INTRODUCTION

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The global burden of 8 million active tuberculosis cases annually is overshadowed by the fact that fully one-third of the global population of humans is asymptomatically infected with tubercle bacilli (67). Many cases of clinically active tuberculosis arise from reactivation of an infection acquired years before the onset of overt symptoms, and these reflect the reemergence of actively growing organisms from an apparently nonreplicative state (4, 40, 65). Not all patients latently infected will develop active disease, and the fraction that ultimately develops tuberculosis through reactivation versus reinfection is a topic of current investigation (69). Conventional antibiotic therapy is sufficient to sterilize sputa and bronchoalveolar lavage specimens, whereupon bacilli cannot be detected by either acid-fast staining or culture. DNA from Mycobacterium tuberculosis can still be detected in such samples, and premature termination of therapy often results in recrudescence of disease, suggesting the continued presence of viable organisms (20, 26, 35, 51, 52, 71). During such a latent infection, the bacteria are thought to remain isolated in masses of lymphoid cells called granulomas, wherein they are encased in an impermeable caseous material by a thin layer of activated macrophages, with restricted access to nutrients or oxygen (15, 60).

The details of the dormant state are unclear, but the mechanism probably falls short of true spore formation. Instead, the processes involved in long-term survival within an asymptomatic patient probably reflect the result of bacterial responses to relatively simple signals from the environment. Adaptation of bacilli to long-term survival under these conditions may therefore be associated with coordinated alterations in patterns of gene expression in specific metabolic networks. The stringent response is a broad transcriptional program encompassing at least 80 genes in Escherichia coli that mediates prokaryotic adaptation to survival under conditions of starvation (9). Induction of the stringent response in E. coli stimulates polyphosphate synthesis (58), increases fatty acid cyclopropanation (19), inhibits fatty acid and phospholipid synthesis (27), upregulates glycogen synthesis (8, 18), upregulates the stationary-phase sigma factor RpoS (44), and inhibits stable RNA synthesis (9). The stringent response can be induced by amino acid, carbon, nitrogen, or phosphorous starvation. Additionally, UV light exposure and fatty acid starvation induce the response (39, 61). The stringent response is mediated by increased intracellular levels of hyperphosphorylated guanine nucleotides, specifically the 3'-pyrophosphate derivative of GDP (ppGpp) and the 3'-pyrophosphate derivative of GTP (pppGpp), the mixture of both being referred to as (p)ppGpp.

In E. coli and other gram-negative bacteria, two proteins have been identified that are responsible for the synthesis of (p)ppGpp, RelA, and SpoT (9). RelA, or ppGpp synthase I, is ribosome associated and is activated by binding uncharged tRNAs to the ribosome upon depletion of amino acids (52). SpoT, ppGpp synthase II, is not associated with ribosomes and has both (p)ppGpp synthetic and hydrolytic activities (21, 22, 28). E. coli strains lacking RelA or lacking both RelA and SpoT cannot grow in minimal media and survive poorly in the stationary phase (9). Among many gram-positive organisms, including the actinomycetes, there appears to be only one protein with homology to both RelA and SpoT that coordinates the metabolism of (p)ppGpp. This protein has been called Rel and has been identified in Streptomyces coelicolor and Streptomyces antibioticus as well as in Corynebacterium glutamicum and Streptococcus equisimilis (10, 11, 32, 46-49, 76). In both species of Streptomyces, the stringent response and Rel protein activity appear to be tightly coupled to stationary-phase adaptation and production of unique and specific antibiotics, such as actinomycin D and actinorhodine. Antibiotic production typically occurs coincident with the formation of aerial mycelia and entry into stationary phase (12). Disruption of the rel gene destroys the ability of both Streptomyces species to produce antibiotics and interferes with spore formation (32, 46).

M. tuberculosis also has only a single RelA or SpoT homolog (Rv2583c), designated Rel_Mtb (13). The Rel_Mtb protein of M. tuberculosis has the most identity to the Rel protein of three other gram-positive actinomycetes, C. glutamicum (67% identity), S. antibioticus (66% identity), and S. coelicolor (62% identity). It has significantly less homology to non-actinomycete gram-positive organisms, for example, the RelA or SpoT homolog of Bacillus subtilis (43% identity), and even less to gram-negative organisms such as Escherichia coli (39% identity to spoT and 37% identity to relA). Purified recombinant Rel_Mtb is a protein of 738 amino acids that is an ATP:GTP/GDP/ITP 3'-pyrophosphoryltransferase as well as an Mn²⁺-dependent (p)ppGpp 3'-pyrophosphorylhydrolase (2).

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Nucleotide labeling and analysis. Bacteria were grown to early log phase (optical density [OD] [650 nm] of 0.2 to 0.3) in Difco Middlebrook 7H9-ADC-Tween medium (containing [per liter] ammonium sulfate, 0.5 g; L-glutamate, 0.5 g; sodium citrate, 0.1 g; pyridoxine, 1 mg; biotin, 0.5 mg; disodium phosphate, 2.5 g; monopotassium phosphate, 1 g; ferric ammonium citrate, 40 mg; magnesium sulfate, 50 mg; calcium chloride, 0.5 mg; zinc sulfate, 1 mg; and copper sulfate, 1 mg; with 5 g of albumin [fraction V; bovine], 2 g of dextrose, 0.2% glycerol, and 0.05% Tween 80 added after sterilization). Where indicated, this medium was made with a lowered phosphate concentration to increase ³²P incorporation containing 1/25 normal phosphate levels (1 mM final concentration) and with 40 mM MOPS (morpholinepropanesulfonic acid) added to maintain pH at 6.6. Bacilli were grown for 48 h in low-phosphate medium, and then ³²P_i was added at 1 mCi/ml and cells were labeled for 3 to 4 h. Labeled M. tuberculosis was pelleted by centrifugation, washed once with Tris-buffered saline with Tween (TBST) (50 mM Tris-HCl [pH 7], 150 mM NaCl, 0.05% Tween 20), and then resuspended in the desired medium. Time points were generally taken at 0, 20, 40, 60, 90, and 120 min. Samples were pelleted by centrifugation and then lysed in 1 M formic acid by bead beating with 0.1-mm-diameter glass beads (BioSpec Products, Bartlesville, Okla.) with three pulses of 40 s each. After high-speed centrifugation to remove cell debris, samples were then directly spotted onto anion-exchange (polyethylenimine-cellulose) plates (EM Science, Gibbstown, N.J.). The two-dimensional thin-layer chromatography (2D-TLC) system employed was adapted from Bochner and Ames (5). First-dimension separation (by charge) was performed in 0.75 M Tris-HCl-25 mM EDTA (pH 8). The second dimension (by base content) solvent was saturated ammonium sulfate plus 5 mM EDTA, with the pH adjusted to 3.5 with sulfuric acid. Plates were dehydrated by a 5-min immersion in methanol before and between developments. Radioactivity was detected with a Storm 860 PhosphorImager (Molecular Dynamics, Sunnyvale, Calif.). Nonradioactive standards (Sigma) were run and visualized by fluorescence quenching to identify spots.

Bacterial strains, media, and growth conditions. The bacterial strains and plasmids used in this study are shown in Table 1. Unless otherwise indicated, M. tuberculosis was grown with constant stirring in 7H9-ADC-Tween and on Middlebrook 7H11-ADC as the solid medium (containing [per liter] pancreatic digest of casein, 1 g; L-glutamate, 0.5 g; sodium citrate, 0.4 g; pyridoxine, 1 mg; biotin, 0.5 mg; ferric ammonium citrate, 40 mg; ammonium sulfate, 0.5 g; disodium phosphate, 1.5 g; monopotassium phosphate, 1.5 g; magnesium sulfate, 50 mg; Bacto agar, 15 g; and malachite green, 1 mg; with 5 g of albumin [fraction V; bovine], 2 g of dextrose, and 0.2% glycerol added after sterilization). E. coli DH5 was grown in Luria-Bertani broth or on agar. Kanamycin and hygromycin were used at 50 and 200 µg/ml, respectively, for selection in E. coli and at 20 and 50 µg/ml, respectively, for selection in M. tuberculosis. Suicide plasmids for targeted gene knockout were electroporated into M. tuberculosis as described by Gordhan and Parish (25). Analysis of cell wall composition and mycolic acid subclass distribution was conducted as previously described (80).

Construction of the rel_Mtb::hyg allele. DNA manipulations were carried out according to standard procedures (59). A cosmid, Pac6, containing the rel_Mtb gene was isolated by screening the pYUB328::H37Rv cosmid library of M. tuberculosis (3) with an internal rel_Mtb probe that was generated by PCR amplification with the degenerate primers RELA1 [5'-CATGGATCCAACGG-(GC)TACGAG(AT)(GC)(GC)(AC)T(GC)CACAC] and RELA2 [5'-CATGGATCCGTGTG(GC)A(CT)(GC)GCGTA(GC)GCGAAGTC]. PCR amplifications were carried out on a Hybaid PCRExpress thermal cycler with TaqI DNA polymerase (Roche Molecular Biochemicals) at an annealing temperature of 55°C. The plasmid pRelS, carrying the rel_Mtb allele, which encodes an in-frame-deleted form of Rel_Mtb lacking the N-terminal region between His94 and Ala413, was constructed by ligating the 1,865-bp BamHI-SphI fragment from Pac6 (containing 1,581 bp of upstream sequence and 284 bp of rel_Mtb coding sequence) and the 1,749-bp SphI-KpnI fragment from Pac6 (containing 1,136 bp of coding sequence and 613 bp of downstream sequence) in BamHI-KpnI-pGEM3Z(+)f. A hyg marker, carried on a 1,739-bp BamHI-BglII fragment from pIJ963 (29), was cloned in the unique BglII site, located 219 bp into the rel_Mtb coding region, to form pRelSH. In this construct, the hyg gene contained in the marked rel_Mtb::hyg allele was codirectional with the rel_Mtb gene. The rel_Mtb::hyg allele could theoretically encode a polypeptide comprising the N-terminal 73 amino acids of Rel_Mtb fused to a 72-amino-acid sequence derived from the 5'-untranslated region of hyg. This fusion is unlikely to possess Rel-associated synthetase or phosphohydrolase activities (22). Expression of the C-terminal part of the mutilated Rel_Mtb as a fusion of the His94-Ala95 region to the His412-Ala413 region would require the improbable presence of a promoter downstream of the hyg gene terminator and a start codon (see Fig. 2).

Construction of rel_Mtb::hyg mutant strains. The hsp60-lacZ reporter from pSMT3lacZ, in which the E. coli lacZ gene was expressed under the control of the Mycobacterium bovis BCG groEL promoter of pSMT3 (55), was cloned as a 3,100-bp XbaI-HindIII fragment into the unique XbaI and HindIII sites of pRelSH to create pSA1. M. tuberculosis was electroporated with 1 to 5 µg of UV-irradiated pSA1 (25, 30, 56), and cells were plated on 7H11-ADC agar containing hygromycin and 5-bromo-4-chloro-3-indolyl--D-galactopyranoside (X-Gal [50 µg/ml]). Chromosomal DNA was extracted from Hyg^r transformants for Southern blot analysis, as previously described (24). A second knockout vector containing the Bacillus subtilis sacB counterselectable marker (57) was constructed as follows. The 5,361-bp BamHI-KpnI fragment, containing the partially deleted rel_Mtb::hyg allele, was excised from pSA1 and cloned in p2NIL (25; T. Parish, B. Gordhan, D. A. Smith, G. J. Bancroft, V. Mizrahi, R. A. McAdam, and N. G. Stoker, Fourth Int. Conf. Pathog. Mycobacterial Infect., abstr. 01, 1999). The PacI fragment from pGOAL13 (Parish et al., Fourth Int. Conf. Pathog. Mycobacterial Infect.), containing an hsp60-sacB cassette in which the sacB gene is expressed by the M. bovis BCG groEL promoter, was then introduced into this vector to produce pSA3. This vector was electroporated into M. tuberculosis following UV irradiation, as described above. Transformants were selected on 7H11-ADC agar containing hygromycin and kanamycin. Since kanamycin selects for the hyg marker contained in the p2NIL-based vector, colonies growing on kanamycin plus hygromycin are predicted to be the result of a site-specific single-crossover event. Hyg^r Km^r transformants were streaked on 7H11-ADC plates containing hygromycin only, to allow double-crossover events to occur. The positive selection option presented by the presence of the sacB gene was utilized to select for double-crossover recombinants by plating on 7H11-ADC containing hygromycin and 2% sucrose. Hyg^r Suc^r (sucrose-resistant) colonies were patched onto fresh medium to test for kanamycin sensitivity, since this would be indicative of vector loss. Hyg^r Suc^r Km^s colonies obtained by this two-step process were selected as candidate allelic exchange mutants.

Construction of a rel_Mtb-complemented strain. We first PCR amplified the upstream region with a small amount of the N terminus of the rel_Mtb gene. The N-terminal primer was 5'-AATATGGATCCGACGAAAATGTATGCGGTGA-3', which included a BamHI site, and the C-terminal primer was 5'-CTCGTCGCAAGATCGACAGGTC-3', which included a BglII site. The rel_Mtb gene was then PCR amplified alone. The N-terminal primer for this amplification was 5'-ACGTCATATGACCGCCCAGCGCAGCACCACCAAT-3', which included an NdeI site, and the C-terminal primer was 5'-ACGTGGTACCCTACGCGGCCGAGGTCACCCGGTA-3', which included a KpnI site. The rel_Mtb gene was then cut with BglII and ligated to the upstream region to reconstruct the complete rel_Mtb gene with intact upstream sequence. This fragment was then ligated into pMV306 by using the BamHI and KpnI sites. This vector, which carries the attP site of mycobacteriophage L5, integrates site specifically in single copy at the L5 phage integration site, attB (41). The rel_Mtb strain was electroporated with pMV306K-rel, and Km^r Hyg^r colonies were selected. The complemented strain thus has a single chromosomal copy of the rel_Mtb gene under the native promoter.

Growth curves. M. tuberculosis strains were grown in 7H9-ADC-Tween as the reference media. Log-phase cultures (OD of 0.1 to 1) were used to inoculate test media to be analyzed for growth. Bacteria were cultured in ~50-ml volumes in 250-ml bottles rolling in a 37°C incubator. Individual ingredients were added or removed from the 7H9-ADC-Tween base medium as indicated in the figures. Growth was measured by determining the A₆₅₀ of the culture. The growth rate in Table 3 is a linear fit to the OD versus time in days at the most rapid growth phase; these results were repeated at least twice in each case with similar results. Dipalmitoylphosphatidylcholine (DPPC) was obtained from Sigma.

Competition starvation survival assay. The rel_Mtb (Hyg^r) strain and H37Rv transformed to Kan^r with the pMV306K vector were grown to early log phase in 7H9-ADC-Tween. Bacilli were then pelleted by centrifugation and washed twice with 0.1% Tween 80 to remove traces of medium. Bacteria were then resuspended in TBST, the OD of each culture was adjusted to 0.2, and then the cultures were mixed at a 1:1 ratio in a 50-ml final volume and incubated by rolling at 37°C. Bacterial clumping was minimized by vortexing a 1-ml aliquot of the culture for 2 to 3 min in a 1.5-ml tube containing ~300 mg of glass beads. In control experiments, this procedure increased the apparent number of CFU of a clumpy M. smegmatis culture, but did not lower the number of CFU of a log-phase culture. For long-term nutrient run-out experiments with 7H9-ADC-Tween, bacteria were diluted to approximately 10⁴ CFU/ml in fresh 7H9-ADC-Tween and grown aerobically at 37°C. Aliquots were removed at the indicated times and plated as described above. For anaerobic survival assays, bacteria were diluted to an OD of 0.05 in fresh 7H9-ADC-Tween and then mixed in a 1:1 ratio. This mixture was aliquoted into 1.5-ml screw-cap tubes with rubber septa with no headspace and incubated stationary at 37°C. Control tubes with methylene blue indicator dye demonstrated that all oxygen was consumed after 4 to 5 days. For all experiments, the number of CFU per milliliter was determined by plating in triplicate at 3 to 5 dilutions onto 7H11-ADC plates containing hygromycin or kanamycin on the indicated days. Cell viability was determined by plating 10-fold dilutions in 7H9-ADC-Tween onto 7H11-ADC plates with kanamycin or hygromycin selection and counting colonies approximately 3 weeks after inoculation at the indicated times.

Ribosome isolation. Two liters of cells of wild-type M. tuberculosis and rel_Mtb M. tuberculosis was grown to an OD of 1.3 in 7H9-ADC-Tween, pelleted, and resuspended in TBST for 24 h. The cells were repelleted and resuspended in buffer 1 (10 mM Tris-HCl [pH 7.6], 30 mM KCl, 15 mM MgCl₂, 6 mM -mercaptoethanol) before being lysed with a bead beater and centrifuged at 15,000 × g followed by 30,000 × g each for 20 min. The supernatant was then centrifuged at 150,000 × g for 3 h. The pellet containing ribosomes was again resuspended in buffer 1 and layered over buffer 2 (buffer 1 containing 30% [wt/vol] sucrose) and centrifuged at 150,000 × g for 15 h. This pellet was washed and resuspended in ribosome buffer (50 mM Tris-HCl [pH 7.6], 50 mM KCl, 10 mM MgCl₂). Ribosome content was estimated by using the conversion factor of 1 OD₂₆₀ unit = 25 pmol of 70S ribosomes in 1 ml of distilled water.

Macrophage infection. Bacterial inocula were prepared as previously described from a 1:400 dilution into RPMI 10 medium (GIBCO/BRL) of a well-dispersed OD of 0.2 7H9-ADC-Tween culture (79). The human macrophage-like cell line THP-1 (ATCC 202-TIB) was seeded at 8 × 10⁵ cells per well in 24-well plates. A 250-µl-per-well bacterial suspension was applied to the adherent cells (for a final multiplicity of infection of approximately 1), and these cells were incubated at 37°C for 1 h. Extracellular bacteria were removed by four washes with 0.5 ml of RPMI 10, and macrophages were subsequently fed with 1 ml of RPMI 10 per well and incubated at 37°C under 5% CO₂. Luciferase-reporting strains were generated by transformation with pMV306K-hsp60-luc, in which the strong constitutive M. tuberculosis groEL promoter drives luciferase expression (16). At each time point, macrophages were lysed with 250 µl of 0.1% Triton X-100, and then 50 µl was removed and mixed with 50 µl of assay buffer (140 µg of luciferin per ml [Molecular Probes] and 0.4% Triton X-100 in distilled water). Macrophages were cultured in triplicate identical wells, and luciferase assays were read in duplicate with a TopCount 96-well reader (Hewlett Packard).

	RESULTS

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Starvation induces the formation of intracellular (p)ppGpp in M. tuberculosis. To assess whether M. tuberculosis utilized a conventional stringent response involving (p)ppGpp, we labeled the total cellular nucleotides of M. tuberculosis with ³²P_i during growth in vitro in low-phosphate media. Labeled bacilli were then shifted to various conditions, and the intracellular nucleotide responses were analyzed by 2D-TLC (see Fig. 2). M. tuberculosis was found to have a very low basal level of (p)ppGpp when grown aerobically and in log phase in minimal medium. (Middlebrook 7H9-ADC-Tween medium contains no complex source of nutrients [see Materials and Methods]). These 2D-TLCs do not differentiate between ppGpp and pppGpp. Several published 1D-TLC systems were tried, but incorporation of label was low in any medium, and unambiguous determination of the ppGpp/pppGpp ratio was not possible due to heavy sample loading requirements. Inhibition of the respiratory chain by azide treatment (5 mM) for 120 min and complete starvation by incubation in Tris-buffered saline with Tween for 120 min strongly increased (p)ppGpp levels (Table 2). The frontline drugs isoniazid and ethambutol at concentrations well above the MIC had no significant effect over similar time intervals. In contrast to the (p)ppGpp induction observed in E. coli, resuspension of log-phase M. tuberculosis in serine hydroxamate, a competitive inhibitor of the seryl-tRNA charging enzyme, had no effect on (p)ppGpp levels, whereas it induces the accumulation of (p)ppGpp in E. coli. While this may imply a significant divergence in amino acid metabolism, M. tuberculosis may simply be impermeable to serine hydroxamate, or the M. tuberculosis tRNA-Ser charging enzyme may be insensitive to such reagents.

Construction and genotypic characterization of rel_Mtb::hyg mutants. To directly demonstrate the linkage between the Rel_Mtb protein and the production of (p)ppGpp, the gene encoding Rel_Mtb was deleted from the H37Rv strain by allelic exchange. Construction of a deletion-replacement construct allowed the substitution of the rel_Mtb gene for a hygromycin resistance determinant (hyg). The Southern blot analysis used to determine the genotype of transformants obtained with pSA1 is shown in Fig. 1. PvuII digestion of the wild-type strain produces a 2,803-bp rel_Mtb-containing fragment that cross-hybridizes with the upstream 2,247-bp SmaI probe used in this analysis. Site-specific integration of pSA1 in the chromosome by a single-crossover event would result in the formation of a second, 3,587-bp PvuII fragment containing the rel_Mtb::hyg allele from pSA1, which cross-hybridizes to the same probe. Allelic exchange by double crossover would therefore result in the disappearance of the wild-type allele and its replacement by the larger mutant allele. Southern blot analysis of the DNA extracted from 10 transformants obtained with pSA1 revealed that in one clone, SJA16, the wild-type allele was absent. Further analysis of SJA16 confirmed that the new PvuII allele contained the hyg gene. In addition, probing with the 945-bp SphI fragment that had been removed from the rel_Mtb gene to generate the rel_Mtb allele confirmed its absence from the genome of SJA16. However, plating of SJA16 on indicator medium containing X-Gal resulted in the unexpected formation of blue colonies, indicating the presence of lacZ in this clone and ruling out the possibility that SJA16 was the product of simple allelic exchange by double crossover. Additional Southern blot analysis suggested that a site-specific double-crossover event had occurred, but had been followed by a subsequent crossover event resulting in the integration of a second copy of pSA1 (Fig. 1). This may have been due to the relatively large amount of UV-irradiated plasmid DNA (5 µg) used in the electroporation experiment that yielded this transformant. Since the second vector copy could theoretically be lost from SJA16 by a further crossover event, the strain was grown, serially diluted, and plated on indicator media in order to identify white colonies. However, no white colonies were found among 108 colonies that were screened.

View larger version (27K): [in this window] [in a new window]   FIG. 1.   Construction and genotypic characterization of relMtb::hyg mutants. (A) Locus of the relMtb gene showing the restriction sites that were used to construct the relMtb::hyg allele contained in pSA1 and pSA3. The BamHI-SphI and SphI-KpnI chromosomal DNA fragments that were used to form the relMtb allele contained in pRelS are denoted by thick, horizontal lines. B, BamHI; Bg, BglII; K, KpnI; P, PvuII; S, SphI. (B) Schematic representation of the genotype of the relMtb::hyg mutant strain, SJA16, showing two copies of the relMtb::hyg allele and the absence of a wild-type relMtb allele. The additional copy of the pSA1 vector, carrying the lacZ and bla genes, is shown as a thick horizontal line. (C) Southern blot analysis of homologous recombinants obtained with pSA1 and pSA3. Chromosomal DNA was digested with PvuII and probed either with the upstream 2,247-bp SmaI fragment () showing the wild-type allele of 2,803 bp and mutant allele of 3,587 bp or with the internal 945-bp SphI fragment () showing the presence of this fragment in the wild type (WT) and single crossovers, but its absence from the relMtb::hyg mutants. KO, knockout. Lanes: 1, wild-type H37Rv; 2, SJA14 (single crossover carrying pSA1 integrated at the relMtb locus); 3, SJA16 (relMtb::hyg mutant carrying additional, integrated copy of pSA1); 4, SJA32 (site-specific single crossover carrying pSA3 integrated at the relMtb locus); 5, SJA33 (relMtb::hyg mutant).

Phenotypic analysis of the rel_Mtb::hyg strain in vitro. As expected, the rel_Mtb strain failed to synthesize (p)ppGpp in response to starvation (Fig. 2). Complementation of the rel_Mtb::hyg mutant with an intact rel_Mtb gene on a single-copy-integrating plasmid restored the ability of the strain to produce (p)ppGpp (data not shown). There were no significant differences in gross surface morphology or apparent growth rate on several types of solid media. The cell wall permeability of the mutant appeared grossly similar to that of the wild type, since the MIC for the rel_Mtb strain was the same as the wild type with a variety of compounds in the broth microdilution assay, including isoniazid, rifampin, cycloserine, hydrochloric acid, and hydrogen peroxide. One exception was that the mutant was twofold more sensitive to azide, which also appeared to induce (p)ppGpp synthesis (Table 2). There were also no significant differences in the mycolic acid subclass distribution or modification in either log- or stationary-phase bacilli, suggesting that, unlike in gram-negative bacteria, cyclopropanation of fatty acids (mycolic acids in this case) is not under rel_Mtb control (19, 80).

View larger version (61K): [in this window] [in a new window]   FIG. 2.   Analysis of intracellular (p)ppGpp in M. tuberculosis by 2D-TLC. (A) Control nucleotides extracted from 32Pi-labeled M. tuberculosis H37Rv aerobically grown in normal 7H9 medium during the log phase. (B) Nucleotides extracted from stationary-phase culture of H37Rv (2-week-old culture). These cultures label significantly less well than logarithmically growing cultures, and, thus, this panel has been exposed more heavily. (C) Nucleotides extracted from H37Rv cells labeled and then placed under starvation conditions (resuspension in TBST). (D) Sample prepared as in panel C, but with the SJA16 rel strain of H37Rv. (E) Schematic representation of nonradioactive standards run in the same 2D-TLC system. Complementation of the relMtb strain with the relMtb gene restored the ability to produce (p)ppGpp under these conditions.

View larger version (15K): [in this window] [in a new window]   FIG. 3.   In vitro growth curves. (A) Growth of wild-type H37Rv (wt) (), the rel mutant (), and the complemented strain C7 () in 7H9 medium at 37°C, determined by OD650. Panel B is the same, but at 42°C. (C) Growth at 37°C in 7H9 with the carbon sources of glucose and glycerol replaced with 0.2 mM DPPC.

View this table: [in this window] [in a new window]   TABLE 3.   Growth of the relMtb strain in liquid media

The rel_Mtb::hyg strain is impaired for survival during long-term starvation. The ability of the rel_Mtb::hyg strain to survive under conditions of long-term nutrient deprivation was also investigated. Preliminary experiments comparing CFU determined from separate cultures of antibiotic-marked wild-type H37Rv and the rel_Mtb mutant revealed higher-than-acceptable error due to clumping of both strains. Although the degree of clumping did not appear to be different between the two strains, it did limit the accuracy of the CFU determinations. To circumvent this problem, equal amounts of a Km^r wild-type strain (created by integration of a single-copy control plasmid into H37Rv) and the Hyg^r rel_Mtb mutant were mixed under starvation conditions and coincubated. Identical samples were removed at various time points, vortexed with sterile glass beads, and plated separately onto both antibiotics. When starved for several months by resuspension in TBST to induce sudden starvation, the rel_Mtb strain lost viability much more rapidly than wild-type H37Rv (Fig. 4A). The mutant rate of loss of viability is higher than the wild-type rate across the entire experiment, suggesting that an initial adaptation event accounts for the disparity in survival.

View larger version (14K): [in this window] [in a new window]   FIG. 4.   Starvation survival. (A) Kanamycin-resistant wild-type H37Rv(pMV306K) (wt) and rel mutant (hygromycin resistant) were mixed in a competition starvation assay in TBST at an initial wild-type/rel ratio of 1.75. The number of CFU per milliliter was determined by plating in triplicate at 3 to 5 dilutions onto 7H11 plates containing hygromycin or kanamycin on the indicated days. Control plates at low dilution with both hygromycin and kanamycin gave no colonies. (B) As in panel A, both organisms were simultaneously inoculated to an initial cell density of 104 CFU/ml, and at sequential time points, the cells were removed and dilutions were plated onto selective media. (C) Anaerobic survival of wild-type H37Rv(pMV306K) and the rel mutant in sealed tubes. A mid-log-phase culture was divided into replicate sealed tubes at an initial cell density of 107 CFU/ml, and at the indicated time points, the tubes were unsealed and viable CFU were determined by plating the cells onto selective media.

rel_Mtb::hyg has a wild-type growth rate in macrophages. Wild-type H37Rv and rel_Mtb strains were analyzed for growth in the THP-1 human macrophage-like cell line (66). To facilitate evaluation of the growth rates of these organisms, we first integrated a groEL promoter-driven firefly luciferase gene (conferring kanamycin resistance on the mutant) into the L5 phage integration site (79). Growth was monitored both by CFU determination on plates and by luciferase activity from a strong constitutive promoter construct. Whole-cell luciferase activities in M. tuberculosis have been shown to accurately report culture and intracellular viability (1, 6, 63). In two independent experiments, there was no significant difference in the growth rates between wild-type H37Rv(pMV306-hsp60-luc) and H37Rvrel_Mtb::hyg(pMV306-hsp60-luc) in THP-1 cells (Fig. 5). The growth rate determined by plating for CFU also showed no significant difference between the two strains (data not shown).

View larger version (13K): [in this window] [in a new window]   FIG. 5.   Growth curve in macrophages. Growth of wild-type H37Rv (wt) and rel mutant strains in THP-1 cells was analyzed by using constitutive luciferase-expressing strains. Shown are data from one experiment, with a second experiment having similar results. In a control in vitro experiment, H37Rv grew faster than the rel mutant (data not shown), consistent with growth determined by absorbance (A).

	DISCUSSION

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Our understanding of the adaptation of mycobacteria to long-term survival within the eukaryotic host has been guided by our estimation of the likely characteristics of their environment during persistence. To date, these efforts have focused on two hypothetical characteristics of this environment: oxygen limitation and nutrient deprivation.

Oxygen limitation induces some dramatic and specific changes in mycobacteria, including enhanced resistance to some drugs (like isoniazid and rifampin) and sensitivity to nitroaromatic compounds, such as metronidazole (43, 75). Oxygen limitation also upregulates the synthesis of specific proteins, such as -crystallin and a flavohemoglobin, and induces enzymes such as glycine dehydrogenase and alanine dehydrogenase (33, 36, 74, 78). Such organisms become thermotolerant, decrease overall protein synthesis, have lost acid fastness and the ability to grow on malachite green-containing media, and have ultramicroscopically thickened cell walls (14, 23, 35, 70). Adaptation to low oxygen tension is a coordinated activity at many levels, and rapid alteration can lead to cell death (71, 73). The coordination of these events is especially evident in that reoxygenation of microaerophilic cultures results in synchronous replication (17, 72).

Nutrient deprivation, in the form of amino acid and carbohydrate depletion, is also likely to coincide with the formation of intact granulomas in a process thought to be essential for curtailing growth of the microorganism (14, 37). Recent speculation has centered on the role of lipid metabolism in maintaining mycobacterial viability in the absence of robust growth, since the caseous intragranulomar environment is likely to be lipid rich and mycobacteria appear well endowed with suitable enzymes for utilizing lipids as a sole carbon source (the so-called "lipolytic hypothesis") (13). There may also be shifts between the primary source of nutrients during infection, because M. tuberculosis growing within a macrophage phagolysosome may well prove to have access to different nutrients than M. tuberculosis persisting within a caseous granuloma.

To adapt to such changing situations, M. tuberculosis may utilize a variety of transcriptional control mechanisms. Some of this environment-dependent gene expression (including expression of -crystallin) is controlled by the expression of an alternative sigma factor, SigF (45, 51). A second sigma factor, SigB, has been shown to be associated with stationary-phase adaptation and general stress (34). The interplay between these two regulons may prove important for distinguishing components important specifically for persistence. In addition to the use of such alternative sigma factors for such adaptation, many microorganisms translate the stress of amino acid or carbon source depletion into an intracellular accumulation of (p)ppGpp, leading to alterations in gene expression that suppress the synthesis of stable RNA species (rRNA and tRNA), induce degradative pathways, activate certain stationary-phase genes, and modulate genes that regulate DNA replication and growth rate (7, 9-11, 64, 77).

In this study, we have demonstrated that there is a very low basal level of (p)ppGpp in log-phase wild-type M. tuberculosis strains CDC1551 and H37Rv grown axenically on glucose with accumulation starting in early stationary-phase cultures and reaching a maximum in long-term stationary-phase cultures. When log-phase cultures were shifted into isotonic buffer with no nutrients (TBST), (p)ppGpp began to accumulate within 20 min, peaked by 40 to 60 min, and declined to a new steady state by 90 to 120 min (data not shown). This temporal pattern is similar to that determined from the kinetic studies of the metabolism of (p)ppGpp in E. coli, where the stringent response occurs on a more abbreviated time scale, being induced within seconds of starvation (9, 50). No (p)ppGpp is detectable in the M. tuberculosis H37Rv strain with a deleted rel_Mtb gene (Fig. 2).

Adaptation to nutrient deprivation is essential for long-term survival of nongrowing cells. M. tuberculosis is capable of surviving under nongrowing starvation conditions for up to 2 years in vitro while retaining the ability to resuscitate (54). In M. smegmatis it has been reported that carbon, nitrogen, or phosphorus-starved organisms retain viability for over 650 days, with an initial 2- to 3-log drop in CFU followed by long-term maintenance of stable numbers (62). These authors speculate that sensing and responding to carbon starvation allowed an adaptation to stationary phase that facilitated long-term bacterial survival. In this study, we demonstrate that an effect of such carbon limitation is to elevate levels of (p)ppGpp in the cell through the action of the Rel_Mtb protein. Rel_Mtb-mediated production of (p)ppGpp presumably induces proteins involved in stationary-phase survival. Furthermore, late-log-phase cultures of the rel_Mtb strain that were subjected to starvation stress contained five times more ribosomes per unit of protein than the wild-type, highlighting the inability of this strain to adapt to the stationary phase (data not shown). This failure to reduce the amount of stable RNA and ribosomal proteins supports the notion that the stringent response is required for growth rate control (7, 42). Thus, as we previously speculated (2), in the absence of this response, M. tuberculosis fails to adapt to the stationary phase and long-term survival is severely compromised.

The Rel_Mtb-deficient strain consistently grows more slowly than the wild type or the complemented strain in normal growth media, suggesting that during aerobic growth under these conditions, some level of (p)ppGpp is required for optimum growth. This apparent defect is not complemented by addition of additional sources of nutrients such as peptone or glycerol. Addition of such supplements does, however, effectively double the growth rate and the maximal OD of the rel_Mtb cultures, suggesting some of the growth defect may occur in response to uncharged tRNA concentrations, an observation consistent with biochemical data (H. Rubin and D. Avarbock, unpublished results). The wild-type strain shows more modest effects of these additives, suggesting that the effect is not strictly due to provision of a general growth factor. In light of the aforementioned theory that the major intracellular carbon source for persistent bacteria is lipid, it is particularly interesting that the Rel_Mtb-deficient strain is not different in growth rate from the wild type under only two conditions: when grown within macrophages and when grown upon lipid. These results were surprising because of the connection of Rel with amino acid starvation in gram-negative organisms and the known defect in growth of amino acid auxotrophs of M. tuberculosis in cultured macrophages (31, 38). It is noteworthy that organisms with genetic deletion of isocitrate lyase, an enzyme essential for growth upon lipid substrates, are defective for persistence in mouse models of latent tuberculosis (J. McKinney, Rockefeller University, personal communication). Taken together, these data are consistent with the hypothesis that intracellular growth relies primarily on lipid catabolism as the major source of carbon.

The evaluation of this mutant in animal models of persistent infection will allow the direct assessment of the relevance of this and other proteins involved in stationary-phase survival to latency and long-term persistence. Validation of the importance of this (p)ppGpp-mediated response network in animal models of persistence would lead to consideration of the Rel_Mtb protein as a target for the development of chemotherapeutic agents with unique activity in the treatment of asymptomatic tuberculosis infections.