Advertisement
JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

Originally published In Press as doi:10.1074/jbc.M313491200 on May 25, 2004

J. Biol. Chem., Vol. 279, Issue 33, 34183-34190, August 13, 2004
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
279/33/34183    most recent
M313491200v1
Right arrow Submit a Letter to Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Song, M.
Right arrow Articles by Choy, H. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Song, M.
Right arrow Articles by Choy, H. E.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

ppGpp-dependent Stationary Phase Induction of Genes on Salmonella Pathogenicity Island 1*

Miryoung Song{ddagger}§, Hyun-Ju Kim{ddagger}§, Eun Young Kim{ddagger}§, Minsang Shin{ddagger}§, Hyun Chul Lee{ddagger}§, Yeongjin Hong{ddagger}§, Joon Haeng Rhee{ddagger}§, Hyunjin Yoon¶, Sangryeol Ryu¶, Sangyong Lim¶, and Hyon E. Choy{ddagger}§||

From the {ddagger}Genome Research Center for Enteropathogenic Bacteria and Research Institute of Vibrio Infection and the §Department of Microbiology, Chonnam National University Medical College, Kwangju 501-746, South Korea and the Department of Food Science and Technology, School of Agricultural Biotechnology, Center for Agricultural Biomaterials, Seoul National University, Seoul, 151-742, South Korea

Received for publication, December 10, 2003 , and in revised form, April 30, 2004.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
We have examined expression of the genes on Salmonella pathogenicity island 1 (SPI1) during growth under the physiologically well defined standard growth condition of Luria-Bertani medium with aeration. We found that the central regulator hilA and the genes under its control are expressed at the onset of stationary phase. Interestingly, the two-component regulatory genes hilC/hilD, sirA/barA, and ompR, which are known to modulate expression from the hilA promoter (hilAp) under so-called "inducing conditions" (Luria-Bertani medium containing 0.3 M NaCl without aeration), acted under standard conditions at the stationary phase induction level. The induction of hilAp depended not on RpoS, the stationary phase sigma factor, but on the stringent signal molecule ppGpp. In the ppGpp null mutant background, hilAp showed absolutely no activity. The stationary phase induction of hilAp required spoT but not relA. Consistent with this requirement, hilAp was also induced by carbon source deprivation, which is known to transiently elevate ppGpp mediated by spoT function. The observation that amino acid starvation elicited by the addition of serine hydroxamate did not induce hilAp in a RelA+ SpoT+ strain suggested that, in addition to ppGpp, some other alteration accompanying entry into the stationary phase might be necessary for induction. It is speculated that during the course of infection Salmonella encounters various stressful environments that are sensed and translated to the intracellular signal, ppGpp, which allows expression of Salmonella virulence genes, including SPI1 genes.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Infection with Salmonella enterica serovar Typhimurium can cause a systemic, typhoid-like disease in mice. Following ingestion, bacteria can colonize the intestinal tract, penetrate the intestinal epithelium, and access systemic sites such as the spleen and liver through lymphatic and blood circulation (1). Passage of the bacteria through the intestinal lining is initiated by bacterial invasion into enterocytes and M cells (1–4). The invasion is mediated by a bacterial type III secretion system (TTSS)1 encoded by genes on Salmonella pathogenicity island 1 (SPI1) (5). The TTSS translocates bacterial effector proteins, also encoded on a SPI, into the host cell cytosol to reorganize the cytoskeleton, resulting in membrane ruffling and eventual bacterial uptake (6). Expression of the SPI1 secretion system and its secreted effectors is coordinately regulated by HilA encoded on SPI1, a member of the OmpR/ToxR family of transcriptional regulators (7). The genes on SPI1 regulated by HilA include invF and sicA (8–10). InvF, a member of the AraC/XylS family of transcriptional regulators, in conjunction with SicA, a TTSS chaperone, takes part in the coordinated regulation of SPI1-encoded genes.

Regulation of hilA expression has been studied extensively because of its central role in invasion gene activation. Environmental signals such as oxygen concentration, osmolarity, and the growth state of bacteria have been shown to influence the expression of hilA and the secretion of invasion-associated proteins (11, 12). Thus, most studies have been carried out using bacteria grown under so-called inducing conditions, namely high osmolarity and low oxygen conditions (LB containing 0.3 M NaCl without aeration). Studies of bacteria grown under these conditions have, to date, revealed that hilA expression is regulated by a complex array of regulatory systems including hilC/sirC/sprA (13–15), hilD (15), sirA/barA (16, 17), fis (18, 19), csrAB (16, 20), envZ/ompR (21), phoB (7), fadD (7), fliZ (7), hha (22), H-NS (19), and HU (19). Two of these genes, hilC and hilD, encode AraC-like transcriptional activators that activate hilA transcription by binding upstream of the hilA promoter DNA (15, 23, 24). Members of the phosphorylated response regulator superfamily involved in hilA expression include sirA/barA, envZ/ompR, phoR/phoB, and phoP/phoQ (7, 12, 17, 21). However, none of these regulatory systems has been shown to directly relay environmental signals to hilA expression.

Enteric bacteria elicit stringent control of ribosome production during the transition from exponential growth to the stationary phase (25, 26). The effector molecule of the stringent control modulation is the alarmone guanosine tetraphosphate ppGpp (27, 28). The ppGpp is synthesized by two synthetases, PSI and PSII, which are encoded by the relA and spoT genes, respectively. These two enzymes respond differently to environmental conditions. PSI is activated during amino acid starvation but is largely inactive during exponential growth; in contrast, PSII is mostly inactive during amino acid starvation but is active during exponential growth to determine basal levels and to respond to certain environmental stress factors, including deprivation of carbon or energy (29–34). Accumulation of ppGpp during the exponential phase of growth results in the reduction of stable RNA synthesis and the activation of certain types of mRNA synthesis.

In this study, we examined expression of SPI1 genes, including hilA under physiologically well defined standard growth conditions (LB with vigorous aeration), and observed that these genes were induced at the onset of the stationary phase. This stationary phase induction was, however, not dependent on the stationary phase-specific sigma factor {sigma}38 but on the stringent signal molecule ppGpp. Most interestingly, we found that the stationary phase hilAp induction depended not on RelA but on SpoT function. This suggests an unusual inducing role of the SpoT protein distinct from its ability to produce the stringent signal molecule ppGpp. We conclude that Salmonella virulence genes, including SPI1 genes, are expressed under stressed conditions in a ppGpp-dependent manner.


   MATERIALS AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Strains and Plasmids—The Salmonella strains, which were derived from 14028s, and the plasmids used in this study are listed in Table I. All bacterial strains were constructed by P22HT int transduction as described previously (35). The hilC::kan strain was constructed following the method developed by Datsenko and Wanner (36). The hilC carrying kan in the place of its open reading frame was generated by PCR amplification using the following pair of 60-nucleotide primers that included 40-nucleotide homology extensions and 20-nucleotide priming sequences with pKD13 as a template: 5'-TTCAATGAATAAATCAGTTGAGGCCATTAGCAATAATCACGTGTAGGCTGGAGCTGCTTC-3' (5' primer); and 5'-CTAATCCATTTATTAATGGAAATTTGTTCGGCTGTTGAAGATTCCGGGGATCCGTCGACC-3' (3' primer). The hilC sequences are underlined.


View this table:
[in this window]
[in a new window]
  		TABLE I
Strains and plasmids

 
The 1.4-kbp PCR products were purified and transformed into bacteria carrying a Red helper plasmid (pKD46) by electroporation. The electrocompetent cells were grown in LB broth with ampicillin and L-arabinose (1 mM) at 30 °C to an A600 of {approx}0.5. The mutants were confirmed by PCR using the original and common test primers 5'-CAGTCATAGCCGAATAGCCT-3' (k1) and 5'-CGGCCACAGTCGATGAATCC-3' (kt) for kan.

Growth Conditions—Except when indicated otherwise, cultures were grown in LB medium (Difco Laboratories) containing 1% NaCl with vigorous aeration at 37 °C. For solid support medium, 1.5% granulated agar (Difco Laboratories) was included. MacConkey lactose, nutrient broth, and brain heart infusion media were purchased from Difco Laboratories. Antibiotics were from Sigma. When present, the following antibiotics were added at the given concentrations: ampicillin, 50 µg/ml; chloramphenicol, 15 µg/ml; and tetracycline, 15 µg/ml. X-gal (Sigma) was used at 20 µg/ml. The carbon source starvation experiment was carried out in LB plus 0.1% glucose with {alpha}-methyl glucoside ({alpha}-MG; Sigma). Amino acid starvation experiment was carried out as described in Shand et al. (37) using DL-serine hydroxamate (SerHX; Sigma) in nutrient broth supplemented with serine (0.75 mM).

Analysis of Culture Supernatant—Cultures were grown overnight in 5 ml of LB broth with antibiotics and vigorous aeration and then harvested. Bacteria were pelleted at 8,000 x g for 15 min, and supernatants were immediately transferred to clean tubes. The supernatants were filtered through a 0.45-µm pore size syringe filter (Sartorius), and proteins were precipitated with cold trichloroacetic acid at a final concentration of 10%. The proteins were collected by centrifugation at 8,000 x g at 4 °C and resuspended in 1 ml of cold acetone. These mixtures were centrifuged for 10 min at 8,000 rpm at 4 °C, and pellets were resuspended in 20 µl of 1x PBS. The protein sample buffer containing {beta}-mercaptoethanol was added to the samples, which were boiled for 5 min, and proteins were separated by SDS-PAGE (7.5%). Proteins were visualized with silver stain (38).

{beta}-Galactosidase Assays—{beta}-galactosidase assays were performed as described by Miller (39) using cells permeabilized with Koch's lysis solution (40). {beta}-galactosidase-specific activity was expressed as Miller units (A420/min/A600/ml x 1000). To measure {beta}-galactosidase levels in bacteria at different stages of growth, fresh overnight cultures were diluted 1:50 into LB or the medium condition described in the text and grown at 37 °C until the cultures reached the stationary phase. Samples were taken for enzyme assay at regular time intervals. Each strain was assayed in triplicate, and average enzyme activities were plotted as a function of time.

Primer Extension Analysis—Total RNA was isolated from Salmonella grown statically using TRIzol reagent (Invitrogen). To study hilA and hisG transcriptions, the primers with 5'-TAATAATATTGTTATAACTAACTGTGATTA-3', which is complementary to positions 134–114 of the transcription start site of hilA, and 5'-ACTGGAAGATCTGAATGTCTTCCAGCACAC-3', which is complementary to positions 124–95 of the transcription start site of hisG, were used. 32P-labeled primers (50,000 cpm) were co-precipitated with 30 µg of total RNA. Primer extension reactions were performed as described by Shin et al. (41).

Invasion Assay—The assays were performed essentially as described previously (42). Monolayers for bacterial invasion were prepared by seeding 5 x 105 HEp-2 cells into each well of 24-well plates. The HEp-2 cells were grown in Dulbecco's modified Eagle's modified (Invitrogen) plus 10% fetal bovine serum (Invitrogen) at 37 °C with 5% CO2. Salmonellae prepared as described in the text were added to HEp-2 cells at a ratio of 10:1, and the mixture was incubated at 37 °C under 5% CO2 for 30 min. Infected cells were washed three times with phosphate-buffered saline (pH 7.4), Dulbecco's modified Eagle's medium containing gentamicin (5 mg/ml; Sigma) was added, and the mixture was incubated for an additional 60 min. Intracellular bacteria were harvested by extraction with lysis buffer (0.05% Triton X-100 in phosphate-buffered saline, pH 7.4), and replica was plated for colony counting on brain heart infusion agar plates.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Growth Phase-dependent Invasiveness of Bacteria Grown under Standard Conditions—The ability of Salmonellae to invade cultured nonphagocytic cells has been correlated with the expression of SPI1-encoded genes (43). In an attempt to investigate the regulation of invasion genes under a physiologically well defined standard growth conditions, we determined the invasiveness of bacteria grown under standard conditions (LB with aeration). In this experiment, an overnight culture of bacteria grown in LB was diluted 40-fold in the same media or a high salt media (LB plus 0.3 M NaCl) and grown with or without aeration, respectively. The high salt media without aeration was considered the "inducing condition" for the expression of SPI1 genes (11, 12). Fig. 1A shows Salmonellae growth under the two conditions. Under the standard condition, bacteria grew rapidly and reached the stationary phase in ~4 h. Under the inducing condition, the culture entered into the stationary phase at a much lower A600, <1 A600. Bacteria were sampled from the middle of the exponential phase (~2 h) and from the early (~4 h) and late (~12 h) stationary phases grown under the two conditions, and the invasiveness of each growth phase culture was determined using HEp-2 cells. In this experiment, the number of bacteria from various growth phases was adjusted to a multiplicity of infection of 10 (bacteria, 5 x 106; host cells, 5 x 105). Fig. 1B shows the actual number of intracellular bacteria that survived gentamicin treatment (10 µg/ml) and were recovered from the host cells following a 1-h incubation of bacteria and host cells. When grown under the standard condition (Fig. 1B, filled bars), the early stationary phase bacteria were found to be ~10–20-fold more invasive than the exponential phase and late stationary phase bacteria. By contrast, the invasiveness of bacteria grown under the inducing condition showed a different pattern; the early stationary phase culture was ~3-fold more invasive than the exponential phase culture but slightly less invasive than the late stationary culture (Fig. 1B, open bars). The maximum invasion was obtained with the early stationary culture grown under the standard condition. It was thought that the loss of invasiveness with the late stationary culture grown under the standard condition was due to the destruction of TTSS by continuous agitation of the culture. Thus, although the inducing condition might closely represent the intestinal milieu (11, 12), bacteria grown under the standard condition were used in the subsequent experiments to identify the factor(s) conferring the maximum invasiveness at the early stationary phase.



View larger version (16K):
[in this window]
[in a new window]
  		FIG. 1.
Host cell (Hep-2) invasion by the bacteria (14028s) grown in the inducing condition or standard growth condition (A and B) and the expression of representative secreted TTSS components (C). A, bacterial growth (A600) under the inducing condition (open circles) and the standard condition (closed circles). B, the actual number of intracellular gentamicin-resistant bacteria after the incubation of Hep-2 cells and bacterial cultures at different growth phases. Closed bars represent the invasiveness of bacteria grown under the standard condition, and open bars represent the invasiveness of bacteria grown under the inducing condition. C, proteins excreted into media during Salmonella growth under the standard condition on 7.5% SDS-PAGE gel. The secreted proteins SipA (89 kDa), SipB (67 kDa), SigD (62 kDa), and SipC (42 kDa), were identified by their sizes as described in Hong and Miller (38). Protein markers (Bio-Rad) are shown in the far left lane. MW, molecular mass.

 
Next, we determined the presence of secreted effector proteins encoded within SPI1 (38) in the cultures at different times grown under the standard condition (see Fig. 1C). Total supernatants of cultures at different phases were collected, precipitated with trichloroacetic acid, and analyzed on 7.5% SDS-PAGE gel (Fig. 1C). The volume of the supernatant was proportionally adjusted to the number of bacteria at each growth phase. The secreted effector proteins, namely SipA (89 kDa), SipB (67 kDa), SigD (62 kDa), and SipC (42 kDa), were detected only in the supernatant of cultures entering the stationary phase (4 h) and thereafter (6 h). Thus, Salmonellae at the entry of the stationary phase were most invasive because SPI1-encoded genes, including those constituting the TTSS apparatus and effector proteins, were expressed exclusively at this growth phase under the standard condition (see below).

Growth Phase-dependent Expression from the Promoters in SPI1—We analyzed the activity of the promoters driving expression of the genes involved in Salmonella invasion of host cells encoded on SPI1, namely the hilA, invF, and sicA promoters (abbreviated hilAp, invFp, and sicAp, respectively), during growth under the standard condition. To determine activity of these promoters, Salmonella typhimurium strains carrying lacZY genes transcriptionally fused to individual promoters on the chromosome (SMR2063; Fig. 2A) or a plasmid in the 14028s strain background (Fig. 3) were used. Bacteria were taken at regular time intervals, and {beta}-galactosidase activity representing the activity of each promoter during the course of growth was determined. Fig. 2 shows the hilAp activity determined under the standard and inducing growth conditions. Under the inducing condition, hilAp activity was about the same throughout the exponential and stationary phases. By contrast, hilAp activity under the standard growth condition was induced ~30-fold when the culture entered the stationary phase. hilAp activity under the standard condition was ~10-fold less during the exponential phase but ~3.5-fold more at the entry of the stationary phase as compared with the activities under the inducing condition. Thus, this result accounts for the different invasiveness of the cultures grown under the two conditions; the central regulator hilAp is selectively expressed at the onset of the stationary phase under the standard condition but is maintained at more or less the same level irrespective of the growth phase under the inducing condition. To further verify the hilAp induction under the standard growth condition, the hilAp specific transcript was monitored during the course of growth by the primer extension assay (Fig. 2B). The hilAp-specific RNA was detected at 3 h as culture entered the stationary phase, peaked at 5 h, and disappeared at 7 h.



View larger version (44K):
[in this window]
[in a new window]
  		FIG. 2.
Expression of hilAp::lacZY during Salmonella growth under the inducing (triangles) or standard condition (circles) (A) and expression of hilA under the standard growth condition (B). A, the curves with open symbols represent growth (A600), and the curves with closed symbols represent chromosomal hilAp activity as determined by {beta}-galactosidase assay (Miller units). B, right panel, expression of hilA under the standard growth condition as determined by primer extension analysis. Thirty micrograms of total Salmonella RNA extracted at each time point during growth was co-precipitated and annealed with end-labeled hilA primer. Reactions were performed as described under "Materials and Methods." The products were resolved on a 6% sequencing gel. Left panel shows the DNA sequencing ladder of the region around the hilA transcription initiation site. Arrow indicates the first nucleotide of the hilA transcript, the T in the circle.

 



View larger version (14K):
[in this window]
[in a new window]
  		FIG. 3.
Expression from hilAp (pMS009) (A), sicAp (pMS011) (B), and invFp (pMS010) (C) on the transcription fusion plasmid pRS415 during Salmonella growth under the standard growth condition. The curves with open symbols represent growth (A600), and the curves with closed symbols represent the activity of each promoter activity as determined by the {beta}-galactosidase assay (Miller units).

 
Subsequently, invF and sicA as well as hilA promoters on the pRS415 plasmid (44) were determined during growth under the standard condition (Fig. 3). The episomal hilAp activity (Fig. 3A) showed a similar pattern of induction at the onset of the stationary phase, but the magnitude of induction was significantly reduced to ~4-fold. The reduction was ascribed to the huge increase in the basal level activity at the exponential phase, as if a repressor acting at the exponential phase was titrated out by the episomal hilAp DNA. The invFp and sicAp activities were determined using the strain carrying the individual promoters fused to lacZYA on the pRS415. Both invFp (Fig. 3C) and sicAp (Fig. 3B) were increased >50-fold as the culture entered the stationary phase. The extension in the activation of downstream activators invF and sicA, as compared with that of the upstream activator hilA, might represent a magnification of the physiological response in cascade regulation. Taken together, these results clearly establish that the early stationary phase bacteria grown under the standard condition are the most invasive because of the selective expression of the central activator, hilA, and the consequent expression of the downstream activators invF and sicA under its control.

Regulation of Stationary Phase Induction of hilA Expression—We then set out to establish the molecular mechanism underlying the stationary phase induction of hilA under the standard growth condition. Stationary phase induction of gene expression in enteric bacteria is due at least in part to the stationary phase sigma factor {sigma}38, the rpoS gene product (45). The heat shock sigma factor ({sigma}24), the rpoE product, has also been shown recently to be strongly induced upon the entry of Salmonellae into the stationary phase (46, 47). We determined the chromosomal hilAp activity in the RpoS– mutant background and found that the stationary phase activation pattern was even greater than in the wild type (WT) (Fig. 4). In the RpoE– mutant background, no difference was observed. Thus, the stationary phase induction of hilAp is apparently independent of rpoS or rpoE.



View larger version (32K):
[in this window]
[in a new window]
  		FIG. 4.
Chromosomal hilAp activity in the WT (SMR2063, closed circles), RpoS– (SMR2065, closed triangles), and RpoE– (SMR2090, closed squares) backgrounds during growth under the standard condition. Dotted curve with open circles shows representative growth (A600). hilAp::lacZY activity was as determined by the {beta}-galactosidase assay (Miller units).

 
Subsequently, we examined the regulation of hilA by those two-component regulatory systems that are known to activate hilA under the inducing condition, namely hilC/hilD, sirA/barA, and envZ/ompR (7, 48) (Fig. 5). Under the standard growth condition, hilAp activity in the HilC– mutant in the exponential phase was equivalent to that in the WT but was not induced at the entry of the stationary phase. On the other hand, hilAp activity in the HilD– mutant in the exponential phase was ~10-fold lower than that in the WT, and the activity remained reduced throughout the course of growth. The hilAp activity in either the SirA– or the BarA– mutant in the exponential phase was not much different from that in the WT but was only partially induced at the entry of the stationary phase. The hilAp activity was virtually undetected in the OmpR– mutant throughout the growth period. However, in the EnvZ– mutant strain hilAp was induced at the entry of the stationary phase, although ~2.5-fold less than in the WT. The differences in hilAp induction in OmpR– and EnvZ– suggest that OmpR could be phosphorylated by a protein(s) other than EnvZ (49) if phosphorylated OmpR induces hilAp activity. Nevertheless, a defect in the two-component regulatory systems resulted in a failure to induce hilAp at the entry of the stationary phase under the standard condition. It is speculated that these activators might respond to a certain signal at the entry of the stationary phase.



View larger version (37K):
[in this window]
[in a new window]
  		FIG. 5.
Chromosomal hilAp activity in WT (SMR2063, closed circles), SirA– (SMR2094, open triangles), BarA– (SMR2095, closed triangles), OmpR– (SMR2064, open squares), EnvZ– (SMR2084, closed squares), HilC– (SMR2106, open inverted triangles), and HilD– (SMR2099, closed inverted triangles). Dotted curve with open circles represents growth (A600). hilAp::lacZY activity was as determined by {beta}-galactosidase assay (Miller units). Note that hilAp activity in OmpR– and HilD– was virtually undetected (open squares and closed inverted triangles overlapped at the bottom).

 
ppGpp-dependent Induction of hilA and SPI1 Genes—In an attempt to identify the global regulatory system responsible for the stationary phase induction of hilAp, we examined hilAp activity in a strain lacking ppGpp, the effector molecule of the stringent response (28). ppGpp is produced and maintained by PSI and PSII, the respective relA and spoT gene products. We examined the hilAp activity in the {Delta}relA and {Delta}relA{Delta}spoT strains, which lack PSI or both PSI and PSII, respectively (Fig. 6). Growth of the mutants did not differ much from the WT strain under the standard growth condition in LB. We observed that, in the {Delta}relA mutant strain, hilAp activity was indistinguishable from that in the WT strain. However, hilAp activity was completely silent throughout the growth phase in the {Delta}relA{Delta}spoT mutant strain lacking ppGpp. These observations suggest that hilAp induction at the entry of the stationary phase is mediated by ppGpp, which is synthesized primarily by SpoT activity. To further verify the route of ppGpp synthesis leading to hilAp induction, hilAp activity was determined during carbon source starvation, which is known to elevate ppGpp in a SpoT-dependent manner (34, 50–52). Carbon starvation was elicited by the addition of 2.5% {alpha}-MG, a competitive inhibitor of glucose uptake, into LB containing 0.1% glucose (Fig. 7). The addition of {alpha}-MG only slightly reduced the growth rate; generation time shifted from ~30 min to ~40 min for all three strains, i.e. WT, {Delta}relA, and {Delta}relA{Delta}spoT. Fig. 7A shows a representative growth curve for all three strains. The basal hilAp activity levels prior to {alpha}-MG addition in the strains fell within a 2-fold range, with WT > {Delta}relA > {Delta}relA{Delta}spoT in order (Fig. 7B). Upon the addition of {alpha}-MG, hilAp activity increased drastically in the WT and {Delta}relA strains but not in the {Delta}relA{Delta}spoT strain. We also examined the hilAp activity during amino acid starvation that elevates ppGpp levels in a RelA-dependent manner (37) (Fig. 8). The condition of amino acid starvation was elicited by the addition of 2 mM SerHX to a culture grown in nutrient broth supplemented with 0.75 mM serine. Both WT and {Delta}relA{Delta}spoT strains grew with more or less the same generation time (~30 min) prior to the addition of SerHX (Fig. 8A). The addition of SerHX in the middle of exponential phase of growth immediately reduced the growth rate for the WT strain (Fig. 8A, top panel). By contrast, the cell mass (A600) of {Delta}relA{Delta}spoT (Fig. 8A, bottom panel) increased at the same rate for some period (~1 h) as the rate prior to the addition of SerHX and then ceased (data not shown). It has been shown that under this growth condition the addition of SerHX drastically increased the ppGpp level ~10-fold in a RelA-dependent manner (37). Under this condition, we first determined an amino acid histidine biosynthesis operon promoter (hisGp), which is a classical promoter known to respond in parallel with the change in ppGpp level (37, 62, 63). The promoter activity was determined by measuring the transcripts. The addition of SerHX increased hisGp activity in WT (~30-fold) within 5 min but not in the {Delta}relA{Delta}spoT mutant strain (Fig. 8B, top). Under the same condition, hilAp activity remained unchanged by the addition of SerHX in either WT or the {Delta}relA{Delta}spoT strain (Fig. 8B, bottom). These results confirm that the induction of hilAp and, consequently, those genes under its control at the entry of the stationary phase results from the elevation of ppGpp levels in a SpoT-dependent manner.



View larger version (26K):
[in this window]
[in a new window]
  		FIG. 6.
Chromosomal hilAp activity in WT (SMR2063, circles), {Delta}relA (SHJ2070, triangles), and {Delta}relA{Delta}spoT (SHJ2057, squares) backgrounds. The curves with open symbols represent growth (A600), and the curves with closed symbols represent hilAp activity as determined by {beta}-galactosidase assay (Miller units).

 



View larger version (14K):
[in this window]
[in a new window]
  		FIG. 7.
Chromosomal hilAp activity in WT (SMR2063, circles), {Delta}relA (SHJ2070, triangles), and {Delta}relA{Delta}spoT (SHJ2057, squares) backgrounds during carbon source deprivation elicited by the addition of {alpha}-MG during exponential growth. {alpha}-MG was added at time 0(arrow). A, a representative growth curve (A600) before and after the addition of {alpha}-MG. The growth patterns for WT, {Delta}relA, and {Delta}relA{Delta}spoT were indistinguishable. Closed and open circles represent A600 with and without {alpha}-MG addition, respectively. B, hilAp activity as determined by {beta}-galactosidase assay (Miller units); closed and open symbols represent the hilAp activities with and without {alpha}-MG addition, respectively.

 



View larger version (21K):
[in this window]
[in a new window]
  		FIG. 8.
hilAp and hisGp activities as determined by primer extension analysis in WT (SMR2110) and {Delta}relA{Delta}spoT (SMR2112) backgrounds during amino acid starvation elicited by the addition of SerHX into cultures grown in nutrient broth supplemented with 0.75 mM serine. SerHX was added at time 0 (arrow) when A600 was 0.15 and 0.3 for WT and {Delta}relA{Delta}spoT, respectively. A, growth (A600) of WT (top) and {Delta}relA{Delta}spoT (bottom) strains as a function of time. Closed and open symbols represent the measurements with and without SerHX addition, respectively. B, hisGp (top) and hilAp (bottom) activities determined by primer extension assay in WT and {Delta}relA{Delta}spoT strains.

 
Lastly, we evaluated the WT and {Delta}relA{Delta}spoT strains for their abilities to invade HEp-2 cells to access the in vivo role of ppGpp in Salmonella virulence (Table II). The early stationary phase bacteria were used in this assay. The analysis revealed that the invasion by the {Delta}relA{Delta}spoT strain was <1% of the level of invasion by the WT bacteria. Thus, the lack of hilA expression in the {Delta}relA{Delta}spoT strain and, consequently, the lack of expression of those genes under its control, including SPI1-encoded TTSS and effector proteins, caused an apparent reduction in invasiveness.


View this table:
[in this window]
[in a new window]
  		TABLE II
Invasiveness of WT and {Delta} relA{Delta} spoT strains in Hep-2 cells

Invasiveness was determined as described under "Materials and Methods."

 

   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
Stationary Phase Induction of hilA under the Standard Growth Condition—In this study we reported that hilA and, therefore, those genes under its control are expressed under the standard growth condition at the onset of the stationary phase based on the following observations: 1) invasiveness culminating at the early stationary phase culture (Fig. 1); 2) some representative secreted proteins encoded in SPI1 being detected in the supernatant from early stationary phase cultures but not in supernatant from exponential phase cultures (Fig. 1); and 3) hilAp and those promoters under its control, i.e. sicAp and invFp, being induced at the onset of the stationary phase (Fig. 2 and 3). Similarly, early stationary phase bacteria grown under the standard condition are reportedly most cytotoxic to cultured mammalian cells (53). The primer extension analysis revealed that hilAp was transitionally expressed during transition from the exponential phase to the stationary phase, demonstrating a pattern of growth phase-dependent expression. The induction of hilA was, however, independent of the stationary phase sigma factor, {sigma}38, or the heat shock sigma factor, {sigma}24, which have both been implicated in Salmonella pathogenesis in animals and are induced at the entry of the stationary phase (45–47) (Fig. 4). Therefore, hilAp seems be induced in response to an unidentified environmental signal built up as culture enters the stationary phase.

We have observed that hilAp induction on a multicopy plasmid was lower than that on the chromosome (~4-fold versus ~30-fold), largely due to a huge increase in hilAp activity at the exponential phase (~1000-fold). Therefore, the stationary phase induction of hilAp activity could, at least in part, be ascribed to the removal of a repressor acting during the exponential phase. In this case, the hypothetical repressor might be titrated out by episomal hilAp DNA, resulting in the elevation of hilA activity during the exponential phase. Because a plethora of regulatory systems has been proposed to regulate hilAp (7), the titratable factors should include an activator(s) as well as a repressor(s).

Interestingly, it was noted that the two-component regulatory systems known to activate hilAp under the inducing condition acted at the level of its induction at the entry of the stationary phase under the standard growth condition (Fig. 5). Among the regulatory components, hilC/hilD has been shown to exert its regulatory effect by directly binding to a site upstream of hilAp (15, 23, 54). We observed under the standard growth condition that hilAp activity remained at the basal level in the HilC– or HilD– mutant background, although the defect was more severe in the HilD– mutant. In fact, hilAp activity was reduced ~10-fold in the HilD– mutant background even during the exponential phase. This result suggests that the mechanism of hilAp activation by hilC/hilD might be different depending on whether the cells are in the exponential growth phase or at the entry into the stationary phase. We obtained similar results with the strains lacking the two-component regulatory systems reported to up-regulate hilAp activity under the inducing condition, i.e. barA/sirA and envZ/ompR (16, 20, 48, 55). Under the standard growth condition, hilAp in the BarA– or SirA– mutant was defective at the level of its induction in the stationary phase but not in the exponential phase. The hilAp activity in the OmpR– mutant was virtually undetected, whereas that in the EnvZ– was almost normally induced, although the peak activity was ~2.5-fold less than that in the WT. It is well established that EnvZ phosphorylates OmpR upon sensing an increase in osmolarity in the environment (49). Under the standard condition, if the phosphorylated OmpR was responsible for hilAp induction, the phosphorylation must occur through a route(s) other than EnvZ. In fact, an EnvZ-independent mechanism of OmpR phosphorylation has been postulated (56, 57). OmpR might take part in hilAp induction at the onset of the stationary phase by sensing an unknown environmental signal through a currently unknown sensor. In this case, OmpR is unlikely to be responding to a change in media osmolarity, because we did not detect any noticeable change in the media osmolarity as the culture entered stationary phase (data not shown). Further study is required to elucidate the underlying mechanism of hilA induction and its regulation by two-component regulatory systems under the standard growth condition.

Implication of ppGpp in hilAp Induction—After establishing hilAp induction at the entry of the stationary phase under the standard growth condition, we searched for the global regulatory signal responsible for the induction and found ppGpp. hilAp activity remained at the basal level in the {Delta}relA{Delta}spoT strain, although it was normally induced in the {Delta}relA strain (Fig. 6). SPI1-encoded sicA and invF promoters also remained at their basal levels in the {Delta}relA{Delta}spoT mutant strain (data not shown). Consistently, the {Delta}relA{Delta}spoT strain showed reduced invasiveness by >100-fold as determined by an in vitro assay using HEp-2 cells (Table II). RelA is known to sense an imbalance or lack of amino acid supply and to synthesize ppGpp, resulting in the reduction of stable RNA synthesis, the phenomenon known as "stringent response" (29, 26, 28). Alternatively, the basal level of ppGpp during balanced growth is regulated by spoT, which carries both ppGpp synthetase (PSII) and hydrolase (34, 58). Therefore, the basal level of ppGpp depends on the balance of two activities. Some conditions, including carbon and energy starvation, have been shown to result in the accumulation of ppGpp in a SpoT-dependent manner (34, 59, 60). Under the standard laboratory growth conditions, the transition from the exponential phase to the stationary phase presumably represents a stressed condition. It was reported recently that changes in the proteome pattern of Escherichia coli entering the stationary phase were significantly different between WT and the {Delta}relA1{Delta}spoT mutant, which had a proteome pattern that appeared to be locked in the exponential growth mode (61). We speculate that the transitional stress at the entry of stationary phase must be sensed and translated to ppGpp synthesis primarily by the SpoT function.

Most interestingly, it was observed that hilAp was induced during the exponential phase of growth by carbon source starvation, which is known to elevate ppGpp level in a SpoT-dependent manner (34, 50–52), but it was not induced by amino acid starvation, which is known to elevate ppGpp level in a RelA-dependent manner (37) (Figs. 7 and 8). Whereas, the amino acid histidine biosynthesis operon promoter (hisGp), a classical promoter positively regulated by ppGpp (37, 62, 63), responded in parallel with the RelA-dependent increase in ppGpp level in this study (Fig. 8). It has been reported that the amino acid starvation elicited by the addition of SerHX causes an immediate increase in ppGpp level in RelA-dependent manner, i.e. from 28.7 pmol/A650 to 1,042 pmol/A650 (37). The carbon source deprivation could also increase ppGpp concentration up to ~500 pmol/A650 in WT bacteria (51). However, it must be noted that hilAp was induced normally in the {Delta}relA strain following the carbon source starvation in which ppGpp pool was measured as being increased by only a few fold, a little more than 100 pmol/A650 (34). Thus, regulation of gene expression following carbon source starvation and amino acid starvation seem to be mechanistically different. Likewise, gene induction at the entry of the stationary phase and the induction observed during the classical stringent response following amino acid deprivation must also be different. In addition to ppGpp, some other alteration accompanying entry into the stationary phase may be necessary for gene induction, including hilAp activation. The physiological consequence of the two routes of ppGpp elevation, the RelA- and SpoT-dependent mechanisms, remains unknown.

During the course of animal infection, Salmonella bacteria encounter diverse environments in the intestinal lumen and inside various host cells. Thus, it is imperative that Salmonellae must be able to sense and respond to changing environments in order to survive (64). We speculate that environmental stress is sensed and translated to the intracellular signal ppGpp, which enables expression of various Salmonella virulence genes, including those encoded on SPI1 that are required for the invasion of host cells and induction of macrophage apoptosis (1, 65).


   FOOTNOTES
 
* This work was supported by the Ministry of Health and Welfare, Republic of Korea Health 21 Research and Development Grant 01-PJ10-PG6-01GM02-002. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Back

|| To whom correspondence should be addressed. Tel.: 82-62-220-4137; Fax: 82-62-228-7294; E-mail: hyonchoy{at}chonnam.ac.kr.

1 The abbreviations used are: TTSS, type III secretion system; {alpha}-MG, {alpha}-methyl glucoside; LB, Luria-Bertani; SerHX, serine hydroxamate; SPI1, Salmonella pathogenicity island 1; WT, wild type. Back


   ACKNOWLEDGMENTS
 
We thank C. Lee (Boston) and K. Tedin (Berlin) for providing important Salmonella strains.



   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Carter, P. B., and Collins, F. M. (1974) J. Exp. Med. 139, 1189–1203[Abstract]
  2. Hohmann, A. W., Schmidt, G., and Rowley, D. (1978) Infect. Immun. 22, 763–770[Abstract/Free Full Text]
  3. Jones, B. D., Ghori, N., and Falkow, S. (1994) J. Exp. Med. 180, 15–23[Abstract/Free Full Text]
  4. Takeuchi, A. (1967) Am. J. Pathol. 50, 109–136[Medline] [Order article via Infotrieve]
  5. Mills, D. M., Bajaj, V., and Lee, C. A. (1995) Mol. Microbiol. 15, 749–759[CrossRef][Medline] [Order article via Infotrieve]
  6. Galan, J. E. (2001) Annu. Rev. Cell Dev. Biol. 17, 53–86[CrossRef][Medline] [Order article via Infotrieve]
  7. Lucas, R. L., and Lee, C. A. (2000) Mol. Microbiol. 36, 1024–1033[CrossRef][Medline] [Order article via Infotrieve]
  8. Darwin, K. H., and Miller, V. L. (1999) J. Bacteriol. 181, 4949–4954[Abstract/Free Full Text]
  9. Darwin, K. H., and Miller, V. L. (2000) Mol. Microbiol. 35, 949–960[CrossRef][Medline] [Order article via Infotrieve]
  10. Darwin, K. H., and Miller, V. L. (2001) EMBO J. 20, 1850–1862[CrossRef][Medline] [Order article via Infotrieve]
  11. Lee, C. A., and Falkow, S. (1990) Proc. Natl. Acad. Sci. U. S. A. 87, 4304–4308[Abstract/Free Full Text]
  12. Bajaj, V., Lucas, R. L., Hwang, C., and Lee, C. A. (1996) Mol. Microbiol. 22, 703–714[CrossRef][Medline] [Order article via Infotrieve]
  13. Eichelberg, K., Hardt, W. D., and Galan, J. E. (1999) Mol. Microbiol. 33, 139–152[CrossRef][Medline] [Order article via Infotrieve]
  14. Rakeman, J. L., Bonifield, H. R., and Miller, S. I. (1999) J. Bacteriol. 181, 3096–3104[Abstract/Free Full Text]
  15. Schechter, L. M., Damrauer, S. M., and Lee, C. A. (1999) Mol. Microbiol. 32, 629–642[CrossRef][Medline] [Order article via Infotrieve]
  16. Altier, C., Suyemoto, M., Ruiz, A. I., Burnham, K. D., and Maurer, R. (2000) Mol. Microbiol. 35, 635–646[CrossRef][Medline] [Order article via Infotrieve]
  17. Johnston, C., Pegues, D. A., Hueck, C. J., Lee, A., and Miller, S.I. (1996) Mol. Microbiol. 22, 715–727[CrossRef][Medline] [Order article via Infotrieve]
  18. Wilson, R. L., Libby, S. J., Freet, A. M., Boddicker, J. D., Fahlen, T. F., and Jones, B. D. (2001) Mol. Microbiol. 39, 79–88[CrossRef][Medline] [Order article via Infotrieve]
  19. Schechter, L. M., Jain, S., Akbar, S., and Lee, C. A. (2003) Infect. Immun. 71, 5432–5435[Abstract/Free Full Text]
  20. Altier, C., Suyemoto, M., and Lawhon, S. D. (2000) Infect. Immun. 68, 6790–6797[Abstract/Free Full Text]
  21. Lindgren, S. W., Stojiljkovic, I., and Heffron, F. (1996) Proc. Natl. Acad. Sci. U. S. A. 93, 4197–4201[Abstract/Free Full Text]
  22. Fahlen, T. F., Wilson, R. L., Boddicker, J. D., and Jones, B. D. (2001) J. Bacteriol. 183, 6620–6629[Abstract/Free Full Text]
  23. Schechter, L. M., and Lee, C. A. (2001) Mol. Microbiol. 40, 1289–1299[CrossRef][Medline] [Order article via Infotrieve]
  24. Olekhnovich, I. N., and Kadner, R. J. (2002) J. Bacteriol. 184, 4148–4160[Abstract/Free Full Text]
  25. Sands, M. K., and Roberts, R. B. (1952) J. Bacteriol. 63, 505–511[Free Full Text]
  26. Stent, G. S., and Brenner, S. (1961) Proc. Natl. Acad. Sci. U. S. A. 47, 2005–2014[Free Full Text]
  27. Cashel, M., and Gallant, J. (1968) J. Mol. Biol. 34, 317–330[CrossRef][Medline] [Order article via Infotrieve]
  28. Cashel, M., Gentry, D. R., Hernandez, V. J., and Vinella, D. (1996) in Escherichia Coli and Salmonella: Cellular and Molecular Biology (Neidhardt, F. C., Curtiss, R., III, Ingraham, J. L., Lin, E. C. C., Low, K. B., Magasanik, B., Reznikoff, W. S., Riley, M., Schaechter, M., and Umbarger, H. E., eds) Vol. 1, pp. 1458–1496, ASM Press, Washington D. C.
  29. Cashel, M. (1969) J. Biol. Chem. 244, 3133–3141[Abstract/Free Full Text]
  30. Lazzarini, R. A., Cashel, M., and Gallant, J. (1971) J. Biol. Chem. 246, 4381–4385[Abstract/Free Full Text]
  31. Harshman, R. B., and Yamazaki, H. (1971) Biochemistry 10, 3980–3982[CrossRef][Medline] [Order article via Infotrieve]
  32. Lagosky, P. A., and Chang, F. N. (1980) J. Bacteriol. 144, 499–508[Abstract/Free Full Text]
  33. Ryals, J., Little, R., and Bremer, H. (1982) J. Bacteriol. 151, 1425–1432[Abstract/Free Full Text]
  34. Murray, K. D., and Bremer, H. (1996) J. Mol. Biol. 259, 41–57[CrossRef][Medline] [Order article via Infotrieve]
  35. Davis, R. W., Botstein, D., and Roth, J. R. (1980) Advanced Bacterial Genetics: A Manual for Genetic Engineering, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
  36. Datsenko, K. A., and Wanner, B. L. (2000) Proc. Natl. Acad. Sci. U. S. A. 97, 6640–6645[Abstract/Free Full Text]
  37. Shand, R. F., Blum, P. H., Mueller, R. D., Riggs, D. L., and Artz, S. W. (1989) J. Bacteriol. 171, 737–743[Abstract/Free Full Text]
  38. Hong, K. H., and Miller, V. L. (1998) J. Bacteriol. 180, 1793–1802[Abstract/Free Full Text]
  39. Miller, J.H. (1972) Experiments in Molecular Genetics, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
  40. Putnam, S. L., and Koch, A. L. (1975) Anal. Biochem. 63, 350–360[CrossRef][Medline] [Order article via Infotrieve]
  41. Shin, D., Lim, S., Seok, Y. J., and Ryu, S. (2001) J. Biol. Chem. 276, 25871–25875[Abstract/Free Full Text]
  42. Lee, C. A., Jones, B. D., and Falkow, S. (1992) Proc. Natl. Acad. Sci. U. S. A. 89, 1847–1851[Abstract/Free Full Text]
  43. Hueck, C. J. (1998) Microbiol. Mol. Biol. Rev. 62, 379–433[Abstract/Free Full Text]
  44. Simons, R. W., Houman, F., and Kleckner, N. (1987) Gene 53, 85–96[CrossRef][Medline] [Order article via Infotrieve]
  45. Hengge-Aronis, R. (1996) Mol. Microbiol. 21, 887–893[CrossRef][Medline] [Order article via Infotrieve]
  46. Humphreys, S., Stevenson, A., Bacon, A., Weinhardt, A. B., and Roberts, M. (1999) Infect. Immun. 67, 1560–1568[Abstract/Free Full Text]
  47. Testerman, T. L., Vazquez-Torres, A., Xu, Y., Jones-Carson, J., Libby, S. J., and Fang, F. C. (2002) Mol. Microbiol. 43, 771–782[CrossRef][Medline] [Order article via Infotrieve]
  48. Lucas, R. L., and Lee, C. A. (2001) J. Bacteriol. 183, 2733–2745[Abstract/Free Full Text]
  49. Pratt, L. A., and Silhavy, T. J. (1995) Mol. Microbiol. 17, 565–573[Medline] [Order article via Infotrieve]
  50. Friesen, J. D., Fiil, N. P., and von Meyenburg, K. (1975) J. Biol. Chem. 250, 304–309[Abstract/Free Full Text]
  51. Hansen, M. T., Pato, M. L., Molin, S., Fill, N. P., and von Meyenburg, K. (1975) J. Bacteriol. 122, 585–591[Abstract/Free Full Text]
  52. De Boer, H. A., Bakker, A. J., Weyer, W. J., and Gruber, M. (1976) Biochim. Biophys. Acta. 432, 361–368[Medline] [Order article via Infotrieve]
  53. Lundberg, U., Vinatzer, U., Berdnik, D., von Gabain, A., and Baccarini, M. (1999) J. Bacteriol. 181, 3433–3437[Abstract/Free Full Text]
  54. Akbar, S., Schechter, L. M., Lostroh, C. P., and Lee, C. A. (2003) Mol. Microbiol. 47, 715–728[CrossRef][Medline] [Order article via Infotrieve]
  55. Lawhon, S. D., Frye, J. G., Suyemoto, M., Porwollik, S., McClelland, M., and Altier, C. (2003) Mol. Microbiol. 48, 1633–1645[CrossRef][Medline] [Order article via Infotrieve]
  56. Forst, S., Delgado, J., Rampersaud, A., and Inouye, M. (1990) J. Bacteriol. 172, 3473–3477[Abstract/Free Full Text]
  57. Heyde, M., Laloi, P., and Portalier, R. (2000) J. Bacteriol. 182, 198–202[Abstract/Free Full Text]
  58. Xiao, H., Kalman, M., Ikehara, K., Zemel, S., Glaser, G., and Cashel, M. (1991) J. Biol. Chem. 266, 5980–5990[Abstract/Free Full Text]
  59. Ishiguro, E. E. (1979) Can. J. Microbiol. 25, 1206–1208[Medline] [Order article via Infotrieve]
  60. VanBogelen, R. A., Kelley, P. M., and Neidhardt, F. C. (1987) J. Bacteriol. 169, 26–32[Abstract/Free Full Text]
  61. Magnusson, L. U., Nystrom, T., and Farewell, A. (2003) J. Biol. Chem. 278, 968–973[Abstract/Free Full Text]
  62. Stephens, J. C., Artz, S. W., and Ames, B. N. (1975) Proc. Natl. Acad. Sci. U. S. A. 72, 4389–4393[Abstract/Free Full Text]
  63. Da Costa, X. J., and Artz, S. W. (1997) J. Bacteriol. 179, 5211–5217[Abstract/Free Full Text]
  64. Marcus, S. L., Brumell, J. H., Pfeifer, C. G., and Finlay, B. B. (2000) Microbes Infect. 2, 145–156[CrossRef][Medline] [Order article via Infotrieve]
  65. Murray, R. A., and Lee, C.A. (2000) Infect. Immun. 68, 5050–5055[Abstract/Free Full Text]
  66. Bang, I. S., Kim, B. H., Foster, J. W., and Park, Y. K. (2000) J. Bacteriol. 182, 2245–2252[Abstract/Free Full Text]
  67. Tedin, K., and Norel, F. (2001) J. Bacteriol. 183, 6184–6196[Abstract/Free Full Text]
  68. Bang, I. S., Audia, J. P., Park, Y. K., and Foster, J. W. (2002) Mol. Microbiol. 44, 1235–1250[CrossRef][Medline] [Order article via Infotrieve]

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
 J. Bacteriol.Home page
C.-H. Baek, S. Wang, K. L. Roland, and R. Curtiss III
Leucine-Responsive Regulatory Protein (Lrp) Acts as a Virulence Repressor in Salmonella enterica Serovar Typhimurium
J. Bacteriol., February 15, 2009; 191(4): 1278 - 1292.
[Abstract] [Full Text] [PDF]

Home page
 J. Bacteriol.Home page
J.-H. Jeong, M. Song, S.-I. Park, K.-O. Cho, J. H. Rhee, and H. E. Choy
Salmonella enterica Serovar Gallinarum Requires ppGpp for Internalization and Survival in Animal Cells
J. Bacteriol., October 1, 2008; 190(19): 6340 - 6350.
[Abstract] [Full Text] [PDF]

Home page
 J. Bacteriol.Home page
J. Yun, B. Jeon, Y.-W. Barton, P. Plummer, Q. Zhang, and S. Ryu
Role of the DksA-Like Protein in the Pathogenesis and Diverse Metabolic Activity of Campylobacter jejuni
J. Bacteriol., July 1, 2008; 190(13): 4512 - 4520.
[Abstract] [Full Text] [PDF]

Home page
 Nucleic Acids ResHome page
S. C. Viegas, V. Pfeiffer, A. Sittka, I. J. Silva, J. Vogel, and C. M. Arraiano
Characterization of the role of ribonucleases in Salmonella small RNA decay
Nucleic Acids Res., December 3, 2007; 35(22): 7651 - 7664.
[Abstract] [Full Text] [PDF]

Home page
 J. Bacteriol.Home page
J. Wang, N. Gardiol, T. Burr, G. P. C. Salmond, and M. Welch
RelA-Dependent (p)ppGpp Production Controls Exoenzyme Synthesis in Erwinia carotovora subsp. atroseptica
J. Bacteriol., November 1, 2007; 189(21): 7643 - 7652.
[Abstract] [Full Text] [PDF]

Home page
 Nucleic Acids ResHome page
S. Lim, J. Yun, H. Yoon, C. Park, B. Kim, B. Jeon, D. Kim, and S. Ryu
Mlc regulation of Salmonella pathogenicity island I gene expression via hilE repression
Nucleic Acids Res., March 19, 2007; 35(6): 1822 - 1832.
[Abstract] [Full Text] [PDF]

Home page
 J. Bacteriol.Home page
R. Balbontin, G. Rowley, M. G. Pucciarelli, J. Lopez-Garrido, Y. Wormstone, S. Lucchini, F. Garcia-del Portillo, J. C. D. Hinton, and J. Casadesus
DNA Adenine Methylation Regulates Virulence Gene Expression in Salmonella enterica Serovar Typhimurium
J. Bacteriol., December 1, 2006; 188(23): 8160 - 8168.
[Abstract] [Full Text] [PDF]

Home page
 J. Bacteriol.Home page
F. Rodrigues, M. Sarkar-Tyson, S. V. Harding, S. H. Sim, H. H. Chua, C. H. Lin, X. Han, R. K. M. Karuturi, K. Sung, K. Yu, et al.
Global Map of Growth-Regulated Gene Expression in Burkholderia pseudomallei, the Causative Agent of Melioidosis
J. Bacteriol., December 1, 2006; 188(23): 8178 - 8188.
[Abstract] [Full Text] [PDF]

Home page
 J. Biol. Chem.Home page
A. Thompson, M. D. Rolfe, S. Lucchini, P. Schwerk, J. C. D. Hinton, and K. Tedin
The Bacterial Signal Molecule, ppGpp, Mediates the Environmental Regulation of Both the Invasion and Intracellular Virulence Gene Programs of Salmonella
J. Biol. Chem., October 6, 2006; 281(40): 30112 - 30121.
[Abstract] [Full Text] [PDF]

Home page
 Infect. Immun.Home page
M. M. Nakamura, S.-Y. Liew, C. A. Cummings, M. M. Brinig, C. Dieterich, and D. A. Relman
Growth Phase- and Nutrient Limitation-Associated Transcript Abundance Regulation in Bordetella pertussis.
Infect. Immun., October 1, 2006; 74(10): 5537 - 5548.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
279/33/34183    most recent
M313491200v1
Right arrow Submit a Letter to Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Song, M.
Right arrow Articles by Choy, H. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Song, M.
Right arrow Articles by Choy, H. E.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 2004 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement