Mammalian natural resistance–associated macrophage protein (Nramp) homologues are important determinants of susceptibility to infection by diverse intracellular pathogens including mycobacteria. Eukaryotic Nramp homologues transport divalent cations such as Fe2+, Mn2+, Zn2+, and Cu2+. Mycobacterium tuberculosis and Mycobacterium bovis (bacillus Calmette-Guérin [BCG]) also encode an Nramp homologue (Mramp).
RNA encoding Mramp induces ∼20-fold increases in 65Zn2+ and 55Fe2+ uptake when injected into Xenopus laevis oocytes. Transport is dependent on acidic extracellular pH and is maximal between pH 5.5 and 6.5. Mramp-mediated 65Zn2+ and 55Fe2+ transport is abolished by an excess of Mn2+ and Cu2+, confirming that Mramp interacts with a broad range of divalent transition metal cations.
Using semiquantitative reverse transcription PCR, we show that Mramp mRNA levels in M. tuberculosis are upregulated in response to increases in ambient Fe2+ and Cu2+ between <1 and 5 μM concentrations and that this upregulation occurs in parallel with mRNA for y39, a putative metal-transporting P-type ATPase. Using a quantitative ratiometric PCR technique, we demonstrate a fourfold decrease in Mramp/y39 mRNA ratios from organisms grown in 5–70 μM Cu2+. M. bovis BCG cultured axenically and within THP-1 cells also expresses mRNA encoding Mramp.
Mramp exemplifies a novel prokaryotic class of metal ion transporter. Within phagosomes, Mramp and Nramp1 may compete for the same divalent cations, with implications for intracellular survival of mycobacteria.
The macrophage vacuole is an especially hostile microenvironment for intracellular pathogens, as it is the arena in which multiple host defences operate. Many phylogenetically unrelated pathogens, including Mycobacteria, Salmonella, and Leishmania species, have successfully adapted to this niche 1,2. A critical determinant of susceptibility to infection by these organisms is the natural resistance–associated macrophage protein (Nramp)1 family 3. Nramp homologues are phylogenetically ancient integral membrane proteins first identified in mice 4. A mutation in Nramp1 (originally designated Bcg/Lsh/Ity) renders mice susceptible to uncontrolled proliferation of many organisms (Mycobacterium bovis [BCG], Mycobacterium avium, Mycobacterium lepraemurium, Leishmania donovani, and Salmonella typhimurium) within the reticuloendothelial system during the early phase of infection 5,6,7. Genetic analyses have now linked polymorphisms in and around the Nramp1 locus with susceptibility to tuberculosis 8 and leprosy 9 in humans.
Nramp homologues in yeast 10 and rats 11,12 transport cations such as Fe2+, Cu2+, and Zn2+, and deficient Mn2+ uptake is implicated in Drosophila mutants without a functional Nramp homologue 13. These cation substrates of Nramp are important in monocytes, neutrophils, and macrophages because they are involved in generating reactive oxygen intermediates during the respiratory burst. For example, hydrogen peroxide generated by the respiratory burst interacts with Fe2+/Fe3+, and produces reactive hydroxyl and superoxide radicals that are crucial in early defence against intracellular microorganisms. Consistent with this function, Nramp1 (a mammalian homologue) expression is restricted to phagosomes of myelocytic cells 14. Some transition metals are also components of bacterial metalloenzymes (such as the superoxide dismutases and catalases) that protect bacteria against oxidative stresses encountered, for example, in phagosomes 15,16.
We 17 and others 18,19 have hypothesized that both mycobacteria and macrophages use Nramp homologues to compete for intraphagosomal metal ions. We now provide evidence that Mramp (the mycobacterial homologue of Nramp) is a pH-dependent divalent cation transporter of broad specificity. Mramp expression is modulated by variation in ambient Cu2+ and Fe2+ concentrations as well as being expressed in intracellular mycobacteria.
Materials And Methods
Isolation and Cloning of Mramp Sequence.
We used the previously identified M. leprae sequence encoding an Nramp homologue to search the EMBL database using TBLASTN 20. PCR on genomic DNA from M. tuberculosis (H37Rv) and BCG using Pfu polymerase (Stratagene, Inc.) was carried out with primers designed to introduce BglII restriction sites and a strong eukaryotic Kozak consensus (TTGGTGG to ATGATGG, initiation codon underlined). PCR primers were as follows: 5′-GTA GCC AGA TCT ATG ATG GCG GGC GAA TTT CGG-3′ and 5′-GCG GTC AGA TCT TCA GCC GGT CAC CGT GAG ATA-3′ (BglII sites are underlined and the translational start codon is in bold). Cycle conditions were as follows: 1 min at 94°C, 35 cycles of 30 s at 94°C, 30 s at 66°C, 2 min at 72°C, with a final 4-min hold at 72°C. The reaction was supplemented with Mg2+ (1 mM) and Betaine (1 M) (Sigma Chemical Co.). The PCR product from M. tuberculosis was subcloned into BglII sites in pSP, which contains 5′ and 3′ untranslated Xenopus β-globin sequences 21 and was verified by sequence analysis. Constructs containing both orientations of Mramp were obtained and designated pXmramp (sense) and pXpmarm (antisense).
Expression of Mramp in Xenopus Oocytes and Fe2+ and Zn2+ Uptake Studies.
Xenopus laevis oocytes were prepared as described previously 22. Capped cRNA encoding Mramp was transcribed (MEGAscript™ SP6; Ambion) from Xba1-linearized templates (pXmramp and pXpmarm), and oocytes were injected with cRNA (5 ng in 50 nl of water) or a corresponding volume of RNAse-free water. Fe2+ and Zn2+ uptake assays were performed after 48–96 h incubation in Barth's solution (88 mM NaCl, 1 mM KCl, 2.4 mM NaHCO3, 15 mM Hepes [pH 7.6], 0.3 mM Ca(NO3)2.4H2O, 0.41 mM CaCl2.6H2O, 0.82 mM MgCl2.7H2O, 10 μg/ml penicillin, 10 μg/ml streptomycin) at 19°C 23.
65Zn2+ uptake assays were performed on batches of 10–15 oocytes washed 4 times in freshly made up standard uptake medium (SUM: 90 mM KCl, 10 mM NaCl, 10 mM morpholinoethane sulfonic acid [MES], pH 5.0–pH 6.5; as before but with 10 mM Hepes at pH 7.0) and incubated in SUM for 1–4 h at room temperature with 100 μM 65ZnCl2 (Nycomed Amersham plc). Transport was terminated by washing oocytes in excess ice-cold SUM. 65Zn2+ uptake was quantitated in individual oocytes on a Wallac Wizard 1480 gamma counter and corrected for uptake into water or antisense cRNA–injected controls.
55Fe2+ uptakes were performed with 55Fe2+ (5 μM in 100 μM total Fe2+; Nycomed Amersham plc) in SUM containing ascorbic acid (2 mM) to maintain iron in a ferrous state, and all studies used fresh solutions to minimize reoxidation of Fe2+. The amount of ferrous iron was verified by a ferrozine assay 24. Quantitation of 55Fe uptake was by scintillation counting (Wallac Microbeta Plus).
Maximal expression of both 65Zn2+ and Fe2+ uptake occurred between 2 and 4 d after microinjection. Competitions with divalent cations were performed using 65Zn2+ or Fe2+ as permeants and 100-fold excess (10 mM) concentrations of CuCl2, MnCl2, FeCl2, ZnCl2, and MgCl2.
Media for M. tuberculosis Cultures.
All glassware was autoclaved after rinsing in 0.2 N HCl followed by deionized water to remove trace quantities of iron. Low Fe (∼5 μM) Sauton's medium for starter cultures consisted of asparagine (15 mM), MgSO4 (1 mM), sodium citrate (4 mM), KH2PO4 (7 mM), and glycerol (2% vol/vol, pH 7.1). Fe-depleted Sauton's medium (<1 μM) was prepared as above, omitting MgSO4, and stirred overnight at 4°C with Chelex 100 (10 g/l). After filter sterilization, the medium was supplemented (MgSO4 [1 mg/ml equivalent to 8.3 mM final concentration], ZnSO4.4H2O [0.2 μg/l final concentration ∼ 1 nM], and MnCl2.4H2O [0.2 μg/l ∼ 1 nM]) to compensate for losses during chelation. Media containing “low Fe” (<1 μM), “medium Fe” (4 μM), or “high Fe” (48 μM) and “low Cu” (<0.5 μM), “medium Cu” (5 μM), or “high Cu” (69.8 μM) were prepared by additionally supplementing aliquots of this medium with ferric ammonium citrate (∼16% Fe content) or CuCl2. To ensure that concentrations of cations not being studied were above limiting concentrations, the Fe-modified media were supplemented with Cu (∼1 μM), and Cu-modified media with Fe (4 μM). Concentrations of Fe and Cu in these media were verified by ferrozine assay 24 and atomic absorption spectrophotometry, respectively. All chemicals were obtained from Sigma-Aldrich.
Growth of M. tuberculosis in Varying Iron and Copper Concentrations.
Starter cultures in Dubos broth supplemented with 10% Dubos medium albumin (Difco) were initiated from glycerol stocks and grown at 37°C to mid-log phase. These were inoculated (1:10) into low iron Sauton's medium, grown for 1 wk (37°C, 5% CO2, without shaking), and subcultured to ensure complete depletion of iron and copper. 10 ml of these cultures was inoculated into Fe/Cu-depleted Sauton's medium (10 ml into 190 ml) supplemented to give low, medium, or high concentrations of iron or copper and grown for 5 wk.
Infection of Macrophages with BCG.
As BCG encodes an Mramp sequence (available from EMBL/GenBank/DDBJ under accession no. AJ005699) identical to that of M. tuberculosis, we used BCG as a model to examine the expression of Mramp during intracellular infection. The human macrophage cell line, THP-1, was maintained as suspended cells and passaged at a density of 2–5 × 106 cells/ml. Before infection with BCG, the cells were passaged at least three times in antibiotic-free RPMI 1640 (ICN Biochemicals) supplemented with heat-inactivated FCS (10%), grown to a density of 2–5 × 106 cells/ml, and stimulated with PMA (20 mM; Sigma Chemical Co.) for 24 h to induce adherence. Nonadherent cells were removed by washing twice in PBS, and the resulting monolayers (∼3–5 × 107 cells/flask) were covered with supplemented RPMI 1640. Mid-log phase bacteria were pelleted from Dubos broth (500 g, 10 min), resuspended in medium, and sonicated (Rinco Ultrasonics) for 15 s (five 3-s bursts at 70% amplitude) to disaggregate bacterial clumps. The sonicate was added to macrophages (10 bacilli/macrophage) and left for 24 h (37°C, 5% CO2). Extracellular mycobacteria were removed by decanting the supernatant and extensively washing the adherent cells twice in PBS. Efficiency of phagocytosis was estimated to be ∼30% by counting CFU in the collected washings and microscopic examination of Ziehl-Nielsen–stained macrophages. Macrophage viability (>90%) throughout these experiments was assessed by Trypan blue exclusion, with further details given in reference 25.
Recovery of RNA from Intracellular BCG.
After extensive washing of the macrophage monolayer, mycobacteria were recovered from differentially lysed THP-1 cells by the addition of 20 ml GTC solution (4 M guanidinium thiocyanate [GTC; Fluka] containing 0.5% sodium N-lauroylsarcosine, 25 mM sodium citrate, pH 7, and 0.1 M 2-ME) to each flask 25. Total RNA was then extracted from the washed bacterial pellets as described previously 26.
Identification of Open Reading Frames.
First strand cDNA synthesis on total RNA used random hexamer primers (Promega) and Moloney murine leukemia virus reverse transcriptase (Superscript II™; GIBCO BRL) according to the manufacturer's instructions. Contamination of RNA by genomic DNA was excluded by PCR on RNA template made without reverse transcriptase and on template made from RNA pretreated with RNAse A (Qiagen).
PCR was carried out using primers spanning the junction between the 3′ end of the Mramp gene and the open reading frame (ORF) immediately downstream under the following cycling conditions: 30 cycles of 1 min at 94°C, 2 min at 55°C, 3 min at 72°C. Primers were 5′-ACGATCACCCATAACAACAGG-3′ and 5′-CAGAGAACGACTTCACCAACC-3′.
Generation of Competitor for Tandem Competitive PCR.
Templates for quantitative PCR assays were generated by oligonucleotide restriction site mutagenesis 27, using M. tuberculosis genomic DNA as template, and corresponded to the following fragments: for Mramp (467 bp, 820–1287), and for two “P”-type ATPases: yhho (503 bp, 79–582) and y39 (503 bp, 100–603). Spanning primer pairs were as follows: for Mramp, 5′-CTGGTTGCCGCGCTGAACATG-3′ and 5′-GAACTGAAACCCCATTCAGCCGGTCACCGT-3′; for y39, 5′-GTTGGGGCCTCGAAGGAATTCGTTGACGCCGCA-3′ and 5′-CTTGCTGAACCACGCCAGCTT-3′; for yhho, 5′-ACCGGCTGAATGGGGTTTCAGTTCGACGCGGG-3′ and 5′-AACGAATTCCTTCGAGGCCCCAACCGCCAGCGC-3′.
Primers were designed so that the Mramp antisense primer overlapped with the yhho sense primer, and the yhho antisense primer overlapped with the y39 sense primer, giving a tandemly organized construct after synthesis by PCR 28. PCR cycle conditions, identical for each fragment, were as follows: 3 min at 94°C, 35 cycles of 30 s at 94°C, 30 s at 65°C, 2 min at 72°C, followed by a 4-min hold at 72°C. To discriminate competitor from target in tandem competitive (TC)-PCR reactions, a mutant asymmetrical Kpn1 restriction site was introduced ∼200 bp internal to the 5′ end of each fragment. These fragments were cloned in tandem into pGEM-T Easy (Promega). We chose “P”-type ATPase sequences (y39, putative Ca2+ transporter; and yhho, atypical heavy metal transporter reviewed in Agranoff et al. ) in order to quantitate the relative amounts of Mramp expression in mRNA obtained from mycobacteria cultured in different ionic microenvironments.
As an internal control for RNA preparations, we amplified 16S ribosomal RNA sequence using the primers 5′-CCC TTG TCT CAT GTT GCC AG and 5′-CTG GCA ACA TGA GAC AAG GG.
Quantitation of mRNA for Mramp and P-type ATPases.
First strand cDNA synthesis on total RNA was carried out as described above. Semiquantitative estimates of mRNA expression were derived by conventional reverse transcription (RT)-PCR carried out under identical conditions for each primer pair and identical starting cDNA concentrations for all three genes. Products were quantified using a GDS 7600 system (Ultraviolet Products) and normalized to the most abundant product for each gene. Precise quantitation of relative amounts of cDNA for Mramp and y39 under different growth conditions was carried out by TC-PCR. A series of PCR amplifications of each gene was carried out on a template mixture consisting of a fixed quantity of cDNA and serial dilutions (at 1/4 log intervals) of competitor molecule (linearized by Sac1 digestion). Products derived from competitor template could be distinguished from target product by KpnI digestion and were quantified as above. The plasmid competitor/cDNA ratio was calculated for individual reactions after heteroduplex correction and analyzed as published previously 29.
Comparison of radioisotope uptake rates between two conditions was by the Mann Whitney U test, and comparison of uptakes at different pH values and with competitors was after Box-Cox transformation (to normalize distributions) and used MANOVA (v5.2 SYSTAT).
Sequence Analysis of Mramp.
A single Nramp homologue (designated Mramp) is located on cosmid MTY21C12 (GenBank/EMBL/DDBJ accession no. Z95210; gene number Rv0924c) in a 5286-bp region containing 5 ORFs oriented in the same direction 30. A potential ribosome binding site is immediately upstream of the first ORF with Mramp as the fourth gene in this series. To ascertain if Mramp is cotranscribed with neighboring ORFs, we carried out RT-PCR on total RNA extracted from cultured H37Rv using primers spanning the junction between the 3′ end of Mramp and the next ORF. A product of expected size (407 bp) was obtained (data not shown), indicating that Mramp is transcribed at least as a bicistronic operon. Database searches failed to identify functionally characterized homologues of this second ORF.
Mramp encodes a predicted 428–amino acid protein with a molecular mass of 44.9 kD and 10 transmembrane segments consistent with proposed topologies for yeast homologues (smf1 and 2) (31; Fig. 1). Compared with eukaryotic homologues, the hydrophilic NH2-terminal region of Mramp, like those of other prokaryotic Nramp homologues, is shorter but exhibits a similar clustering of polar residues 31. The COOH terminus is also shorter and probably lacks the two final transmembrane segments predicted in some eukaryotic homologues. The amphiphilic properties of transmembrane segments M3, M5, and M9, in which the polar and nonpolar residues are segregated to opposite faces of the predicted α-helices (possibly forming a transmembrane channel), are also found in Mramp.
Sequence analysis of Mramp confirms that certain amino acid residues are highly conserved between all members of the Nramp family (Fig. 1). Mramp sequences from M. tuberculosis and BCG are identical and are most closely related to other bacterial homologues (72.4, 40, and 40% sequence identities with M. leprae, Bacillus subtilis, and Escherichia coli, respectively), whereas comparison with eukaryotic homologues gives overall amino acid identities of 21–24%. There is an asymmetrical distribution of charged amino acid residues between the endo- and exofacial regions of Mramp. This is consistent with similar patterns of charge distribution observed in many integral membrane proteins 32.
Mramp Induces 65Zn2+ Uptake in Oocytes.
Initially we cloned Mramp into pGEM-T Easy after mutating the mycobacterial GTG start codon to ATG without strengthening the Kozak consensus sequence. Microinjection of oocytes with RNA made from this construct induced up to twofold increases in 55Fe2+ and 65Zn2+ uptake compared with water-injected oocytes (data not shown). To optimize Mramp expression in oocytes, we retained the modified start codon, introduced a strong Kozak consensus, and cloned Mramp into a vector containing flanking X. laevis 5′ and 3′ untranslated regions (see Materials and Methods).
In 10 independent experiments, RNA derived from this latter construct induced large increases (up to 22-fold) in the accumulation of 65Zn2+ by Mramp-expressing oocytes compared with water-injected (Fig. 2 A) or Mramp antisense–injected controls (Fig. 2 A, inset). To confirm that these induced 65Zn2+ uptakes were specific to Mramp, we also examined the uptake of 65Zn2+ in oocytes injected with RNA made from the Trypanosoma brucei hexose transporter (THT1 33; Fig. 2 B). As expected, there was no increase in 65Zn2+ uptake associated with expression of THT1, confirming the requirement for Mramp to induce 65Zn2+ uptake. Conversely, we demonstrated 2′-deoxy-d[14C]-glucose (2-DOG) uptake by THT1 but not by Mramp (Fig. 2 C). To confirm that accumulation of 65Zn2+ continued beyond these experimental time points, we monitored 65Zn2+ uptake for up to 4 h. The increase in uptake of 65Zn2+ was linear during this period, which encompasses the uptake times of experiments shown (slope 3.8 ± 0.63, P < 0.001).
Mramp-induced 65Zn2+ Uptake Is pH Dependent.
In oocytes, translocation of divalent cations by DCT1 (the rat Nramp2 homologue) depends on cotransport of protons, with maximal activity of DCT1 at an extraoocytic pH of 5.5. To determine if cation transport by Mramp displays a similar pH dependence, we measured 65Zn2+ uptake by oocytes incubated in extracellular pH values between 5.0 and 7.0. In nine independent experiments, 65Zn2+ uptake by oocytes was confined to extracellular pH values between 5.5 and 6.5 (Fig. 3) and was completely abolished at pH 7 or 5.
Mramp Has Broad Cation Transport Specificity.
As a first step to determine the specificity of Mramp for divalent cations in the d-block series, we measured the uptake of 65Zn2+ in the presence of an excess of unlabeled Mn2+. Mn2+ (10 mM) completely abolished uptake of 65Zn2+ (Fig. 4 A), indicating that Mn2+ competes with 65Zn2+ for binding to or uptake by Mramp.
We next used 55Fe2+ as a permeant to investigate in detail the substrate specificity of Mramp for divalent cations. Mramp mediates large increases in the uptake of 55Fe2+ at pH 5.5 (up to 18-fold) above water-injected oocytes (Fig. 4 B). This induced 55Fe2+ uptake is abolished by Mn2+ and Cu2+ (Fig. 4 C). In contrast, Mg2+, a divalent cation that does not belong to the d-block series, enhanced 55Fe2+ accumulation by oocytes ninefold compared with 55Fe2+ uptake in its absence (Fig. 4 C).
Mramp and y39 Expression Are Modulated by Changes in Ambient Iron and Copper Concentrations.
Mycobacterial growth varied in media containing different concentrations of Fe2+ and Cu2+. At relatively high concentrations (>45 μM), Fe2+ and Cu2+ inhibited bacterial growth by 29 and 38%, respectively (Fig. 5 B). Mramp mRNA transcript was detectable in bacteria grown at all Fe2+ and Cu2+ concentrations tested (Fig. 5 A), including a faint band in bacteria grown in Fe2+-depleted culture medium, which was quantifiable using the GDS 7600 system but is not visible on the photograph. mRNA for y39 was similarly detectable at all Fe2+ and Cu2+ concentrations. In contrast, mRNA for yhho gave much fainter bands in bacteria grown in high Fe2+ concentrations and medium and high Cu2+ concentrations, and was undetectable in other conditions. rRNA (16S) RT-PCR analysis of these templates confirmed that initial total RNA template quantities were comparable for all conditions (Fig. 5 A, bottom).
Semiquantitative analysis of PCR products from Mramp and y39 (a putative Ca2+-translocating P-type ATPase ) using identical template concentrations and PCR conditions showed large increases in mRNA for Mramp (∼50-fold) as Fe2+ concentration increases from <1 to 48 μM (Fig. 5 A). As Cu2+ concentrations increase over a similar range, mRNA for Mramp increases ∼10-fold, and is maximal at 5 μM Cu2+. There is less increase in mRNA for y39 under these conditions (∼17- and 5-fold, respectively).
To investigate the regulation of Mramp and y39 transcription more precisely, we used a ratiometric PCR technique called TC-PCR to quantitate mRNA for Mramp in relation to y39 in M. tuberculosis cultured in media containing these different concentrations of Fe2+ and Cu2+. The mRNA ratios for Mramp/y39 fell fourfold (from 0.44 to 0.11) when Cu2+ concentrations increased from 5 to 70 μM. The relatively low PCR yields of product from y39 except for bacteria grown in medium and high Cu2+ concentrations precluded more accurate quantitation of Mramp/y39 mRNA ratios in these conditions.
Mramp Is Expressed by BCG in the Intracellular Environment.
Fig. 5 C (top) shows that mRNA encoding Mramp is detectable in RNA extracted from intracellular BCG. For comparison, we show that Mramp mRNA is also detectable in axenically cultured BCG under identical PCR conditions. Comparability of template concentrations in this experiment was verified by RT-PCR analysis of rRNA (16S) (Fig. 5 C, bottom).
Although approximately 1.7 billion people (one third of the world's population) are infected with M. tuberculosis at any one time, it is striking that, in the absence of coinfection with HIV, fewer than 10% of these will develop active disease during their lifetimes 34. Host genetic factors such as polymorphisms in Nramp1 clearly influence susceptibility to infection or disease caused by Mycobacteria species 35. For example, tuberculosis in a tribally mixed Gambian population was associated with two pairs of Nramp1 polymorphisms 8, and in another study involving members of Chinese and Vietnamese families with leprosy, haplotypes associated with Nramp1-linked polymorphisms were observed to be distributed nonrandomly between affected and unaffected family members 9.
The Nramp family of proteins is highly conserved between bacteria and mammals, and two eukaryotic examples have been shown to transport divalent cations such as Fe2+ and Mn2+ 12,36,37. Nramp1 is likely to perform similar transport functions to Nramp2, which mediates pH-dependent Fe2+ uptake in heterologous expression studies and in vivo 12,36. Defining the transport specificities for Nramp1 has proved difficult 38, and all studies characterizing Nramp homologues have been carried out exclusively on eukaryotic sequences. Recent studies in RAW264.7 cells overexpressing Nramp1 suggest that Nramp1 does contribute to iron mobilization from vesicles 39. Nramp1 also circumvents maturation arrest of phagosomes containing live BCG, permitting the increase in acidification normally seen in phagosomes containing killed BCG or latex beads 40. These observations point to the possibility that competition for transition metal ions may be important in determining maturational dynamics of phagosomes as well as their lethality for certain intracellular pathogens.
We studied a mycobacterial homologue of the Nramp family because of its potential relevance to intracellular survival. Nramp homologues are found in M. tuberculosis, M. leprae, M. smegmatis, and BCG 7,17. These homologues (called Mramp) have been suggested to mediate the uptake of cations such as Fe2+, Mn2+, and Zn2+, which may be important in defence by microbial superoxide dismutase against the macrophage respiratory burst 17,18. Our studies now provide direct evidence for a function of Mramp as a transporter of Zn2+ and Fe2+.
Furthermore, the enhanced uptake of 65Zn2+ and 55Fe2+ induced in oocytes expressing Mramp is abrogated by an excess of Mn2+ and Cu2+, but not by unrelated divalent cations such as Mg2+, suggesting important interactions between Mramp and these transition elements. In spite of divergence in primary sequence between Nramp1, DCT1 (a rat intestinal homologue of Nramp2), and Mramp and their diverse phylogeny, all three sequences can mediate the uptake of Fe2+ into Xenopus oocytes 12. DCT1 transports other members of the transition metal series, and this broad specificity is also observed for Mramp. Therefore, Mramp represents a novel class of prokaryotic metal ion transporter with representatives in other bacteria such as E. coli and B. subtilis (Fig. 1).
We examined the pH dependence of cation transport by Mramp using 65Zn2+ as a permeant, because at pH > 6.0 it is difficult to manipulate the equilibrium between Fe2+ and Fe3+ even in the presence of reducing agents such as ascorbic acid 41. There is a narrow range of extracellular acid pH values that allows Mramp-induced uptake of 65Zn2+ by oocytes. This pH range (5.5–6.5) coincides with estimates of ambient pH in the microenvironment of intraphagosomal mycobacteria 42. This observation also provides evidence for the direction in which cation transport is likely to be taking place, namely from the relatively acidic phagosome into mycobacteria. By contrast, an uninfected phagolysosome (for example, one containing inert particles) has a significantly lower pH (<5.5 ), and would therefore be unlikely to allow efficient transport of divalent cations by Mramp.
To assess the expression of Mramp in M. tuberculosis cultured axenically, we applied a precise assay to quantitate mRNA for Mramp obtained from organisms grown in media containing defined Cu2+ and Fe2+ concentrations. These studies permitted assessment of the growth characteristics of bacteria as well as the relative expression of mRNA for Mramp compared with mRNA encoding a putative Ca2+ P-type ATPase (y39). Mramp is expressed poorly in bacteria grown in relatively Cu2+- and Fe2+-deficient media, and expression is enhanced at higher concentrations of these metal ions (≥5 μM). Similar patterns of mRNA expression are observed for the putative Ca2+-transporting P-type ATPase (y39), but in contrast, mRNA encoding an atypical heavy metal-translocating P-type ATPase (yhho) is barely detectable under any of the conditions tested (Fig. 5). This stimulation of expression of mRNA for Mramp and y39 at higher ambient concentrations of Cu2+and Fe2+ is associated with retardation of bacterial growth by ∼30%.
mRNA for Mramp encoded by BCG is clearly expressed in the intracellular environment (Fig. 5 C). We used BCG as a model for M. tuberculosis because M. tuberculosis is frequently cytopathic when cultured in THP1 cells, compromising yields of RNA. BCG is well recognized as a convenient model to study mycobacterial gene expression in these circumstances 25.
Mramp may act in concert with mechanisms inhibiting acidification of phagosomes to permit intracellular survival of mycobacteria. The deployment of Nramp1 in the host's phagosomal membrane is clearly important in defence against infection, as established by classical studies on the genetics of Nramp1. If Nramp1 also uses phagosomal protons to extrude cations, thereby competing with Mramp, the pH dependence of this phenomenon will be critical in establishing which of the two transporters (Mramp or Nramp1) functions most efficiently in the infected macrophage. Experiments to examine this hypothesis in greater detail can now be formulated on the basis of Mramp's function as defined by heterologous expression. Mramp is the first mycobacterial gene to be expressed in oocytes, exemplifying the utility of this system for the functional characterization of other prokaryotic transporters (E. coli glycerol facilitator glpF, and E. coli water channel AqpZ 43).
We thank Dr. T. Balz for the THT1 clone, and Dr. G. Gould for the pSPGT1 clone.
D. Agranoff is a Medical Research Council Training Fellow, and S. Krishna is a Wellcome Trust Senior Research Fellow in Clinical Science. I.M. Monahan, J.A. Mangan, and P.D. Butcher acknowledge the support of the European Union and Medical Research Council (UK), and J.A. Mangan, P.D. Butcher, and S. Krishna acknowledge Medical Research Council Co-operative Grant G9800300 for support.
1used in this paper: BCG, bacillus Calmette-Guérin; 2-DOG, 2′-deoxy-[14C]d-glucose; Mramp, mycobacterial homologue of Nramp; Nramp, natural resistance–associated macrophage protein; ORF, open reading frame; RT, reverse transcription; SUM, standard uptake medium; TC, tandem competitive