or hemin are expected to have no significant difference (i.e. LTnSeq-FC values near 0).

The Hidden markov model (HMM) analysis of TRANSIT (version 3.0.0) was used on the biological replicate 1 dataset of each condition (S5 Table) to assess essentiality of the Mtb genes under different iron conditions as previously described [80]. The HMM models Tn insertion counts as coming from geometric distributions conditioned on four different states of essentiality with increasing mean insertion count: essential (ES), growth defect (GD), nonessential (NE), and growth advantage (GA). Genes are labeled based on the most frequent state label among individual TA sites in the gene (as assiged by the Viterbi algorithm). The numbers of genes in each state under different iron conditions are shown in S2 Fig.

Construction of the M. tuberculosis deletion mutants

The Mtb deletion mutants Δrv2047c, ΔmmpL4, ΔmmpL5, ΔmmpL4/mmpL5 and ΔsmtB-zur deletion mutants were constructed by allelic exchange using homologous recombination as previously described [81]. The parent strain Mtb mc²6230 harboring the rv2047c deletion vector pML3622 was grown on selective 7H10 plates containing 10% ADS, 0.5% glycerol, 24 μg/mL pantothenate, 0.2% casamino acids, 20 μM hemin, 2% sucrose and 50 μg/mL hygromycin. The plates were cultured at 40 ^oC for 4 weeks to select for double cross-overs (DCO). 6 out of 8 clones were validated as double cross-over (DCO) by PCR. One of the Δrv2047c::hyg^r clones was selected and named Mtb ML2256 (S4 Fig). The rv2047c expression vector pML4211 was constructed and integrated into the chromosome of Mtb ML2256 at the L5 attB site to generate the rv2047c complemented strain Mtb ML2257. The deletion of the smtB-zur operon was done using the same protocol. The Mtb mc²6206 strain harboring the smtB-zur deletion vector pML3606 was grown on selective 7H10 plates at 40 ^oC for 4 weeks. 2 out of 3 clones were validated as double cross-over (DCO) by PCR. One of the ΔsmtB-zur::hyg^r clones was selected and named Mtb ML2277 (S5 Fig). The L5 integration vectors pML4218 (smtB), pML4219 (zur) and pML4220 (smtB-zur) were transformed into Mtb ML2277 to generate the complemented strains Mtb ML2278, Mtb ML2279 and Mtb ML2280, respectively. All Mtb strains are listed in S1 Table and the deletion and expression vectors are listed in S4 Table.