Skip to main page content

• HOME
• Current Issue
• Archive
• Alerts
• About ASM
• Contact us
• Tech Support
• Journals.ASM.org

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Abranches, J. Articles by Lemos, J. A. Search for Related Content PubMed PubMed Citation Articles by Abranches, J. Articles by Lemos, J. A.

 Previous Article  |  Next Article 

Journal of Bacteriology, April 2009, p. 2248-2256, Vol. 191, No. 7
0021-9193/09/$08.00+0     doi:10.1128/JB.01726-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

The Molecular Alarmone (p)ppGpp Mediates Stress Responses, Vancomycin Tolerance, and Virulence in Enterococcus faecalis

Jacqueline Abranches,^1,2 Alaina R. Martinez,¹ Jessica K. Kajfasz,¹ Violeta Chávez,³ Danielle A. Garsin,³ and José A. Lemos^1,2*

Center for Oral Biology,¹ Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York 14642,² Department of Microbiology and Molecular Genetics, The University of Texas Health Science Center at Houston, Houston, Texas 77030³

Received 9 December 2008/ Accepted 15 January 2009

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
The stringent response is a global bacterial response to stress that is mediated by accumulation of the alarmone (p)ppGpp. In this study, treatment with mupirocin was shown to induce high levels of (p)ppGpp production in Enterococcus faecalis, indicating that this nosocomial pathogen can mount a classic stringent response. In addition, (p)ppGpp was found to accumulate in cells subjected to heat shock, alkaline shock, and inhibitory concentrations of vancomycin. Sequence analysis of the E. faecalis genome indicated that (p)ppGpp synthesis is catalyzed by the bifunctional synthetase/hydrolase RelA and the RelQ small synthase. The (p)ppGpp profiles of relA, relQ, and relAQ strains revealed that RelA is the major enzyme responsible for the accumulation of (p)ppGpp during antibiotic or physical stresses, while RelQ appears to be responsible for maintaining basal levels of alarmone during homeostatic growth. Compared to its parent, the relA strain was more susceptible to several stress conditions, whereas complete elimination of (p)ppGpp in a relAQ double mutant restored many of the stress-sensitive phenotypes of relA. Interestingly, growth curves and time-kill studies indicated that tolerance to vancomycin is enhanced in the relA strain but diminished in the relQ and relAQ strains. Finally, virulence of the relAQ strain but not of the relA or relQ strain was significantly attenuated in the Caenorhabditis elegans model. Taken together, these results indicate that (p)ppGpp pools modulate environmental stress responses, vancomycin tolerance, and virulence in this important nosocomial pathogen.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Enterococcus faecalis is a natural inhabitant of the human and animal intestinal flora. Although normally harmless to healthy individuals, enterococcal infections rank among the top three most common causes of nosocomial infections (43), with E. faecalis representing nearly 90% of the total cases of enterococcal infections (44). The strong association of this organism with infections in hospital settings has been attributed to its inherent capacity to withstand environmental stresses and to its innate and acquired resistance to many antibiotics (15, 17, 33). In particular, the appearance of vancomycin-resistant enterococcus (VRE) strains in the late 1980s gave these organisms a tremendous selective advantage, increasing the likelihood of their propagation and persistence in hospitals (33). From a clinical standpoint, E. faecalis is an opportunistic pathogen that causes a myriad of diseases in humans, infecting the bloodstream, abdomen, endocardium, urinary tract, biliary tract, burn wounds, and indwelling foreign devices (17, 32, 43, 44). Moreover, E. faecalis has also been involved in the dissemination of antibiotic resistance to other medically relevant bacterial species (51).

The stringent response is a global bacterial response to nutritional stress that is mediated by accumulation of the alarmones guanosine tetraphosphate and guanosine pentaphosphate, collectively known as (p)ppGpp (8, 42). These nucleotides are synthesized by enzymatic phosphorylation of GDP and GTP using ATP as a phosphate donor and are produced at low basal levels during favorable growth conditions. Accumulation of (p)ppGpp results in strong downregulation of genes for rRNAs and anabolic processes and upregulation of genes involved in amino acid biosynthesis and stress survival (5, 8, 35, 36, 48, 49). Thus, the (p)ppGpp alarmones function as chemical messengers that allow bacteria to switch their metabolism from a "growth mode" to a "survival mode."

In Escherichia coli and its close relatives, two homologous proteins are involved in (p)ppGpp metabolism, the ribosome-associated (p)ppGpp-synthetase RelA and the bifunctional synthetase/hydrolase SpoT (8, 41). In gram-positive bacteria, a bifunctional Rel/Spo ortholog, herein designated RelA, harbors both degradation and synthesis activities (30, 52). Recently two small proteins, designated RelP and RelQ, with weak (p)ppGpp-synthase activities were found in the oral pathogen Streptococcus mutans (26). It was demonstrated that while relA encoded a strong bifunctional synthetase/hydrolase enzyme responsible for the rapid accumulation of (p)ppGpp upon amino acid starvation, the RelP and RelQ proteins were responsible for constitutive expression of (p)ppGpp in nonstressed cells (26, 35). Subsequent work with Bacillus subtilis and Streptococcus pneumoniae further confirmed the functionality of these enzymes as (p)ppGpp synthases (3, 34). Homologues of at least one of the two small (p)ppGpp synthases are found in the genomes of gram-positive bacteria but absent in the genomes of proteobacteria (26, 34).

In the past few years, the role of (p)ppGpp in bacterial virulence has become an area of extensive research. Studies have correlated changes in (p)ppGpp levels to the expression of virulence traits, including stress survival (12, 20, 25, 54), biofilm formation (2, 25, 46), antibiotic resistance (14, 19, 20, 40), and persistence (5, 14, 20, 21, 35, 42). In some cases, animal models have been used to provide unequivocal evidence of the role of (p)ppGpp in virulence (6, 9, 10, 16, 39, 46). Despite its strong association with bacterial virulence, the stringent response has not been studied for E. faecalis. In this article, we characterize the stringent response of E. faecalis and demonstrate that (p)ppGpp pools play a fundamental role in growth under adverse conditions and may be a key factor regulating tolerance and growth in the presence of antibiotics, in particular vancomycin. Finally, we show that virulence of a (p)ppGpp⁰ strain was highly attenuated in a Caenorhabditis elegans killing assay.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Bacterial strains and culture conditions. Bacterial strains and plasmids used in this study are listed in Table 1. E. faecalis strains were routinely grown in brain heart infusion (BHI) medium at 37°C. E. coli strains were grown in Luria broth and used for plasmid construction and propagation. When required for selective growth of strains, erythromycin (10 µg ml^–1 for E. faecalis, 300 µg ml^–1 for E. coli), spectinomycin (1,000 µg ml^–1), fusidic acid (25 µg ml^–1), or rifampin (rifampicin) (200 µg ml^–1) was added to the growth medium. To evaluate the capacity of E. faecalis strains to grow under different stress conditions, mid-exponential-phase cultures were diluted 1:100 into fresh medium and growth was monitored using a Bioscreen C growth monitor (Oy Growth Curves AB Ltd., Helsinki, Finland). Disc inhibition assays were used to assess the sensitivity of the strains to H₂O₂, HCl, or sodium hypochlorite. Briefly, a uniform layer of exponentially grown cells was spread onto BHI agar plates using a sterile swab, and paper filter discs (1 mm in diameter) saturated with 5% H₂O₂, 3 N HCl, or 10% sodium hypochlorite were placed onto the agar. All plates were incubated at 37°C for 48 h before the inhibition halo was recorded.

View this table: [in this window] [in a new window]

TABLE 1. Bacterial strains and plasmids used in this study

Construction of mutant strains. A markerless genetic exchange system (22) was used to construct relA, relQ, and relAQ mutants in E. faecalis OG1RF. Briefly, two PCR products flanking the relA or relQ gene were obtained with the primers listed in Table 2. The PCR amplicons were approximately 1 kb in size and included the first 10 to 15 residues and the last 10 to 15 residues of the relA or relQ gene, which were retained in the mutants to avoid unanticipated effects on the expression of adjacent genes. After digestion with the appropriate restriction enzymes, the two PCR products flanking the gene of interest were simultaneously cloned onto pGEM5 (Promega, Madison, WI) to give the plasmids pGrelA and pGrelQ. The 2-kb fragments containing the relA (pGrelA) and relQ (pGrelQ) up-down fragments were subcloned into pCJK47 (22) using E. coli EC1000 (24) as the host strain. The resulting plasmids, pCJK-relA and pCJK-relQ, were electroporated into competent E. faecalis CK111 (donor strain) (23). E. faecalis CK111 containing the pCJK-relA or pCJK-relQ plasmids was conjugated with wild-type E. faecalis OG1RF, and single-crossover insertions were selected on BHI agar medium containing rifampin and erythromycin. Single colonies were subjected to the PheS* negative counterselection system to isolate double-crossover deletions as described elsewhere (22). The relA and relQ gene deletions were confirmed by PCR sequencing of the insertion site and flanking sequences. Subsequently, a double relA relQ strain was constructed by conjugation of the donor strain harboring pCJK-relQ with the relA mutant.

View this table: [in this window] [in a new window]

TABLE 2. Primers used for gene deletion

Detection of (p)ppGpp accumulation patterns. For (p)ppGpp measurements in E. faecalis, cells were grown in the chemically defined FMC medium (47) containing a lower phosphate concentration (8.6 mM) in order to improve ³²P labeling (26). Overnight cultures grown in FMC were diluted 1:100 in fresh low-phosphate FMC, grown to an optical density at 600 nm of 0.2, and prelabeled with 50 µCi of carrier-free [³²P]orthophosphate (Amersham Biosciences, Piscataway, NJ) for one generation. At this point, experimental cells were treated with mupirocin (50 µg ml^–1), vancomycin (10 µg ml^–1), or ampicillin (32 µg ml^–1) or subjected to acid shock (pH 5, using 3 N HCl), alkaline shock (pH 10, using 2 N NaOH), and heat shock (60°C). Control cells consisted of aliquots that were labeled for the duration of the experimental cultures. Nucleotide pools were extracted by adding an equal volume of 13 M formic acid, followed by two freeze-thaw cycles. Acid extracts were centrifuged briefly, and the supernatant fluids were spotted onto polyethyleneimine (PEI)-cellulose plates (Selecto Scientific, Inc., Suwanee, GA) for separation by thin-layer chromatography (TLC) in 1.5 M KH₂PO₄ (pH 3.4).

Biofilm assay. Biofilm formation on polystyrene microtiter plates was quantified essentially as described previously (1). Biofilms were grown in a semidefined biofilm medium (28) containing glucose as the carbohydrate source for 24 h at 37°C before adherent bacteria were stained with 0.1% crystal violet. The bound dye was extracted from the stained cells with 33% acetic acid solution in water, and the biofilms were quantified by measuring the optical density of the solution at 575 nm.

Determination of MIC. The MIC for ampicillin, mupirocin, or vancomycin was determined in BHI using twofold serial dilutions prepared in the wells of microtiter plates. Bacteria from mid-log-phase cultures were inoculated into each well at 10⁵ CFU ml^–1. Microtiter plates were incubated at 37°C for 24 h before the optical density at 600 nm of each well was measured using the Benchmark Plus microplate spectrophotometer (Bio-Rad, Hercules, CA). The lowest concentration of antibiotic that prevented cell growth was assigned as the MIC.

Time-kill kinetics. Cultures were grown in BHI to exponential phase and then diluted 1:10 in fresh BHI to obtain a starting inoculum of 5 x 10⁶ to 1 x 10⁷ CFU ml^–1. Time-kill studies were initiated by adding five times the MIC of vancomycin for the wild-type strain. Viable counts were determined at time zero and then every 24 h for up to 6 days.

C. elegans killing assay. The ability of E. faecalis OG1RF and its derivatives to kill C. elegans was investigated as described previously (11). Briefly, a single colony of OG1RF was inoculated in BHI broth and grown at 37°C overnight, and 10 µl of culture was spread on a 35-mm BHI plate containing 50 µg ml^–1 gentamicin. The plates were allowed to incubate overnight at 37°C and were brought to room temperature before 60 to 90 L4-stage, wild-type (N2) worms (obtained from the Caenorhabditis Genetics Center) were set on the bacterial lawns. The Kaplan-Meier method was used to determine survival over time, and curves were compared using the log-rank test to generate P values testing the null hypothesis that a given pair of survival curves was identical. P values of 0.05 or less were considered statistically significant. All data were analyzed with the GraphPadPrism 5.0 software program.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
E. faecalis strains can mount a classic stringent response. To determine whether E. faecalis can mount a stringent response, the accumulation of (p)ppGpp during mupirocin treatment was examined. Mupirocin is an inhibitor of isoleucyl-tRNA synthetase that has been shown to elicit a potent stringent response in streptococci (26, 31, 53). In S. mutans, we have previously determined that (p)ppGpp accumulation is best observed when cells are treated with 5 to 10 times the MIC for mupirocin (26). Thus, we determined the MIC for mupirocin in E. faecalis OG1RF and V583 and found that E. faecalis was intrinsically more resistant to mupirocin than S. mutans (MIC of 10 µg ml^–1 for the E. faecalis strains versus MIC of 50 ng ml^–1 for S. mutans). Time-course experiments using 50 µg ml^–1 mupirocin showed dramatic increases in (p)ppGpp pools in E. faecalis OG1RF (Fig. 1A), with (p)ppGpp levels remaining elevated for up to 90 min (data not shown). Consistent with increases in (p)ppGpp pools was a fast drop in GTP levels, the acceptor nucleotide necessary for pppGpp synthesis (8). Similar results, e.g., rapid accumulation of (p)ppGpp at the expense of GTP upon mupirocin treatment, were obtained when using clinical isolates of E. faecalis (Fig. 1B), suggesting that this response is conserved among E. faecalis strains. Notably, the amounts of (p)ppGpp accumulated by the different isolates showed significant differences. Since all strains displayed the same MIC for mupirocin (data not shown), it appears that the differences in (p)ppGpp levels are due to inherent heterogeneity among different isolates. Based on the fact that all isolates can mount a classic stringent response, the experiments described below were conducted using strain OG1RF and its isogenic mutants. The advantages of using strain OG1RF is that it is readily transformable, does not carry plasmids, and is not resistant to antibiotics commonly used for genetic studies (4).

View larger version (68K): [in this window] [in a new window]

FIG. 1. Accumulation of (p)ppGpp in E. faecalis after mupirocin treatment. (A) E. faecalis OG1RF treated with mupirocin for 15 or 30 min. (B) E. faecalis clinical isolates treated with mupirocin for 30 min. Exponentially grown cells were labeled with [32P]orthophosphate in FMC and treated with 50 µg ml–1 mupirocin for the times (minutes) indicated. Nucleotide acid extracts were spotted onto PEI-cellulose plates for TLC in 1.5 M KH2PO4. The identities of the radioactive spots were confirmed by comigration with GTP, GP5, and GP4 standards.

(p)ppGpp accumulates under selected environmental stress conditions. Enterococci are well known for their capacity to survive in harsh environments. Here we assessed (p)ppGpp levels in OG1RF cells subjected to acid, alkaline, or heat shock. Under the conditions tested, (p)ppGpp was found to accumulate in cells subjected to heat (60°C) or alkaline (pH 10) shock but not in cells subjected to acid shock (pH 5) ( Fig. 2). Time course experiments confirmed the transient accumulation of (p)ppGpp pools in cells subjected to heat or alkaline shock (data not shown).

View larger version (68K): [in this window] [in a new window]

FIG. 2. (p)ppGpp profile of E. faecalis OG1RF under selected stress conditions. Exponentially grown cells were labeled with [32P]orthophosphate in FMC and subjected to the stress condition indicated for 60 min. Acid extracts were spotted onto PEI-cellulose plates for TLC in 1.5 M KH2PO4.

Vancomycin treatment triggers (p)ppGpp accumulation. The spread of VRE strains constitutes a major clinical problem in hospital settings. Vancomycin is a glycopeptide that acts on gram-positive organisms by inhibiting cell wall biosynthesis. This molecule attaches to the lipid II precursor at its D-Ala-D-Ala peptide side chain, thereby inhibiting transglycosylation of cell wall subunits. Cell envelope stress responses have been linked to general stress responses (7) and to the overall homeostasis of gram-positive bacteria (18). Moreover, it has been reported that the intracellular concentration of (p)ppGpp is linked to the intrinsic resistance to antimicrobial agents in bacteria (14, 19, 20, 40). TLC analysis of nucleotide extracts clearly indicated that (p)ppGpp accumulates to significantly high levels in OG1RF cells treated with inhibitory concentrations of vancomycin (Fig. 3). Interestingly, treatment with inhibitory concentrations of ampicillin, a β-lactam antibiotic that also inhibits cell wall biosynthesis, did not result in (p)ppGpp accumulation (Fig. 3). The kinetics of (p)ppGpp accumulation, peaking after 60 min, were considerably slower than the kinetics observed in mupirocin-treated cells.

View larger version (80K): [in this window] [in a new window]

FIG. 3. Accumulation of (p)ppGpp in E. faecalis OG1RF after vancomycin treatment. Exponentially grown cells were labeled with [32P]orthophosphate in FMC and treated with 32 µg ml–1 ampicillin (A) or 10 µg ml–1 vancomycin (V) for 60 min. Control cells (C) were kept untreated and labeled for the duration of the experiment. Acid extracts were spotted onto PEI-cellulose plates for TLC in 1.5 M KH2PO4.

Identification of genes encoding (p)ppGpp synthetases in E. faecalis. Previously we have shown that production of (p)ppGpp by S. mutans is catalyzed by three enzymes: RelA, RelP, and RelQ (26). While RelA and RelQ appear to be ubiquitously distributed in the genome of low-GC gram-positive bacteria, BLAST searches indicated that RelP homologues are not ubiquitously distributed in gram-positive cocci, including E. faecalis V583 (37). The E. faecalis RelA (EF1974) and RelQ (EF2671) putative proteins share high levels of identity with their counterparts in S. mutans (78% and 80% similarities, respectively). Recently the complete genome of E. faecalis OG1RF became available (4). BLAST searches of the OG1RF genome and searches in the preliminary sequences of strains TX0104 and H22 available at the Baylor College of Medicine Human Genome Sequencing Center (http://www.hgsc.bcm.tmc.edu) identified putative RelA and RelQ homologues but not RelP. Thus, it appears that (p)ppGpp synthesis is catalyzed by only two enzymes in E. faecalis: RelA and RelQ.

RelA is the major synthetase responsible for (p)ppGpp accumulation. A markerless genetic exchange system was used to construct in-frame deletions in the relA and relQ genes of E. faecalis OG1RF. In order to rule out the possibility that polar effects on genes downstream of relA and relQ (ef1974 and ef2671, respectively) may have contributed to phenotypes of the relA and relQ strains, real-time PCR was used to confirm that expression of the genes apparently cotranscribed with relA and relQ, ef1973 and ef2670, respectively, was not affected in the mutant strains (data not shown). The (p)ppGpp profile of relA, relQ, and relAQ indicates that RelA is the major enzyme responsible for the transient accumulation of (p)ppGpp during mupirocin or vancomycin treatment (Fig. 4). Although it does not appear to be involved in the transient accumulation of (p)ppGpp, RelQ appears to be responsible for maintaining basal levels of alarmone during homeostatic growth, since only the relAQ double mutant displayed an apparent (p)ppGpp⁰ phenotype (Fig. 4).

View larger version (85K): [in this window] [in a new window]

FIG. 4. Accumulation of (p)ppGpp in E. faecalis OG1RF, relA, relQ, and relAPQ strains after mupirocin or vancomycin treatment. Exponentially grown cells were labeled with [32P]orthophosphate in FMC and treated with 50 µg ml–1 mupirocin for 15 min or 10 µg ml–1 vancomycin for 60 min. C, untreated control cells; M, mupirocin-treated cells; V, Vancomycin-treated cells. Acid extracts were spotted onto PEI-cellulose plates for TLC in 1.5 M KH2PO4.

Growth characteristics, stress tolerance, and biofilm formation by the relA, relQ, and relAQ strains. The results described above prompted us to investigate the role of RelA and RelQ in the physiology of E. faecalis. Analysis of growth rates of the mutants in BHI indicated that the relQ and relAQ strains grew as well as the parent strain whereas the relA strain grew slightly slower (Fig. 5). The ability of the relA, relQ, and relAQ strains to grow under a variety of stress conditions was examined (Fig. 6). No differences in growth between the mutants and parent strain were observed when cells were grown at pH 9 or in the presence of detergents (0.003% sodium dodecyl sulfate or 0.02% deoxycholate) (data not shown). In comparison to its parent, the relA strain grew poorly or considerably slower at 48°C, at pH 5, or in the presence of 5% NaCl or 2 mM H₂O₂ (Fig. 6). Inactivation of relQ alone did not affect cell growth under any of the conditions tested (Fig. 6). Complete elimination of (p)ppGpp in the relAQ strain restored many of the growth defects of the relA strain, with the exception of growth at 48°C or in the presence of H₂O₂. Compared to the parent strain, the relAQ strain grew slowly and had low growth yields at 48°C. Surprisingly, the relAQ strain grew faster and to a higher growth yield than its parent in the presence of H₂O₂ (Fig. 6).

View larger version (34K): [in this window] [in a new window]

FIG. 5. Growth curves of E. faecalis OG1RF, relA, relQ, and relAQ strains in BHI, determined using the Bioscreen growth reader monitor. The results represent the means ± standard deviations of three independent experiments.

View larger version (22K): [in this window] [in a new window]

FIG. 6. Growth of E. faecalis OG1RF, relA, relQ, and relAQ strains under stress conditions, determined using the Bioscreen growth reader monitor. The results represent the means ± standard deviations of three independent experiments.

We also tested the susceptibilities of the mutant strains to HCl, H₂O₂, and sodium hypochlorite using disk diffusion assays. Based on the diameters of the zone of inhibition for each compound tested, the relA strain was more sensitive to HCl and H₂O₂, but no differences were observed in the inhibition zone caused by sodium hypochlorite (Table 3). No significant differences in sensitivity to any of the tested conditions were observed among wild-type, relQ, and relAQ strains. To test the abilities of the strains to grow on BHI plates at high temperatures, exponentially growing cells were serially diluted and aliquots were spotted onto BHI plates that were incubated at 45° and 50°C. No differences were observed when strains were grown at 45°C. However, consistent with the slow-growth phenotype at 48°C in broth, the relAQ strain was more sensitive to growth at 50°C by 1 log (Table 3).

View this table: [in this window] [in a new window]

TABLE 3. Phenotypes of the relA, relQ, and relAQ strains in relation to that of OG1RF (wild-type strain) in disc diffusion and plate titration assays

The capacity of the mutants to form biofilms on polystyrene microtiter plates was also assessed. Quantitative analysis of biofilms formed by the relA, relQ, and relAQ mutants did not differ from that of biofilms formed by the parent OG1RF strain (data not shown). However, it is important to acknowledge the limitations of the microtiter plate assay. This method is based on batch cultures grown under static conditions that fail to reproduce the physicochemical environment that is encountered in vivo. Therefore, these data must be interpreted with caution, and it is possible that under certain conditions, changes in (p)ppGpp pools may affect biofilm formation by E. faecalis.

Tolerance to vancomycin is enhanced in the relA strain but diminished in the relQ and relAQ strains. The accumulation of (p)ppGpp in cells treated with vancomycin suggests that these nucleotides could be involved in the intrinsic tolerance of the organism to this antimicrobial drug. Compared to the wild-type strain (MIC = 8 µg ml^–1), the relQ and relAQ strains exhibited lower MICs for vancomycin (4 µg ml^–1). No differences in the MICs were observed between the parent and relA strains. Next, we tested the ability of E. faecalis OG1RF and its rel derivatives to grow in the presence of subinhibitory concentrations of vancomycin. Compared to the growth of the wild-type strain in the presence of 2.5 µg ml^–1 vancomycin, the relQ strain grew slower whereas growth of the relAQ strain was severely impaired (Fig. 7A). Surprisingly, the relA strain grew considerably faster than the wild-type strain (Fig. 7A). Time-kill kinetic studies were conducted using a concentration equal to five times the MIC of vancomycin for OG1RF (40 µg ml^–1). In comparison to the parent strain, OG1RF, the relQ and relAQ strains were more rapidly killed whereas the relA strain was more resistant to vancomycin killing (Fig. 7B).

View larger version (15K): [in this window] [in a new window]

FIG. 7. Growth and time-kill curves of E. faecalis OG1RF, relA, relQ, and relAQ strains in the presence of vancomycin. (A) Growth curves in BHI containing 2.5 µg ml–1 vancomycin. (B) Time-kill curves of logarithmic-phase cultures treated with 40 µg ml–1 vancomycin. Viable counts were determined by plating known dilutions of the samples on BHI plates every 24 h.

Virulence of the relAQ mutant was attenuated in the C. elegans model. To determine whether disruption of one or both (p)ppGpp synthetases affected E. faecalis virulence, the relA, relQ, and relAQ mutants were tested for their ability to kill C. elegans (Fig. 8). Compared with the wild-type strain, OG1RF, virulence of the relAQ strain was highly attenuated (P < 0.0001). There were no significant differences in killing among the relA and relQ strains.

View larger version (18K): [in this window] [in a new window]

FIG. 8. Killing of C. elegans by E. faecalis OG1RF and its derivatives. Exposure of C. elegans to the relA and relQ mutants did not cause a significant difference in killing from that with the wild-type strain, OG1RF (P = 0.8089 and 0.8895, respectively). However, the relAQ mutant was significantly attenuated (P < 0.0001). This experiment was repeated three times with similar results.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
In this report, (p)ppGpp profiles of cells subjected to stress and mutational analysis of genes involved in alarmone metabolism provided unequivocal evidence that production of (p)ppGpp is an integral part of the core stress responses of E. faecalis. More specifically, it was demonstrated that E. faecalis accumulates the alarmone (p)ppGpp in response to amino acid starvation, and more importantly, it reveals that (p)ppGpp modulates environmental stress responses, vancomycin tolerance, and virulence in this important nosocomial pathogen.

Until recently, bifunctional RelA was considered the sole enzyme responsible for controlling (p)ppGpp metabolism in gram-positive bacteria. However, two related small enzymes, designated RelP and RelQ, were recently identified and shown to function as true alarmone synthetases in S. mutans, S. pneumoniae, and B. subtilis (3, 26, 34). While RelA and RelQ appear to be ubiquitous in the genome of many gram-positive organisms, RelP was found to be absent in several organisms, including E. faecalis (4, 37). The contributions of each enzyme to (p)ppGpp metabolism have been partially assigned in S. mutans and B. subtilis. It was demonstrated that RelP and RelQ play an important role in cell homeostasis by producing low levels of alarmone during nonstressful conditions, whereas RelA appears to have retained the function of Rel/Spo-like proteins and is the major enzyme responsible for the stringent response, i.e., the rapid accumulation of (p)ppGpp in response to amino acid starvation (26, 35). Notably, RelA is the only enzyme also acting as a (p)ppGpp phosphohydrolase, suggesting that in addition to being responsible for the rapid and transient accumulation of (p)ppGpp during starvation, RelA plays a key role by controlling the intracellular (p)ppGpp/GTP/GDP ratios during homeostatic growth.

The (p)ppGpp measurements using the E. faecalis relA, relQ, and relAQ mutants reveal a pattern similar to that described for S. mutans and B. subtilis (26, 34), with the caveat that RelP is not found in E. faecalis (4, 37). Moreover, the growth characteristics of the E. faecalis relA, relQ, and relAQ mutant strains mirrored the growth behavior of the relA, relQ, and relAPQ strains of S. mutans and B. subtilis (26, 34). In both S. mutans and B. subtilis, the slow-growth phenotype of relA strains could be restored when the RelP and RelQ synthases were simultaneously inactivated, resulting in a (p)ppGpp⁰ phenotype (26, 34). Similarly, the E. faecalis relAQ strain grew as well as the parental strain; thus, the slow growth of the E. faecalis relA mutant is most likely a result of the inability of the strain to hydrolyze (p)ppGpp synthesized by RelQ.

The association of (p)ppGpp levels with resistance to antibiotics has been observed in E. coli (14, 19, 38, 40, 50). In most cases, antibiotic resistance was linked to low growth rates due to the stringent response and to reductions in autolytic activity (19, 50). Moreover, it has been demonstrated that artificially raising (p)ppGpp levels increased β-lactam tolerance in E. coli (19), and mutant cells lacking RelA were more susceptible to β-lactams (38). More recently, a direct correlation between intracellular (p)ppGpp levels and resistance to microcin J25, a plasmid-encoded antibacterial peptide, was established (40). In this latter case, resistance to microcin J25 was shown to involve (p)ppGpp-dependent induction of an efflux pump responsible for lowering the intracellular levels of the peptide (40). Despite its association with antibiotic resistance in E. coli, the role of (p)ppGpp in multitolerant bacteria, such as VRE, has not been evaluated. Here, we demonstrated that tolerance to vancomycin is intimately associated with (p)ppGpp pools. Although RelA is the enzyme responsible for rapid accumulation of (p)ppGpp, when exposed to inhibitory concentrations of vancomycin, the relA mutant had the same MIC as the wild-type strain, grew faster in the presence of subinhibitory concentrations of the drug, and survived better in time-kill studies. On the other hand, the relQ and relAQ strains had a lower MIC and slow or impaired growth in the presence of subinhibitory concentrations and were killed more rapidly by vancomycin, characteristics that were exacerbated in the relAQ strain. Considering that the relA strain, which is unable to break down (p)ppGpp, has high background levels of alarmone (synthesized by RelQ), that the relQ mutant produces lower basal (p)ppGpp pools (through RelA), and that the relAQ strain is completely unable to synthesize (p)ppGpp, one can speculate that higher basal levels of (p)ppGpp increase the expression of vancomycin tolerance/resistance determinants in E. faecalis. In many ways, because the relA strain grew better in the presence of subinhibitory concentrations of vancomycin, this result is in stark contrast with earlier findings for E. coli that indicated that antibiotic tolerance was linked to slow growth and reduced autolysis that was dependent on a functional RelA (13, 50). However, it is important to note that recent studies revealed that bacteria have evolved different modes of (p)ppGpp regulation and that the effects of (p)ppGpp on cell physiology vary greatly among different organisms (26, 34, 41). Presently it is not clear whether (p)ppGpp has a direct role in the expression of genes that confer vancomycin tolerance to E. faecalis or if it initiates a regulatory cascade that leads to tolerance. Future efforts aiming to dissect the scope of the (p)ppGpp regulon will help us identify potential downstream genes and pathways responsible for these effects.

It was interesting to note that there were clear phenotypic differences between strains expressing different levels of (p)ppGpp. While it appears that basal levels of (p)ppGpp produced by RelQ play a fundamental role in vancomycin tolerance, a functional RelA protein seems to be of greater relevance when cells are under environmental stress. However, it is possible that the reduced ability of the relA strain to grow under stress was due to toxic accumulation of (p)ppGpp through RelQ. If this is true, the key function of RelA during environmental stress may be to fine-tune basal levels of (p)ppGpp by virtue of its unique capacity to control (p)ppGpp/GTP ratios. This appears to be the case in S. mutans, since several experiments have suggested that one of the key roles of RelA is to limit the amount of (p)ppGpp that is allowed to accumulate in the cells from the action of RelP and RelQ (26, 35).

In the nematode C. elegans model, adult worms feeding on lawns of E. faecalis were killed over the course of several days in an infectious process that reproduces several aspects of human gram-positive pathogenesis (11). Furthermore, known virulence factors required for E. faecalis pathogenesis in mammalian model systems were also shown to be important for nematode killing and vice-versa (11, 29, 45). Here we showed that virulence of the relAQ double mutant, which is completely unable to produce (p)ppGpp, was highly attenuated in the C. elegans model. Interestingly, this was not the case for the relA and relQ single mutants, which produce basal levels of (p)ppGpp, and in the case of relQ, the mutant is capable of synthesizing large amounts of (p)ppGpp as part of a RelA-dependent stringent response. Therefore, it appears that basal levels of (p)ppGpp, rather than the stringent response, constitute the key factor controlling E. faecalis virulence in the C. elegans model.

In summary, this report reveals that (p)ppGpp plays an important role in stress tolerance and may be a key factor regulating tolerance and growth in the presence of vancomycin, two major factors that contribute to the emergence of E. faecalis as a pathogen. In addition, by using the C. elegans model of infection, we were able to demonstrate that (p)ppGpp is required for full virulence of E. faecalis. The discovery that the (p)ppGpp alarmone is associated with vancomycin tolerance in E. faecalis and possibly tolerance to other antibiotics is of particular importance. Although tolerant strains are not drug resistant, these strains retain the capacity to grow once the drug is discontinued and are thereby implicated in treatment failure and relapsing disease, especially when grown in biofilms (27). Moreover, bacterial tolerance facilitates the appearance of drug resistance, especially in organisms such as enterococci and Staphylococcus aureus, which can rapidly acquire resistance determinants from its surrounding environment. Although the (p)ppGpp-mediated stringent response is well known to protect the cells during starvation by shutting down global gene expression and by selectively activating transcription of genes involved in amino acid biosynthesis and stress survival, this report and others (26, 34) indicate that subtle changes in (p)ppGpp pools can dramatically affect cell homeostasis. Studies are under way to fully understand how and to what extent (p)ppGpp pools control virulence-related events in E. faecalis.

 
We are most grateful to Maria da Gloria Carvalho and Bernard Beall for clinical isolates of E. faecalis, Gary Dunny for strains and plasmids, and Roberta Faustoferri for critical reading of the manuscript.

This study was partially supported by the NIDCR Training Program in Oral Science Grant T32 DE007202 to J.A. and J.K.K., NIH, R21AI078104 to D.A.G., and a Ralph H. & Ruth J. McCullough Foundation award to V.C.

 
* Corresponding author. Mailing address: Center for Oral Biology, Box 611, 601 Elmwood Ave., University of Rochester Medical Center, Rochester, NY 14642. Phone: (585) 275-1850. Fax: (585) 276-0190. E-mail: jose_lemos{at}urmc.rochester.edu

Published ahead of print on 23 January 2009.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 

1
1. Ahn, S. J., J. A. Lemos, and R. A. Burne. 2005. Role of HtrA in growth and competence of Streptococcus mutans UA159. J. Bacteriol. 187:3028-3038.[Abstract/Free Full Text]
2
2. Balzer, G. J., and R. J. McLean. 2002. The stringent response genes relA and spoT are important for Escherichia coli biofilms under slow-growth conditions. Can. J. Microbiol. 48:675-680.[CrossRef][Medline]
3
3. Battesti, A., and E. Bouveret. 7 November 2008. Bacteria possessing two RelA/SpoT-like proteins have evolved a specific stringent response involving the acyl carrier protein-SpoT interaction. J. Bacteriol. doi:10.1128/JB.01195-08.[Abstract/Free Full Text]
4
4. Bourgogne, A., D. A. Garsin, X. Qin, K. V. Singh, J. Sillanpaa, S. Yerrapragada, Y. Ding, S. Dugan-Rocha, C. Buhay, H. Shen, G. Chen, G. Williams, D. Muzny, A. Maadani, K. A. Fox, J. Gioia, L. Chen, Y. Shang, C. A. Arias, S. R. Nallapareddy, M. Zhao, V. P. Prakash, S. Chowdhury, H. Jiang, R. A. Gibbs, B. E. Murray, S. K. Highlander, and G. M. Weinstock. 2008. Large scale variation in Enterococcus faecalis illustrated by the genome analysis of strain OG1RF. Genome Biol. 9:R110.[CrossRef][Medline]
5
5. Braeken, K., M. Moris, R. Daniels, J. Vanderleyden, and J. Michiels. 2006. New horizons for (p)ppGpp in bacterial and plant physiology. Trends Microbiol. 14:45-54.[CrossRef][Medline]
6
6. Bugrysheva, J. V., A. V. Bryksin, H. P. Godfrey, and F. C. Cabello. 2005. Borrelia burgdorferi rel is responsible for generation of guanosine-3'-diphosphate-5'-triphosphate and growth control. Infect. Immun. 73:4972-4981.[Abstract/Free Full Text]
7
7. Cao, M., T. Wang, R. Ye, and J. D. Helmann. 2002. Antibiotics that inhibit cell wall biosynthesis induce expression of the Bacillus subtilis sigma(W) and sigma(M) regulons. Mol. Microbiol. 45:1267-1276.[CrossRef][Medline]
8
8. Cashel, M., D. R. Gentry, V. J. Hernandez, and D. Vinella. 1996. The stringent response, p. 1458-1496. In F. C. Neidhardt, R. C. Curtiss III, J. L. Ingraham, E. C. C. Lin, K. B. Low, B. Magasanik, W. S. Reznikoff, M. Riley, M. Schaechter, and A. E. Umbarger (ed.), Escherichia coli and Salmonella: cellular and molecular biology, 2nd ed., vol. 1. ASM Press, Washington, DC.
9
9. Dahl, J. L., C. N. Kraus, H. I. Boshoff, B. Doan, K. Foley, D. Avarbock, G. Kaplan, V. Mizrahi, H. Rubin, and C. E. Barry III. 2003. The role of RelMtb-mediated adaptation to stationary phase in long-term persistence of Mycobacterium tuberculosis in mice. Proc. Natl. Acad. Sci. USA 100:10026-10031.[Abstract/Free Full Text]
10
10. Erickson, D. L., J. L. Lines, E. C. Pesci, V. Venturi, and D. G. Storey. 2004. Pseudomonas aeruginosa relA contributes to virulence in Drosophila melanogaster. Infect. Immun. 72:5638-5645.[Abstract/Free Full Text]
11
11. Garsin, D. A., C. D. Sifri, E. Mylonakis, X. Qin, K. V. Singh, B. E. Murray, S. B. Calderwood, and F. M. Ausubel. 2001. A simple model host for identifying Gram-positive virulence factors. Proc. Natl. Acad. Sci. USA 98:10892-10897.[Abstract/Free Full Text]
12
12. Gaynor, E. C., D. H. Wells, J. K. MacKichan, and S. Falkow. 2005. The Campylobacter jejuni stringent response controls specific stress survival and virulence-associated phenotypes. Mol. Microbiol. 56:8-27.[CrossRef][Medline]
13
13. Goodell, W., and A. Tomasz. 1980. Alteration of Escherichia coli murein during amino acid starvation. J. Bacteriol. 144:1009-1016.[Abstract/Free Full Text]
14
14. Greenway, D. L., and R. R. England. 1999. The intrinsic resistance of Escherichia coli to various antimicrobial agents requires ppGpp and sigma S. Lett. Appl. Microbiol. 29:323-326.[CrossRef][Medline]
15
15. Huycke, M. M., D. F. Sahm, and M. S. Gilmore. 1998. Multiple-drug resistant enterococci: the nature of the problem and an agenda for the future. Emerg. Infect. Dis. 4:239-249.[Medline]
16
16. Jeong, J. H., M. Song, S. I. Park, K. O. Cho, J. H. Rhee, and H. E. Choy. 2008. Salmonella gallinarum requires ppGpp to internalize and survive in animal cells. J. Bacteriol. 190:6340-6350.[Abstract/Free Full Text]
17
17. Jett, B. D., M. M. Huycke, and M. S. Gilmore. 1994. Virulence of enterococci. Clin. Microbiol. Rev. 7:462-478.[Abstract/Free Full Text]
18
18. Jordan, S., M. I. Hutchings, and T. Mascher. 2008. Cell envelope stress response in Gram-positive bacteria. FEMS Microbiol. Rev. 32:107-146.[Medline]
19
19. Joseleau-Petit, D., D. Thevenet, and R. D'Ari. 1994. ppGpp concentration, growth without PBP2 activity, and growth-rate control in Escherichia coli. Mol. Microbiol. 13:911-917.[CrossRef][Medline]
20
20. Kim, S., K. Watanabe, H. Suzuki, and M. Watarai. 2005. Roles of Brucella abortus SpoT in morphological differentiation and intramacrophagic replication. Microbiology 151:1607-1617.[Abstract/Free Full Text]
21
21. Korch, S. B., T. A. Henderson, and T. M. Hill. 2003. Characterization of the hipA7 allele of Escherichia coli and evidence that high persistence is governed by (p)ppGpp synthesis. Mol. Microbiol. 50:1199-1213.[CrossRef][Medline]
22
22. Kristich, C. J., J. R. Chandler, and G. M. Dunny. 2007. Development of a host-genotype-independent counterselectable marker and a high-frequency conjugative delivery system and their use in genetic analysis of Enterococcus faecalis. Plasmid 57:131-144.[CrossRef][Medline]
23
23. Kristich, C. J., V. T. Nguyen, T. Le, A. M. Barnes, S. Grindle, and G. M. Dunny. 2008. Development and use of an efficient system for random mariner transposon mutagenesis to identify novel genetic determinants of biofilm formation in the core Enterococcus faecalis genome. Appl. Environ. Microbiol. 74:3377-3386.[Abstract/Free Full Text]
24
24. Leenhouts, K., G. Buist, A. Bolhuis, A. ten Berge, J. Kiel, I. Mierau, M. Dabrowska, G. Venema, and J. Kok. 1996. A general system for generating unlabelled gene replacements in bacterial chromosomes. Mol. Gen. Genet. 253:217-224.[CrossRef][Medline]
25
25. Lemos, J. A., T. A. Brown, Jr., and R. A. Burne. 2004. Effects of RelA on key virulence properties of planktonic and biofilm populations of Streptococcus mutans. Infect. Immun. 72:1431-1440.[Abstract/Free Full Text]
26
26. Lemos, J. A., V. K. Lin, M. M. Nascimento, J. Abranches, and R. A. Burne. 2007. Three gene products govern (p)ppGpp production by Streptococcus mutans. Mol. Microbiol. 65:1568-1581.[CrossRef][Medline]
27
27. Lewis, K. 2007. Persister cells, dormancy and infectious disease. Nat. Rev. Microbiol. 5:48-56.[CrossRef][Medline]
28
28. Loo, C. Y., D. A. Corliss, and N. Ganeshkumar. 2000. Streptococcus gordonii biofilm formation: identification of genes that code for biofilm phenotypes. J. Bacteriol. 182:1374-1382.[Abstract/Free Full Text]
29
29. Maadani, A., K. A. Fox, E. Mylonakis, and D. A. Garsin. 2007. Enterococcus faecalis mutations affecting virulence in the Caenorhabditis elegans model host. Infect. Immun. 75:2634-2637.[Abstract/Free Full Text]
30
30. Mechold, U., M. Cashel, K. Steiner, D. Gentry, and H. Malke. 1996. Functional analysis of a relA/spoT gene homolog from Streptococcus equisimilis. J. Bacteriol. 178:1401-1411.[Abstract/Free Full Text]
31
31. Mechold, U., and H. Malke. 1997. Characterization of the stringent and relaxed responses of Streptococcus equisimilis. J. Bacteriol. 179:2658-2667.[Abstract/Free Full Text]
32
32. Mohamed, J. A., and D. B. Huang. 2007. Biofilm formation by enterococci. J. Med. Microbiol. 56:1581-1588.[Abstract/Free Full Text]
33
33. Murray, B. E. 2000. Vancomycin-resistant enterococcal infections. N. Engl. J. Med. 342:710-721.[Free Full Text]
34
34. Nanamiya, H., K. Kasai, A. Nozawa, C. S. Yun, T. Narisawa, K. Murakami, Y. Natori, F. Kawamura, and Y. Tozawa. 2008. Identification and functional analysis of novel (p)ppGpp synthetase genes in Bacillus subtilis. Mol. Microbiol. 67:291-304.[Medline]
35
35. Nascimento, M. M., J. A. Lemos, J. Abranches, V. K. Lin, and R. A. Burne. 2008. Role of RelA of Streptococcus mutans in global control of gene expression. J. Bacteriol. 190:28-36.[Abstract/Free Full Text]
36
36. Paul, B. J., M. B. Berkmen, and R. L. Gourse. 2005. DksA potentiates direct activation of amino acid promoters by ppGpp. Proc. Natl. Acad. Sci. USA 102:7823-7828.[Abstract/Free Full Text]
37
37. Paulsen, I. T., L. Banerjei, G. S. Myers, K. E. Nelson, R. Seshadri, T. D. Read, D. E. Fouts, J. A. Eisen, S. R. Gill, J. F. Heidelberg, H. Tettelin, R. J. Dodson, L. Umayam, L. Brinkac, M. Beanan, S. Daugherty, R. T. DeBoy, S. Durkin, J. Kolonay, R. Madupu, W. Nelson, J. Vamathevan, B. Tran, J. Upton, T. Hansen, J. Shetty, H. Khouri, T. Utterback, D. Radune, K. A. Ketchum, B. A. Dougherty, and C. M. Fraser. 2003. Role of mobile DNA in the evolution of vancomycin-resistant Enterococcus faecalis. Science 299:2071-2074.[Abstract/Free Full Text]
38
38. Pisabarro, A. G., M. A. De Pedro, and E. E. Ishiguro. 1990. Dissociation of the ampicillin-induced lysis of amino acid-deprived Escherichia coli into two stages. J. Bacteriol. 172:2187-2190.[Abstract/Free Full Text]
39
39. Pizarro-Cerda, J., and K. Tedin. 2004. The bacterial signal molecule, ppGpp, regulates Salmonella virulence gene expression. Mol. Microbiol. 52:1827-1844.[CrossRef][Medline]
40
40. Pomares, M. F., P. A. Vincent, R. N. Farias, and R. A. Salomon. 2008. Protective action of ppGpp in microcin J25-sensitive strains. J. Bacteriol. 190:4328-4334.[Abstract/Free Full Text]
41
41. Potrykus, K., and M. Cashel. 2008. (p)ppGpp: still magical? Annu. Rev. Microbiol. 62:35-51.[Medline]
42
42. Primm, T. P., S. J. Andersen, V. Mizrahi, D. Avarbock, H. Rubin, and C. E. Barry III. 2000. The stringent response of Mycobacterium tuberculosis is required for long-term survival. J. Bacteriol. 182:4889-4898.[Abstract/Free Full Text]
43
43. Richards, M. J., J. R. Edwards, D. H. Culver, and R. P. Gaynes. 2000. Nosocomial infections in combined medical-surgical intensive care units in the United States. Infect. Control Hosp. Epidemiol. 21:510-515.[CrossRef][Medline]
44
44. Ruoff, K. L., L. de la Maza, M. J. Murtagh, J. D. Spargo, and M. J. Ferraro. 1990. Species identities of enterococci isolated from clinical specimens. J. Clin. Microbiol. 28:435-437.[Abstract/Free Full Text]
45
45. Sifri, C. D., E. Mylonakis, K. V. Singh, X. Qin, D. A. Garsin, B. E. Murray, F. M. Ausubel, and S. B. Calderwood. 2002. Virulence effect of Enterococcus faecalis protease genes and the quorum-sensing locus fsr in Caenorhabditis elegans and mice. Infect. Immun. 70:5647-5650.[Abstract/Free Full Text]
46
46. Taylor, C. M., M. Beresford, H. A. Epton, D. C. Sigee, G. Shama, P. W. Andrew, and I. S. Roberts. 2002. Listeria monocytogenes relA and hpt mutants are impaired in surface-attached growth and virulence. J. Bacteriol. 184:621-628.[Abstract/Free Full Text]
47
47. Terleckyj, B., N. P. Willett, and G. D. Shockman. 1975. Growth of several cariogenic strains of oral streptococci in a chemically defined medium. Infect. Immun. 11:649-655.[Abstract/Free Full Text]
48
48. Traxler, M. F., D. E. Chang, and T. Conway. 2006. Guanosine 3',5'-bispyrophosphate coordinates global gene expression during glucose-lactose diauxie in Escherichia coli. Proc. Natl. Acad. Sci. USA 103:2374-2379.[Abstract/Free Full Text]
49
49. Traxler, M. F., S. M. Summers, H. T. Nguyen, V. M. Zacharia, G. A. Hightower, J. T. Smith, and T. Conway. 2008. The global, ppGpp-mediated stringent response to amino acid starvation in Escherichia coli. Mol. Microbiol. 68:1128-1148.[CrossRef][Medline]
50
50. Tuomanen, E., and A. Tomasz. 1986. Induction of autolysis in nongrowing Escherichia coli. J. Bacteriol. 167:1077-1080.[Abstract/Free Full Text]
51
51. Weigel, L. M., D. B. Clewell, S. R. Gill, N. C. Clark, L. K. McDougal, S. E. Flannagan, J. F. Kolonay, J. Shetty, G. E. Killgore, and F. C. Tenover. 2003. Genetic analysis of a high-level vancomycin-resistant isolate of Staphylococcus aureus. Science 302:1569-1571.[Abstract/Free Full Text]
52
52. Wendrich, T. M., and M. A. Marahiel. 1997. Cloning and characterization of a relA/spoT homologue from Bacillus subtilis. Mol. Microbiol. 26:65-79.[CrossRef][Medline]
53
53. Whitehead, K. E., G. M. Webber, and R. R. England. 1998. Accumulation of ppGpp in Streptococcus pyogenes and Streptococcus rattus following amino acid starvation. FEMS Microbiol. Lett. 159:21-26.[CrossRef][Medline]
54
54. Zhang, S., and W. G. Haldenwang. 2003. RelA is a component of the nutritional stress activation pathway of the Bacillus subtilis transcription factor sigma B. J. Bacteriol. 185:5714-5721.[Abstract/Free Full Text]

---

Journal of Bacteriology, April 2009, p. 2248-2256, Vol. 191, No. 7
0021-9193/09/$08.00+0     doi:10.1128/JB.01726-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Yan, X., Zhao, C., Budin-Verneuil, A., Hartke, A., Rince, A., Gilmore, M. S., Auffray, Y., Pichereau, V. (2009). The (p)ppGpp synthetase RelA contributes to stress adaptation and virulence in Enterococcus faecalis V583. Microbiology 155: 3226-3237 [Abstract] [Full Text]  

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Abranches, J. Articles by Lemos, J. A. Search for Related Content PubMed PubMed Citation Articles by Abranches, J. Articles by Lemos, J. A.